Xizhi Wang1
Benson O. A. Botchway
Xuehong Liu- 1Department of Histology and Embryology, Medical College, Shaoxing University, Zhejiang, China
- 2Institute of Neuroscience, Zhejiang University School of Medicine, Hangzhou, China
Spinal cord injury (SCI) can result in an irreversible disability due to loss of sensorimotor function below the lesion. Presently, clinical treatments for SCI mainly include surgery, drugs and postoperative rehabilitation. The prospective roles of bioscaffolds and exosomes in several neurological diseases have been reported. Bioscaffolds can reconnect lesion gaps as well as transport cells and bioactive factors, which in turn can improve axonal and functional regeneration. Herein, we explicate the respective roles of bioscaffolds and exosomes in SCI, and elucidate on the usage of combinational therapy involving bioscaffolds and extracellular vesicles (EVs) in improving SCI.
Introduction
Spinal cord injury (SCI) is a severe neurological trauma with high morbidity and mortality (Ni et al., 2015). The pathophysiological mechanism of SCI is still unclear. SCI pathological processes are divided into primary and secondary injury processes (Ozturk et al., 2018). We have extensively elucidated these SCI pathological processes in our previous reports (Liu et al., 2018; Xu L. et al., 2018; Zhou et al., 2018). In the event of SCI, the routine management will involve surgical, medicinal and rehabilitation therapies (Sandrow-Feinberg and Houlé, 2015; Frank and Roynard, 2018). Owing to the ineffectiveness of these therapies, the search for effective treatment strategies for SCI is of prime importance, most especially to clinicians and patients. There have been suggestions that the potential usage of bioscaffold and stem cell therapies could improve spontaneous functional recovery in SCI. Extracellular vesicles (EVs), a form of endogenous nanovesicles, have been and are still being studied extensively in some neurological disorders (Chopp and Zhang, 2015; Ojha et al., 2017; Osier et al., 2018). In this report, we delve into some of the studies that have been conducted pertaining to the contributory roles of bioscaffolds and EVs in SCI and present our perspective on the usage of combined bioscaffold-EVs in SCI.
The Effects of Bioscaffolds in SCI Treatment
Regeneration is hampered after SCI. This is because the microenvironment created following SCI is not conducive for cell migration and axonal growth. Axonal regulation is a vital part in nerve repair. Bioscaffolds can ameliorate the spinal cord microenvironment and direct cell behaviors such as migration, proliferation and differentiation (Caicco et al., 2013). Current research studies are focused on developing scaffolds that could steer axonal regeneration and reduce scar tissue formation. The combination of biomaterials with stem cells did improve SCI functional recovery (Khaing et al., 2014; Zweckberger et al., 2016). Biomaterial scaffolds have the ability to create a substrate where cell growth could be engineered in a highly controlled fashion (Mackenzie and Rademakers, 2008; Hakim et al., 2015). The combination of growth factors and biomaterial scaffolds demonstrated effective SCI repair by decreasing lesion cavity, promoted vascular formation and increased neural cell attachment and axonal outgrowth (Grulova et al., 2015). Spinal cord injured neurons have limited growth potential, and an adverse microenvironment could potentiate the differentiation of neural stem cells (NSCs) into astrocytes and oligodendrocytes rather than neurons (Fan et al., 2017; Piltti et al., 2017). Thus, in the event of SCI, a favorable microenvironment that has the capacity to promote NSCs differentiation and improve neurological functions will be paramount. Scaffolds possess superior biocompatibility and low immunogenicity, thus being able to establish a favorable microenvironment for SCI (Altinova et al., 2014; Takashima et al., 2015). Although the application of an ideal bioscaffold for SCI treatment in the clinical setting is presently of great interest, its potentiality in instigating inflammation is a drawback. Scaffolds can potentially induce immune responses in patients (Theodore et al., 2016; Zhao et al., 2017).
The capability of scaffolds in maintaining the normal state in cell differentiation processes is required for SCI recovery (Kadoya et al., 2016). Scaffold features, which include non-toxicity, non-carcinogenic, biocompatible and biodegradable are imperative for SCI therapy (Novikova et al., 2018). In the event of SCI, stem cell transplantations could potentially replace lost tissue components, contribute to remyelination of damaged axons and secrete growth factors (Karamouzian et al., 2012; Shin et al., 2018). Transplanted cells include embryonic/neuronal stem cells, mesenchymal stem cells (MSCs), Schwann cells and olfactory ensheathing cells (Vismara et al., 2017; Yang et al., 2017). Scaffold and transplantation of selective stem cells might remedy the issue of regeneration in SCI. Bioscaffolds could combine with stem cells; with the combination providing physical support for the lesion gap and steering cell migration, proliferation and differentiation. In favorable conditions, stem cells could differentiate into neurons and secrete growth factors. Bioscaffold-based stem cell therapy could provide a favorable microenvironment. Taken together, the features of combined bioscaffold-stem cell could improve SCI (Figure 1).
Figure 1. Ideal bioscaffold-based stem cell therapy for spinal cord injury (SCI).
Prospective Role of EVs in SCI Treatment
EVs
EVs are membrane vesicles that are released from a variety of cell types into the extracellular space (van der Pol et al., 2012). EVs mainly consist of exosomes (diameter: 30–100 nm), microvesicles (diameter: 100–1,000 nm) and apoptotic bodies (diameter: 1,000–5,000 nm; van der Pol et al., 2012; Iessi et al., 2017; Caruso Bavisotto et al., 2019). EVs have gained much attention in recent years (Verma et al., 2015). EVs were first discovered in sheep reticulocytes in 1983, with its name, “exosome,” coined in 1987 (Pan and Johnstone, 1983; Johnstone et al., 1987). EVs are small vesicles that contain nucleic acids such as DNA, messenger RNA (mRNA), long non-coding RNA (lncRNA), microRNA (miRNA), proteins and lipids (Hong et al., 2017; Mo et al., 2018; Torralba et al., 2018). EVs originate from the inward budding of cells called multivesicular bodies (MVBs). Undergoing a maturation process, intraluminal vesicles (pre-exosomes) that have accumulated in the MVBs blend with the plasma membrane, subsequently releasing EVs (Caruso Bavisotto et al., 2019). EVs’ life journey includes endosome biogenesis, transport, release and re-uptake by endocytosis (Wang et al., 2017).
EVs can be extricated by several methods including ultracentrifugation, filtration centrifugation, density gradient centrifugation and immunomagnetic separation (Schageman et al., 2013; Brownlee et al., 2014; Muller et al., 2014). A number of cells can secrete EVs in both normal and pathological conditions. EVs are naturally present in body fluids, including blood, saliva, urine, cerebrospinal fluid (CSF) and breast milk (Prada and Meldolesi, 2016). The numerous sources of EVs show their potentiality of being employed in the clinical setting, as they are readily available in the event that they are needed. In other words, EVs could be used extensively if they are effective and easy to obtain. That said, EVs derived from human plasma could potentially be unsafe. For example, EVs delivering pathological prions could affect normal cells and EVs carrying miR-29b could impede the neuroprotective function in HIV patients (Hu et al., 2012; Berrone et al., 2015; Caruso Bavisotto et al., 2019). Cellular prion protein (PrPC) from plasma-derived EVs might contribute to the pathogenesis and propagation of prion diseases such as transmissible spongiform encephalopathies (TSEs), a type of neurodegenerative disease (Berrone et al., 2015; Properzi et al., 2015b). The study by Nonaka et al. (2013) reported TAR DNA-binding protein 43 (TDP-43) aggregates to be potentially conveyed from one cell to the other, to some extent, via EVs. Aggregates of TDP-43 are implicated in both frontotemporal dementia and amyotrophic lateral sclerosis (ALS) with all these studies put across, choosing the safest source of exosomes is paramount. In this regard, we refer to the article by Campanella et al. (2019). One of the suggested choices out across by the authors was the employment of EVs that had could be extracted from the same patient so as to avoid the issue of immunogenicity-associated complications. These EVs, of course, would have to be subjected to therapies and tinkering. The only hindrance to this choice, however, will be the lengthened time that it will take for the therapy to be initiated following injury. The secretion of EVs by host cells to recipient cells could regulate the biological activities of the recipient cells through the substances that the EVs carry (De Toro et al., 2015). The molecular mechanisms involved in the secretion, uptake, transmission of signals and corresponding functions between cells are still unclear.
Potential Applications of EVs
EVs are involved in intercellular communication and play important roles in the regulation of stem cell maintenance, tissue repair and immunosurveillance (Katsman et al., 2012; Robbins and Morelli, 2014; Benito-Martin et al., 2015; Rani et al., 2015). EVs can transport molecules and modulate biological functions within recipient cells (Montecalvo et al., 2012; Logozzi et al., 2019). The multiple functions of EVs and their superiority such as small size have raised the possibilities for their development and usage as therapeutic, diagnostic and screening purposes for some diseases. For instance, miRNA-derived EVs could be used as non-invasive biomarkers to screen and diagnose lung cancer (Cazzoli et al., 2013). As a messenger of information exchange between cells, EVs could potentially transmit genetic information and proteins through the following manner: (1) EVs membrane can fuse with target cell membrane and directly release its RNAs or proteins directly; (2) EVs membrane protein can bind to target cell membrane protein and activate a series of signaling pathways; and (3) EVs membrane proteins can be cleaved by proteases in the extracellular matrix, with the cleaved fragments acting as ligands to bind to receptors on the target cell membrane and cause a cascade reaction (Wahlgren et al., 2012; Mulcahy et al., 2014; Yoon et al., 2014). EVs could be internalized by recipient cells through mechanisms such as endocytosis including clathrin-mediated endocytosis, phagocytosis, macropinocytosis and plasma or endosomal membrane fusion. Endocytosis is an energy-dependent process and is indicative of endocytic pathways (Mulcahy et al., 2014). The size, contents and membrane composition of EVs are heterogeneous and depend on the cellular source, state and environmental conditions. The function of exosomes also depends on the type of cells where they are derived, which could be utilized in many applications such as immune response, antigen presentation, cell migration and differentiation, and tumor invasion (Frydrychowicz et al., 2015; Pusic et al., 2016). Tumor-derived EVs were involved in the exchange of genetic information between tumor cells and normal cells, which was impetus to tumor invasion or inhibition (Zech et al., 2012). The study by Cossetti et al. (2014) reported the possible key role of EVs in serving as carriers in the soma-to-germline transmission of nucleic acids (specifically RNA). EVs are involved in tumor metastasis and chemotherapeutic drug resistance, which might be the cause of tumor refractoriness (Federici et al., 2014; Xiao et al., 2014; Kreger et al., 2016; Lugini et al., 2016). Exactly, in turn, EVs-mediated treatments in tumors attracted the attention of many researchers (Jang et al., 2013; Pascucci et al., 2014; Saari et al., 2015; Kim M. S. et al., 2018). The use of EVs as a delivery mechanism of chemotherapeutics such as cisplatin, doxorubicin and highly cytotoxic drugs such as acridine orange increases the therapeutic index of a tumor (Toffoli et al., 2015; Hadla et al., 2016; Agrawal et al., 2017; Iessi et al., 2017). While the vast majority of these studies showed a promising drug delivery system of EVs in cancer, EVs could be applied in other conditions such as SCI owing to its delivery efficacy, low immunogenicity and high biocompatibility.
EVs act on the innate immune system as paracrine messengers and have been described as pro-inflammatory mediators in many chronic inflammatory diseases, such as rheumatoid arthritis and atherosclerosis (Boilard et al., 2010; Holder et al., 2012; Hoyer et al., 2012). They also exert immunomodulatory properties against both infectious agents and tumors, and alleviate immune abnormalities such as graft-vs.-host disease (Kordelas et al., 2014). On the basis of these features, EVs could play a contributory role in both the diagnosis and treatment of immune-related or inflammatory diseases. Recently, researches on EVs in many fields are in full swing (Bei et al., 2017; Fang et al., 2018; Huang et al., 2018; Li H. et al., 2018; Nojehdehi et al., 2018). Also, EVs could be used for cell co-culturing in vitro or in vivo injection with biological activity. Another key feature of EVs is their ability to cross the blood-brain barrier (BBB; Zhuang et al., 2011; Chen et al., 2016). EVs in both circulation and the CSF could make these vesicles unfold long-distance communication and transport bioactive molecules to selected targets. Circulating EVs could reveal the status of the tissue origin and provide an accurate means for minimally invasive diagnosis of neurological diseases. EVs have been applied as drug delivery vehicles in Parkinson’s disease (Haney et al., 2015). Experiments in rats showed MSCs-derived EVs attenuated inflammation and demyelination of the central nervous system (CNS; Li Z. et al., 2018).
Contribution of EVs in SCI Treatment (Table 1)
Results from published EVs studies have been encouraging, which in turn may increase their potential of being applied in SCI (Xin et al., 2013; Properzi et al., 2015a; Zhang et al., 2015; Kim et al., 2016; Liu et al., 2019; Ren et al., 2019). The innate immune response plays a role in neuroinflammation following CNS injury via activation of inflammasomes (Haneklaus et al., 2013; de Rivero Vaccari et al., 2016). The expressions of nucleotide-binding-and-oligomerization domain (NOD)-like receptor protein-1 (NLRP-1) inflammasome, apoptosis-associated speck-like protein containing a caspase recruitment domain (ASC) and caspase-1 are significantly elevated in spinal cord neurons following trauma. NLRP1 inflammasome proteins are present in EVs derived from CSF after SCI. EVs-mediated short-interfering RNA (siRNA) delivery inhibited the inflammatory process following SCI (de Rivero Vaccari et al., 2016). Owing to the lack of effective treatment for the primary phase of SCI, the inhibition of the secondary phase of SCI by effective measures could potentially curtail SCI-associated disabilities. One of these effective measures, we believe, lies in the application of EVs due to its numerous beneficial factors. EVs released from mesenchymal stromal cells attenuated apoptosis, inflammation and promoted angiogenesis following SCI (Huang et al., 2017). Human umbilical cord MSCs-derived EVs promoted functional recovery in SCI mice by curtailing inflammation (Sun et al., 2018). EVs derived from miR-133b-modified MSC promoted recovery after SCI (Li D. et al., 2018). MSC-derived EVs reduced SCI-induced A1 astrocytes and exerted anti-inflammatory and neuroprotective effects following SCI (Wang et al., 2018). The EVs isolated from differentiated PC12 cells and MSCs exerted a protective role in SCI treatment by inhibiting the expression of phosphatase and tensin homolog (PTEN; Xu G. et al., 2018). All these published studies evince the therapeutic role of exosomes in SCI. Although the specific mechanisms pertaining to the therapeutic effects of EVs in SCI have not been clearly defined, there is the possibility that the mechanisms might involve an inhibitory effect on neuronal cell apoptosis and inhibition of inflammatory responses in a series of signaling pathways: (1) Active Wnt proteins are secreted on EVs; (2) EVs could transfer epidermal growth factor receptor (EGFR) to endothelial cells, and subsequently activate both MAPK and Akt pathways; (3) Exosomal miR-9 could stimulate angiogenesis by activating JAK-STAT signal pathway; (4) EVs from activated CD8+ T-cell could activate ERK and NF-κB pathways; and (5) nanovesicles could activate the JNK and c-Jun signaling cascades in MSCs (Al-Nedawi et al., 2009; Cai et al., 2012; Zhuang et al., 2012; Kim H. Y. et al., 2018). In view of the fact that the precise pathophysiology of EVs in SCI presently remains unclear, these related signaling pathways warrant further studies as they could potentially shed light on EVs’ pathophysiology.
Table 1. Summary of applications of exosomes.
EVs are characterized by their ability to transfer proteins and genetic information to instruct intercellular communication. Through the employment of EVs, we are of the view that the alteration of detrimental messages produced in damaged tissues could potentially be instrumental in SCI treatment. SCI could be improved by loading certain substances that have anti-inflammatory effects. Since the instigation of signaling pathways by inflammatory factors is one of SCI pathogenesis, EVs could be employed to inhibit the inflammatory process following injury. For example, a specific inhibitor of certain signaling pathways could be combined with EVs and injected into the injured spinal cord. Also, the encapsulation and transportation of proteins, RNAs and drugs might provide novel insights for the treatment of diseases such as SCI. RNAs and proteins packaged within EVs are stable, thus, increasing their potential application in clinical therapies. In two separate animal studies, mesenchymal stromal cells-derived EVs promoted neurovascular plasticity and functional recovery in stroke and traumatic brain injury (Xin et al., 2013; Zhang et al., 2015). Since EVs have the potential to exert beneficial therapeutic effects in these neurological diseases, we believe it might exert similar effects in SCI. That said, a thorough pre-clinical and clinical studies are still needed to further evidence its suitability in SCI therapy (Figure 2).
Figure 2. Prospective role of extracellular vesicles (EVs) combined with bioscaffold in stem cell therapy for SCI.
Combination of EVs and Biological Scaffolds
We do believe a substantial improvement in SCI repair could lie in the usage of combinational treatment methods. Though several combinations have been evidenced to be significantly better than single treatments, the complete recovery following severe SCI has not been found (Tabesh et al., 2009). One of the promising SCI therapies would be to incorporate biodegradable polymer grafts with other therapeutic strategies. The study by Huleihel et al. (2016) showed that vesicles (from “exomere”-sized particles to “microvesicles” of 1,000 nm) are associated with scaffolds placed in different organ sites and that those vesicles have different miRNA signatures, implying they might come from tissue-specific cellular sources. These “inherent” vesicles exhibited certain ex-vivo effects on neurite-like outgrowth from neuroblastoma cells and promoted an M2-type macrophage phenotype. Thus, the vesicles already present might influence the surrounding cellular composition. It would, therefore, be safe and logical to hypothesize that activated astrocytes and microglia in a SCI setting could release pro-inflammatory vesicles that could reside for potentially long periods of time on these scaffolds, and possibly aid in the maintenance of the inflammatory environment. Implantation of an ideal scaffold could potentially inhibit glial scar formation and guide the orientated axonal growth along the scaffold. This, in turn, could reconnect neuronal relays between nascent and host neurons and facilitate recovery of neurological function after SCI. Additionally, an ideally modified scaffold integrating bioactive factors might potentially exhibit neuroprotective effects through its dispensation of physical support to bridge the lesion gap following spinal cord transection or resection, as well as providing guidance cues in nerve fiber regrowth and functional regeneration of neural stem cells. Owing to the microenvironment affecting spinal cord repair after injury, the provision of a suitable microenvironment as well as the inhibition of adverse environments during SCI repair is paramount. Scaffold implantation could potentially induce immune responses or inflammation. This, of course, would not be conducive to SCI repair and would limit its clinical therapeutic employment. In view of this, we hypothesize that EVs combined with biological scaffold might hold promise for spinal cord regeneration across the injured site with fewer side effects. Also, the delivery of selective cargo in EVs that attenuates adverse effects while exerting their therapeutic effects would improve SCI. Stem cells have the potential of serving as effective therapeutics for severe SCI provided that: (1) the activation of biological factors is strictly controlled; (2) the differentiation profiles of stem cells are properly regulated; and (3) the microenvironment is suitable. One risk of stem cells application is their potential of resulting in tumorigenesis (Rodriguez et al., 2012). MSCs administration might cause a stoppage in the distal blood vessels due to their relatively large cell size (Furlani et al., 2009). Thus, fully using the advantages of stem cells while avoiding disadvantages is a critical step toward applying them to SCI. Studies have attributed the main therapeutic functions of stem cells to the paracrine mechanisms, where EVs might be the most valuable therapeutic factor (Ratajczak et al., 2014). EVs have low immunogenicity, can cross the BBB and effectively deliver functional molecules such as siRNA, miRNA and drugs to target cells (Alvarez-Erviti et al., 2011; Zhuang et al., 2011; Fais et al., 2016). Through the employment of receptor-mediated endocytosis for internalization, EVs assisted in the delivery of drugs to target cells; this was irrespective of the concentration gradient (Wang et al., 2017). These characteristics support the feasibility of being used in SCI treatment. Also, the release of functional cargo in EVs from a suitable scaffold might play a significant role in cell surface interactions, cell proliferation and migration and interconnectivity. We do believe that in the event of SCI, stem cells-derived EVs could reduce the complication associated with scaffolds and improve the conveyance of nutrients to the injured site, which, in turn, could potentially enhance axonal regeneration.
MSC-derived EVs have been reported to be non-immunogenic in the autologous setting and is well tolerated in humans (Kusuzaki et al., 2017). Several studies have evinced the feasibility of MSC-derived EVs in SCI treatment (Kim H. Y. et al., 2018; Li D. et al., 2018; Sun et al., 2018; Wang et al., 2018; Xu G. et al., 2018; Liu et al., 2019). In the light of these, MSC-derived EVs could potentially be employed in SCI therapy. With multifarious advantages such as diverse sources, small size and ability to cross the BBB, the combination of EVs with bioscaffold might improve SCI recovery. Just as stem cells can combine with scaffold, EVs could also combine with scaffolds in a similar manner as evidenced in several studies (Gao et al., 2014; Gurruchaga et al., 2017; DeBrot and Yao, 2018). Briefly, through a series of techniques such as cell culture, stimulation and EVs isolation and identification, EVs could be blotted onto scaffold under sterile conditions and left still for hours for the EVs to be completely absorbed to finalize the combination of EVs and scaffolds (Zhang et al., 2016, 2017; Wei et al., 2019). EVs derived from human-induced pluripotent stem cell-derived MSC combined with tricalcium phosphate (β-TCP) effectively promoted bone repair and regeneration in a rat model of calvarial bone defects (Zhang et al., 2016). This study established a strong possibility and regulation for the practical study of biological scaffolds combined with EVs. On the basis of EVs features such as information communication, signaling intervention, drug delivery, stem cell sustenance and immunosurveillance, the employment of bioscaffold-based EVs therapy could potentially improve SCI.
Conclusion and Future Perspective
Axonal regeneration of CNS in their native environment is intricate due to inhibitory functions in their extracellular environment. This, in turn, complicates the management of neurological disorders, including SCI. Several natural and synthetic polymers have been used as either scaffolds or within scaffolds for nerve regeneration. EVs that can be modified and loaded with drugs or therapeutic agents are emerging to improve SCI therapy efficiency, and exosomal cargo is an ideal biomarker that can elucidate the complex mechanisms appertaining to SCI. The stability of EVs in peripheral circulation suggests that they can be used in SCI recovery. EVs can transfer their contents to recipient cells, and can also be combined with either scaffold or stem cells, resulting in augmented neuronal differentiation and favorable microenvironment for SCI repair. In order to expedite the usage of combinational therapy involving EVs and bioscaffolds for SCI treatment in the clinical setting, we do suggest the following:
1. Thorough elucidation of the specific type of EVs/parental cells to employ in the event of SCI.
2. Thorough investigation of the gold standard approach to isolating EVs and the tools for tracking EVs production, uptake and long-term distribution;
3. Comprehensive elucidation of the precise mechanisms underlying the application of EVs such as signaling pathways;
4. Exploration of inexpensive but excellent bioscaffolds that could effectively bind and release EVs in a rational manner (i.e., exosomes that could be released at the right time and place);
5. Extensive investigation of the long-term possible adverse reactions and response measures to these adverse reactions.
Additionally, larger clinical studies together with the suggested points are also warranted. We do intend to systematically investigate some of these suggestions in our future studies.
Author Contributions
XL designed the study. XW, BB, YZ, JY and XL prepared the first draft of the manuscript and revised the manuscript. All authors approved the final article.
Funding
This work was supported by the Natural Science Foundation of Zhejiang Province (No. LY19H170001) and Public Technology Applied Research Projects Foundation of Shaoxing City (No. 2017B70066).
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.
Abbreviations
SCI, spinal cord injury; NSCs, neural stem cells; EVs, extracellular vesicles; mRNA, messenger RNA; lncRNA, long non-coding RNA; miRNA, microRNA; MVBs, multivesicular bodies; CSF, cerebrospinal fluid; PrPC, cellular prion protein; TSEs, transmissible spongiform encephalopathies; BBB, the blood-brain barrier; CNS, the central nervous system; NOD, nucleotide-binding-and-oligomerization domain; NLRP-1, nucleotide-binding-and-oligomerization domain-like receptor protein-1; ASC, apoptosis-associated speck like protein containing a caspase recruitment domain; siRNA, short-interfering RNA; MSCs, mesenchymal stem cells; PTEN, phosphatase and tensin homolog; EGFR, epidermal growth factor receptor; TCP, tricalcium phosphate.
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Keywords: spinal cord injury, stem cell therapy, neuronal damage, functional and axonal regeneration, bioscaffolds, extracellular vesicles
Citation: Wang X, Botchway BOA, Zhang Y, Yuan J and Liu X (2019) Combinational Treatment of Bioscaffolds and Extracellular Vesicles in Spinal Cord Injury. Front. Mol. Neurosci. 12:81. doi: 10.3389/fnmol.2019.00081
Received: 24 January 2019; Accepted: 14 March 2019;
Published: 12 April 2019.
Edited by:
Juan Pablo de Rivero Vaccari, University of Miami, United StatesReviewed by:
Stefano Fais, Istituto Superiore di Sanità (ISS), ItalyMichael Graner, University of Colorado Denver, United States
Copyright © 2019 Wang, Botchway, Zhang, Yuan and Liu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Xuehong Liu, bGl1eHVlaDY1ODhAMTI2LmNvbQ==