Hydrogen sulfide (H2S) is an important gasotransmitter in mammals. Despite physiological changes induced by exogenous H2S donor NaHS to plants, whether and how H2S works as a true cellular signal in plants need to be examined. A self-developed specific fluorescent probe (WSP-1) was applied to track endogenous H2S in tomato (Solanum lycopersicum) roots in site. Bioimaging combined with pharmacological and biochemical approaches were used to investigate the cross-talk among H2S, nitric oxide (NO), and Ca2+ in regulating lateral root formation. Endogenous H2S accumulation was clearly associated with primordium initiation and lateral root emergence. NO donor SNP stimulated the generation of endogenous H2S and the expression of the gene coding for the enzyme responsible for endogenous H2S synthesis. Scavenging H2S or inhibiting H2S synthesis partially blocked SNP-induced lateral root formation and the expression of lateral root-related genes. The stimulatory effect of SNP on Ca2+ accumulation and CaM1 (calmodulin 1) expression could be abolished by inhibiting H2S synthesis. Ca2+ chelator or Ca2+ channel blocker attenuated NaHS-induced lateral root formation. Our study confirmed the role of H2S as a cellular signal in plants being a mediator between NO and Ca2+ in regulating lateral root formation.
Citation: Li Y-J, Chen J, Xian M, Zhou L-G, Han FX, Gan L-J, et al. (2014) In Site Bioimaging of Hydrogen Sulfide Uncovers Its Pivotal Role in Regulating Nitric Oxide-Induced Lateral Root Formation. PLoS ONE 9(2): e90340. https://doi.org/10.1371/journal.pone.0090340
Editor: Hiroyasu Nakano, Juntendo University School of Medicine, Japan
Received: October 15, 2013; Accepted: January 30, 2014; Published: February 27, 2014
Copyright: © 2014 Li et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was financed by the grant from the Hi-Tech R & D Program of China (2011AA10A202). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Hydrogen sulfide (H2S) is considered as the third gasotransmitter in medical biology after nitric oxide (NO) and carbon monoxide (CO) . The clinical relevance of H2S as a signaling molecule has been highly appreciated in mammals –. In mammals and bacteria, two multifunctional pyridoxal 5′-phosphate (PLP)-dependent enzymes, cystathionine γ-lyase (CSE) and cystathionine β-synthase (CBS), are demonstrated to be the major sources of endogenous H2S production . H2S can also be produced by 3-mercaptopyruvate sulfurtransferase (3SMT) along with cysteine aminotransferase (CAT) in brain . In plants H2S is considered to be a by-product from cysteine desulfuration catalyzed by L-cysteine desulfhydrase (LCD, EC184.108.40.206) and D-cysteine desulfhydrase (DCD, EC220.127.116.11), both of which belonging to the PLP protein family . Both genes (LCD and DCD) have been characterized in Arabidopsis . A recent study suggests that O-acetylserine(thiol)lyase (OASTL), a cysteine synthase-like protein, also possesses the activity of cysteine desulfuration .
The detailed studies in the biological role of H2S in plants are very limited compared to those in mammals . Exogenous application of NaHS, a H2S donor, confers the tolerance of plants to oxidative stress –. H2S is also proposed to be involved in regulating stomatal closure –, photosynthesis , and seed germination , . However, the major challenge of identifying the nature of H2S as a plant signaling molecule is the lack of data of tracking endogenous H2S in site in plants. The traditional approaches of determining H2S from biological tissues include colorimetric in-tube assay , sulfide electrode assay , and gas chromatography/mass spectrometry . These methods require tissue pre-processing (e.g. homogenization), leading to the unavoidable loss of H2S. Therefore, in the last two years, a group of chemists have developed some specific fluorescent probes for capturing and tracking H2S in vivo through instantaneous bioimaging , which show great potential for revealing the biological behavior of H2S. However, the application of these probes in biological study, especially for plants, is rarely reported.
NO-modulated lateral root formation is a well characterized signaling event in plants , . NO can modulate the expression of cell cycle regulatory genes (e.g. CYCD and CDKA), which are essential for lateral root initiation from primordia , . The key of lateral root formation is lateral root emergence, which is a process that new primordia break through the outer layer cells from primary roots . Auxin has been confirmed as a regulatory star in this process by positively regulating Auxin Response Factors (ARFs) (e.g. ARF4/7/19) – and endogenous NO . In addition, a recent study suggests that cytosolic Ca2+ combined with its sensor calmodulin (CaM) acts downstream of NO during lateral root formation . The auxin-NO signaling event has been considered to play a vital role in regulating lateral root growth, but the detailed regulatory network needs to be illuminated by mining novel components. The biological interplay among H2S, NO, and Ca2+ has been well investigated in mammals , . Thus, it is of interest to study whether and how H2S acts as a gasotransmitter in NO signaling cassette for the regulation of lateral root formation. WSP-1 (Washington State Probe-1) is a self-developed fluorescent probe for detecting H2S within living cells with high-sensitivity and selectivity , . In the present study, tracking and bioimaging endogenous H2S with WSP-1 in plant cells provide direct evidence that H2S is a novel regulator in NO-modulated lateral root formation. This study confirmed the role of H2S as a cellular signal molecule in plant signaling events.
Materials and Methods
Plant culture and treatments
Tomato (Solanum lycopersicum, Suhong2003 wild type) seeds were surface-sterilized with 1% NaClO for 10 min followed by washing with distilled water. Seeds were germinated in Petri dishes on filter papers imbibed with distilled water. Then the selected identical seedlings with radicles 1.5 cm were transferred to another Petri dish containing various treatment solutions in a chamber with a photosynthetic active radiation of 200 μmol/m2/s, a photoperiod of 12 h, and the temperature at 25±1°C.
SNP (sodium nitroprusside) and GSNO (S-Nitrosoglutathione) as NO donors were applied at concentrations of 0.05–0.4 mM and 0.5 mM, respectively. The 0.1 mM of cPTIO [2-(4-carboxy-2-phenyl)-4,4,5,5-tetramethylinidazoline-1-oxyl-3-oxide] was applied as NO scavenger. The 0.2–2 mM of NaHS (sodium hydrosulphide) was applied as H2S donor. PAG (DL-propargylglicine) (0.1 mM) and HT (hypotaurine) (0.1 mM) are H2S biosynthesis inhibitors and H2S scavengers, respectively. Na2SO4, Na2SO3, and NaHSO3 at the concentration of 2 mM are applied as NaHS homologues to identify the specificity for NaHS as H2S donor. EGTA [ethylene glycol-bis(2-aminoethylether)-N,N,N,N-tetraacetic acid] (0.1 mM) and LaCL3 (0.5 mM) are Ca2+ chelators and Ca2+ channel blockers, respectively. The treatment solution is composed of different chemicals as mentioned above according to the experimental design. After treatments, the roots were washed with distilled water for physiological, histochemical, and biochemical analysis.
Histochemical detection of endogenous H2S and cytosolic Ca2+ in vivo
Intracellular NO was visualized using DAF-FM DA (3-Amino, 4-aminomethyl-2′,7′- difluorescein, diacetate) fluorescent probe described by Guo et al . The roots of seedlings after treatment were transferred to 20 mM of Hepes-NaOH (pH 7.5) buffer solution containing 15 μM of DAF-FM DA. After being incubated in darkness at 25°C for 15 min, the roots were rinsed with distilled water for three times and were visualized (excitation 490 nm and emission 525 nm) by a fluorescence microscope (ECLIPSE, TE2000-S, Nikon).
The intracellular H2S was visualized using WSP-1 [3′- methoxy- 3- oxo- 3H- spiro[isobenzofuran- 1, 9′- xanthen]- 6′- yl 2- (pyridin- 2- yldisulfanyl)benzoate]. The roots of seedlings after treatments were transferred to 20 mM Hepes-NaOH (pH 7.5) buffer solution containing 15 μM of WSP-1. After being incubated in darkness at 25°C for 40 min, the roots were washed with distilled water three times and were visualized immediately by a fluorescence microscope with a 465/515 nm and an excitation/emission filter set (ECLIPSE, TE2000-S, Nikon).
For the detection of WSP-1 fluorescence in different reactive sulfur species, WSP-1 with final concentration of 15 μM were added into the following solutions, SDS (sodium dodecyl sulfate, 2 mM), NaHSO4 (2 mM), NaHSO3 (2 mM), Na2SO4 (2 mM), Na2SO3 (2 mM), Na2S2O4 (2 mM), GSSG (glutathione disulfide, 2 mM), sulfonamide (2 mM), GSNO (2 mM), and NaHS (2 mM), respectively. Twenty μL of the above solutions were transferred to a glass slide for the visualization with a fluorescence microscope with a 465/515 nm and an excitation/emission filter set (ECLIPSE, TE2000-S, Nikon).
The cytosolic Ca2+ was visualized using Ca2+-sensitive fluorescent probe Fluo-3 AM. Similarly, the probe was loaded to roots in 20 mM Hepes-NaOH (pH 7.5) buffer solution containing 15 μM of Fluo-3 AM in darkness at 25°C for 30 min. Then, the fluorescent image was captured using a fluorescence microscope with 488/525 nm and an excitation/emission filter set (ECLIPSE, TE2000-S, Nikon).
The relative fluorescent density of the fluorescent images was analyzed using Image-Pro Plus 6.0 (Media Cybernetics, Inc.).
Analysis of transcripts
Semiquantitative RT-PCR was performed with the total RNA for the transcription analysis. Total RNA was extracted from root samples using Trizol (Invitrogen) according to the manufacturer's instructions. Reverse transcription was performed at 42°C in a 25 μl reaction mixture including 3 μg of RNA, 0.5 μg of oligo(dT) primers, 12.5 nmol of dNTPs, 20 units of RNase inhibitor and 200 units of MLV. The first cDNA was used as a template for PCR to analyze the transcripts of genes. The total 25 μl of PCR reaction mixture in Tris-HCl buffer (pH 8.3, 10 mM) was composed of 1 μl of normalized cDNA template, 10 pmol of sense primer, 10 pmol of antisense primer, 5 nmol of dNTPs, 32.5 nmol of Mg2+, and 0.5 U of Tag DNA polymerase. PCR was performed as follows: 95°C for 3 min, 30 cycles at 94°C for 30 s, different annealing temperature for 30 s, 68°C for 1.5 min, and a final extension step at 68°C for 7 min. All the tested genes were retrieved from tomato genome (Sol Genomics Network, http://solgenomics.net/organism/Solanum_lycopersicum/genome) or NCBI (National Center for Biotechnology Information, http://www.ncbi.nlm.nih.gov/). The following primers and annealing temperatures were used to amplify the genes: CYCD3;1 (Sol accession number SGN-U583476), sense 5′-TTATCTTTCATTGATCATATTATGAGG-3′ and antisense 5′-CTAGGTAATCTAGAGAACAAGATATCG-3′ (amplifying a 526 bp fragment, 45°C); CDKA1 (Sol accession number SGN-U572518), sense 5′-GCTTATTGTCATTCTCATAGAGTTCTT-3′ and antisense 5′-TCGTTGAAGCACTCATGCTCAAGGGC-3′ (Sol amplifying a 521 bp fragment, 45°C); ARF4 (Sol accession number SGN-U569639), sense 5′-ATGCTTGTGCTGGTCC-3′ and antisense 5′-CTCCGTGCAGATCCTT-3′ (amplifying a 477 bp fragment, 45°C); ARF7 (NCBI accession number EF121545.1), sense 5′-TCAGAGTTATGGCACG-3′ and antisense 5′-GACGAGGAACAGAAAA-3′ (amplifying a 373 bp fragment, 45°C); CaM1 (Sol accession number SGN-U580544), sense 5′-TGAATCTGATGGCACGGAAG-3′ and antisense 5′-TACTTGAACCGCTCCTGAGT-3′ (amplifying a 338 bp fragment, 50°C); Actin (Sol accession number SGN-U580422), sense 5′-AGAGCTATGAGCTCCCAGATGG-3′ and antisense 5′-TTAATCTTCATGCTGCTAGGAGC-3′ (amplifying a 272 bp fragment, 50°C). The relative abundance of Actin was used as internal standard.
Each result was presented as the mean of at least three replicated measurements. The significant differences between treatments were statistically evaluated by standard deviation and one-way analysis of variance (ANOVA) using Microsoft Excel 2010 (Microsoft Corporation, USA). The data between different treatments were compared statistically by ANOVA, followed by F-test if the ANOVA result is significant at P<0.05.
NO induced lateral root formation
NO donors were used to assess the regulatory effect of NO on tomato lateral root formation. The NO donor SNP stimulated lateral root growth in both dose- and time-dependent manner (Figure 1a and b). On the contrary, treatments with NO scavenger cPTIO alone remarkably inhibited lateral root formation (Figure 1c and d). Another NO donor GSNO could stimulate lateral root formation as well (Figure 1c and d). However, the addition of cPTIO could abolish the promoting effect of both NO donors on lateral roots(Figure 1c and d). These results confirmed the promoting effect of NO on tomato lateral root formation.
(a) The roots of three-day old tomato seedlings were exposed to 0, 0.05, 0.1, 0.2, and 0.4 mM of SNP for 6 days for the measurement of the lateral root number. (b) The roots of three-day old tomato seedlings were exposed to 0.2 mM of SNP for 3–8 days for the measurement of the lateral root number. (c–d) The roots of three-day old tomato seedlings were exposed to cPTIO (0.1 mM), SNP (0.2 mM), SNP (0.2 mM) + cPTIO (0.1 mM), GSNO (0.5 mM), and GSNO (0.5 mM) + cPTIO (0.1 mM) for 6 days for photographing root phenotype (c) and measuring the lateral root number (d). Vertical bars represent standard deviations of the mean (n = 6). Asterisk indicates that mean values are significantly different (P<0.05) between the treatment and the control (a, b) or between different treatments (d).
WSP-1 can be used for the selective detection of H2S in tomato root
In order to investigate the potential of WSP-1 in the detection of H2S in plant system, tomato roots treated with NaHS at different concentrations (0.2, 0.4, and 2 mM) were loaded with WSP-1. These concentrations were within the range of those that have been used to elicit physiological responses of H2S in plants , , , . The strong fluorescent density was observed in roots in the presence of NaHS in a dose-dependent manner (Figure 2a and b). This result was similar to the detection of H2S with WSP-1 in mammalian system . To further identify the selectivity of WSP-1 probe for H2S, several kinds of reactive sulfur species (e.g. sulfane sulfur, inorganic sulfur derivatives, ploysulfide, sulfenic acid derivative, and S-nitrosothiol) were detected in solution. As expected, compared to the significant fluorescence signal yielded from the reaction of WSP-1 with NaHS solution, other tested reactive sulfur species did not lead to significant fluorescence increase (Figure 2c). Analysis of fluorescent density showed that several sulfur compounds (e.g. NaHSO4, Na2SO4, Na2S2O4, and sulfonamide) had little fluorescence, but their values are too small as compared with NaHS (Figure 2d). These results suggested that WSP-1 could be used for the selective detection of endogenous H2S in tomato roots.
(a–b) The roots of three-day old tomato seedlings were exposed to NaHS solution (0, 0.2, 0.4, and 2 mM) for 2 h. Then the roots were loaded with WSP-1 for fluorescent imaging (a) and the calculation of relative fluorescent density (b). (c) WSP-1 was loaded into different sulfur compounds solutions as mentioned in “Materials and Methods” for fluorescent imaging. (d) The calculation of relative fluorescent density from (c). Vertical bars represent standard deviations of the mean (n = 3). Asterisk indicates that mean values are significantly different (P<0.05) between the treatment and the control.
Endogenous H2S was involved in lateral root formation
Next, we investigate the link between lateral root emergency and endogenous H2S. The bright green fluorescence of WSP-1 was clearly linked to the primordium initiation and lateral root emergence (Figure 3a). In a cross section of primary roots with lateral root primoidium, the fluorescence of WSP-1 was clearly concentrated in the region of primordium (Figure 3b). To further ascertain the role of H2S in regulating lateral root formation, we measured lateral root number by altering endogenous H2S level in roots. Both H2S biosynthesis inhibitor PAG and H2S scavenger HT induced significant decreases in lateral root number (Figure 3c and e). However, the treatment with NaHS significantly enhanced lateral root number compared to the control (Figure 3c and e). Treatments with several homologues of Na or S (e.g. Na2SO4, Na2SO3, and NaHSO3) did not affect lateral root number (Figure 3d and f), suggesting that NaHS-released H2S contributed to the promotion of lateral root formation. This was further confirmed by in vivo fluorescent detection of endogenous H2S level in roots. Both PAG and HT led to the significant decrease in endogenous H2S levels (Figure 3g and h). NaHS, but not its homologues, remarkably enhanced endogenous H2S level in roots (Figure 3g and h).
(a) WSP-1 was loaded into the roots during lateral root formation for fluorescent imaging. (b) The cross section of primary roots loaded with WSP-1. Arrows indicate lateral roots (LR) primordium; BF, bright field; Fl, fluorescence. (c–f) The roots of three-day old tomato seedlings were exposed to NaHS (2 mM), PAG (0.1 mM), HT (0.1 mM), Na2SO4 (2 mM), Na2SO3 (2 mM), and NaHSO3 (2 mM) for 6 days for photographing root phenotype (c–d) and measuring lateral root numbers (e–f). Vertical bars represent the standard deviations of the mean (n = 6). (g–h) The roots of three-day old tomato seedlings were exposed to NaHS (2 mM), PAG (0.1 mM), HT (0.1 mM), Na2SO4 (2 mM), Na2SO3 (2 mM), and NaHSO3 (2 mM) for 3 days. Then, the roots were loaded with WSP-1 for fluorescent imaging (g) and the calculation of relative fluorescent density (h). Vertical bars represent standard deviations of the mean (n = 3). Asterisk indicates that mean values are significantly different (P<0.05) between the treatment and the control.
NO induced lateral root formation by regulating endogenous H2S generation
To determine the role of H2S in NO-induced lateral root formation, we first investigated the effect of NO donors on the generation of endogenous H2S in roots detected by WSP-1. Treatments with NO scavenger cPTIO induced a significant decrease in endogenous H2S level in roots (Figure 4a and b). Two NO donors (SNP and GSNO) stimulated the generation of endogenous H2S, which could be blocked by the addition of cPTIO (Figure 4a and b). SNP stimulated the generation of endogenous NO and H2S in dose-dependent manners (Figure 4c).
(a–b) The roots of three-day old tomato seedlings were exposed to cPTIO (0.1 mM), SNP (0.2 mM), SNP (0.2 mM)+cPTIO (0.1 mM), GSNO (0.5 mM), and GSNO (0.5 mM)+cPTIO (0.1 mM) for 3 days. Then, the roots were loaded with WSP-1 for fluorescent imaging (a) and the calculation of relative fluorescent density (b). Vertical bars represent standard deviations of the mean (n = 3). (c) The roots of three-day old tomato seedlings were exposed to 0, 0.05, 0.1, 0.2, and 0.4 mM of SNP for 3 days. Then, the roots were loaded with DAF-FM DA and WSP-1 for fluorescent imaging, respectively. (d–g) The roots of three-day old tomato seedlings were exposed to cPTIO (0.1 mM), cPTIO (0.1 mM) + NaHS (2 mM), SNP (0.2 mM), and SNP (0.2 mM) + PAG (0.1 mM) for 6 days for photographing root phenotype (d–e) and measuring lateral root number (f–g). (h–i) The roots of three-day old tomato seedlings were exposed to cPTIO (0.1 mM), cPTIO (0.1 mM) + NaHS (2 mM), SNP (0.2 mM), and SNP (0.2 mM) + PAG (0.1 mM) for 2 days for the measurement of lateral root primordia. Vertical bars represent standard deviations of the mean (n = 6). (j) The roots of three-day old tomato seedlings were exposed to SNP (0.2 mM), NaHS (2 mM), and SNP (0.2 mM)+PAG (0.1 mM) for 2 days for the analysis of genes transcripts. (k) Quantitative analysis of genes transcript levels under different treatment conditions. The data were obtained by densitometric analysis of the relative abundance of the transcripts with respect to the loading control Actin. Asterisk indicates that mean values are significantly different (P<0.05) between the treatment and the control. Actin was used for cDNA normalization.
Since NO was able to stimulate H2S generation in tomato roots, it is essential to know whether NO-governed H2S generation is able to manipulate lateral root formation. The addition of NaHS reversed the inhibitory effect of cPTIO on lateral root formation (Figure 4d and f). Furthermore, the addition of PAG abolished the stimulatory effect of SNP on lateral root formation (Figure 4e and g). These effects could be observed in the emergence of lateral root primordia as well (Figure 4h and i). Then we tested the effect of the interplay between NO and H2S on the expression of four genes related to lateral root emergence, including two cell cycle regulatory genes (CYCD3;1 and CDKA1) and two ARF genes (ARF4 and ARF7). As expected, both SNP and NaHS could stimulate the expression of these genes while the addition of PAG could block the stimulatory effect of SNP (Figure 4j and k).
Ca2+/CaM1 acted downstream of H2S in NO-induced lateral root formation
By using Fluo-3 AM to detect cytosolic Ca2+ in tomato roots, we found that both SNP and NaHS stimulated the accumulation of cytosolic Ca2+ in roots while the addition of PAG reversed the stimulatory effect of SNP and NaHS (Figure 5a and b). The changes in the CaM1 expression showed similar patterns with cytosolic Ca2+ under the above treatments (Figure 5c and d).
(a–c) The roots of three-day old tomato seedlings were exposed to SNP (0.2 mM), NaHS (2 mM), and SNP (0.2 mM) + PAG (0.1 mM) for 4 days. Then, the roots were loaded with Fluo-3 AM for fluorescent imaging (a) and the calculation of relative fluorescent density (b). Vertical bars represent standard deviations of the mean (n = 3). The roots were also used for the analysis of the CaM1 transcripts (c). (d) Quantitative analysis of CaM1 transcript levels under different treatment conditions. The data were obtained by densitometric analysis of the relative abundance of the transcripts with respect to the loading control Actin. (e–f) The roots of three-day old tomato seedlings were exposed to NaHS (2 mM), NaHS (2 mM)+La3+ (0.5 mM), and NaHS (2 mM)+EGTA (0.1 mM) for 6 days for photographing root phenotype (e) and measuring lateral root numbers (f). Vertical bars represent standard deviations of the mean (n = 6). (g) The roots of three-day old tomato seedlings were exposed to NaHS (2 mM), NaHS (2 mM)+La3+ (0.5 mM), and NaHS (2 mM)+EGTA (0.1 mM) for 2 days for the analysis of genes transcripts. (h) Quantitative of genes transcript levels under different treatment conditions. The data were obtained by densitometric analysis of of the relative abundance of the transcripts with respect to the loading control Actin. Asterisk indicates that mean values are significantly different (P<0.05) between different treatments. Actin was used for cDNA normalization.
Next, we determined the cross-talk between H2S and Ca2+ on lateral root formation. As expected, both Ca2+ channel blocker La3+ and Ca2+ chelator EGTA could abolish the stimulatory effect of NaHS on lateral root formation (Figure 5e and f) and the expression of CYCD3;1, CDKA1, ARF4, and ARF7 (Figure 5g and h).
In plants, both NO and CO have been already identified as vital signaling molecules participating in an array of intrinsic signaling events , . But the biology of H2S in plants is not well understood. Many physiological changes in plants resulting from the exposure of exogenous H2S have been summarized by Lisjak et al. . In order to identify whether H2S is a true cellular signal in plants, the in site concentration and the locality of endogenous H2S in plants need to be determined . In the present study, we overcome the obstacle of tracking endogenous H2S in plants in site. The endogenous H2S in tomato roots have been successfully detected in site by specific fluorescent probe WSP-1, which provides the direct evidence supporting the interplay among NO, H2S, and Ca2+ in regulating lateral root formation.
Basically, we provide three lines of evidence indicating that H2S is an important messenger operating downstream of NO during lateral root formation in tomato seedlings. First, endogenous H2S accumulation accompanies with lateral root emergency while lateral root formation is positively correlated with the changes of endogenous H2S concentration in pharmacological experiments. Second, PAG- or HT-induced decreases in endogenous H2S blocked NO-induced lateral root formation. Third, PAG is able to attenuate the stimulatory effect of NO on cytosolic Ca2+ accumulation and CaM1 transcripts. Both Ca2+ channel blocker and Ca2+ chelator can inhibit H2S-induced lateral root formation.
The development of specific fluorescent probes provides a powerful tool for studying the biological function of gasotransmitters. WSP-1 has been demonstrated to be efficient fluorescence probe for selectively detecting H2S in mammalian system . Whether WSP-1 is suitable for the detection of H2S in plants remains unclear because of the abundant reactive sulfur species in plants . In the present study, NaHS, but not other five kinds of tested reactive sulfur species, can react with WSP-1 to produce significant fluorescence in vitro. Tomato roots treated with NaHS showed well-increased fluorescence detected by WSP-1. These evidences support that WSP-1 shows great potential for selectively detecting H2S in tomato roots. Our study widens the application of WSP-1 for detecting H2S in biological system.
According to the detection of endogenous NO using famous fluorescent probe DAF-2 DA, NO accumulation is clearly associated to lateral root primodium initiation . Interestingly, the link between endogenous H2S accumulation and primodium emergence has been established successfully with using specific fluorescent probe WSP-1 in the present study. Based on our data, the endogenously generated NO induced lateral root formation through endogenous H2S generation. This can be confirmed by the fact that the decreases in the concentration of endogenous NO and H2S caused the inhibition of lateral root formation while treatment with NO donor SNP enhanced the concentration of endogenous NO, resulting in the increase in the concentration of endogenous H2S in roots. The promoting effect of NO on lateral root formation has been well characterized by Correa-Aragunde et al . Here, we demonstrate that H2S is a new component of the signaling event for NO-induced lateral root formation, and that H2S acts downstream of NO signal. But Zhang et al. has reported that H2S may act upstream of NO in inducing adventitious root formation. However, a possible feedback regulation of H2S by NO has also been suggested because plant roots treated with SNP maintained higher levels of endogenous H2S in comparison to control . Our present study provides the detailed evidence that NO induces lateral root formation by regulating endogenous H2S. Therefore, it can be proposed that H2S is required for root organogenesis by functioning probably both upstream and downstream of NO. However, whether and how NO induces H2S generation by regulating LCD or DCD in tomato roots remains to be further investigated.
The function of Ca2+ as a mediator in NO-induced lateral root formation of Arabidopsis has recently been studied by Wang et al . In tobacco suspension cultured cells, the application of Ca2+ chelator or CaM antagonists can decrease NaHS-induced heat tolerance, supporting that Ca2+ may act downstream of H2S . Here we suggests that H2S is a mediator between NO and Ca2+ in lateral root development of tomato plants by fluorescently bioimaging intracellular H2S and cytosolic Ca2+. In the vascular tissues of mammals, H2S-induced cytosolic Ca2+ rise is attributed to Ca2+ release from multiple intracellular sources rather than extracellular Ca2+ influx . The different regulatory styles of cytosolic Ca2+ by H2S between plants and mammals would be an interesting topic to be investigated further.
H2S regulates various physiological processes by targeting KATP channels in mammals. H2S is an endogenous opener of KATP channels by interacting with Cys6 and Cys26 in rvSUR1 (Sulphonylurea Receptor 1) subunit of KATP channel complex through S-sulfhydration . In plants, MRP5 (Multidrug Resistance-associated Protein 5) is a homologue of mammalian SUR . In Arabidopsis, AtMRP5 not only works as an auxin conjugate transporter in modulating lateral root formation but also acts as a regulator of Ca2+ channel in regulating guard cell signaling , . MRP5 can be possibly regulated by H2S due to the fact that the treatment with Gli (glibenclamide), a typical SUR inhibitor, blocks NaHS-induced stomatal closure . Thus, whether H2S regulates Ca2+ signaling through the S-sulfhydration of MRP5 during lateral root formation needs to be further investigated. In addition, NO may induce Ca2+ influx by post-transcriptionally modified Ca2+ channel proteins directly , . Therefore, it is possible that NO may act parallelly with H2S in inducing cytosolic Ca2+.
The biology of H2S in mammals has been significantly advanced, but mining the signaling role of H2S in plants is just emerging. Based on our observation, a model could be proposed of the crosstalk between NO and H2S in regulating lateral root formation (Figure 6). The current regulatory network involving NO, H2S, and Ca2+ in regulating later root formation is largely unknown, but our data suggest that H2S acting between NO and Ca2+ is one of the possible signaling pathway in the complicated network for the regulation of lateral root formation. However, a possible feedback mechanism between NO and H2S maybe operating for the induction of lateral root formation. Our present study is the first report of bioimaging endogenous H2S in plants, which provides the direct evidence of identifying H2S as a true cellular signaling molecule in regulating lateral root formation. These results not only propose a novel component in lateral root signaling but also shed new light on the study of the biological role of H2S in plants.
Conceived and designed the experiments: JC Z-QS L-JG. Performed the experiments: JC Y-JL. Analyzed the data: JC Y-JL. Contributed reagents/materials/analysis tools: MX. Wrote the paper: JC Y-JL L-GZ FH.
- 1. Wang R (2010) Hydrogen sulfide: the third gasotransmitter in biology and medicine Antioxid Redox Signal. 12: 1061–1064.
- 2. Vandiver MS, Snyder S (2012) Hydrogen sulfide: a gasotransmitter of clinical relevance. J Mol Med 90: 255–263.
- 3. Kimura H, Shibuya N, Kimura Y (2012) Hydrogen sulfide is a signaling molecule and a cytoprotectant. Antioxid Redox Signal 17: 45–57.
- 4. Kimura H (2011) Hydrogen sulfide: its production, release and functions. Amino Acids 41: 113–121.
- 5. Kimura H (2013) Production and physiological effects of hydrogen sulfide. Antioxid Redox Signal: doi:10.1089/ars.2013.5309.
- 6. Shibuya N, Tanaka M, Yoshida M, Ogasawara Y, Togawa T, et al. (2009) 3-Mercaptopyruvate sulfurtransferase produces hydrogen sulfide and bound sulfane sulfur in the brain. Antioxid Redox Signal 11: 703–714.
- 7. Papenbrock J, Riemenschneider A, Kamp A, Schulz-Vogt HN, Schmidt A (2007) Characterization of cysteine-degrading and H2S-releasing enzymes of higher plants – from the field to the test tube and back. Plant Biol 9: 582–588.
- 8. Jin Z, Shen J, Qiao Z, Yang G, Wang R, et al. (2011) Hydrogen sulfide improves drought resistance in Arabidopsis thaliana. Biochem Biophys Res Commun 414: 481–486.
- 9. Álvarez C, Calo L, Romero LC, Garcia I, Gotor C (2010) An O-acetylserine(thiol)lyase homolog with L-cysteine desulfhydrase activity regulates cysteine homeostasis in Arabidopsis. Plant Physiol 152: 656–669.
- 10. Lisjak M, Teklic T, Wilson ID, Whiteman M, Hancock JT (2013) Hydrogen sulfide: environmental factor or signalling molecule? Plant Cell Environ: DOI: 10.1111/pce.12073.
- 11. Christou A, Manganaris GA, Papadopoulos I, Fotopoulos V (2013) Hydrogen sulfide induces systemic tolerance to salinity and non-ionic osmotic stress in strawberry plants through modification of reactive species biosynthesis and transcriptional regulation of multiple defence pathways. J Exp Bot 64: 1953–1966.
- 12. Wang Y, Li L, Cui W, Xu S, Shen W, et al. (2012) Hydrogen sulfide enhances alfalfa (Medicago sativa) tolerance against salinity during seed germination by nitric oxide pathway. Plant Soil 351: 107–119.
- 13. Li Z-G, Gong M, Xie H, Yang L, Li J (2012) Hydrogen sulfide donor sodium hydrosulfide-induced heat tolerance in tobacco (Nicotiana tabacum L) suspension cultured cells and involvement of Ca2+ and calmodulin. Plant Sci 185–186: 185–189.
- 14. Zhang H, Ye Y-K, Wang S-H, Luo J-P, Tang J, et al. (2009) Hydrogen sulfide counteracts chlorophyll loss in sweetpotato seedling leaves and alleviates oxidative damage against osmotic stress. Plant Growth Regul 58: 243–250.
- 15. Dawood M, Cao F, Jahangir MM, Zhang G, Wu F (2012) Alleviation of aluminum toxicity by hydrogen sulfide is related to elevated ATPase, and suppressed aluminum uptake and oxidative stress in barley. J Hazard Mater 209–210: 121–128.
- 16. Zhang H, Tan Z-Q, Hu L-Y, Wang S-H, Luo J-P, et al. (2010) Hydrogen sulfide alleviates aluminum toxicity in germinating wheat seedlings. J Integr Plant Biol 52: 556–567.
- 17. Li L, Wang Y, Shen W (2012) Roles of hydrogen sulfide and nitric oxide in the alleviation of cadmium-induced oxidative damage in alfalfa seedling roots. Biometals 25: 617–631.
- 18. Wang B-L, Shi L, Li Y-X, Zhang W-H (2010) Boron toxicity is alleviated by hydrogen sulfide in cucumber (Cucumis sativus L.) seedlings. Planta 231: 1301–1309.
- 19. Zhang H, Hu L, Li P, Hu K, Jiang C, et al. (2010) Hydrogen sulfide alleviated chromium toxicity in wheat. Biol Plant 54: 743–747.
- 20. Zhang H, Hu L-Y, Hu K-D, He Y-D, Wang S-H, et al. (2008) Hydrogen sulfide promotes wheat seed germination and alleviates oxidative damage against copper stress. J Integr Plant Biol 50: 1518–1529.
- 21. García-Mata C, Lamattina L (2010) Hydrogen sulphide, a novel gasotransmitter involved in guard cell signalling. New Phytol 188: 977–984.
- 22. Hou Z, Wang L, Liu J, Hou L, Liu X (2013) Hydrogen sulfide regulates ethylene-induced stomatal closure in Arabidopsis thaliana. J Integr Plant Biol 55: 277–289.
- 23. Lisjak M, Teklic T, Wilson ID, Wood M, Whiteman M, et al. (2011) Hydrogen sulfide effects on stomatal apertures. Plant Signal Behav 6: 1444–1446.
- 24. Chen J, Wu FH, Wang WH, Zheng CJ, Lin GH, et al. (2011) Hydrogen sulphide enhances photosynthesis through promoting chloroplast biogenesis, photosynthetic enzyme expression, and thiol redox modification in Spinacia oleracea seedlings. J Exp Bot 62: 4481–4493.
- 25. Zhang H, Dou W, Jiang C, Wei Z, Liu J, et al. (2010) Hydrogen sulfide stimulates β-amylase activity during early stages of wheat grain germination. Plant Signal Behav 5: 1031–1033.
- 26. Li Z-G, Gong M, Liu P (2012) Hydrogen sulfide is a mediator in H2O2-induced seed germination in Jatropha Curcas. Acta Physiol Plant 34: 2207–2213.
- 27. Sekiya J, Schmidt A, Wilson LG, Filner P (1982) Emission of hydrogen sulfide by leaf tissue in response to L-cysteine. Plant Physiol 70: 430–436.
- 28. Liang GH, Adebiyi A, Leo MD, McNally EM, Leffler CW, et al. (2011) Hydrogen sulfide dilates cerebral arterioles by activating smooth muscle cell plasma membrane KATP channels. Am J Physiol Heart Circ Physiol 300: H2088–H2095.
- 29. Duan CX, Liu YG (2013) Recent advances in fluorescent probes for monitoring of hydrogen sulfide. Curr Med Chem 20: 2929–2937.
- 30. Correa-Aragunde N, Graziano M, Lamattina L (2004) Nitric oxide plays a central role in determining lateral root development in tomato. Planta 218: 900–905.
- 31. Tian Q-Y, Sun D-H, Zhao M-G, Zhang W-H (2007) Inhibition of nitric oxide synthase (NOS) underlies aluminum-induced inhibition of root elongation in Hibiscus moscheutos. New Phytol 174: 322–331.
- 32. Correa-Aragunde N, Graziano M, Chevalier C, Lamattina L (2006) Nitric oxide modulates the expression of cell cycle regulatory genes during lateral root formation in tomato. J Exp Bot 57: 581–588.
- 33. Péret B, De Rybel B, Casimiro I, Benkova E, Swarup R, et al. (2009) Arabidopsis lateral root development: an emerging story. Trends Plant Sci 14: 399–408.
- 34. Okushima Y, Fukaki H, Onoda M, Theologis A, Tasaka M (2007) ARF7 and ARF19 regulate lateral root formation via direct activation of LBD/ASL genes in Arabidopsis. Plant Cell 19: 118–130.
- 35. Yoon EK, Yang JH, Lim J, Kim SH, Kim S-K, et al. (2010) Auxin regulation of the microRNA390-dependent transacting small interfering RNA pathway in Arabidopsis lateral root development. Nucleic Acids Res 38: 1382–1391.
- 36. Wang H, Niu Y, Chai R, Liu M, Zhang Y (2013) Cross–talk between nitric oxide and Ca2+ in elevated CO2-induced lateral root formation. Plant Signal Behav 8: e23106.
- 37. Li L, Rose P, Moore PK (2011) Hydrogen sulfide and cell signaling. Annu Rev Pharmacol Toxicol 51: 169–187.
- 38. Liu Y-H, Lu M, HU L-F, Wong PTH, Webb GD, et al. (2012) Hydrogen sulfide in the mammalian cardiovascular system. Antioxid Redox Signal 17: 141–185.
- 39. Devarie-Baez NO, Bagdon PE, Peng B, Zhao Y, Park C-M, et al. (2013) Light-induced hydrogen sulfide release from “Caged” gem-dithiols. Org Lett 15: 2786–2789.
- 40. Liu C, Pan J, Li S, Zhao Y, Wu LY, et al. (2011) Capture and visualization of hydrogen sulfide by a fluorescent probe. Angewandte Chemie 123: 10511–10513.
- 41. Guo K, Xia K, Yang ZM (2008) Regulation of tomato lateral root development by carbon monoxide and involvement in auxin and nitric oxide. J Exp Bot 59: 3443–3452.
- 42. Zhang H, Hu S-L, Zhang Z-J, Hu L-Y, Jiang C-X, et al. (2011) Hydrogen sulfide acts as a regulator of flower senescence in plants. Postharvest Biol Technol 60: 251–257.
- 43. Besson-Bard A, Pugin A, Wendehenne D (2008) New insights into nitric oxide signaling in plants. Annu Rev Plant Biol 59: 21–39.
- 44. Xuan W, Xu S, Yuan X, Shen W (2008) Carbon monoxide: A novel and pivotal signal molecule in plants? Plant Signal Behav 3: 381–382.
- 45. Gruhlke MCH, Slusarenko AJ (2012) The biology of reactive sulfur species (RSS). Plant Physiol Biochem 59: 98–107.
- 46. Zhang H, Tang J, Liu X-P, Wang Y, Yu W, et al. (2009) Hydrogen Sulfide Promotes Root Organogenesis in Ipomoea batatas, Salix matsudana and Glycine max. J Integr Plant Biol 51: 1086–1094.
- 47. Jiang B, Tang G, Cao K, Wu L, Wang R (2010) Molecular mechanism for H2S-induced activation of KATP channels. Antioxid Redox Signal 12: 1167–1178.
- 48. Martinoia E, Klein M, Geisler M, Bovet L, Forestier C, et al. (2002) Multifunctionality of plant ABC transporters – more than just detoxifiers. Planta 214: 345–355.
- 49. Gaedeke N, Klein M, Kolukisaoglu U, Forestier C, Muller A, et al. (2001) The Arabidopsis thaliana ABC transporter AtMRP5 controls root development and stomata movement. EMBO J 20: 1875–1887.
- 50. Suh SJ, Wang Y-F, Frelet A, Leonhardt N, Klein M, et al. (2007) The ATP binding cassette transporter AtMRP5 modulates anion and calcium channel activities in Arabidopsis guard cells. J Biol Chem 282: 1916–1924.
- 51. Yao X, Huang Y (2003) From nitric oxide to endothelial cytosolic Ca2+: a negative feedback control. Trends Pharmacol Sci 24: 263–266.
- 52. Jeandroz S, Lamotte O, Astier J, Rasul S, Trapet P, et al.. (2013) There's more to the picture than meets the eye: Nitric oxide cross-talk with Ca2+ signaling. Plant Physiol: DOI: 10.1104/1113.220624.