Anett Stéger
Michael Palmgren- Department of Plant and Environmental Sciences, University of Copenhagen, Copenhagen, Denmark
Root hairs are tubular outgrowths of epidermal cells that increase the root surface area and thereby make the root more efficient at absorbing water and nutrients. Their expansion is limited to the root hair apex, where growth is reported to take place in a pulsating manner. These growth pulses coincide with oscillations of the apoplastic and cytosolic pH in a similar way as has been reported for pollen tubes. Likewise, the concentrations of apoplastic reactive oxygen species (ROS) and cytoplasmic Ca2+ oscillate with the same periodicity as growth. Whereas ROS appear to control cell wall extensibility and opening of Ca2+ channels, the role of protons as a growth signal in root hairs is less clear and may differ from that in pollen tubes where plasma membrane H+-ATPases have been shown to sustain growth. In this review, we outline our current understanding of how pH contributes to root hair development.
Introduction
Root hairs are single tubular extensions of root cells that enhance water and nutrient uptake by increasing the root surface area. Furthermore, they facilitate beneficial microbial interactions. Root hairs develop from a subset of epidermal cells, the trichoblasts, but not from the hairless atrichoblasts. The fate of root epidermal cells seems to be determined at an early stage of development as trichoblasts are distinguishable from atrichoblasts prior to the emergence of the root hair, partially due to their shorter cell length (Dolan et al., 1994; Masucci et al., 1996). When epidermal cells enter the maturation zone, root hair-promoting transcription factors are activated and then the root hair initiation site is determined (Balcerowicz et al., 2015).
Several events during root hair initiation and subsequent growth are already well characterized. After the determination of the initiation site, the first morphological sign of root hair development is the appearance of a “bulge” on the outer wall of the trichoblast (Dolan et al., 1993); (Figure 1A). In Arabidopsis thaliana, it is followed by two phases of root hair growth: an initial period of slow growth (0.2–0.5 μm/min) and subsequent rapid growth (1–2.5 μm/min) (Dolan et al., 1994). The initial period is likely used for organizing the elements of the growth machinery to prepare the cell for the second phase: tip growth. Tip growth is a form of polar growth during which root hairs expand at the tip (Bibikova and Gilroy, 2003). In growing root hairs, the subapical region contains the endoplasmic reticulum, mitochondria, and Golgi bodies, while a large central vacuole fills the basal region (Miller et al., 2000); (Figure 1B). The extreme apex is the destination for high levels of secretory vesicles that carry the building materials for the growing plasma membrane and cell wall (Sherrier and VandenBosch, 1994; Galway et al., 1997; Miller et al., 2000). At the end of the tip-growing phase, Arabidopsis root hairs reach a final length of approximately 1 mm and are 10 μm in diameter (Grierson and Schiefelbein, 2002).
Figure 1. Schematic representation of a growing root hair. (A) The pH changes during bulge formation in Arabidopsis. The pH values are based on data in Bibikova et al. (1998). Colors indicate a localized pH increase (blue) and decrease (red) at the site of initiation in trichoblasts. (B) Schematic representation of the cytosolic pH gradient and the organelles within a growing root hair. The figure is adapted from Datta et al. (2011). A more alkaline cytosolic pH at the root hair tip compared to the base reflects measurements by Bai et al. (2014). (C) Graphical illustration of proton fluxes and oscillatory pH changes at the tip during root hair growth. Light purple arrows indicate net proton fluxes. The pH values are based on the analysis of Monshausen et al. (2007). (D) Growth rate, intracellular Ca2+, extracellular pH, and ROS oscillations on a time scale. The figure is adapted from Cárdenas (2009). Time values are from Monshausen et al. (2007) and Monshausen et al. (2008). The dashed curve represents the expected cytosolic pH oscillations. (E) Graphical illustration of how the cell wall pH could influence cell wall cross-linking. The figure is adapted from Schoenaers et al. (2017). (F) Overview of how cytoplasmic pH changes might influence actin polymerization and depolymerization based on the hypothesis from Lovy-Wheeler et al. (2006).
The mechanism of tip growth is complex and involves the transport of secretory vesicles toward the tip, dynamic actin and microtubule cytoskeletal networks, changes in reactive oxygen species (ROS) and Ca2+ gradients, as well as changes in the activity of cell wall-modifying enzymes and other processes (Mendrinna and Persson, 2015; Eljebbawi et al., 2020; Mase and Tsukagoshi, 2021). Furthermore, it has long been known that a current of protons (H+) enters root hairs at the tip and leaves at the base (Weisenseel et al., 1979); (Figure 1C), but its role in root hair development and growth is uncertain (Cárdenas, 2009; Schoenaers et al., 2017; Siao et al., 2020). In this review, we summarize what is known about the role of protons and pH changes in the emergence and growth of root hairs, and we highlight aspects that merit further investigation. As tip growth is not unique to root hairs, such knowledge could be useful for understanding how other tip-growing structures develop, such as pollen tubes, fungal hyphae, fucoid algal cells, moss protonemata, and nerve fibers in animals.
pH changes during bulging: An effect or a cause?
Bulging at the trichoblast has long been known to correlate with pH changes at both the apoplast (acidification) and cytoplasm (alkalinization) (Bibikova et al., 1998; Fasano et al., 2001); (Figure 1A). A drop in pH (from ~5 to 4.5) occurs at the root hair initiation site of the cell wall. This localized cell wall acidification is not present before bulging and lasts just until the root hair reaches the tip-growing stage (Bibikova et al., 1998). When the cell wall is acidified, the cytoplasm is alkalinized, suggesting that the pH changes are due to the cellular export of protons (Bibikova et al., 1998). Inhibiting the extracellular pH drop with strong buffers prevents root hair initiation, but as the cell wall returns to acidic pH, bulging restarts. These observations have been interpreted as evidence that the pH change is the cause and not the result of cell wall bulge initiation. However, cell wall acidification alone is not sufficient to cause bulging, as lowering the pH of the entire trichoblast to 4.5 does not lead to the emergence of bulges or general cell wall swelling (Bibikova et al., 1998), which does not exclude the possibility that localized pH changes might cause bulging.
A cytosolic pH gradient and oscillating pH
Cytosolic pH can be measured with genetically encoded biosensors (Walia et al., 2018) that are less prone to artifacts associated with trapped or injected fluoroprobic dyes (Graber et al., 1986). In growing root hairs expressing a pH-sensitive ratiometric variant of Aequorea victoria green fluorescent protein (GFP-H148D; Elsliger et al., 1999), the cytosolic pH at the tip was measured and shown to oscillate between pH 7.4 and 7.6 (Monshausen et al., 2007); (Figure 1C). In this work, cytosolic pH at the base of root hairs was not reported. A subsequent study employed a pH-sensitive GFP from Ptilosarcus gurneyi (Pt-GFP; Schulte et al., 2006) and found tip cytosolic pH to be more alkaline than that at the base of root hairs (Bai et al., 2014); (Figure 1B). This observation is surprising considering that protons enter at the tip and leave the cytosol at the base (Weisenseel et al., 1979) and is different from the pH profile observed in pollen tubes, another tip-growing system. In lily (Lilium longiflorum) pollen tubes, cytosolic pH at the extreme apex was measured using an injected ratiometric pH sensitive dye (2′,7′-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein (BCECF)-dextran) and was found to be more acidic than a constitutive cytosolic alkaline band in the subapical region (Feijó et al., 1999); (Figure 2A). In this system, proton influx was revealed at the extreme apex, while efflux was reported in the region of the alkaline band (Feijó et al., 1999); (Figure 2A). Ratiometric pHluorin is another pH-sensitive GFP variant (Haseloff et al., 1997; Miesenböck et al., 1998) that has been used to image cytosolic pH in Arabidopsis pollen tubes (Hoffmann et al., 2020). This study found the cytosolic pH at the tip to be more acidic than that in the base of the pollen tube but failed to detect a subapical alkaline band (Hoffmann et al., 2020); (Figure 2B). Higher resolution cytosolic pH measurements in root hairs may resolve whether cytosolic pH at the extreme apex of root hairs is indeed acidic compared to the basal parts.
Figure 2. Schematic representation of growing pollen tubes from the pH point of view. (A) The cytosolic pH gradient and pH oscillations in growing Lilium longiflorum pollen tubes. Values for the pH gradient and the cytosolic pH oscillation in the alkaline band are based on measurements in Feijó et al. (1999). Question marks indicate undetermined pH values or unknown distribution of plasma membrane H+-ATPases. Color codes represent the cytosolic pH gradient, where red indicates slightly more acidic pH and blue more alkaline pH compared to the rest of the cytoplasm. (B) The cytosolic pH gradient and pH oscillations in growing Arabidopsis pollen tubes. Values for the pH gradient and the cytosolic pH oscillation are based on Hoffmann et al. (2020). Red indicates a more acidic pH, while blue indicates a more alkaline pH. Question marks indicate undetermined pH values.
Growth analysis suggests that a consistent oscillatory root hair growth is associated with the pH oscillations at the tip with approximately two pulses per minute (Monshausen et al., 2007; Wu et al., 2007); (Figures 1C,D). These pH oscillations occur with the same periodicity as growth but out of phase. Cross-correlation analysis revealed that a decrease in extracellular pH precedes rhythmic root hair growth, whereas the maximal increase in extracellular pH lags behind growth by approximately 7 seconds (Monshausen et al., 2007); (Figure 1D). These pH oscillations are observed exclusively at the apical 5 to 10 μm of the root hair tip, not along the shanks and base, and no such changes were reported for non-growing root hairs (Monshausen et al., 2007). At the root hair apex, each extracellular alkalinization event is accompanied by transient cytosolic acidification likely due to a flux of protons from the cell wall toward the cytosol (Monshausen et al., 2007). As a result, the apoplastic pH shifts from approximately 5.4 to 5.8 and the cytosolic pH from 7.6 to 7.4; the difference in amplitude is likely due to the different buffering capacity of the apoplast and cytosol (Oja et al., 1999); (Figure 1C). There appears to be a limit to the tolerance to such pH changes, as growing root hairs tend to burst at the tip when the pH of the growth medium is artificially lowered to 4.5, while root hair growth is rapidly inhibited when the medium pH is increased to pH 8 (Monshausen et al., 2007).
These oscillatory pH changes may be required for control of actin dynamics in the growing root hair. In root hairs, long actin bundles run longitudinally along the root hair and branch out close to the tip (Cárdenas et al., 1998), and root hair growth is associated with constant polymerization of actin (Vazquez et al., 2014). Dynamic actin reorganization involves the assembly and disassembly of actin filaments that are likely regulated by pH-sensitive actin-binding proteins (Vazquez et al., 2014); (Figure 1F). In pollen tubes, alkalinization of cytosolic pH promotes actin-depolymerizing factor (ADF) protein activity so it becomes more efficient in actin depolymerization at the minus end and supports growth at the plus end (Chen et al., 2002; Lovy-Wheeler et al., 2006). It remains to be determined whether an oscillatory cytosolic pH controls actin dynamics in root hairs.
Role of pH change in cell wall loosening
The root hair cell wall has different characteristics at the apex and in the non-expanding parts: it is thin at the growing tips and turns into a thicker, stronger, multi-layered cell wall in the shanks of root hairs (Galway, 2006). The root hair cell wall is composed mainly of (xylo)glucans, pectins, and O-glycoproteins (Galway et al., 2011; Velasquez et al., 2011; Peña et al., 2012). Lack of any of these polymers inhibits tip growth, suggesting that they operate together to control polarized growth (Bernhardt and Tierney, 2000; Favery et al., 2001; Pang et al., 2010; Ringli, 2010; Park et al., 2011; Velasquez et al., 2011; Zabotina et al., 2012; Wang et al., 2014). In response to oscillating pH changes in the tip, cell wall-loosening enzymes with different pH optima could in principle contribute to oscillating growth by alternating between loosening and rigidifying the cell wall (Schoenaers et al., 2017); (Figure 1E).
Possible cell wall-loosening enzymes in root hairs could be expansins. These proteins mediate acid-induced expansion by disrupting the bonds between cellulose and hemicellulose residues. Expansins are most active at acidic pH; for example, alpha and beta expansins (EXPs) have a pH optimum of around 4.5 (McQueen-Mason et al., 1992). EXP7 and EXP18 were detected in the cell walls of trichoblasts but not atrichoblasts, pointing to their role in root hair development (Cho and Cosgrove, 2002). Expansins were also shown to localize at the bulge site of maize (Zea mays) roots (Baluška et al., 2000). Their important role in root hair initiation is also supported by the finding that in barley (Hordeum vulgare), a root hairless mutant (rhl1.a) is defective in expression of the HvEXPB1 gene, which encodes a β-expansin (Kwasniewski and Szarejko, 2006).
While the acidic pH shift activates expansins, it may actually inhibit other cell wall proteins, e.g., pectate lyases. Pectate lyases cleave glycosidic linkages with an alkaline pH optimum of ~7.5 to 8 (Ouattara et al., 2010). These enzymes are expressed in pollen tubes, and it was suggested that they are required for pectin degradation during tip growth (Wing et al., 1990). A pectate lyase, ROOT HAIR-SPECIFIC 14 (RHS14), was shown to be expressed in Arabidopsis root hairs, suggesting that pectate lyases might also be involved in regulating cell wall loosening in these tubular structures (Su-Kyung et al., 2009).
Xyloglucan endotransglycosylases (XETs) are also expressed in root hairs. A highly localized up-regulation of their activity was reported exclusively at the root hair initiation site before any visible bulge formation (Vissenberg et al., 2001), which points to an important role of XETs during the initial phase. However, XET activity was uniform along the length of the growing root hair suggesting that it does not have a key role in guiding polar growth in this system. Known XETs have a pH optimum of approximately 5 to 6.5 (Han et al., 2016). However, such a pH range is higher than the reported pH 4.5 of the cell wall during bulging (Bibikova et al., 1998). Vissenberg et al. (2001) showed that this lower pH of 4.5 does not substantially affect XET activity in initiating root hairs, while no activity is detected at the initiation site if the pH is increased to 7. Therefore, it seems that XET activity is also pH dependent and that an acidophilic XET isoform accumulates at the root hair initiation site (Vissenberg et al., 2001). Accordingly, transient pH changes at the cell wall could affect cell wall dynamics.
A putative role of plasma membrane H+-ATPases in root hair growth
Work on pollen tubes has shown that autoinhibited plasma membrane H+-ATPases (AHAs; AHA6, AHA8, and AHA9) sustain pollen tube growth, as a triple mutant deficient in these ATPases shows severe growth defects (Hoffmann et al., 2020). In pollen tubes, reverse fountain cytoplasmic streaming has been described where protons are exported at the shanks and imported at the pollen tube tip. This movement of protons likely is made possible by the presence of these plasma membrane H+-ATPases in the shanks and their absence from the tip (Hoffmann et al., 2020); (Figure 2B).
The first experiments pointing toward the involvement of plasma membrane H+-ATPases in root hair growth were performed with pharmacological inhibitors. Cyanide indirectly inhibits plasma membrane H+-ATPases by depleting cytosolic ATP (Lew and Spanswick, 1984), while vanadate competes with phosphate at the catalytic site of P-type ATPases, leading to direct inhibition of these pumps (Cantley et al., 1977; Sze, 1984). Both compounds inhibit root hair initiation and root hair growth (Bibikova et al., 1998). Even though these compounds are not specific for plasma membrane H+-ATPases, the results suggest that root hair growth is ATP dependent and is possibly carried out by P-type ATPases, a large family of primary active pumps to which plasma membrane H+-ATPases belong.
Of the 11 AHAs present in the Arabidopsis genome, AHA1, AHA2, AHA4, AHA5, AHA7, AHA9, and AHA10 are expressed in root hairs (Moriau et al., 1999; Palmgren, 2001; Santi and Schmidt, 2009; Młodzińska et al., 2014). The presence of almost all AHA isoforms in Arabidopsis root hairs suggests a high level of redundancy. Functional redundancy of plasma membrane H+-ATPases has been reported previously in pollen tubes where single aha6, aha8, and aha9 mutants show very mild phenotypes, whereas a triple aha6 aha8 aha9 mutant is strongly compromised in growth (Hoffmann et al., 2020).
Strong enrichment of AHA7 transcripts was reported in Arabidopsis root hairs that was two orders of magnitude higher in root hairs compared to other root cells (Lan et al., 2013). Furthermore, in the hairless Arabidopsis mutant rhd2, AHA7 was 3.6-fold less abundant than in the wild type (Jones et al., 2006). Analysis of loss of function aha7 mutants in Arabidopsis showed that the pump is important during special conditions as the number of root hairs decreased under Fe (Santi and Schmidt, 2009) and phosphate (Yuan et al., 2017) deficiency. This would suggest that in Arabidopsis, AHA7 is involved in the root hair initiation process under limiting conditions (Santi and Schmidt, 2009). However, no significant changes in root hair length and density could be observed in aha7 mutant lines grown under control conditions. This suggests that at least under normal conditions AHA7 serves a redundant function with other plasma membrane H+-ATPases (Hoffmann et al., 2019). AHA7 is unique among AHAs in that it is equipped with a pH-sensitive loop exposed to the apoplastic side of the plasma membrane, which inactivates the pump when the extracellular pH dips below pH 6.0 through protonation of an acidic group in the loop. Thus, proton export by AHA7 may be inhibited when the apoplast is acidified to a certain extent and reactivated as the apoplastic pH increases again. This could imply a mechanism for generating pH oscillations during tip growth (Hoffmann et al., 2019).
AHA2, a predominant plasma membrane H+-ATPase in roots (Harper et al., 1990; Fuglsang et al., 2007), is also expressed in Arabidopsis root hairs (Młodzińska et al., 2014). Loss of AHA2 does not alter root hair density under control conditions but leads to increased root hair length, just like the lack of both AHA2 and AHA7 (Hoffmann et al., 2019). This phenotype is not likely to be due to overcompensation from other AHAs, as application of the P-type ATPase inhibitor vanadate at low concentrations (25 μM), which is sufficient to inhibit AHAs (O'Neill and Spanswick, 1984; Regenberg et al., 1995), also increases root hair length (Lin et al., 2015). As a decreased proton motive force would be expected to reduce nutrient uptake, stimulation of root hair growth in response to reduced plasma membrane H+-ATPase activity could be a developmental response to nutrient starvation. Previous observations support this hypothesis as they show that low availability of nutrients leads to longer root hairs (Bates and Lynch, 1996; Schmidt et al., 2000; López-Bucio et al., 2003; Müller and Schmidt, 2004).
Another puzzling observation is that in Arabidopsis root hairs, both AHA7 and AHA2 were equally distributed between the shanks and the tip (Fuglsang et al., 2007; Młodzińska et al., 2014; Hoffmann et al., 2019); (Figure 1C), in contrast to the distribution of plasma membrane H+-ATPases in pollen tubes, where they are absent from the extreme apex (Certal et al., 2008; Hoffmann et al., 2020). The presence of the proton extruding pumps at the apex seems to act against the described inside-directed proton current at the tip.
It has been suggested that expansion of root hairs and pollen tubes is driven by turgor pressure (e.g., Mendrinna and Persson, 2015), and by energizing uptake of K+ followed by water, plasma membrane H+-ATPase could play a role in this process. However, in pollen tubes, the turgor pressure was shown to remain unaltered in the aha6 aha8 aha9 triple mutant when compared to the wild type despite a much reduced growth efficiency (Hoffmann et al., 2020). Thus, maybe other processes drive pollen tube extension, such as cytoskeleton buildup. This does not rule out the possibility that in root hairs plasma membrane H+-ATPases contribute to a buildup of turgor pressure. However, if this is the case, a reduced plasma membrane H+-ATPase activity would be expected to lead to reduced tip growth, but the opposite was observed in the aha2 aha7 double mutant in which the root hairs are significantly longer compared to the wild type (Hoffmann et al., 2019).
Control of H+ dynamics by FERONIA and RALF
Phosphorylation of specific Thr and Ser residues within the C-terminal regulatory domain of AHAs causes either activation or inactivation of pump activity (Falhof et al., 2016; Fuglsang and Palmgren, 2021); (Figure 3A). A number of plant receptor-like kinases (RLKs) involved in this process have been identified (Falhof et al., 2016), including FERONIA, a CrRLK1L subfamily member. FERONIA binds members of a unique peptide ligand family, RAPID ALKALINIZATION FACTOR (RALF) (Haruta et al., 2014). Following binding to the receptor at the apoplastic side of the plasma membrane, Ca2+ influx into the cytoplasm is initiated, with one of the downstream effects being inhibition of the plasma membrane H+-ATPase (Haruta et al., 2014); (Figure 3B) and, as a consequence, alkalinization of the apoplast.
Figure 3. Graphical illustration of plasma membrane H+-ATPase regulation. (A) Phosphorylation of specific Thr, Ser, and Tyr residues in the C-terminal autoinhibitory domain plasma membrane H+-ATPases that either promote or inhibit proton efflux by this pump. (B) Another layer of regulation of plasma membrane H+-ATPases involves their inactivation by FERONIA after RALF binding.
In Nicotiana attenuata, silencing of the NaRALF transcript by transformation with an inverted-repeat construct of RALF results in plants with normal wild-type shoots but longer roots and trichoblasts that evolve into abnormal root hairs (Wu et al., 2007). The affected trichoblasts develop bulges that expand into spherical structures that eventually burst. The negative effect on growth is strongest at neutral pH (pH 6.8), whereas in a medium strongly buffered at a more acidic pH (pH 5.5), root hair growth partially resembles that of the wild type. Furthermore, silencing NaRALF results in slower extracellular pH oscillations and reduced magnitude. These pH oscillations are linked to the regulation of cell wall cross-linking, which is related to the control of tip growth (Wu et al., 2007). Taken together, these observations demonstrate that RALF has an important role in root hair development, and, since its action is associated with the alteration of proton fluxes, its effect may be linked to the inactivation of the plasma membrane H+-ATPase.
A role for RALF signaling in root hair development was confirmed recently following the isolation of an Arabidopsis temperature-sensitive FERONIA mutant (fer-ts) (Kim et al., 2021). This mutant grows like the wild type at 20°C, but at 30°C, fer-ts seedlings are resistant to added RALF1 peptide and do not develop root hairs. The mutant receptor carries a G41S substitution in a highly conserved glycine residue in the extracellular domain of the FERONIA receptor protein, at a position distant from the peptide binding site. Thus, the deficiency in root hair formation is probably not due to a loss of RALF1 binding as such but rather to impairment of FERONIA (Kim et al., 2021).
Root hair phenotypes of the FERONIA and RALF mutants are likely a result of crosstalk between different signaling pathways that need not involve plasma membrane H+-ATPase at all. For example, the RALF1-FERONIA complex phosphorylates a translation initiation factor, eIF4E1, which regulates the synthesis of root hair proteins, e.g., a Rho GTPase (ROP2) (Zhu et al., 2020) that controls root hair initiation and tip growth (Jones et al., 2002) and the transcription factor ROOT HAIR DEFECTIVE 6-LIKE 4 (RSL4) that controls the expression of hundreds of genes in root hairs (Yi et al., 2010). However, the effect of the RALF-FERONIA complex on plasma membrane H+-ATPase and its possible involvement in root hair growth control requires further investigation.
The big picture: How pH changes affect ROS, Ca2+, and growth oscillations
Like pH, both apoplastic and cytoplasmic ROS and Ca2+ concentrations oscillate during root hair growth and are considered to sustain root hair tip growth (Monshausen et al., 2007); (Figure 1D). Mutants of RESPIRATORY BURST OXIDASE HOMOLOG C (RBOHC)/ROOT HAIR DEFECTIVE 2 (RHD2) have short root hairs and are impaired in tip growth (Foreman et al., 2003). The encoded RBOHC/RHD2 protein is an NADPH oxidase that localizes to the root hair tip where it produces superoxide, which is converted to hydrogen peroxide (H2O2) (Foreman et al., 2003; Chapman et al., 2019). This results in a tip-focused ROS gradient in the elongating root hair (Jones et al., 2007). This tip-focused ROS gradient is hypothesized to regulate the cytoplasmic Ca2+ dynamics that control delivery by exocytosis of cellular material to the tip and subsequent elongation (Foreman et al., 2003). ROS act as signaling molecules in small amounts, but they may cause cellular damage and cell death at higher concentrations (Czarnocka and Karpiński, 2018). In pollen tubes, flavonols were shown to prevent ROS from accumulating at damaging levels during heat stress and thereby promote pollen tube growth even at elevated temperatures (Muhlemann et al., 2018). Consistent with flavonols acting as ROS scavengers, disrupting flavonol synthesis in tomato (Solanum lycopersicum) leads to higher levels of ROS in root hairs but also increased root hair formation (Maloney et al., 2014). Root hair-producing trichoblasts were shown to express ROS-producing enzymes and accumulate high levels of ROS when compared to atrichoblasts (Gayomba and Muday, 2020). Thus, the elevated levels of ROS might result in increased frequency of trichoblasts (Maloney et al., 2014).
ROS production in the apoplast seems to correlate with a cytosolic pH increase (Gonugunta et al., 2009), and an increased cytosolic Ca2+ concentration might promote ROS production at the root hair tip (Zhang et al., 2017); (Figure 4). ROS molecules are transported from the apoplast into the cytosol through the PLASMA MEMBRANE INTRINSIC PROTEIN (PIP) aquaporin, and this transport is inhibited by high extracellular Ca2+ levels and by low apoplastic pH (Byrt et al., 2017); (Figure 4). Therefore, these results suggest an association not only between Ca2+ and ROS, but also between pH and ROS.
Figure 4. Graphical illustration of how pH, ROS, and Ca2+ possibly interact with each other in root hairs. These hypothesized interactions are indicated with dashed lines. In general, green represents pH, brown ROS, and blue Ca2+-related effects or proteins. Whether there are causative links between H+ and Ca2+ fluxes remains to be investigated.
Oscillating ROS levels have been proposed to contribute to a change in the active state of AHAs, and in this way ROS could control apoplastic pH oscillations (Mangano et al., 2018). However, plasma membrane H+-ATPases are quite insensitive to ROS due to a conserved and buried cysteine residue in close proximity to the pivotal aspartate that is phosphorylated in every catalytic cycle (Welle et al., 2021). In Arabidopsis AHA2, this Cys residue protects the pump from oxidation by ROS (Welle et al., 2021). This observation argues against a role for ROS in directly controlling plasma membrane H+-ATPase activities but does not exclude the possibility that plasma membrane H+-ATPases could be part of a mechanism that involves ROS.
However, an essential role of ROS oscillations in tip growth is challenged by the observation that a simple increase of the extracellular pH from 5 to 6 partly restored the short root hair phenotype of the rhd2 mutant, which lacks a NADPH oxidase responsible for ROS production. How alkalinization of the growth medium results in a restored phenotype is unclear. Under these conditions, the mutant showed decreased ROS accumulation but a normal tip-focused Ca2+ gradient (Monshausen et al., 2007), which was supposed to be modulated by the localized accumulation of ROS. Thus, ROS may not be essential for root hair development as such and Ca2+ channels can be activated in another way than through ROS accumulation.
As proposed for ROS, Ca2+ ions function as secondary messengers. High Ca2+ levels trigger vesicle exocytosis and thereby the delivery of the building material of the growing root hair apex (Campanoni and Blatt, 2007). However, a direct correspondence between Ca2+ oscillations, vesicle secretion, and growth is not evident as the peak in Ca2+ oscillations follows the peak in growth rate (Monshausen et al., 2008); (Figure 1D). A concerted effect of H+ and Ca2+ is like to impact actin dynamics via Ca2+- and pH-sensitive actin binding proteins such as actin-depolymerizing factor (ADF), gelsolin, and villin (Ketelaar, 2013; Qian and Xiang, 2019). During Ca2+ oscillations, Ca2+ ions could be imported from the apoplast or released from subcellular components (such as vacuoles and the endoplasmic reticulum). The negatively charged pectins and arabinogalactan are capable of binding Ca2+ ions in the cell wall (Tian et al., 2006; Lamport and Várnai, 2013). Apoplastic pH changes mediated by plasma membrane H+-ATPases might regulate the release of Ca2+ ions from the cell wall (Virk and Cleland, 1988; Peaucelle et al., 2012); (Figure 4). The removal of Ca2+ from the cytoplasm requires active transport, which may be carried out by autoinhibitory P-type IIB Ca2+-ATPases (ACAs) or Ca2+/H+ antiporters (CAXs). Thus, H+ and Ca2+ may act together in root hair tip growth. Whether Ca2+ influx precedes H+ influx (Behera et al., 2018) or Ca2+ influx is lagging behind H+ influx (Li et al., 2021) is still a matter of debate in ion signaling and remains to be tested in root hairs.
Conclusions and perspectives
The emergence of root hairs and their subsequent growth coincide with changes in apoplastic and cytosolic pH, which seem to involve dynamic changes in plasma membrane H+-ATPase activity. However, there appear to be differences with another tip-growing system, pollen tubes. In both systems, proton influx at the apex and efflux at the shank is reported. However, in root hairs, AHA2 and AHA7 proton pumps appear to be equally distributed along the root hair plasma membrane, whereas in pollen tubes a polar distribution of plasma membrane H+-ATPases explains mechanistically how the proton circuit can occur. We still do not understand why the cytosolic pH gradient from tip to base in root hairs and pollen tubes is apparently oriented in different directions. Moreover, it remains to be investigated what role RALF and FERONIA play in regulating plasma membrane H+-ATPase activity during root hair development. Furthermore, the puzzling positive effect on root hair growth exhibited by the aha2 aha7 double knockout mutant compared to the negative effect of the aha6 aha8 aha9 triple knockout on pollen tube growth suggests the possibility of an at least partially different mechanism for growth. The pH changes involved in root hair growth are likely a result of the crosstalk of several signaling pathways. As it stands, a broader understanding of the effect of pH on root hair growth and the role of plasma membrane H+-ATPases is required to develop potential general models for tip growth in diverse biological systems.
Data availability statement
The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author/s.
Author contributions
All authors listed have made a substantial, direct, and intellectual contribution to the work and approved it for publication.
Funding
This work was supported by grants from the Danish National Research Foundation (PUMPkin; MP) the Carlsberg Foundation (RaisingQuinoa; project number CF18-1113; MP), the Innovation Fund Denmark (LESSISMORE; MP), and the Novo Nordisk Foundation (NovoCrops; project number 2019OC53580; MP).
Conflict of interest
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.
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Keywords: root hair, tip growth, polar growth, pH, ROS, Ca2+, plasma membrane H+ -ATPase, protons
Citation: Stéger A and Palmgren M (2022) Root hair growth from the pH point of view. Front. Plant Sci. 13:949672. doi: 10.3389/fpls.2022.949672
Received: 21 May 2022; Accepted: 07 July 2022;
Published: 27 July 2022.
Edited by:
Agepati S. Raghavendra, University of Hyderabad, IndiaReviewed by:
Maria Teresa Portes, University of São Paulo, BrazilXiangpei Kong, Shandong University, China
Copyright © 2022 Stéger and Palmgren. 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: Michael Palmgren, cGFsbWdyZW4mI3gwMDA0MDtwbGVuLmt1LmRr