Lysophosphatidic Acid and Glutamatergic Transmission

Signaling through bioactive lipids regulates nervous system development and functions. Lysophosphatidic acid (LPA), a membrane-derived lipid mediator particularly enriched in brain, is able to induce many responses in neurons and glial cells by affecting key processes like synaptic plasticity, neurogenesis, differentiation and proliferation. Early studies noted sustained elevations of neuronal intracellular calcium, a primary response to LPA exposure, suggesting functional modifications of NMDA and AMPA glutamate receptors. However, the crosstalk between LPA signaling and glutamatergic transmission has only recently been shown. For example, stimulation of presynaptic LPA receptors in hippocampal neurons regulates glutamate release from the presynaptic terminal, and excess of LPA induce seizures. Further evidence indicating a role of LPA in the modulation of neuronal transmission has been inferred from animal models with deficits on LPA receptors, mainly LPA₁ which is the most prevalent receptor in human and mouse brain tissue. LPA₁ null-mice exhibit cognitive and attention deficits characteristic of schizophrenia which are related with altered glutamatergic transmission and reduced neuropathic pain. Furthermore, silencing of LPA₁ receptor in mice induced a severe down-regulation of the main glutaminase isoform (GLS) in cerebral cortex and hippocampus, along with a parallel sharp decrease on active matrix-metalloproteinase 9. The downregulation of both enzymes correlated with an altered morphology of glutamatergic pyramidal cells dendritic spines towards a less mature phenotype, indicating important implications of LPA in synaptic excitatory plasticity which may contribute to the cognitive and memory deficits shown by LPA₁-deficient mice. In this review, we present an updated account of current evidence pointing to important implications of LPA in the modulation of synaptic excitatory transmission.

Introduction

Phosphatidic acid (PA) or phosphatidate (diacylglycerol 3-phosphate) is the simplest phosphoglyceride and the precursor of important glycerophospholipids. Only small amounts of PA are present in eukaryotic membranes; however, the molecule is a key intermediate in the biosynthesis of the other phosphoglycerides. Lipids are one of the most abundant biomolecules in mammalian brain; in fact, they outnumber the amount of proteins and other cellular components in human brain accounting for 60%–70% of total dry weight (Svennerholm et al., 1994). Apart from their structural role forming the lipid bilayer of cell membranes, where proteins are embedded, many lipids also possess key cell signaling functions and the term “bioactive lipids” has been coined to refer to those non-structural regulatory functions. Lysophosphatidic acid (LPA; 1 or 2-acyl-sn-glycero-3-phosphate) is a naturally occurring lysophospholipid derived from cell membranes that belong to the growing list of bioactive lipids. It may act as an intercellular signaling molecule after recognition by G protein-coupled receptors (GPCRs; Ye et al., 2002; Fukushima, 2004; Choi and Chun, 2013). LPA is a heterogeneous molecule, with distinct variants regarding the length and degree of saturation of its acyl chains (Moolenaar and Hla, 2012), which can be recognized by at least six cognate GPCRs (named LPA₁ to LPA₆) present in many different cell types (Mutoh et al., 2012); hence, a plethora of biological responses have been described for this phospholipid messenger, including differentiation, proliferation, migration, vascular regulation, cell survival and cytoskeletal remodeling (Choi and Chun, 2013; Figure 1). In this review article, we will focus on LPA actions in synaptic transmission, plasticity and neuropathic pain. We will present a succinct account of experimental results dealing with primary cell cultures of neurons and astrocytes, neuronal cell lines as well as knock-out (KO) mouse models of different LPA receptors with special emphasis on KOLPA₁ mice.

FIGURE 1

Figure 1. Main functional effects of lysophosphatidic acid (LPA) in cells related to the nervous system. In this scheme, we highlight the main functional effects elicited by LPA in neuronal cell lines and in primary cultures of neurons and astrocytes. Neurite retraction, growth cone collapse and cell rounding have been described to be mediated by all LPA receptor subtypes, except LPA₃. This last receptor has been recently shown to induce neurite branch formation. In neurons, LPA also induces a sustained elevation of intracellular calcium, with strong repercussions on cytoskeletal remodeling as neurite outgrowth. The morphological changes induced by LPA in neurons can be also mediated by autocrine effects coming from neighbor astrocytes, which promote neuronal differentiation and increases in arborization and neurite outgrowth. Finally, LPA-treated astrocytes show a range of different effects including the inhibition of glutamate uptake and increases in intracellular calcium concentration.

LPA and Synaptic Plasticity

Glutamate, the main excitatory neurotransmitter in the nervous system, activates both ionotropic (NMDAR and AMPAR) and metabotropic receptors. NMDAR is composed of heteromultimeric subunits and display slow channel kinetics and a marked permeability to Ca²⁺. However, at rest, they are blocked by Mg²⁺ and only upon neuronal depolarization they become fully functional. On the other hand, AMPAR isoforms display lower voltage-dependence and faster kinetics than NMDARs and permeate predominantly Na⁺. Furthermore, AMPARs display a lower affinity for glutamate and rapidly desensitize upon their selective stimulation. In neurons, AMPARs undergo constitutive and activity dependent-trafficking which is relevant for synaptic plasticity—reviewed in Lüscher and Malenka (2012).

The first direct evidence showing that LPA had a modulatory role on glutamate receptors came from early studies in Xenopus oocytes and isolated hippocampal neurons, where glutamate- and NMDA-mediated currents were potentiated by direct application of LPA (Tabuchi et al., 1997; Lu et al., 1999). This effect was indirectly mediated by protein kinase C (PKC)-dependent phosphorylation of the NMDAR (Lu et al., 1999) upon extracellular Ca²⁺ entering the cell via this channel type (Holtsberg et al., 1997). Since then, a series of experimental evidence have shown that LPA acts as a fine-tuning regulatory mechanism of glutamatergic transmission in the nervous system.

NMDA-mediated Ca²⁺ increases in the postsynaptic neuron are able to induce long-term forms of either potentiation (LTP) or depression (LTD) at both excitatory and inhibitory synapses (Bliss and Schoepfer, 2004). LTP and LTD represent well established experimental correlates of learning and memory (Bliss and Collingridge, 1993). Since LPA₁-null mice showed impairments in spatial learning and memory (Santin et al., 2009; Castilla-Ortega et al., 2010), it is reasonable to assume a modulatory role of LPA₁ in these processes. Despite the cellular and molecular mechanisms are still poorly understood, the described behavioral alterations could be explained by an abnormal development of certain brain areas (further discussion in “LPA and Structural Plasticity” section) but also by a reduced signaling via NMDAR (Blanco et al., 2012; Shin et al., 2012). Chronic exposure to cocaine and other drugs of abuse induce an abnormal increase in basal locomotion—i.e., conditioned locomotion—which correlates with the strengthening of glutamatergic synapses via LTP mechanisms (Kauer and Malenka, 2007) but also with a reduction in the density of dendritic spines (Scofield et al., 2016). LPA₁-null mice exhibited reduced cocaine-induced conditioned locomotion, which was accompanied by a reduction of metabotropic mGluR3 receptor (Blanco et al., 2012). Therefore, it is plausible to assume a role of LPA in conditioned locomotion both through NMDAR mediated synapse, but also by means of morphological changes (further discussed in next section). Ginseng (the root of Panax ginseng), widely used in traditional medicine, contains gintonin, a unique LPA-ginseng protein complex which can deliver LPA to is cognate receptors with high affinity (Hwang et al., 2012b; Choi et al., 2015). It has been shown that application of gintonin enhanced NMDA current in oocytes, induced transient elevations of intracellular Ca²⁺ in cultured hippocampal neurons and favored LTP in rat hippocampal slices (Shin et al., 2012). Besides, long-term oral administration of this compound was able to attenuate memory impairments in a transgenic mouse model of Alzheimer’s disease (Hwang et al., 2012a; Choi et al., 2015).

Direct evidence on the regulatory effects of LPA in synaptic strength comes from in vitro studies in hypoglossal motoneurons expressing AMPAR and gamma-aminobutyric acid receptor type A (GABA_AR). During inspiration, these motoneurons are synaptically excited by glutamatergic brain stem afferents and activate tongue muscles to maintain air inflow towards the lungs. They present a pattern of rhythmic firing in bursts that follows the respiratory phases (Peever et al., 2002). Studies using brain stem slices obtained from neonatal mice, demonstrated that LPA, via LPA₁, induced a rapid and reversible depression on synaptic strength (García-Morales et al., 2015), which is another form of functional synaptic plasticity (Schneggenburger et al., 2002). The authors demonstrated that LPA signaling on excitatory glutamatergic transmission takes place at the presynaptic neuron, as the attenuation of excitatory AMPA-current by LPA was related to a reduction in glutamate release probability. The LPA-induced mechanism is mediated by a phospholipase C (PLC)-dependent phosphorylation of the myosin light chain (MLC) by MLC kinase at the presynaptic neuron (García-Morales et al., 2015). Thus, the pool-size of available synaptic vesicles within excitatory boutons is reduced. Such depletion of available vesicles usually underlies short-term forms of synaptic depression (Schneggenburger et al., 2002). By this means, LPA released from the postsynaptic neuron acts as a retrograde messenger by reducing the strength of the synapse and, hence, acting as a negative-feedback mechanism preventing hyperactivity (Figure 2A). In the context of synaptic plasticity, it has already been proposed the synthesis of a retrograde messenger that diffuses to the presynaptic ending, whereby interacts with specific targets and regulates neurotransmitter release (Regehr et al., 2009). On the other hand, at GABAergic synapses, LPA exerts a post-synaptic effect by favoring receptor internalization, leading to neuronal disinhibition. This mechanism is mediated by dephosphorylation of the GABA_Aγ2 subunit upon recruitment of RhoA/ROCK-calcineurin (García-Morales et al., 2015) and resembles typical LTD (Bliss and Schoepfer, 2004). Modest opening of NMDARs—i.e., less Ca²⁺ entry—leads to the activation of calcineurin—calcium/calmodulin-dependent protein phosphatase due to its higher affinity for calcium/calmodulin than CaMKII (Bliss and Schoepfer, 2004). Experiments performed in vivo showed that blockade of LPA signaling by LPA_1–3 antagonists increased the frequency of the spikes fired per burst. This demonstrated that endogenous LPA signaling contributes to normal patterns of motor output commands in adult mice (García-Morales et al., 2015) and could help to explain the impairment in suckling behavior—regulated by hypoglossal neurons—described in LPA₁-null mice (Contos et al., 2000). The apparent mismatch of LPA effects in hypoglossal neurons might be related with activity-dependent LPA synthesis and/or release, promoting neuronal disinhibition (increased firing) at low concentrations and depressing excitation (reduced firing) upon increased activity.

FIGURE 2

Figure 2. (A) Upon high levels of LPA, glutamatergic pre-synaptic neurons decrease the pool of available glutamate-containing vesicles acting as a negative feed-back to decrease excitability of hypoglossal motoneurons. Low concentration of LPA induces gamma-aminobutyric acid receptor type A (GABA_AR) internalization at the post-synaptic membrane, increasing briefly the excitability of the hypoglossal motoneuron by disinhibition (García-Morales et al., 2015). (B) Loss of functional plasticity-related gene 1 (PRG-1) at the post-synaptic membrane leads to increased LPA accumulation at the synaptic cleft. Activation of LPA₂ facilitates now glutamate release from the presynaptic neuron. In addition, the release of autotaxin (ATX) from astrocytes is now further increased by the enhanced concentration of glutamate (Trimbuch et al., 2009; Vogt et al., 2016; Thalman et al., 2018).

Further experimental data obtained from different research groups also suggest a facilitator role of LPA during glutamatergic transmission. Plasticity-related gene 1 (PRG-1) is a specific membrane protein present at the postsynaptic spines of glutamatergic synapses in the brain cortex and hippocampus, where it has a key role modulating excitability (Vogt et al., 2016). PRG-1 is involved in LPA uptake into intracellular postsynaptic compartments (Trimbuch et al., 2009), thereby controlling LPA levels in the synaptic cleft. When PRG-1 is absent, mice develop severe seizures; however, double PRG-1/LPA₂ null mice do not exhibit an epileptic phenotype. When PRG-1 function is restored, the excitability levels examined in vitro in individual cells returned to normal. Interestingly, when the LPA-PRG-1 interacting site was altered, hyperexcitability remained (Trimbuch et al., 2009). Later on, a mutation of the Prg-1 gene was found which blocks its ability to regulate cellular LPA uptake, leading to an increased hyperexcitability (Vogt et al., 2016). In PRG-1^+/− mice, inhibition of the LPA-synthesizing enzyme autotaxin (ATX) normalized cortical hyperexcitability and behavior (Thalman et al., 2018). The expression of ATX was restricted to the astrocytes located in excitatory synapses, while its secretion to the synaptic cleft was regulated by glutamatergic signaling (Thalman et al., 2018; Figure 2B).

Both PRG-1^+/− and LPA₁ null-mice display deficits in prepulse inhibition (PPI) during the startle reflex in comparison with their respective wild-types (WTs; Harrison et al., 2003; Thalman et al., 2018). PPI is considered as a useful tool to study the neurobiology of schizophrenia, although it is also a common phenotype of other neuropsychiatric disorders (Swerdlow et al., 2008). The exact mechanisms underlying schizophrenia are poorly understood and beyond the scope of this review, but it has been proposed that the dysregulation of glutamatergic neurotransmission is a key component in this pathophysiology (Moghaddam and Javitt, 2012; McNally and McCarley, 2016). Increasing evidence points to an enhanced glutamatergic transmission through activation of AMPAR due to the presence of defective NMDAR (Hardingham and Do, 2016; Moghaddam and Javitt, 2012). But also LPA₁-null mice show a reduction in the generation of gamma-osciliations (Cunningham et al., 2006). This type of rhythmic activity at 30–100 Hz allows coherent synchronous communication between different brain areas to evoke adequate perception. It has been postulated that a reduction of NMDAR activity in a subset of GABAergic interneurons results in a disruption of the synchrony, leading to an “integration disorder” (McNally and McCarley, 2016). Abnormal gamma-band activity frequently observed in patients with schizophrenia is strongly correlated with perceptual impairments (McNally and McCarley, 2016). In this line, ketamine (a non-competitive NMDAR antagonist) superfusion in entorhinal slices from WT littermates of LPA₁-null mice was able to reduce gamma-oscillations (Cunningham et al., 2006). Taken together, the results point to a reduction in glutamatergic transmission via NMDAR, at least in some brain areas, but the exact mechanisms by which glutamate release is altered or which NMDAR is malfunctioning are still unknown.

A deficit in LPA-LPA₁ leading to a reduction in NMDAR transmission could be explained by experimental data obtained from LPA₁-null mice: low hippocampal levels of both glutamine and GABA (Harrison et al., 2003; Roberts et al., 2005), a reduced release of glutamate at the hippocampus (Roberts et al., 2005) or a decreased hippocampal synaptic activity (Musazzi et al., 2011). However, Harrison and coworkers did not observe changes in synaptic function at the hippocampus (Harrison et al., 2003) while an enhanced level of SNARE proteins were described at the presynaptic site (Musazzi et al., 2011), which would point to a favored neurotransmitter release. On the other hand, and in apparent contradiction, a lack of functional PRG points to an excess of LPA as a contributing factor during the development of mental disorders present with PPI deficits (Vogt et al., 2016). Thus inhibition of LPA synthesis reduced excess of glutamate release and restored PPI in PRG^+/− mice (Vogt et al., 2016).

Proper brain functioning requires an adequate balance between excitatory and inhibitory inputs. Despite the mechanisms of actions are not fully understood, LPA regulates glutamatergic transmission in such a way that a disruption in these signaling pathways seems to have an impact in the development of cognitive disorders.

LPA and Structural Plasticity

The role of membrane-derived phospholipids as key regulators of synaptic neurotransmission and plasticity was early detected in pioneer works measuring responses of different cell types to these biomediators (reviewed in Moolenaar, 1995; Bieberich, 2012). To discuss the effects of LPA on structural plasticity we should take into account that LPA targets many brain cells, including those forming the tripartite synapse (presynaptic and postsynaptic neurons and astrocytes), as well as neural progenitor cells (NPCs), microglia, oligodendrocytes, Schwan cells and endothelial cells (Noguchi et al., 2009). Thus, LPA was shown to induce a wide range of responses in the central nervous system (CNS) as well as in neural cell lines (Figure 1). LPA elicited sharp changes in cell’s shape and morphology, growth cone collapse and neurite retraction in many neuronal cell lines through activation of the small GTPase Rho which in turn contracts cytoskeleton (Ye et al., 2002; Choi et al., 2010; Fukushima et al., 2011). Several Rho-mediated intracellular signals seem to be involved in the cytoskeletal rearrangements of neuronal cells after activation of protein G13 by LPA binding (reviewed in Fukushima, 2004). The activation of Rho kinase produces phosphorylation of the MLC and inactivation of myosin phosphatase, which triggers actin polymerization and cell contraction (neurite retraction; Figure 1). The LPA-dependent Rho kinase-mediated regulation of neurite outgrowth can be strongly influenced by the intracellular Ca²⁺ levels, as was recently shown in primary hippocampal neurons cultured with agonists and antagonists of Rho kinase and Ca²⁺ (Ji et al., 2017).

LPA strongly influences the intracellular Ca²⁺ levels and thus may play important roles in a variety of functions as cellular shape regulation, motility and apoptosis (Figure 1). Neuronal calcium levels are modulated by many proteins, including ligand- and voltage-gated channels, pumps, transporters and calcium-binding proteins, and play a crucial role in neuronal development, adaptive responses, dendritic spine development and synaptic plasticity, as well as in pathological neuronal processes (Segal and Korkotian, 2016; Jackman and Regehr, 2017). In neurons, LPA induces a sustained elevation of intracellular calcium which has been related to extracellular glutamate levels and modulation of glutamate receptors (Ye et al., 2002), as discussed in the previous section. However, pathophysiological LPA concentrations in brain, as happens after hemorrhagic brain injury when a dramatic increase in LPA concentration is observed in CSF, could lead to persistent Ca²⁺ increases conducive to neuronal necrosis and apoptosis (Holtsberg et al., 1997; Steiner et al., 2002).

The processes of neuronal arborization and neurite outgrowth are strongly influenced by LPA, which has been described as an important regulator of morphological neuroplasticity (Shiono et al., 1993; Figure 1). After being recognized by LPA receptors, cyclic phosphatidic acid (cPA) may also elicit a neurotrophic effect and promotes neurite outgrowth in embryonic hippocampal neurons acting through the same effectors as nerve growth factor (NGF), including a sustained activation of ERK 1/2 and Akt (Fujiwara et al., 2003). Of interest, a novel signaling pathway involving LPA₃ receptor, Gq protein and the Rho family GTPase 2 (Rnd2) has been lately reported to play an important role in neurite branching of hippocampal neurons and, therefore, on neural network formation (Furuta et al., 2012). In sharp contrasts with the reported effects of LPA on neurite retraction in many neuronal cell types, which were mostly mediated by all LPA receptors except LPA₃ (Ishii et al., 2000; Fukushima, 2004), these authors demonstrated a novel signaling pathway linking LPA₃ with enhanced axonal branch formation, both in neuronal cell lines with ectopic expression of LPA₃ as well as in primary neurons with endogenous LPA₃ expression (peak of expression on postnatal day 7; Furuta et al., 2012).

Sprouting, extension and arborization of neurites, formation of novel dendrites and remodeling (maturation) of existing ones are key structural changes with strong implications in synaptic formation and plasticity. In this context, modulation of dendritic spine dynamics by LPA has been previously reported; for instance, LPA₁ was localized in dendritic spines and its overexpression in cultured hippocampal neurons correlated with morphological and functional effects: increases in the density and size of spines and significant changes in the decay time of miniature excitatory synaptic currents (mEPSC; Pilpel and Segal, 2006). Of note, none of the three classic pathways activated by LPA (Gq-mediated activation of PKC, Gi inhibition of adenyl cyclase and G12/13 activation of Rho) mediates the effects on spines of LPA₁ overexpression (Pilpel and Segal, 2006). In agreement with these results, changes in the morphology of excitatory synaptic spines, with potential repercussion in synaptic neurotransmission, were found after genetic deletion of LPA₁ receptor in a murine model; namely, hippocampal dendritic spines showed a clear immature phenotype as compared with WT counterparts, with predominance of filopodia in detriment of the mushroom and stubby spines, and marked reduction in mushroom spine head-width (Figure 3; Peñalver et al., 2017).

FIGURE 3

Figure 3. Golgi staining of CA1 pyramidal neurons from wild-type (WT) and KOLPA₁ mice demonstrating the morphological differences between KOLPA₁ and WT spines. (A) Overall spine length values showed significant differences between genotypes (WT 1.4 ± 0.05 μm, KOLPA₁ 2.12 ± 0.09 μm; Mann-Whitney, ****p < 0.0001). (B) Significant differences were found in the distribution of dendritic spine morphologies within stratum oriens from KOLPA₁ model compared to the same region of WT mice. Filopodia type was significantly more frequent in KOLPA₁ mice in detriment of both mushroom and stubby categories (t-test, Filopodia ****p < 0.0001, Stubby **p = 0.0073 and Thin, n.s.; Mann-Whitney, Mushroom ****p < 0.0001). (C,D) Spine head of mushroom subtype was smaller in KOLPA₁ (D; D2, D3 depict details from D1 and D4, respectively) than in WT mice (C; C2, C3 depict details from C1 and C4, respectively). (E) Quantitative analysis demonstrated a significant decrease in the head-width of mushroom spines from KOLPA₁ mice (0.52 ± 0.02 μm) compared to WT (0.91 ± 0.02 μm); t-test, ****p < 0.0001. Scale bar: C1, C4, D1 and D4 (2 μm); C2, C3, D2, D3 (1 μm). Matrix metalloproteinase (MMP) activities (F) and protein expression levels (G) in cerebral cortex and hippocampus of WT and KOLPA₁ mice. Significant differences were found in MMP-9 proteolytic activity of both brain areas (F), showing a decreased activity in knock-out (KO) mice (****p < 0.0001), while MMP-2 remained unchanged. Immunoblot analysis of MMP-9 protein expression in cerebral cortex and hippocampus from WT and KOLPA₁ mice (G). Quantitive analysis of proactive (92 kDa) and active (82 kDa) MMP-9 were determined by densitometry and relative to β-actin expression (WT n = 4; KO n = 5). A reduction in active MMP-9 expression was detected in KOLPA₁ compared to WT mice (*p < 0.05, **p < 0.01), while no changes were detected in pro-active MMP-9 expression (Adapted from Peñalver et al., 2017).

LPA-induced effects on neuronal network formation are multiple and highly depending on the physiological and developmental states. Moreover, the effects of LPA on neuronal differentiation could be also mediated in an indirect way through previous stimulation of surrounding astrocytes. In fact, LPA induces a wide range of responses in cultured astrocytes, including proliferation and inhibition of glutamate uptake (Steiner et al., 2002; Shano et al., 2008; Figure 1), inhibition of glucose uptake, stimulation of lipid peroxidation and increases in intracellular calcium concentration (Keller et al., 1997). Interestingly, LPA-primed astrocytes promote neuronal differentiation of cortical cerebral progenitors and developing neurons, which showed increases in arborization and neurite outgrowth (de Sampaio e Spohr et al., 2008, 2011). These effects were exclusively ascribed to astrocytic LPA₁ and/or LPA₂ receptors, but not LPA₃ (de Sampaio e Spohr et al., 2008). Furthermore, the contribution of LPA-activated astrocytes to neuronal differentiation is also supported by data on expression levels of LPA receptors during mouse brain development. Thus, LPA₁ receptor was found in astrocytes and oligodendrocytes, as well as in neurons, during embryonic and postnatal development (Suckau et al., 2019). However, LPA₁ protein was not detectable in mature hippocampal neurons (14-day-old cultures), when an extensive network of synaptic connections was established, but was strongly detected in glial cells and immature neurons (only 2 days in culture; Suckau et al., 2019). In addition, the production of NGF is also enhanced by astrocytes’ exposure to LPA, which may further contribute to neuronal differentiation (Furukawa et al., 2007).

On the other hand, LPA signaling via LPA₁ receptor has been associated with invasive and metastatic properties of cancer cells, particularly through the induction of proteolytic enzymes like matrix metalloproteinases (MMPs) 2 (Kato et al., 2012) and 9 (Park et al., 2011). Interestingly, we also found a link between LPA₁ and MMP-9 expression in brain: silencing LPA₁ expression in mouse brain induced a marked reduction in MMP-9 activity in hippocampus and cortex of KOLPA₁ mice compared with WT counterparts, while no changes were detected for MMP-2 (Figure 3; Peñalver et al., 2017). A considerable body of evidence has recently shown a key role for MMP-9 in synaptic remodeling, synaptic plasticity and cognitive processes (Rivera et al., 2010; Michaluk et al., 2011). In neurons, MMP-9 is located at the postsynaptic domains of excitatory synapses and its inhibition has been linked to memory deficits in behavioral learning paradigms (Nagy et al., 2007). MMP-9 is a key regulator of dendritic spine morphology (Michaluk et al., 2011; Dziembowska and Wlodarczyk, 2012); thus, its activation through proteolytic cleavage of an inactive precursor form (pro-active MMP-9) is strictly regulated during spine maturation (Tian et al., 2007; Bilousova et al., 2009). Immunoblot analysis indicates that active MMP-9 protein levels in brain are reduced in KOLPA₁ respect to WT mice, although no significant differences were found for pro-active MMP-9 (Figure 3). The downregulation of MMP-9 activity shown by LPA₁-null mice may play an important role in their cognitive performance and partially explain the neurophysiological phenotype shown by these animals (Santin et al., 2009; Castilla-Ortega et al., 2010). These results suggest that a reduced MMP-9 activity would be a downstream effect of the absence of LPA-induced Rho/ROCK signaling pathway, which is known to produce proteolytic enzymes like MMP-9 (Yu et al., 2014).

A further relationship between LPA signaling and glutamatergic excitatory transmission was recently found in LPA₁-null mice. In this model, a marked down-regulation of the main glutaminase (GA) isoform (KGA) involved in the synthesis of neurotransmitter glutamate was reported (Peñalver et al., 2017). The drastic decrease of KGA protein expression was particularly relevant in cerebral cortex and hippocampus (Figure 4), although correlation between GLS mRNA abundance, KGA protein levels and GA activity was only apparent in prefrontal cortex (PFC) and motor cortex (Figure 4). Despite substantial decrements of KGA protein in key glutamatergic regions, the total GA activity was essentially maintained which immediately suggests activation of compensatory mechanisms. For example, two distinct LPA-related mechanisms, involving other LPA receptors, would compensate this regional KGA loss by enhancing the enzymatic activity of GLS isoforms. The Gls-encoded alternative spliced GAC isoform is activated by Rho GTPases (Wang et al., 2008); interestingly, LPA stimulates activation of Rho in several neuronal cell lines, cortical progenitors and cortical neurons (Ye et al., 2002). Moreover, the Raf-Mek-Erk signaling pathway has been shown to increase KGA activity by phosphorylation after stimulation by several mitogens, including LPA (Thangavelu et al., 2012); therefore, post-translational modifications of the remaining KGA protein pool would cooperate in keeping basal GA activity in mutant KOLPA₁ mice.

FIGURE 4

Figure 4. Comparative analysis of immunostaining for Gls-encoded long GA protein variant (KGA) in WT and KOLPA₁ mice brain. Specific immunolabeling for KGA was detected within the somata/neuropile of several brain regions in WT brain (left column). In general, there was a strong reduction in the staining together with a progressive switch to a perivascular location from control to KO mice. (A,B) Panoramic views of sections containing cerebral cortex and striatum: black arrows indicate KGA-positive blood vessels. (C,D) Progressive change of KGA-staining in deep layers of agranular insular cortex (square; detail of cortical somatic staining, inset in (C). (E,F) KGA-positive staining in the CA1-CA3 hippocampal subfields and DG was dramatically decreased in KO genotype in comparison to WT. Ctx, cortex; St, striatum; bv, blood vessel; CA1, CA3, hippocampal subfields; DG, dentate gyrus; Th, thalamus. Scale bar: (A,B), 1 mm; (C,D), 100 μm; (E,F), 500 μm; Inset (C), 25 μm. Determination of total GA activity in mouse brain regions (G). Significant differences in GA specific activity were found in motor cortex (WT n = 9; KO n = 5) and prefrontal cortex (PFC; WT n = 12; KO n = 8), but not in hippocampus and striatum (results not shown). ***p < 0.001; *p < 0.05 (both panels adapted from Peñalver et al., 2017).

The deficit of KGA protein in null mutant mice lacking LPA₁ receptors may also give rise to developmental defects in cortical and hippocampal neurons with strong implications in synaptic plasticity. Of note, in null mice for the Gls gene the main functional deficit was found in the implementation of more active neural network circuits, stressing the importance of KGA in neuronal maturation, development and differentiation (Masson et al., 2006). In accordance with these findings, GLS isoforms (KGA and GAC) were upregulated during neurogenesis of human NPCs, and their expression pattern positively correlated with the neuronal marker microtubule associated protein 2 (MAP-2; Wang et al., 2014). Most important, studies of cultured human NPCs after siRNA silencing of GLS suggest a critical role of GLS isoforms for proliferation and survival of NPCs (Wang et al., 2014). Furthermore, inhibition of GA activity in cultures of mouse embryonary cortical neurons resulted in impaired neuritogenesis (Velletri et al., 2013), while both mRNA and protein KGA levels strongly increased when cerebellar granule cells differentiate in culture (Thomas et al., 1989). This last study also demonstrated KGA upregulation in parallel with Ca²⁺-dependent glutamate release and formation of neurites, synaptic vesicles and synapses (Thomas et al., 1989). Therefore, it is tempting to speculate that an impairment of KGA in synaptic regions, as expected from the drastic downregulation of KGA shown by KOLPA₁ mice, would also negatively impact developmental processes of the nervous system.

LPA and Neuropathic Pain

The perception of noxious stimuli arises from signals originated at the peripheral branches of specialized primary afferents called nociceptors. The cell bodies of these neurons are located at the dorsal root- and trigeminal ganglia and their central processes enter the spinal cord. Nociceptors contact dorsal horn neurons on both projecting and local circuit neurons in specific nociceptive pathways and exert excitatory activity as they use glutamate as their main neurotransmitter. In addition, unmyelinated C-nociceptors also contain neuropeptides such as substance P (SP), which are usually co-released together with glutamate upon tissue injury or persistent stimulation from peripheral nerves, see Millan (1999) for a review. By this means, neuropeptides exert slow excitatory potentials that maintain the initial depolarization elicited by glutamate which results in long-term changes in the responses of dorsal horn neurons through mechanisms resembling those underlying LTP (Sandkühler, 2009). The prolonged changes in excitability are known as central sensitization and help to explain the hyperalgesia (exaggerated response to noxious stimulation) and allodynia (pain in response to innocuous stimuli) that are developed during chronic pain. Sensitization of dorsal horn neurons involves the recruitment of second messenger pathways and activation of protein kinases resembling NMDAR-mediated LTP in brain areas, where LPA was shown to play a key modulatory role. In a similar way, LPA seems critical in the initiation of central sensitization during neuropathic pain, since hyperalgesia and allodynia were absent in LPA₁ null mice after peripheral nerve damage (Inoue et al., 2004). A single intrathecal injection of LPA in awake mice provoked pain-like behaviors, which were reverted by application of antisense oligonucleotide against LPA₁ prior to the induction of the experimental neuropathy (Inoue et al., 2004).

Intense activation of primary afferents (by capsaicin, or co-application of SP and NMDA) induced de novo LPA synthesis in spinal cord slices by means of an ATX-dependent mechanism (Inoue et al., 2008b). Activity from fast conducting Aδ pain fibers activates primarily AMPAR, causing a rapid depolarization sufficient to release Mg²⁺ block from NMDAR. As a consequence, activity from slow conducting C-nociceptors provokes, in the same post-synaptic neuron, a sustained depolarization via NMDA and metabotropic neurokinin 1 receptors for SP (NK1). The intracellular events that follow NK1 and NMDA signaling and lead to LPA accumulation have been largely studied and are summarized in Figure 5. Briefly, signaling via NK1 receptors induces sustained excitatory postsynaptic potentials that provokes Ca²⁺ release from the endoplasmic reticulum via inositol-1,4,5-triphosphate (IP₃) sensitive receptors. Meanwhile, PKC-mediated NMDAR phosphorylation potentiates accumulation of intracellular Ca²⁺ and promotes synthesis of LPC by means of phospholipase A₂ (PLA₂). LPC leaves the neuron to be converted to LPA by ATX (Inoue et al., 2008a). It has been shown that neuropathic pain behaviors induced by LPC application in the spinal cord were abolished in LPA₁ and LPA₃ null mice (Inoue et al., 2004; Ma et al., 2009) and significantly attenuated in ATX^+/− heterozygous mice (Inoue et al., 2008b). In addition, de novo LPA synthesis was inhibited by PLA₂ antagonists (Ma et al., 2009, 2010b). LPA causes demyelination in dorsal root fibers when applied ex vivo (Fujita et al., 2007); accordingly, nerve-injury induced demyelination was abolished in LPA₁-null mice and markedly attenuated in ATX^+/− heterozygous mice (Inoue et al., 2004; Nagai et al., 2010). In this line, early blockade of LPA₁ receptors with a specific antagonist Ki-16425 (Ohta et al., 2003) inhibits neuronal damage in the sciatic nerve ligation model and in response to intrathecal LPA injection (Ma et al., 2009). In addition, in a rat model of osteoarthritis, early treatment with Ki-16425 reduced demyelination and nerve damage and attenuated hindlimb pain (McDougall et al., 2017).

FIGURE 5

Figure 5. Sustained activity from peripheral nerve as a consequence of nerve damage provokes co-release of glutamate and substance P (SP) from the central terminals of the nociceptors. Activation of NMDA and NK1 receptors provokes a rise in cytosolic Ca²⁺ followed by phospholipase A₂ (PLA₂)-induced lisophosphatidilcholine (LPC) synthesis. LPC leaves the cell and is converted to LPA by ATX. Signaling through LPA₁ initiates a process of demyelination at the central terminals of the primary afferents. Signaling through LPA₃ constitutes a feed-forward mechanism for LPA formation (Inoue et al., 2004; Fujita et al., 2007; Ma et al., 2010a,b).

LPA-induced demyelination involves at least two different mechanisms. The activation of calcium-dependent protease calpain (via G_q/11) degrades myelin proteins of the Schwamm cells around the dorsal root fibers (Xie et al., 2010). In addition, a sustaining downregulation of myelin proteins is induced by LPA₁ signaling via Gα_12/13 which activates RhoA and ROCK kinase pathways to silence transcription factors (such as Erg2 and Sox10) involved in myelin gene expression (Fujita et al., 2007).

An intriguing form of neuropathic pain, whose underlying mechanisms are still a matter of debate, is that produced by antineoplastic agents (Park, 2014). Chemotherapy-induced peripheral neuropathy is a common side effect in cancer patients that might require discontinuing the treatment. In mice, it was shown that paclitaxel application, used for the treatment of solid tumors, provoked a marked increase of LPA in the spinal dorsal horn, which was completely abolished in LPA₁ and LPA₃-null mice and by intrathecal pre-treatment with NK1 or NMDAR antagonists in WT mice (Uchida et al., 2014).

Hence, nerve insult promotes LPA accumulation by an LTP-like mechanism initiated at NMDA/NK1 receptor of post-synaptic dorsal horn neurons. LPA acts as a retrograde messenger and activates LPA₁ and LPA₃ located at the membranes of the Schwann cells and evokes demyelination of the central axon of the primary afferents (Figure 5). At the same time, LPA levels are maintained through de novo LPA synthesis promoted by LPA/LPA₃ interaction at the microglia, since treatment with minocycline reverted both LPA- and nerve damage-induced neuropathic pain and dampened LPA synthesis (Ma et al., 2010b).

Demyelination allows for ectopic relocation of Na_v and K_v channels along the exposed patches of axonal membrane, altering the normal excitability and prompting abnormal spontaneous firing of action potentials (Roza et al., 2003; Campbell and Meyer, 2006; Bernal et al., 2016; Bernal and Roza, 2018; Roza and Lopez-Garcia, 2008). In addition, loss of myelin could favor electrical coupling between fibers (Meyer et al., 1985; Bernal et al., 2016) and promote aberrant sprouting from demyelinated nodes (Griffin et al., 2010). Nerve trauma, metabolic diseases or viral infection trigger neuropathic pain due to an altered excitability at the peripheral axons of the affected primary afferents; in this context, an involvement of LPA at the site of injury should also be expected. Early experiments showed that LPA injection in the hind-paws of awake mice produced withdrawal reflexes (indicative of pain) which were inhibited by specific blockade of NK1 and pertussis toxin, suggesting the activation of SP-containing nociceptors via a signaling mechanism involving PTX sensitive-Gi/o proteins (Renbäck et al., 1999). Furthermore, upregulation of LPA₁ occurs in the distal nerve stump following nerve injury (Weiner et al., 2001).

Neuropathic pain is a pathological expression of the nociceptive system caused by different etiologies which commonly are present with demyelination. The unequivocal contribution of LPA-signaling in the induction, and possible maintenance (Ueda et al., 2018), of central sensitization points to novel therapeutic strategies for modulation of some neuropathic pain symptoms.

Conclusions

The bioactive natural lipid LPA induces multiple cellular responses in the CNS as well as in neural cell lines. Many, but not all, of these effects are mediated through interaction with the LPA₁ receptor, considered the most prevalent receptor type in both embryonic and adult brains of humans and mice. Genetic silencing of LPA₁ in mice causes altered neurotransmitter homeostasis which were previously related to psychiatric diseases. Behavioral studies with LPA₁ deficient mice reported deficiencies in spatial memory retention and abnormal use of searching orientation strategies, defective working and reference memory, independently of exploratory and emotional impairments, attributed to hippocampal malfunction. Recent results reinforce the view of LPA as an important mediator of synaptic plasticity. Signaling through LPA₁ receptor exerts an important impact on KGA expression mainly through a posttranscriptional mechanism, stressing a key relationship between LPA and glutamatergic transmission. Furthermore, the absence of LPA₁ signaling downregulates expression of active MMP-9 and provokes drastic changes in hippocampal dendritic spines toward an immature phenotype. These changes may provide a molecular basis for the role of LPA in influencing synaptic plasticity associated to cognitive and memory processes. In this line, activation of NMDAR at excitatory synapsis in different areas of the CNS leads to production of LPA which may either potentiate or restrain the synaptic strength by enhancing currents through NMDAR and modulating glutamate release. On the other hand, at inhibitory synapses, NMDAR-induced LPA-synthesis leads to a transient disinhibition on GABAergic neurons. Sustained NMDAR activation in dorsal horn neurons within nociceptive circuits elicits LPA production, which is further sustained by means of a positive-feedback mechanism. Such LPA accumulation initiates demyelination of primary afferents inducing the development of neuropathic pain. Nevertheless, much work is needed to completely address the molecular mechanisms underlying the huge number of key processes affected by this multifaceted bioactive lipid.

Author Contributions

CR, JC-S, MG-G, AP and JM conceived and wrote the manuscript.

Funding

This work was financially supported by the Spanish Ministry of Economy and Competitivity, Grant SAF2015-64501-R (to JM) and SAF2016-77585-R (to CR), and by Red de Trastornos Adictivos, Instituto de Salud Carlos III (ISC-III) Grant RD16/0017/001 (JM).

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

Thanks are due to Fernando Rodríguez de Fonseca and Guillermo Estivill for their help in managing the colony of KOLPA₁ mice. The technical assistance of Ms Victoria Enrique is gratefully acknowledged.

References

Bernal, L., Lopez-Garcia, J. A., and Roza, C. (2016). Spontaneous activity in C-fibres after partial damage to the saphenous nerve in mice: effects of retigabine. Eur. J. Pain 20, 1335–1345. doi: 10.1002/ejp.858

PubMed Abstract | CrossRef Full Text | Google Scholar

Bernal, L., and Roza, C. (2018). Hyperpolarization-activated channels shape temporal patterns of ectopic spontaneous discharge in C-nociceptors after peripheral nerve injury. Eur. J. Pain doi: 10.1002/ejp.1226 [Epub ahead of print].

PubMed Abstract | CrossRef Full Text | Google Scholar

Bieberich, E. (2012). It’s a lipid’s world: bioactive lipid metabolism and signaling in neural stem cell differentiation. Neurochem. Res. 37, 1208–1229. doi: 10.1007/s11064-011-0698-5

PubMed Abstract | CrossRef Full Text | Google Scholar

Bilousova, T., Dansie, L., Ngo, M., Aye, J., Charles, J., Ethell, D., et al. (2009). Minocycline promotes dendritic spine maturation and improves behavioural performance in the fragile X mouse model. J. Med. Genet. 46, 94–102. doi: 10.1136/jmg.2008.061796

PubMed Abstract | CrossRef Full Text | Google Scholar

Blanco, E., Bilbao, A., Luque-Rojas, M., Palomino, A., Bermúdez-Silva, F. J., Suárez, J., et al. (2012). Attenuation of cocaine-induced conditioned locomotion is associated with altered expression of hippocampal glutamate receptors in mice lacking LPA1 receptors. Psychopharmacology 220, 27–42. doi: 10.1007/s00213-011-2446-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Bliss, T. V., and Collingridge, G. L. (1993). A synaptic model of memory: long-term potentiation in the hippocampus. Nature 361, 31–39. doi: 10.1038/361031a0

PubMed Abstract | CrossRef Full Text | Google Scholar

Bliss, T., and Schoepfer, R. (2004). Controlling the ups and downs of synaptic strength. Science 304, 973–974. doi: 10.1126/science.1098805

PubMed Abstract | CrossRef Full Text | Google Scholar

Campbell, J. N., and Meyer, R. A. (2006). Mechanisms of neuropathic pain. Neuron 52, 77–92. doi: 10.1016/j.neuron.2006.09.021

PubMed Abstract | CrossRef Full Text | Google Scholar

Castilla-Ortega, E., Sánchez-López, J., Hoyo-Becerra, C., Matas-Rico, E., Zambrana-Infantes, E., Chun, J., et al. (2010). Exploratory, anxiety and spatial memory impairments are dissociated in mice lacking the LPA1 receptor. Neurobiol. Learn. Mem. 94, 73–82. doi: 10.1016/j.nlm.2010.04.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Choi, J. W., and Chun, J. (2013). Lysophospholipids and their receptors in the central nervous system. Biochim. Biophys. Acta 1831, 20–32. doi: 10.1016/j.bbalip.2012.07.015

PubMed Abstract | CrossRef Full Text | Google Scholar

Choi, J. W., Herr, D. R., Noguchi, K., Yung, Y. C., Lee, C.-W., Mutoh, T., et al. (2010). LPA receptors: subtypes and biological actions. Annu. Rev. Pharmacol. Toxicol. 50, 157–186. doi: 10.1146/annurev.pharmtox.010909.105753

PubMed Abstract | CrossRef Full Text | Google Scholar

Choi, S.-H., Jung, S.-W., Lee, B.-H., Kim, H.-J., Hwang, S.-H., Kim, H.-K., et al. (2015). Ginseng pharmacology: a new paradigm based on gintonin-lysophosphatidic acid receptor interactions. Front. Pharmacol. 6:245. doi: 10.3389/fphar.2015.00245

PubMed Abstract | CrossRef Full Text | Google Scholar

Contos, J. J., Fukushima, N., Weiner, J. A., Kaushal, D., and Chun, J. (2000). Requirement for the lpA1 lysophosphatidic acid receptor gene in normal suckling behavior. Proc. Natl. Acad. Sci. U S A 97, 13384–13389. doi: 10.1073/pnas.97.24.13384

PubMed Abstract | CrossRef Full Text | Google Scholar

Cunningham, M. O., Hunt, J., Middleton, S., LeBeau, F. E., Gillies, M. J., Gillies, M. G., et al. (2006). Region-specific reduction in entorhinal gamma oscillations and parvalbumin-immunoreactive neurons in animal models of psychiatric illness. J. Neurosci. 26, 2767–2776. doi: 10.1523/jneurosci.5054-05.2006

PubMed Abstract | CrossRef Full Text | Google Scholar

de Sampaio e Spohr, T. C., Choi, J. W., Gardell, S. E., Herr, D. R., Rehen, S. K., Gomes, F. C., et al. (2008). Lysophosphatidic acid receptor-dependent secondary effects via astrocytes promote neuronal differentiation. J. Biol. Chem. 283, 7470–7479. doi: 10.1074/jbc.M707758200

PubMed Abstract | CrossRef Full Text | Google Scholar

de Sampaio e Spohr, T. C. L., Dezonne, R. S., Rehen, S. K., and Gomes, F. C. A. (2011). Astrocytes treated by lysophosphatidic acid induce axonal outgrowth of cortical progenitors through extracellular matrix protein and epidermal growth factor signaling pathway. J. Neurochem. 119, 113–123. doi: 10.1111/j.1471-4159.2011.07421.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Dziembowska, M., and Wlodarczyk, J. (2012). MMP9: a novel function in synaptic plasticity. Int. J. Biochem. Cell Biol. 44, 709–713. doi: 10.1016/j.biocel.2012.01.023

PubMed Abstract | CrossRef Full Text | Google Scholar

Fujita, R., Kiguchi, N., and Ueda, H. (2007). LPA-mediated demyelination in ex vivo culture of dorsal root. Neurochem. Int. 50, 351–355. doi: 10.1016/j.neuint.2006.09.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Fujiwara, Y., Sebök, A., Meakin, S., Kobayashi, T., Murakami-Murofushi, K., and Tigyi, G. (2003). Cyclic phosphatidic acid elicits neurotrophin-like actions in embryonic hippocampal neurons. J. Neurochem. 87, 1272–1283. doi: 10.1046/j.1471-4159.2003.02106.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Fukushima, N. (2004). LPA in neural cell development. J. Cell. Biochem. 92, 993–1003. doi: 10.1002/jcb.20093

PubMed Abstract | CrossRef Full Text | Google Scholar

Fukushima, N., Furuta, D., and Tsujiuchi, T. (2011). Coordinated interactions between actin and microtubules through crosslinkers in neurite retraction induced by lysophosphatidic acid. Neurochem. Int. 59, 109–113. doi: 10.1016/j.neuint.2011.04.020

PubMed Abstract | CrossRef Full Text | Google Scholar

Furukawa, A., Kita, K., Toyomoto, M., Fujii, S., Inoue, S., Hayashi, K., et al. (2007). Production of nerve growth factor enhanced in cultured mouse astrocytes by glycerophospholipids, shingolipids and their related compounds. Mol. Cell. Biochem. 305, 27–34. doi: 10.1007/s11010-007-9524-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Furuta, D., Yamane, M., Tsujiuchi, T., Moriyama, R., and Fukushima, N. (2012). Lysophosphatidic acid induces neurite branch formation through LPA3. Mol. Cell. Neurosci. 50, 21–34. doi: 10.1016/j.mcn.2012.03.006

PubMed Abstract | CrossRef Full Text | Google Scholar

García-Morales, V., Montero, F., González-Forero, D., Rodríguez-Bey, G., Gómez-Pérez, L., Medialdea-Wandossell, M., et al. (2015). Membrane-derived phospholipids control synaptic neurotransmission and plasticity. PLoS Biol. 13:e1002153. doi: 10.1371/journal.pbio.1002153

PubMed Abstract | CrossRef Full Text | Google Scholar

Griffin, J. W., Pan, B., Polley, M. A., Hoffman, P. N., and Farah, M. H. (2010). Measuring nerve regeneration in the mouse. Exp. Neurol. 223, 60–71. doi: 10.1016/j.expneurol.2009.12.033

PubMed Abstract | CrossRef Full Text | Google Scholar

Hardingham, G. E., and Do, K. Q. (2016). Linking early-life NMDAR hypofunction and oxidative stress in schizophrenia pathogenesis. Nat. Rev. Neurosci. 17, 125–134. doi: 10.1038/nrn.2015.19

PubMed Abstract | CrossRef Full Text | Google Scholar

Harrison, S., Reavill, C., Brown, G., Brown, J., Cluderay, J., Crook, B., et al. (2003). LPA1 receptor-deficient mice have phenotypic changes observed in psychiatric disease. Mol. Cell. Neurosci. 24, 1170–1179. doi: 10.1016/j.men.2003.09.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Holtsberg, F. W., Steiner, M. R., Furukawa, K., Keller, J. N., Mattson, M. P., and Steiner, S. M. (1997). Lysophosphatidic acid induces a sustained elevation of neuronal intracellular calcium. J. Neurochem. 69, 68–75. doi: 10.1046/j.1471-4159.1997.69010068.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Hwang, S., Shin, T.-J., Choi, S.-H., Cho, H.-J., Lee, B.-H., Pyo, M., et al. (2012a). Gintonin, newly identified compounds from ginseng, is novel lysophosphatidic acids-protein complexes and activates G protein-coupled lysophosphatidic acid receptors with high affinity. Mol. Cells 33, 151–162. doi: 10.1007/s10059-012-2216-z

PubMed Abstract | CrossRef Full Text | Google Scholar

Hwang, S., Shin, E.-J., Shin, T.-J., Lee, B.-H., Choi, S.-H., Kang, J., et al. (2012b). Gintonin, a ginseng-derived lysophosphatidic acid receptor ligand, attenuates Alzheimer’s disease-related neuropathies: involvement of non-amyloidogenic processing. J. Alzheimer Dis. 31, 207–223. doi: 10.3233/jad-2012-120439

PubMed Abstract | CrossRef Full Text | Google Scholar

Inoue, M., Ma, L., Aoki, J., Chun, J., and Ueda, H. (2008a). Autotaxin, a synthetic enzyme of lysophosphatidic acid (LPA), mediates the induction of nerve-injured neuropathic pain. Mol. Pain 4:6. doi: 10.1186/1744-8069-4-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Inoue, M., Ma, L., Aoki, J., and Ueda, H. (2008b). Simultaneous stimulation of spinal NK1 and NMDA receptors produces LPC which undergoes ATX-mediated conversion to LPA, an initiator of neuropathic pain. J. Neurochem. 107, 1556–1565. doi: 10.1111/j.1471-4159.2008.05725.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Inoue, M., Rashid, M., Fujita, R., Contos, J. J., Chun, J., and Ueda, H. (2004). Initiation of neuropathic pain requires lysophosphatidic acid receptor signaling. Nat. Med. 10, 712–718. doi: 10.1038/nm1060

PubMed Abstract | CrossRef Full Text | Google Scholar

Ishii, I., Contos, J. J., Fukushima, N., and Chun, J. (2000). Functional comparisons of the lysophosphatidic acid receptors, LPA1/VZG-1/EDG-s LPA2/EDG-4 and LPA3/EDG-7 in neuronal cell lines using a retrovirus expression system. Mol. Pharmacol. 58, 895–902. doi: 10.1124/mol.58.5.895

PubMed Abstract | CrossRef Full Text | Google Scholar

Jackman, S. L., and Regehr, W. G. (2017). The mechanisms and functions of synaptic facilitation. Neuron 94, 447–464. doi: 10.1016/j.neuron.2017.02.047

PubMed Abstract | CrossRef Full Text | Google Scholar

Ji, Z., Cai, Z., Zhang, J., Liu, N., Chen, J., Tan, M., et al. (2017). Rho kinase regulates neurite outgrowth of hippocampal neurons via calcium dependent cytoskeleton regulation. Am. J. Transl. Res. 9, 762–773.

PubMed Abstract | Google Scholar

Kato, H. E., Zhang, F., Yizhar, O., Ramakrishnan, C., Nishizawa, T., Hirata, K., et al. (2012). Crystal structure of the channelrhodopsin light-gated cation channel. Nature 482, 369–374. doi: 10.1038/nature10870

PubMed Abstract | CrossRef Full Text | Google Scholar

Kauer, J. A., and Malenka, R. C. (2007). Synaptic plasticity and addiction. Nat. Rev. Neurosci. 8, 844–858. doi: 10.1038/nrn2234

PubMed Abstract | CrossRef Full Text | Google Scholar

Keller, J. N., Steiner, M. R., Holtsberg, F. W., Mattson, M. P., and Steiner, S. M. (1997). Lysophosphatidic acid-induced proliferation-related signals in astrocytes. J. Neurochem. 69, 1073–1084. doi: 10.1046/j.1471-4159.1997.69031073.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Lu, W. Y., Xiong, Z. G., Lei, S., Orser, B. A., Dudek, E., Browning, M. D., et al. (1999). G-protein-coupled receptors act via protein kinase C and Src to regulate NMDA receptors. Nat. Neurosci. 2, 331–338. doi: 10.1038/7243

PubMed Abstract | CrossRef Full Text | Google Scholar

Lüscher, C., and Malenka, R. C. (2012). NMDA receptor-dependent long-term potentiation and long-term depression (LTP/LTD). Cold Spring Harb. Perspect. Biol. 4:a005710. doi: 10.1101/cshperspect.a005710

PubMed Abstract | CrossRef Full Text | Google Scholar

Ma, L., Nagai, J., and Ueda, H. (2010a). Microglial activation mediates de novo lysophosphatidic acid production in a model of neuropathic pain. J. Neurochem. 115, 643–653. doi: 10.1111/j.1471-4159.2010.06955.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Ma, L., Uchida, H., Nagai, J., Inoue, M., Aoki, J., and Ueda, H. (2010b). Evidence for de novo synthesis of lysophosphatidic acid in the spinal cord through phospholipase A2 and autotaxin in nerve injury-induced neuropathic pain. J. Pharmacol. Exp. Ther. 333, 540–546. doi: 10.1124/jpet.109.164830

PubMed Abstract | CrossRef Full Text | Google Scholar

Ma, L., Uchida, H., Nagai, J., Inoue, M., Chun, J., Aoki, J., et al. (2009). Lysophosphatidic acid-3 receptor-mediated feed-forward production of lysophosphatidic acid: an initiator of nerve injury-induced neuropathic pain. Mol. Pain 5:64. doi: 10.1186/1744-8069-5-64

PubMed Abstract | CrossRef Full Text | Google Scholar

Masson, J., Darmon, M., Conjard, A., Chuhma, N., Ropert, N., Thoby-Brisson, M., et al. (2006). Mice lacking brain/kidney phosphate-activated glutaminase have impaired glutamatergic synaptic transmission, altered breathing, disorganized goal-directed behavior and die shortly after birth. J. Neurosci. 26, 4660–4671. doi: 10.1523/jneurosci.4241-05.2006

PubMed Abstract | CrossRef Full Text | Google Scholar

McDougall, J. J., Albacete, S., Schuelert, N., Mitchell, P. G., Lin, C., Oskins, J. L., et al. (2017). Lysophosphatidic acid provides a missing link between osteoarthritis and joint neuropathic pain. Osteoarthritis Cartilage 25, 926–934. doi: 10.1016/j.joca.2016.08.016

PubMed Abstract | CrossRef Full Text | Google Scholar

McNally, J. M., and McCarley, R. W. (2016). Gamma band oscillations: a key to understanding schizophrenia symptoms and neural circuit abnormalities. Curr. Opin. Psychiatry 29, 202–210. doi: 10.1097/yco.0000000000000244

PubMed Abstract | CrossRef Full Text | Google Scholar

Meyer, R. A., Raja, S. N., Campbell, J. N., Mackinnon, S. E., and Dellon, A. L. (1985). Neural activity originating from a neuroma in the baboon. Brain Res. 325, 255–260. doi: 10.1016/0006-8993(85)90321-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Michaluk, P., Wawrzyniak, M., Alot, P., Szczot, M., Wyrembek, P., Mercik, K., et al. (2011). Influence of matrix metalloproteinase MMP-9 on dendritic spine morphology. J. Cell Sci. 124, 3369–3380. doi: 10.1242/jcs.090852

PubMed Abstract | CrossRef Full Text | Google Scholar

Millan, M. J. (1999). The induction of pain: an integrative review. Prog. Neurobiol. 57, 1–164. doi: 10.1016/s0301-0082(98)00048-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Moghaddam, B., and Javitt, D. (2012). From revolution to evolution: the glutamate hypothesis of schizophrenia and its implication for treatment. Neuropsychopharmacology 37, 4–15. doi: 10.1038/npp.2011.181

PubMed Abstract | CrossRef Full Text | Google Scholar

Moolenaar, W. H. (1995). Lysophosphatidic acid, a multifunctional phospholipid messenger. J. Biol. Chem. 270, 12949–12952. doi: 10.1074/jbc.270.22.12949

PubMed Abstract | CrossRef Full Text | Google Scholar

Moolenaar, W. H., and Hla, T. (2012). SnapShot: bioactive lysophospholipids. Cell 148, 378–378.e2. doi: 10.1016/j.cell.2012.01.013

PubMed Abstract | CrossRef Full Text | Google Scholar

Musazzi, L., Daniel, E., Maycox, P., Racagni, G., and Popoli, M. (2011). Abnormalities in α/β-CaMKII and related mechanisms suggest synaptic dysfunction in hippocampus of LPA1 receptor knockout mice. Int. J. Neuropsychopharmacol. 14, 941–953. doi: 10.1017/S1461145710001240

PubMed Abstract | CrossRef Full Text | Google Scholar

Mutoh, T., Rivera, R., and Chun, J. (2012). Insights into the pharmacological relevance of lysophospholipid receptors. Br. J. Pharmacol. 165, 829–844. doi: 10.1111/j.1476-5381.2011.01622.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Nagai, J., Uchida, H., Matsushita, Y., yano, R., Ueda, M., Niwa, M., et al. (2010). Autotaxin and lysophosphatidic acid1 receptor-mediated demyelination of dorsal root fibers by sciatic nerve injury and intrathecal lysophosphatidylcholine. Mol. Pain 6:78. doi: 10.1186/1744-8069-6-78

PubMed Abstract | CrossRef Full Text | Google Scholar

Nagy, V., Bozdagi, O., and Huntley, G. W. (2007). The extracellular protease matrix metalloproteinase-9 is activated by inhibitory avoidance learning and required for long-term memory. Learn. Mem. 14, 655–664. doi: 10.1101/lm.678307

PubMed Abstract | CrossRef Full Text | Google Scholar

Noguchi, K., Herr, D., Mutoh, T., and Chun, J. (2009). Lysophosphatidic acid (LPA) and its receptors. Curr. Opin. Pharmacol. 9, 15–23. doi: 10.1016/j.coph.2008.11.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Ohta, H., Sato, K., Murata, N., Damirin, A., Malchinkhuu, E., Kon, J., et al. (2003). Ki16425, a subtype-selective antagonist for EDG-family lysophosphatidic acid receptors. Mol. Pharmacol. 64, 994–1005. doi: 10.1124/mol.64.4.994

PubMed Abstract | CrossRef Full Text | Google Scholar

Park, H. J. (2014). Chemotherapy induced peripheral neuropathic pain. Korean J. Anesthesiol. 67, 4–7. doi: 10.4097/kjae.2014.67.1.4

PubMed Abstract | CrossRef Full Text | Google Scholar

Park, S. Y., Jeong, K. J., Panupinthu, N., Yu, S., Lee, J., Han, J. W., et al. (2011). Lysophosphatidic acid augments human hepatocellular carcinoma cell invasion through LPA1 receptor and MMP-9 expression. Oncogene 30, 1351–1359. doi: 10.1038/onc.2010.517

PubMed Abstract | CrossRef Full Text | Google Scholar

Peever, J. H., Shen, L., and Duffin, J. (2002). Respiratory pre-motor control of hypoglossal motoneurons in the rat. Neuroscience 110, 711–722. doi: 10.1016/s0306-4522(01)00594-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Peñalver, A., Campos-Sandoval, J. A., Blanco, E., Cardona, C., Castilla, L., Martín-Rufián, M., et al. (2017). Glutaminase and MMP-9 downregulation in cortex and hippocampus of LPA1 receptor null mice correlate with altered dendritic spine plasticity. Front. Mol. Neurosci. 10:278. doi: 10.3389/fnmol.2017.00278

PubMed Abstract | CrossRef Full Text | Google Scholar

Pilpel, Y., and Segal, M. (2006). The role of LPA₁ in formation of synapses among cultured hippocampal neurons. J. Neurochem. 97, 1379–1392. doi: 10.1111/j.1471-4159.2006.03825.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Regehr, W. G., Carey, M. R., and Best, A. R. (2009). Activity-dependent regulation of synapses by retrograde messengers. Neuron 63, 154–170. doi: 10.1016/j.neuron.2009.06.021

PubMed Abstract | CrossRef Full Text | Google Scholar

Renbäck, K., Inoue, M., and Ueda, H. (1999). Lysophosphatidic acid-induced, pertussis toxin-sensitive nociception through a substance P release from peripheral nerve endings in mice. Neurosci. Lett. 270, 59–61. doi: 10.1016/s0304-3940(99)00464-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Rivera, S., Khrestchatisky, M., Kaczmarek, L., Rosenberg, G. A., and Jaworski, D. M. (2010). Metzincin proteases and their inhibitors: foes or friends in nervous system physiology? J. Neurosci. 30, 15337–15357. doi: 10.1523/jneurosci.3467-10.2010

PubMed Abstract | CrossRef Full Text | Google Scholar

Roberts, C., Winter, P., Shilliam, C. S., Hughes, Z. A., Langmead, C., Maycox, P. R., et al. (2005). Neurochemical changes in LPA1 receptor deficient mice—a putative model of schizophrenia. Neurochem. Res. 30, 371–377. doi: 10.1007/s11064-005-2611-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Roza, C., Laird, J. M., Souslova, V., Wood, J. N., and Cervero, F. (2003). The tetrodotoxin-resistant Na+ channel Nav1.8 is essential for the expression of spontaneous activity in damaged sensory axons of mice. J. Physiol. 550, 921–926. doi: 10.1113/jphysiol.2003.046110

PubMed Abstract | CrossRef Full Text | Google Scholar

Roza, C., and Lopez-Garcia, J. A. (2008). Retigabine, the specific KCNQ channel opener, blocks ectopic discharges in axotomized sensory fibres. Pain 138, 537–545. doi: 10.1016/j.pain.2008.01.031

PubMed Abstract | CrossRef Full Text | Google Scholar

Sandkühler, J. (2009). Models and mechanisms of hyperalgesia and allodynia. Physiol. Rev. 89, 707–758. doi: 10.1152/physrev.00025.2008

PubMed Abstract | CrossRef Full Text | Google Scholar

Santin, L., Bilbao, A., Pedraza, C., Matas-Rico, E., López-Barroso, D., Castilla-Ortega, E., et al. (2009). Behavioral phenotype of maLPA1-null mice: increased anxiety-like behavior and spatial memory deficits. Genes Brain Behav. 8, 772–784. doi: 10.1111/j.1601-183X.2009.00524.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Schneggenburger, R., Sakaba, T., and Neher, E. (2002). Vesicle pools and short-term synaptic depression: lessons from a large synapse. Trends Neurosci. 25, 206–212. doi: 10.1016/s0166-2236(02)02139-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Scofield, M. D., Heinsbroek, J. A., Gipson, C. D., Kupchik, Y. M., Spencer, S., Smith, A. C. W., et al. (2016). The nucleus accumbens: mechanisms of addiction across drug classes reflect the importance of glutamate homeostasis. Pharmacol. Rev. 68, 816–871. doi: 10.1124/pr.116.012484

PubMed Abstract | CrossRef Full Text | Google Scholar

Segal, M., and Korkotian, E. (2016). Roles of calcium stores and store-operated channels in plasticity of dendritic spines. Neuroscientist 22, 477–485. doi: 10.1177/1073858415613277

PubMed Abstract | CrossRef Full Text | Google Scholar

Shano, S., Moriyama, R., Chun, J., and Fukushima, N. (2008). Lysophosphatidic acid stimulates astrocyte proliferation through LPA1. Neurochem. Int. 52, 216–220. doi: 10.1016/j.neuint.2007.07.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Shin, T.-J., Kim, H.-J., Kwon, B.-J., Choi, S.-H., Kim, H.-B., Hwang, S.-H., et al. (2012). Gintonin, a ginseng-derived novel ingredient, evokes long-term potentiation through N-methyl-D-aspartic acid receptor activation: involvement of LPA receptors. Mol. Cells 34, 563–572. doi: 10.1007/s10059-012-0254-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Shiono, S., Kawamoto, K., Yoshida, N., Kondo, T., and Inagami, T. (1993). Neurotransmitter release from lysophosphatidic acid-stimulated PC12 Cells: involvement of lysophosphatidic acid receptors. Biochem. Biophys. Res. Commun. 193, 667–673. doi: 10.1006/bbrc.1993.1676

PubMed Abstract | CrossRef Full Text | Google Scholar

Steiner, M. R., Urso, J. R., Klein, J., and Einer, S. M. (2002). Multiple astrocyte responses to lysophosphatidic acids. Biochim. Biophys. Acta 1582, 154–160. doi: 10.1016/s1388-1981(02)00150-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Suckau, O., Gross, I., Schrötter, S., Yang, F., Luo, J., Wree, A., et al. (2019). LPA1 , LPA2 , LPA4, and LPA6 receptor expression during mouse brain development. Dev. Dyn. 248, 375–395. doi: 10.1002/dvdy.23

PubMed Abstract | CrossRef Full Text | Google Scholar

Svennerholm, L., Boström, K., Jungbjer, B., and Olsson, L. (1994). Membrane lipids of adult human brain: lipid composition of frontal and temporal lobe in subjects of age 20 to 100 years. J. Neurochem. 63, 1802–1811. doi: 10.1046/j.1471-4159.1994.63051802.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Swerdlow, N. R., Weber, M., Qu, Y., Light, G. A., and Braff, D. L. (2008). Realistic expectations of prepulse inhibition in translational models for schizophrenia research. Psychopharmacology 199, 331–388. doi: 10.1007/s00213-008-1072-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Tabuchi, S., Kume, K., Aihara, M., Ishii, S., Mishina, M., and Shimizu, T. (1997). Lipid mediators modulate NMDA receptor currents in a Xenopus oocyte expression system. Neurosci. Lett. 237, 13–16. doi: 10.1016/s0304-3940(97)00792-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Thalman, C., Horta, G., Qiao, L., Endle, H., Tegeder, I., Cheng, H., et al. (2018). Synaptic phospholipids as a new target for cortical hyperexcitability and E/I balance in psychiatric disorders. Mol. Psychiatry 23, 1699–1710. doi: 10.1038/s41380-018-0053-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Thangavelu, K., Pan, C., Karlberg, T., Balaji, G., Uttamchandani, M., Suresh, V., et al. (2012). Structural basis for the allosteric inhibitory mechanism of human kidney-type glutaminase (KGA) and its regulation by Raf-Mek-Erk signaling in cancer cell metabolism. Proc. Natl. Acad. Sci. U S A 109, 7705–7710. doi: 10.1073/pnas.1116573109

PubMed Abstract | CrossRef Full Text | Google Scholar

Thomas, J. W., Novelli, A., Tao-Cheng, J.-H., Henneberry, R., Smith, H. H., and Banner, C. (1989). Developmental induction of glutaminase in primary cultures of cerebellar granule cells. Mol. Brain Res. 6, 47–54. doi: 10.1016/0169-328x(89)90027-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Tian, L., Stefanidakis, M., Ning, L., Lint, P., Nyman-Huttunen, H., Libert, C., et al. (2007). Activation of NMDA receptors promotes dendritic spine development through MMP-mediated ICAM-5 cleavage. J. Cell Biol. 178, 687–700. doi: 10.1083/jcb.200612097

PubMed Abstract | CrossRef Full Text | Google Scholar

Trimbuch, T., Beed, P., Vogt, J., Schuchmann, S., Maier, N., Kintscher, M., et al. (2009). Synaptic PRG-1 modulates excitatory transmission via lipid phosphate-mediated signaling. Cell 138, 1222–1235. doi: 10.1016/j.cell.2009.06.050

PubMed Abstract | CrossRef Full Text | Google Scholar

Uchida, H., Nagai, J., and Ueda, H. (2014). Lysophosphatidic acid and its receptors LPA1 and LPA3 mediate paclitaxel-induced neuropathic pain in mice. Mol. Pain 10:71. doi: 10.1186/1744-8069-10-71

PubMed Abstract | CrossRef Full Text | Google Scholar

Ueda, H., Neyama, H., Nagai, J., Matsushita, Y., Tsukahara, T., and Tsukahara, R. (2018). Involvement of lysophosphatidic acid-induced astrocyte activation underlying the maintenance of partial sciatic nerve injury-induced neuropathic pain. Pain 159, 2170–2178. doi: 10.1097/j.pain.0000000000001316

PubMed Abstract | CrossRef Full Text | Google Scholar

Velletri, T., Romeo, F., Tucci, P., Peschiaroli, A., Annicchiarico-Petruzzelli, M., Niklison-Chirou, M., et al. (2013). GLS2 is transcriptionally regulated by p73 and contributes to neuronal differentiation. Cell Cycle 12, 3564–3573. doi: 10.4161/cc.26771

PubMed Abstract | CrossRef Full Text | Google Scholar

Vogt, J., Yang, J., Mobascher, A., Cheng, J., Li, Y., Liu, X., et al. (2016). Molecular cause and functional impact of altered synaptic lipid signaling due to a prg-1 gene SNP. EMBO Mol. Med. 8, 25–38. doi: 10.15252/emmm.201505677

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, X., Bozdagi, O., Nikitczuk, J. S., Zhai, Z., Zhou, Q., and Huntley, G. W. (2008). Extracellular proteolysis by matrix metalloproteinase-9 drives dendritic spine enlargement and long-term potentiation coordinately. Proc. Natl. Acad. Sci. U S A 105, 19520–19525. doi: 10.1073/pnas.0807248105

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, Y., Huang, Y., Zhao, L., Li, Y., and Zheng, J. (2014). Glutaminase 1 is essential for the differentiation, proliferation and survival of human neural progenitor cells. Stem Cells Dev. 23, 2782–2790. doi: 10.1089/scd.2014.0022

PubMed Abstract | CrossRef Full Text | Google Scholar

Weiner, J. A., Fukushima, N., Contos, J. J., Scherer, S. S., and Chun, J. (2001). Regulation of schwann cell morphology and adhesion by receptor-mediated lysophosphatidic acid signaling. J. Neurosci. 21, 7069–7078. doi: 10.1523/jneurosci.21-18-07069.2001

PubMed Abstract | CrossRef Full Text | Google Scholar

Xie, W., Uchida, H., Nagai, J., Ueda, M., Chun, J., and Ueda, H. (2010). Calpain-mediated down-regulation of myelin-associated glycoprotein in lysophosphatidic acid-induced neuropathic pain. J. Neurochem. 113, 1002–1011. doi: 10.1111/j.1471-4159.2010.06664.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Ye, X., Fukushima, N., Kingsbury, M. A., and Chun, J. (2002). Lysophosphatidic acid in neural signaling. Neuroreport 13, 2169–2175. doi: 10.1097/00001756-200212030-00002

PubMed Abstract | CrossRef Full Text | Google Scholar

Yu, Y., Qin, J., Liu, M., Ruan, Q., Li, Y., and Zhang, Z. (2014). Role of Rho kinase in lysophosphatidic acid-induced altering of blood-brain barrier permeability. Int. J. Mol. Med. 33, 661–669. doi: 10.3892/ijmm.2014.1618

PubMed Abstract | CrossRef Full Text | Google Scholar