Regulation and role of endogenously produced hydrogen sulfide in angiogenesis.

Several studies have investigated the cellular signaling pathways, which regulate the proangiogenic effect of H 2 S. Exogenously added H 2 S promotes the phosphorylation of Akt, ERK1/2 and p38 [ 30 , 72 , 86 ]. The contribution of endogenous H 2 S in the activation of MAPK cascades was demonstrated using VEGF; stimulation of cells with VEGF promoted ERK1/2 and p38 phosphorylation that could be blocked by pharmacological inhibitors or silencing of CSE [ 30 ]. ATP-sensitive potassium channels (K ATP ), a major mediator of the effects of H 2 S, were shown to lie upstream of p38 [ 30 ]. In line with these findings, direct K ATP , channel openers also promote angiogenesis [ 30 , 87 ]. Treatment of tissues or cells with inhibitors of H 2 S synthesis, CSE gene deletion or silencing results in decreased cGMP levels [ 88 , 89 ], while over expression of CSE increases cGMP [ 88 ]. The ability of H 2 S to up regulate cGMP levels is, at least in part, due to the direct inhibition of PDE activity by H 2 S [ 70 , 88 ] ( Fig.2 ). Moreover, H 2 S converts sGC to its ferrous, NO-responsive form and further increases cGMP [ 90 ]. Furthermore, H 2 S production also activates the phosphoinositide 3-kinase (PI3K)/serine/threonine kinase (Akt) pathway, leading to endothelial nitric oxide synthase (eNOS) phosphorylation and eNOS activation [ 70 , 72 , 91 ]. PI3-K/Akt activation might result from the ability of H 2 S to inhibit the lipid phosphatase and tensin homolog (PTEN)[ 92 ]. H 2 S has also been shown to increase eNOS activity by promoting its dimerization [ 93 ] ( Fig.2 ). The increase in NO production, along with the inhibition of cGMP breakdown allows for significant elevations in intracellular cGMP in vascular endothelium [ 70 ]. As expected, endothelial cells incubated with L-cysteine exhibit enhanced VASP phosphorylation on Ser239, proving proof that endogenously generated H 2 S activates the cGMP/PKG axis [ 70 ]. cGMP accumulation, in turn, activates protein kinase G (PKG) stimulating the angiogenic properties of endothelial cells [ 70 ] ( Fig.2 ). The proangiogenic effect of 3-MP/3MST/H 2 S pathway is also associated with the activation of Akt and PKG. 3-MP stimulates Akt phosphorylation on its activating site (Ser473). Similarly, 3-MST silencing results in lower levels of Akt and vasodilator-stimulated phosphoprotein phosphorylation [ 74 ]. Based on the above observations, the concerted action of NO and H 2 S is believed to be crucial for the angiogenic response. Inhibition of NO blocks the proliferation, migration and tube-structure formation [ 70 , 72 ], while inhibiting H 2 S abolishes the NO-stimulated angiogenesis [ 70 , 72 ].

Angiogenesis is a physiological process through which new blood vessels are formed from the existing vasculature [ 1 , 2 ]. In healthy organisms, the rate at which new blood vessels are formed varies with biological age and differs between tissues [ 3 ]. Early in life during embryonic development, organisms exhibit rapid neovascularization [ 4 ]. In contrast, during adulthood the process is tightly controlled; endothelial cells in mature vessels cells are quiescent and have a long-half life [ 5 ]. Angiogenesis in adults is observed only in the context of a limited number of physiological responses and in selected tissues. New vessel growth is restricted to the endometrium during the menstrual cycle, as an adaptive response to exercise in skeletal muscle and in wound healing [ 3 , 6 ]. Dysregulation of angiogenesis is associated with many pathophysiological conditions and diseases [ 3 , 7 ]. On one hand, excessive or abnormal new blood vessel growth is seen in cancer, psoriasis, arthritis, endometriosis, inflammatory bowel disease and diabetic retinopathy [ 3 , 7 , 8 ]. On the other hand, impaired angiogenesis or vessel regression has been linked to neurodegenerative diseases, hair loss and preeclampsia [ 7 , 9 ]. Given the wide array of conditions associated with aberrant angiogenesis, there has been a considerable interest in its physiological regulatory processes and in the opportunities for pharmacological modulation. Work in this field resulted in several drug approvals, mainly for malignancies and ocular diseases [ 10 , 11 ]. Further understanding of the basic mechanisms that regulate angiogenesis are expected to offer new targets with translational potential.

CSE KO mice do not display a major cardiovascular phenotype, apart from a mild hypertension [ 98 ]. Although extensively used in the literature for almost a decade, there are no reports describing developmental angiogenic defects or alterations in vascular structure or density in the organs of these animals. However, as discussed above, vessels isolated from CSE KO animals show reduced responsiveness to VEGF in in vitro assays. On the other hand, very limited information on the 3MST KO mice is available, with no studies evaluating their cardiovascular phenotype [ 99 ]. In contrast, CBS KO mice exhibit a severe phenotype that results in reduced lifespan [ 100 ]. CBS heterozygotes are used in most studies; loss of just one CBS allele results in mild hypehomocysteinemia causing endothelial dysfunction [ 101 ] and vascular complications [ 102 ]. In a hind limb ischemia model, Bosch-Marcé and colleagues observed that arteriogenesis/angiogenesis was reduced in CBS +/− animals; angiogenesis was inversely related to plasma levels of homocysteine [ 103 ]. The observed impairment, was not dependent on reduced expression of VEGF or impaired phosphorylation of its receptor Flk-1, but was rather attributed to impaired Akt phosphorylation associated with hyperhomocysteinemia. The first in vivo model in which the role of CSE-derived H 2 S was investigated was the chicken chorioallantoic membrane (CAM). Treatment of CAMs with the H 2 S synthesis inhibitors PAG and β-Cyano-L-alanine (BCA) lead to reduced vessel length and branching [ 30 ] ( Fig.3 ). The effect of PAG and BCA was reversed following addition of NaHS. Although the CAM is a widely used model and in most cases accurately predicts the angiogenic potential of the tested agents, it is a developmental model of angiogenesis in a non-mammalian organism. To further investigate the contribution of endogenous H 2 S in new blood vessel formation and to extend the in vitro findings that H 2 S is required for VEGF-stimulated proliferation, migration and network formation, we employed the Matrigel® plug assay. In these experiments reduced Matrigel® plugs were implanted into mice that received water for injection or PAG for 15days. Some of the xenografted plugs contained VEGF to drive the angiogenic response, while others contained vehicle. At the end of the experiment plugs were removed and angiogenesis was assessed by measuring hemoglobin content, as an index of vascularization ( Fig.4 ). We observed that VEGF stimulates vessel ingrowth in the Matrigel® plugs and that PAG administration reduced both basal and VEGF-stimulated angiogenesis. In agreement with the angiogenic properties of CSE-derived H 2 S, 3-MP administration to enhance production of H 2 S by 3MST lead to an increase in neovascularization of Matrigel ®plugs implanted in mice [ 74 ]. The role of endogenous H 2 S has also been studied in a number of pathophysiological conditions associated with angiogenesis, including wound healing, critical limb ischemia and cancer [ 30 , 45 , 70 ]. Burn wounds in CSE KO mice healed at a slower rate compared to those of wild-type control mice [ 30 ]. Moreover, administration of 3-MP to boost the 3MST-derived H 2 S facilitated wound closure in a burn wound model in rats [ 74 ]. Wound skin capillary densities were reduced in db/db animals which received the CSE inhibitor PAG; these animals exhibited reduced wound-closure rates [ 77 ]. In the only study to address the role of H 2 S in retinal neovascularization, mice were maintained in 70% oxygen from postnatal day P7 to P12 and room air from P12 to P17. It was observed that this treatment resulted in up regulation of CSE [ 104 ]. Moreover, CSE KO exhibited a 19% reduction in retinal neovascularization and a 31% increase in vaso-obliteration compared to heterozygotes during oxygen-induced retinopathy. Similarly, inhibition of CSE/CBS by aminooxyacetic acid (AOAA) decreased retinal retinal neovascularization, while accelerating vaso-obliteration. These results indicated that the CSE is critically involved in the development of pathological retinal neovascularization during retinal ischemia. In a femoral artery ligation study, arteriogenesis was inhibited in the absence of CSE. Mature vessel density, angiogenic indices and blood flow were significantly reduced in CSE KO mice compared with WT mice with femoral artery ligation [ 45 ]; administration of diallyl disulfide restored these parameters. In line with this notion, patients with critical limb ischemia exhibit reduced levels of all three H 2 S generating enzymes and attenuated H 2 S bioavailability accompanied by increased oxidative stress [ 105 ]. Mechanistically, H 2 S-stimulated angiogenesis is heavily dependent on the presence of eNOS/NO in wound healing, ischemia-driven angiogenesis and in Matrigel® plug neovessel growth [ 45 , 51 , 70 ]. Tumor angiogenesis is an area with significant translational implications. It is, thus, not surprising that production of H 2 S has been studied by several laboratories in the context of cancer [ 27 , 106 – 111 ]. Endogenous H 2 S levels were found to be increased in VHL-deficient clear cell renal cell carcinoma (ccRCC) cell lines. Inhibition of endogenous H 2 S production in the CAM decreased vascularization of ccRCC xenografts [ 112 ]. We have previously demonstrated that CBS, but not CSE or 3MST, is over expressed in human colon adenocarcinomas and colon cancer-derived epithelial cell lines (HCT116, HT- 29, LoVo), resulting in increased H 2 S production [ 27 ]. CBS silencing in HCT116 resulted in reduced tumor growth. Moreover, pharmacological inhibition of CSE/CBS by AOAA reduced the growth of patient-derived tumor xenotransplants and HCT116 tumors. Tumors from AOAA-treated mice also exhibited reduced vessel density [ 27 ], suggesting a significant role of endogenous H 2 S in tumor angiogenesis. CBS expression, was also found increased primary epithelial ovarian cancer and ovarian cancer cell lines; CBS down regulation via siRNA or inhibition of its activity by AOAA impairs proliferation and viability of cancer cells in vitro [ 106 ]. Silencing CBS in a cisplatin-resistant orthotopic ovarian cancer model reduced nodule formation, sensitized tumor cells to cisplatin and inhibited angiogenesis [ 106 ]. Taken together, the studies in colon and ovarian cancer cells clearly establish CBS-produced H 2 S as a novel, endogenous, regulator of tumor progression and angiogenesis [ 113 ].

Hypoxia is one of the most potent stimuli known to drive angiogenesis [ 35 ]. A drop in cellular oxygen tension stabilizes hypoxia inducible factor-1α (HIF-1α) through inhibition of prolyl-hydroxylase activity; lack of HIF-1α hydroxylation prevents recognition and ubiquitination by VHL E3 ubiquitin ligase that labels HIF-1α for degradation[ 35 , 36 ]. HIF-1α can then dimerize with HIF-1β, and bind to HIF-responsive elements in the promoter region of hypoxia-regulated genes [ 37 ]; this leads to the expression of several angiogenesis-related factors, including VEGF [ 38 ]. Several observations have linked H 2 S bioavailability to changes in ambient oxygen concentration [ 39 ]. H 2 S reacts with O 2 , and in spite of the fact that this reaction occurs at slow rates, O 2 can decrease H 2 S concentrations in tissues; highly oxygenated tissues might, thus, contain less H 2 S compared to tissues with lower O 2 tensions [ 40 – 42 ]. Moreover, enzymatic pathways that utilize molecular O 2 , oxidize H 2 S in the mitochondria, converting it to thiosulfate and sulfate for subsequent excretion and limit its biological actions [ 17 , 42 ]. Ischemia/hypoxia and the resulting intracellular acidosis have also been proposed to increase the release of H 2 S from acid labile pools (iron-sulfur clusters) [ 43 ]. Moreover, O 2 has indirect effects on H 2 S; heme-containing proteins react with H 2 S at different rates depending on their redox status [ 42 ]. Limited information is available about the effect of hypoxia on the expression of H 2 S-generating enzymes in the cardiovascular system. HIF binding elements are present in the CBS promoter; hypoxia increased CBS levels in a HIF-dependent manner in cultured glioblastoma cells [ 44 ]. These results were extrapolated in vivo ; rats exposed to hypobaric hypoxic exhibited increased CBS expression and activity in the cerebellum and cortex. Moreover, it was recently shown that chronic hypoxia increased tissue H 2 S levels and CSE activity in a mouse model of hind limb ischemia [ 45 ]. Increases in tissue H 2 S levels, albeit smaller, were also noted in CSE KO. In contrast, intermittent hypoxia decreased endothelial CSE expression in small mesenteric arteries [ 46 ]. Additional links between HIF-1 and H 2 S have been established. Flannigan and colleagues demonstrated that loss of CSE-derived H 2 S production decreased HIF-1α stability, indicating that endogenously generated H 2 S is important for HIF-1 signaling [ 47 ]. Indeed, administration of diallyl disulfide, an H 2 S-releasing molecule, stabilized HIF-1α expression and up-regulated hypoxia-responsive genes [ 47 ]. Similarly, in rat brain capillary endothelial cells incubation with a H 2 S donor, promoted an increase in HIF-1α and VEGF mRNA and protein levels, and enhanced HIF-1 DNA binding [ 48 ]. In cells treated with a H 2 S donor, angiogenic responses were linked to miR-640 down regulation and mediated by a VEGFR2/mTOR/HIF-1α pathway [ 49 ]. However, it should be kept in mind that under certain conditions H 2 S donors have been shown to suppress HIF-1 [ 50 ]. Interestingly, Kevil's group reported that H 2 S enhanced HIF-1α activation in hypoxic conditions and this correlated with a significantly higher stimulation of proliferation compared to normoxic cells [ 51 ]. The same group reported that expression of HIF-1α in skeletal muscle tissue was elevated under ischemia in WT but not in CSE KO mice [ 51 ]. The above observations establish multiple interactions between H 2 S and HIF-regulated pathways and propose that a freed forward cycle between HIF and H 2 S might exist in angiogenesis ( Fig.1 ).

Hydrogen sulfide (H 2 S), is the newest member of the gasotransmitter family [ 12 – 14 ]. Once viewed exclusively as an environmental pollutant and toxicant, H 2 S is now recognized as an endogenous biological mediator with important roles in homeostasis, physiology and disease [ 15 , 16 ]. H 2 S is ubiquitously present in mammalian cells and tissues and can be generated both through enzymatic and non-enzymatic pathways [ 16 ]. Three enzymes are known to be involved in catalytic reactions that yield H 2 S [ 17 , 18 ]. Two of them, cystathionine beta synthase (CBS) [ 19 ] and cystathionine gamma lyase (CSE) [ 20 ] operate in the transsulfuration pathway, the conversion of methionine to cysteine, and require pyridoxal-5′-phosphate (PLP) as a cofactor. The third enzyme is 3-mercaptopyruvate sulfurtransferase (3-MST) and converts 3-mercaptopyruvate (3-MP) to H 2 S and pyruvate [ 21 , 22 ]. Although 3MST itself does not need PLP, generation of 3-MP by cysteine aminotransferase (CAT) is dependent on PLP for its activity. H 2 S producing enzymes exhibit widespread tissue distribution [ 16 ]. CBS is viewed as the predominant H 2 S-producing enzyme in the nervous system, while CSE is believed to be the main enzyme in the cardiovascular system [ 12 , 14 ]. With research in the field advancing and experimental tools improving, CBS was also shown to be expressed in vascular tissues, as well as the heart [ 23 – 25 ]. CSE is mainly a cytosolic enzyme that can translocate to the mitochondria in response to injurious stimuli its presence in liver mitochondria increases after hypoxia [ 26 ]. CBS is found in the mitochondria of normal and tumor cells [ 27 , 28 ]. 3MST appears in both the cytosolic and mitochondrial fractions of cells and is expressed in all tissues studied so far [ 18 ]. 3MST is the least studied enzyme, most likely because no pharmacological inhibitors are available [ 29 ]. All three H 2 S-producing enzymes have been demonstrated to be present in the endothelium [ 30 – 32 ]. Thus, they are well-positioned to influence the angiogenic properties of endothelial cells and modify responses to angiogenic factors. Moreover, H 2 S - similar to the other two gasotransmitters NO and CO - is a freely membrane permeable, diffusible molecule, not requiring transporter of carrier molecules to gain intracellular access [ 33 ]; therefore, H 2 S produced by neighboring cells can also act in a paracrine manner to affect angiogenesis. In this brief review, we will focus on the role of endogenously produced H 2 S in the angiogenic process. H 2 S donors have been shown in a variety of models to promote angiogenic responses; readers interested in the effects of exogenously supplied H 2 S are referred to recent reviews [ 16 , 34 ].

VEGF plays a crucial role in angiogenic responses, both under normal and pathophysiological conditions [ 3 , 8 , 9 ]. As already mentioned in the previous section, VEGF-stimulated angiogenic properties of endothelial cells can be inhibited by the CSE inhibitor PAG or CSE silencing [ 30 , 70 , 78 ]. This observation suggests that incubation of endothelial cells with VEGF promotes H 2 S synthesis. Indeed, incubation of human EC with VEGF leads to increase output of H 2 S [ 30 ]. Although the mechanism through which this occurs has not been studied in detail, it was proposed to be mediated by a calcium/calmodulin-dependent activation of CSE [ 70 ] ( Fig.1 ). However, the reverse effect has also been observed. Adenovirus-mediated triple gene transfer of CBS, CSE and 3MST was found to increase VEGF expression and to diminish the levels of the anti-angiogenic factor endostatin [ 79 ]. These findings (i.e. enhanced VEGF production after H 2 S stimulation) have also been reproduced using various classes of H 2 S donors [ 80 – 82 ]. The above data suggest that H 2 S is a downstream effector of VEGF signaling, but can also exist upstream of VEGF, depending on the conditions/model studied. VEGF binding to VEGFR2 causes it to homodimerize, leading to transautophosphorylation of a series of tyrosine residues, including Tyr951, Tyr996, Tyr1054, Tyr1059, Tyr1175, and Tyr1214 [ 83 ]. Tao and colleagues identified a disulfide bond between Cys1045 and Cys1024 of VEGFR2 that alters the active conformation of the receptor, inhibiting its activity [ 76 ] ( Fig.2 ). Nucleophilic attack of the disulfide bond by H 2 S leads to a disulfide reduction and boosts VEGFR2 tyrosine kinase activity [ 76 ] ( Fig.1 ). Although the authors reported that CSE co-localized at sub-cellular areas at the membrane of vascular endothelial cells with VEGFR2, reduction of the Cys1045-Cys1024 disulfide bond has only been demonstrated with H 2 S donors. In a recent study, silencing CBS in endothelial cells compromised the phenotypic and signaling responses to VEGF that were due to decreased transcription of VEGFR2 and neuropilin (NRP)-1 ( Fig.1 ). Silencing of CBS resulted in transcriptional down-regulation of VEGFR2 and NRP-1 that was mediated by a decreased stability of the transcription factor specificity protein 1 (Sp1) [ 31 ]. Sp1 reduced stability was triggered by lack of sulfhydration on Cys68 and Cys755 that occurred in cells in which CBS had been silenced. H 2 S donor administration in CBS-silenced ECs restored the levels of Sp1 and its binding to the VEGFR2 promoter, as well as functional VEGF responses (proliferation, and migration phenotypes). Thus, maintaining endogenous H 2 S levels is crucial for preserving VEGF-responsiveness. To summarize the interactions between H 2 S and VEGF evidence has been presented to show that i) H 2 S increases after acute exposure of EC to VEGF, ii) prolonged exposure to increased H 2 S concentrations up regulates VEGF expression iii) H 2 S aids VEGFR2 in expressing increased activity by assuming a more activity conformation and maintains its expression levels. Considerably less information is available regarding the interaction between H 2 S and other growth factors. Basic fibroblast growth factor (bFGF) is another factor that is crucial for new blood vessels to form [ 2 ]. Inhibition of H 2 S by PAG did not reduce FGF-stimulated migration, suggesting that the actions of this angiogenic factor are H 2 S-independent [ 30 , 70 ]. Although H 2 S might not be required for bFGF angiogenic signaling, H 2 S up regulates bFGF levels in vivo . bFGF along with VEGF and interleukin-16 were increased following hind limb ischemia in wild-type mice; this response was reduced in CSE KO animals [ 45 ]. Recent reports showed that H 2 S reduced angiopoietin-2 production but none of them studied this effect in the context of angiogenesis [ 84 , 85 ]. The potential role of H 2 S in angiogenic signaling of other key growth factors, including the angiopoietins and Notch remains to be tested in future studies.

The evidence presented above shows that H 2 S derived from CSE, CBS or 3-MST, stimulates the angiogenic properties of endothelial cells. MAPK pathways and NO are the main mediators of the H 2 S-induced angiogenesis. In addition, endogenously produced H 2 S contributes to angiogenesis during development in vivo , as well as angiogenic responses that accompany wound healing and tumor growth, pointing towards translational opportunities. In spite of the compelling evidence in the literature for the role of endogenously generated H 2 S in new blood vessel formation, a multitude of questions regarding the regulation and biology of H 2 S in the context of angiogenesis remain unanswered. In growing, maturing and quiescent vessels, what cell type and which H 2 S-producing enzyme is the major source of H 2 S? Does H 2 S contribute to inflammation-associated angiogenesis? How are H 2 S signaling pathways integrated in vivo in the different settings where angiogenesis occurs? How does H 2 S impact on the endothelial metabolome and how does that contribute to its angiogenic properties? Can H 2 S be used to stimulate therapeutic angiogenesis? In addition to cancer, what other diseases related to angiogenesis can benefit from inhibition of H 2 S production? These questions and many more, some of which are mentioned in the sections above, await answers. Gaining more knowledge on H 2 S in angiogenesis will not only satisfy scientific curiosity, but will only increase the odds of successful translation of basic science findings into clinical applications.

Mammalian cells under normal conditions generate ATP in an oxygen-dependent manner. We recently showed that endogenously produced H 2 S by CBS or 3MST can be used as an inorganic energy source that complements and balances the bioenergetic role of Krebs cycle-derived electron donors [ 27 , 52 ]. Interestingly, the normally cytosolic enzyme CSE can translocate from the cytosol to mitochondria during hypoxia, where L-cysteine levels are 3 times higher than those of the cytosol, under stress-related conditions [ 26 ]. Moreover, CBS in the mitochondrial matrix is degraded by Lon protease in normoxic conditions [ 28 ]; lowering of O 2 tension prevents CBS degradation, allowing CBS accumulation. H 2 S could be used to maintain electron flow and to sustain cellular bioenergetics during hypoxia (but not anoxia as oxygen has to be present to serve as the final elector acceptor) to meet the demands of rapidly dividing endothelial cells during angiogenesis. In comparison to other respiratory chain substrates sulfide's electron yield is low: two molecules of sulfide are needed to provide a pair of electrons [ 53 ]. Moreover, it is costly in terms of oxygen, due to the involvement of the sulfide oxidation unit; sulfide oxidation needs three times more oxygen for the same electron transfer through complexes III and IV [ 54 ]. Therefore, the energy yield per oxygen atom consumed for sulfide is low compared to NADH or FADH2. However, sulfide is still an attractive alternative fuel as H 2 S is freely diffusible across membranes and does not require activation or conversion. Endothelial cells exhibit considerable plasticity and can emerge from prolonged periods of quiescence to assume a rapidly proliferating phenotype during angiogenesis [ 5 ]. Although oxidative phosphorylation is a markedly more efficient mode of ATP generation than glycolysis, it has been recently proposed that endothelial cells heavily rely on glycolysis to cover their ATP needs [ 55 ]. Cultured endothelial cells have glycolytic rates that exceed glucose oxidation rates and fatty acid oxidation flux [ 56 ]. Silencing of the glycolytic enzyme 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 3 (PFKFB3) decreased endothelial cell proliferation and migration, while over expression of PFKFB3 accelerated the angiogenic properties of endothelial cells [ 57 ]. Moreover, knockdown or pharmacologic inhibition of PFKFB3 reduced vessel branching and outgrowth in vivo [ 55 , 58 ]. Since endothelial cells appear to depend on glycolysis during neovascularization, it has been proposed that inhibition of PFKFB3 will only transiently and partially reduce glycolysis in vivo , inhibiting pathological angiogenesis, without affecting blood vessels throughout the body [ 58 ]. In line with its angiogenic effects and the link between glycolysis and angiogenesis, endogenously produced H 2 S was shown to stimulate the activity of another glycolytic enzyme, glyceraldehyde 3-phosphate dehydrogenase (GAPDH); GAPDH undergoes S-sulfhydration on the active site cysteine 150 and stimulates glycolytic flux [ 59 , 60 ]. Although evidence for the contrary (inhibition of GAPDH by H 2 S/persulfidation) has been presented [ 61 ], most studies have shown that H 2 S enhances the efficiency of glycolysis in cells [ 62 , 63 ]. Future studies should aim to quantify the contribution of glycolysis enhancement to the angiogenic actions of H 2 S.

In this section we will refer to pharmacologically active compounds that modify angiogenic responses by modulating endogenous H 2 S. Zofenopril, an SH-containing inhibitor of the angiotensin converting enzyme, was recently demonstrated to up regulate CSE in the cardiovascular system without affecting CBS and 3MST levels [ 23 ]. In a follow up study, Terzuoli et al reported that the zofenoprilat-induced angiogenic properties of endothelial cells were attenuated by CSE inhibition or silencing [ 94 ]. Similarly, PAG administration reduced neovascularization in the Matrigel® plug assay in vivo [ 94 ]. The molecular mechanisms underlying zofenopril-induced angiogenesis were dependent on Akt, eNOS and ERK1/2 cascades, in line with what is known about mediators of H 2 S-triggered angiogenic signaling. S-propargyl-l-cysteine (SPRC) is a H 2 S donor that also increases CSE levels [ 95 ]. Recent findings show that SPRC increased HUVECs proliferation and in vitro angiogenesis in a PAG-inhibitable manner [ 96 ]. Results from in vivo studies using SPRC provided additional evidence for its CSE-mediated effects, as PAG inhibited angiogenesis in an Matrigel® plug model [ 96 ]. Since other H 2 S donors have been shown to increase CSE expression under certain conditions [ 97 ], it is possible that endogenous H 2 S contributes to the angiogenic effects of some H 2 S donors. It should also be mentioned that NO donors require the presence of endogenous H 2 S to exert their angiogenic effects. CSE silencing resulted in the blockade of NO-induced proliferation, migration and in in vitro aortic ring angiogenesis [ 70 ]. Based on what is known about the mechanism of action of H 2 S, we predict that additional pharmacological agents that target cGMP-regulated pathways and promote angiogenesis (e.g. PDE inhibitors, sGC activators/stimulators, natriuretic peptides) could interact with endogenously produced H 2 S to regulate new blood vessel formation.