- Open Access
Pleiotropic effects of statins in distal human pulmonary artery smooth muscle cells
Respiratory Research volume 12, Article number: 137 (2011)
Recent clinical data suggest statins have transient but significant effects in patients with pulmonary arterial hypertension. In this study we explored the molecular effects of statins on distal human pulmonary artery smooth muscle cells (PASMCs) and their relevance to proliferation and apoptosis in pulmonary arterial hypertension.
Primary distal human PASMCs from patients and controls were treated with lipophilic (simvastatin, atorvastatin, mevastatin and fluvastatin), lipophobic (pravastatin) and nitric-oxide releasing statins and studied in terms of their DNA synthesis, proliferation, apoptosis, matrix metalloproteinase-9 and endothelin-1 release.
Treatment of human PASMCs with selected statins inhibited DNA synthesis, proliferation and matrix metalloproteinase-9 production in a concentration-dependent manner. Statins differed in their effectiveness, the rank order of anti-mitogenic potency being simvastatin > atorvastatin > > pravastatin. Nevertheless, a novel nitric oxide-releasing derivative of pravastatin (NCX 6550) was effective. Lipophilic statins, such as simvastatin, also enhanced the anti-proliferative effects of iloprost and sildenafil, promoted apoptosis and inhibited the release of the mitogen and survival factor endothelin-1. These effects were reversed by mevalonate and the isoprenoid intermediate geranylgeranylpyrophosphate and were mimicked by inhibitors of the Rho and Rho-kinase.
Lipophilic statins exert direct effects on distal human PASMCs and are likely to involve inhibition of Rho GTPase signalling. These findings compliment some of the recently documented effects in patients with pulmonary arterial hypertension.
It is recognised that 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors (statins) have beneficial cardiovascular effects beyond cholesterol lowering [1, 2]. These so-called pleiotropic effects depend principally on inhibiting the synthesis of the isoprenoid intermediates farnesylpyrophosphate (FPP) and geranylgeranylpyrophosphate (GGPP), which are essential for the post-translational processing, membrane translocation and activation of the Ras and Rho GTP-binding protein families. These GTPases regulate many cellular functions and couple membrane growth factor receptors to intracellular pathways that affect cell proliferation [3, 4]. Activation of RhoA and its downstream mediator Rho-associated kinase is implicated in the pathogenesis of pulmonary hypertension (PH) and inhibition of the RhoA/Rho-kinase may also contribute to the beneficial effects of established therapies, such as sildenafil [5–8]. Statins inhibit RhoA/Rho-kinase signalling by suppressing mevalonate and GGPP synthesis and have been shown to attenuate the development of PH in several animal models [9–16]. More importantly, simvastatin reversed established experimental pulmonary hypertension [17, 18] and this was associated with increased apoptosis and reduced proliferation of smooth muscle cells in vascular lesions [9, 17]. The addition of simvastatin to sildenafil also reversed hypoxia-induced pulmonary hypertension and remodelling . In keeping with findings in animal experiments, recent clinical study using simvastatin in PAH showed transient but significant effects on right ventricular mass and NT-proBNP .
Differences have emerged in the protective effect of HMG-CoA reductase inhibitors in experimental models of PH [20, 21], raising questions about whether statins as a class of drugs are capable of inducing similar responses in the pulmonary vasculature of humans and laboratory animals. Actually, the potential direct effects of statins on the growth and survival of PASMCs are unclear and cells from different regions of the pulmonary vascular bed may vary in their response .
We hypothesised that statins have the potential to directly affect proliferation and apoptosis of distal human PASMCs. Specifically, we sought to establish (1) the effect of statins on PASMC proliferation, apoptosis and production of factors (endothelin-1 and matrix metalloproteinase-9) implicated in the pathogenesis of PAH; (2) the anti-proliferative effect of statins when used in combination with established therapies for PAH and (3) the intermediates in the mevalonate pathway responsible for the action of statins.
Cell isolation and culture
PASMCs were derived from micro-dissected segments of distal pulmonary arteries (< 1 mm external diameter) [23, 24]. Lung tissues were obtained from patients (8 female/8 male; aged 49.9 ± 2.8 years) undergoing lobectomy or pneumonectomy for bronchial carcinoma (n = 3), lung transplantation for idiopathic PAH (IPAH, n = 3), emphysema or fibrotic lung disease (n = 9) and from unused donor lungs (n = 1). Informed consent and approval from the Hammersmith Hospitals (Ref. No. 2001/6003) and Royal Brompton & Harefield Hospitals (Ref. No. 01-210) ethics committees was obtained. Cells (passages 3 to 12) were phenotyped using immunohistochemical and receptor binding techniques and, like smooth muscle cells in the medial layer of intact distal human pulmonary arteries, they expressed α-smooth muscle actin, calponin, endothelin ETA and ETB receptors and phosphodiesterase type 5 [23, 24]. Cells were quiesced for at least 24 hours in serum-free Dulbeco's modified Eagle medium (DMEM) prior to treatment with statins and other drugs at stated concentrations.
Simvastatin was acquired both as a pro-drug (activated by alkaline hydrolysis) and in active form, whereas other statins were obtained as active compounds (Merck Biosciences Ltd., Nottingham, UK). Nitric oxide (NO)-releasing derivatives of pravastatin (NCX 6550) and fluvastatin (NCX 6553) were provided by the NiCox Research Institute, Milan, Italy . Involvement of specific signalling pathways was assessed by examining the ability of exogenous mevalonic acid (MVA), squalene, geranylgeranylpyrophosphate (GGPP) and farnesylpyrophosphate (FPP) to reverse responses to statin treatment and using inhibitors of geranylgeranyl transferase (GGTI-2133), farnesyl transferase (FTI-277), Rho (exoenzyme C3) and Rho-kinase (Y-27632) (Merck Biosciences Ltd.).
DNA synthesis was assessed by measuring incorporation of [3H-methyl]-thymidine (0.25 μCi/well; GE Healthcare, Little Chalfont, Buck's, UK) over 24 hours in cells stimulated with recombinant human platelet-derived growth factor (PDGF, 5 ng/ml; R&D Systems Europe Ltd., Abingdon, Oxon, UK) [24, 26]. Some experiments were conducted using statins in combination with iloprost (GE Healthcare) and sildenafil (Pfizer Global Research & Development, Sandwich, Kent, UK).
Cell viability and proliferation
Cell viability was assessed by measuring trypan blue exclusion and ATP content using a CellTiter-Glo® Luminescent cell viability assay (Promega Coporation, Southampton, UK). Adherent cells were trypsinized and counted with a multi-chamber haemocytometer.
Apoptosis was assessed by measuring cytoplasmic histone-associated DNA fragments (Roche Diagnostics Ltd, Lewis, Sussex, UK) and Hoechst 33342 staining [24, 26], in the presence and absence of the pan-caspase inhibitor z-VAD-fmk (MP Biomedicals Europe, Illkirch, France).
Endothelin-1 and matrix metalloproteinase-9 production
Production of ET-1 was stimulated with recombinant human transforming growth factor-β1 (TGF-β1, 10 ng/ml; R&D Systems) for 24 hours and matrix metalloproteinase-9 (MMP-9) by tumour necrosis factor-α (TNF-α, 10 ng/ml) and phorbol 12-myrisate 13-acetate (PMA, 0.1 μM). ET-1 and MMP-9 were measured in conditioned medium using QuantiGlo® (R&D Systems, UK) and Biotrack® immunoassays (GE Healthcare, UK) respectively .
Data are expressed as means ± SEM and analysed with GraphPad Prism version 4.0 (GraphPad Software, San Diego, CA). Comparisons were made by one-way ANOVA with Tukey's post test and Student's t test as appropriate. A probability of P < 0.05 indicated statistical significance.
Statin treatment reduces cell proliferation and promotes apoptosis
Treatment of human PASMCs with PDGF increased DNA synthesis ~4-fold (P < 0.001) and was attenuated by statins in a concentration-dependent manner. This effect was most marked when concentrations above 0.1 μM were used, with 1 μM resulting in significant inhibition in both IPAH and non-IPAH cells (Figure 1A-B). However, statins differed in their relative potency, with a rank order of simvastatin (IC50 0.68 ± 0.09 μM, n = 4 isolates) > atorvastatin (IC50 3.11 ± 0.84 μM, n = 3 isolates; P = 0.019) > > pravastatin (IC50 > 100 μM, n = 3 isolates) (Figure 1A). While pravastatin (1-10 μM) failed to significantly inhibit DNA synthesis the NO-releasing derivative NCX 6500 was effective at concentrations of 5-10 μM (5-fold higher concentration as compared to other lipophilic statins) (Figure 1C). Fluvastatin and its NO-releasing derivative NCX 6553 (1 μM ) inhibited DNA synthesis to a similar extent and the effects of all three compounds were reversed by MVA (Figure 1D).
The inhibitory effect of simvastatin was reversed by MVA and GGPP, but not by the cholesterol precursor squalene or by FPP (Figure 2A-B); indicating that the anti-proliferative effect was due to inhibition of HMG-CoA reductase and isoprenylation of Rho proteins and not to the interruption of cholesterol synthesis. Inhibitors of Rho and Rho-kinase also attenuated DNA synthesis, implicating Rho/Rho-kinase signalling in the mitogenic response to PDGF (Figure 2C). In addition, the anti-proliferative effect of the prostacyclin analogue iloprost and PDE5 inhibitor sildenafil on human PASMCs [22, 26] was enhanced when used together with simvastatin, the combined effect being greater than either agent alone (Figure 2D). Serum-stimulated proliferation of PASMCs from patients with IPAH was also attenuated by statins, simvastatin being more potent than atorvastatin at equimolar concentrations (Figure 3A-B). The proportion of adherent, non-viable trypan blue-stained PASMCs was relatively low (1-2%) and no significant acute toxic effects were observed with increasing statin concentrations, as determined by assessing intracellular ATP levels over 24 hours in both the presence and absence of serum (data not shown).
Serum-deprivation increased DNA fragmentation and this was augmented by simvastatin, fluvastatin and NO-releasing derivatives of pravastatin (NCX 6500) and fluvastatin (NCX 6553), but not by pravastatin (Figure 4A-B). Theses pro-apoptotic effects were reversed by MVA, but not by squalene, and mimicked in cells treated with Y-27632 (Figure 4C-D). The effect of statins was also prevented by GGPP, but not FPP, and abolished by the pan-caspase inhibitor z-VAD-fmk (Figure 5A-B). Furthermore, the pro-apoptotic effect was verified by assessment of nuclear chromatin condensation in Hoechst-stained cells (Additional File 1) and accompanied by morphological changes. Cultured cells typically became rounded and isolated from their neighbours following statin treatment and this was prevented by MVA (Figure 5C).
Statin treatment inhibits ET-1 release and MMP-9 production
Human PASMCs represent an important site of ET-1 production, particularly when stimulated with cytokines or growth factors such as TGF-β1 [23, 27]. Lipophilic statins inhibited ET-1 release in a concentration-dependent manner from PASMCs isolated from patients with IPAH (Figure 6A), and these inhibitory effects were reversed by the addition of MVA or GGPP, but not FPP (Figure 6B). Pravastatin was again found to be ineffective, whereas the NO-releasing derivative of pravastatin (NCX 6500), fluvastatin and NCX 6553 all attenuated ET-1 production (Figure 6C). Inhibition of farnesyl transferase resulted in non-significant reduction of ET-1 production. Instead inhibition of geranylgeranyl transferase mimicked the effect of statins (Figure 7A) and, consistent with signalling via geranylgeranylated proteins, inhibitors of Rho and Rho-kinase also attenuated ET-1 production (Figure 7B). Stimulation of PASMCs with TNF-α and PMA markedly induces MMP-9 expression and increases MMP-9 activity in conditioned medium . Simvastatin attenuated MMP-9 production from PASMCs which was reversed by MVA (Figure 7C-D).
As might be expected, the magnitude of statin-induced responses varied between different human PASMC isolates. Nonetheless, statins appeared to exhibit reproducible effects in cells from patients with IPAH and those with other lung diseases or apparently normal lung tissues.
We have shown that statins exhibit several complementary effects in distal human PASMCs derived from patients with IPAH as well as other lung diseases. Specifically, lipophilic statins used at concentrations ≥ 1 μM attenuated proliferation, promoted apoptosis and inhibited production of ET-1 and MMP-9, all of which are implicated in the pathogenesis of PAH and remodelling of pulmonary arteries. When used in combination with established therapies for PAH, simvastatin (0.5 μM) also exhibited an additional inhibitory effect on DNA synthesis.
The anti-proliferative effect of statins was dependent on inhibition of the mevalonate pathway and formation of isoprenoids and was selectively reversed by GGPP and not FPP, suggesting that post-translational geranylgeranylation of proteins contributes to the mitogenic effect of PDGF in PASMCs. The Rho family GTPases are in fact a major target of geranylgeranylation and the inhibition of Rho and Rho-kinase is considered to underlie many of the pleiotropic effects of statins in smooth muscle cells . The anti-mitogenic effect of Rho and Rho-kinase inhibitors in PASMCs supports this view. Moreover, activation of RhoA/Rho-kinase signalling is implicated in the pathogenesis of PH and inhibition of this pathway attenuates the development of the disease in experimental models [5, 6, 16].
Similar effects of statins in other smooth cells have been previously reported. The inhibitory effect of simvastatin was mediated by geranylgeranylation of RhoA but not farnesylation of Ras in bronchial smooth muscle cells . Mevalonate also reversed anti-proliferative effect of simvastatin in human bronchial smooth muscle cells . In addition to the mevalonate pathway, Insulin-like growth factor I/insulin dependent pathway has been implicated in the inhibition of human vascular smooth muscle cells proliferation by lovastatin .
Established therapies, such as iloprost and sildenafil display cAMP- and cGMP-dependent anti-proliferative effects in human PASMCs [22, 26] and when used together with a statin had a greater inhibitory effect than either agent alone. The use of adjunctive simvastatin in patients with PAH resulted in short-term reduction of right ventricular mass and marker of cardiac failure supporting the concept that combination therapies may be of some benefit, although this has not yet been shown to improve functional capacity [19, 31]. Both cAMP and cGMP pathways regulate the activity and expression of RhoA in vascular smooth muscle cells  and the beneficial effects of sildenafil and simvastatin in hypoxia-induced PH depend, at least in part, on the inhibition of RhoA- and Rho-kinase-dependent functions [8, 18].
A number of apoptosis-based strategies have been successful in reversing pulmonary vascular remodelling in animals [33, 34], including the use of simvastatin in monocrotaline- and hypoxia-induced PH [17, 18]. However, the apoptotic response to statins varies between different species and cell types  and here we establish that statins have a pro-apoptotic effect on isolated distal human PASMCs. The growth of these cultured cells depends on the autocrine production of ET-1 , which is a recognized survival factor as well as mitogen and protects against apoptosis in vascular smooth muscle cells . Human PASMCs synthesise substantial amounts of ET-1 when stimulated with TGF-β1  and lipophilic statins such as simvastatin attenuated ET-1 release. In accordance with the Rho-dependent regulation of endothelial ET-1 expression by statins , the effect was also mimicked by inhibition of geranylgeranyl transferase, Rho and Rho-kinase. Thus, a reduction in ET-1 release may contribute to both the anti-proliferative and pro-apoptotic effects of statins in PASMCs. Proteolytic enzymes are also implicated in the migration, proliferation and resistance to apoptosis of PASMCs [38, 39] and represent another potential therapeutic target as PASMCs exhibit increased gelatinase activity in PAH [40, 41] and statins such as simvastatin attenuated MMP-9 production in cultured cells. The precise mechanisms underlying this effect are not fully understood, but include inhibition of RhoA/Rho-kinase activation and reduced MMP-9 mRNA expression .
When used at equimolar concentrations, statins differed in their effectiveness (simvastatin > atorvastatin >> pravastatin) at inhibiting DNA synthesis, proliferation and ET-1 production. The ability of statins to inhibit HMG-CoA reductase activity in other non-hepatic human cells is considered to vary with their lipophilicity, simvastatin being 5- to 40-fold more potent than atorvastatin and ~600-fold more potent than pravastatin . Conversely, these statins were broadly equipotent at inhibiting enzyme activity in a cell-free system . Pravastatin had little or no effect on PASMCs unless it was linked to a NO-releasing moiety. Besides slowly releasing NO, this functional group is thought to increase lipophilicity and aid penetration into cells, thereby contributing to the MVA-dependent effects of the NO-releasing derivative NCX 6550 . Thus, unlike pravastatin, lipophilic fluvastatin and its NO-releasing derivative NCX 6553 displayed comparable inhibitory effects on PASMCs. These novel agents have not been studied before in distal human PASMCs and could be used as tools in interrogating deranged cellular pathways in PAH.
It is worth noting that the response of IPAH and non-IPAH cells to lipophilic statins may be different, although such a difference was not apparent when statins were used at concentrations ≥ 1 μM in our studies. A recent study suggested differences in PDGF (10 ng/ml) induced cell proliferation between IPAH and non-IPAH cells when treated with 0.1 μM of simvastatin . The authors demonstrated greater inhibitory effect of IPAH than non-IPAH cells. However, in the same study 1 μM of simvastatin exhibited significant inhibitory effect in non-IPAH cells consistent with our findings. Thus medium to high concentrations of lipophilic statins affect non-IPAH and IPAH cells equally. Although the doses of statins used in our experiments are similar to other studies, such concentrations are unlikely to be achieved in human plasma. It is conceivable that lipophilic statins used in clinical doses could result in a cumulative response through their effects on a number of cell systems. Speculatively our in vitro observations could explain the short-term effects of simvastatin in the recent clinical study in PAH .
Lipophilic statins directly modulate proliferation, apoptosis and the production of ET-1 and MMP-9 in human PASMCs. These effects are relevant to the pathogenesis of PAH.
- HMG-CoA reductase:
3-hydroxy-3-methylglutaryl-coenzyme A reductase
idiopathic pulmonary arterial hypertension
pulmonary arterial hypertension
pulmonary artery smooth muscle cells
human platelet-derived growth factor
phorbol 12-myrisate 13-acetate
transforming growth factor-β1
tumour necrosis factor-α.
Sadowitz B, Maier KG, Gahtan V: Basic science review: Statin therapy--Part I: The pleiotropic effects of statins in cardiovascular disease. Vasc Endovascular Surg. 2010, 44: 241-251. 10.1177/1538574410362922.
Liao JK, Laufs U: Pleiotropic effects of statins. Annu Rev Pharmacol Toxicol. 2005, 45: 89-118. 10.1146/annurev.pharmtox.45.120403.095748.
Nunes KP, Rigsby CS, Webb RC: RhoA/Rho-kinase and vascular diseases: what is the link?. Cell Mol Life Sci. 2010, 67: 3823-3836. 10.1007/s00018-010-0460-1.
Loirand G, Guerin P, Pacaud P: Rho kinases in cardiovascular physiology and pathophysiology. Circ Res. 2006, 98: 322-334. 10.1161/01.RES.0000201960.04223.3c.
McMurtry IF, Abe K, Ota H, Fagan KA, Oka M: Rho kinase-mediated vasoconstriction in pulmonary hypertension. Adv Exp Med Biol. 2010, 661: 299-308. 10.1007/978-1-60761-500-2_19.
Oka M, Fagan KA, Jones PL, McMurtry IF: Therapeutic potential of RhoA/Rho kinase inhibitors in pulmonary hypertension. Br J Pharmacol. 2008, 155: 444-454.
Ali O, Wharton J, Gibbs JS, Howard L, Wilkins MR: Emerging therapies for pulmonary arterial hypertension. Expert Opin Investig Drugs. 2007, 16: 803-818. 10.1517/135437188.8.131.523.
Guilluy C, Sauzeau V, Rolli-Derkinderen M, Guerin P, Sagan C, Pacaud P, Loirand G: Inhibition of RhoA/Rho kinase pathway is involved in the beneficial effect of sildenafil on pulmonary hypertension. Br J Pharmacol. 2005, 146: 1010-1018. 10.1038/sj.bjp.0706408.
Nishimura T, Faul JL, Berry GJ, Vaszar LT, Qiu D, Pearl RG, Kao PN: Simvastatin attenuates smooth muscle neointimal proliferation and pulmonary hypertension in rats. Am J Respir Crit Care Med. 2002, 166: 1403-1408. 10.1164/rccm.200203-268OC.
Girgis RE, Li D, Zhan X, Garcia JG, Tuder RM, Hassoun PM, Johns RA: Attenuation of chronic hypoxic pulmonary hypertension by simvastatin. Am J Physiol Heart Circ Physiol. 2003, 285: H938-945.
Murata T, Kinoshita K, Hori M, Kuwahara M, Tsubone H, Karaki H, Ozaki H: Statin protects endothelial nitric oxide synthase activity in hypoxia-induced pulmonary hypertension. Arterioscler Thromb Vasc Biol. 2005, 25: 2335-2342. 10.1161/01.ATV.0000186184.33537.48.
Guerard P, Rakotoniaina Z, Goirand F, Rochette L, Dumas M, Lirussi F, Bardou M: The HMG-CoA reductase inhibitor, pravastatin, prevents the development of monocrotaline-induced pulmonary hypertension in the rat through reduction of endothelial cell apoptosis and overexpression of eNOS. Naunyn Schmiedebergs Arch Pharmacol. 2006, 373: 401-414. 10.1007/s00210-006-0082-1.
Taraseviciene-Stewart L, Scerbavicius R, Choe KH, Cool C, Wood K, Tuder RM, Burns N, Kasper M, Voelkel NF: Simvastatin causes endothelial cell apoptosis and attenuates severe pulmonary hypertension. Am J Physiol Lung Cell Mol Physiol. 2006, 291: L668-676. 10.1152/ajplung.00491.2005.
Laudi S, Trump S, Schmitz V, West J, McMurtry IF, Mutlak H, Christians U, Weimann J, Kaisers U, Steudel W: Serotonin transporter protein in pulmonary hypertensive rats treated with atorvastatin. Am J Physiol Lung Cell Mol Physiol. 2007, 293: L630-638. 10.1152/ajplung.00110.2006.
Satoh K, Fukumoto Y, Nakano M, Sugimura K, Nawata J, Demachi J, Karibe A, Kagaya Y, Ishii N, Sugamura K, Shimokawa H: Statin ameliorates hypoxia-induced pulmonary hypertension associated with down-regulated stromal cell-derived factor-1. Cardiovasc Res. 2009, 81: 226-234. 10.1093/cvr/cvn244.
Zhao L, Sebkhi A, Ali O, Wojciak-Stothard B, Mamanova L, Yang Q, Wharton J, Wilkins MR: Simvastatin and sildenafil combine to attenuate pulmonary hypertension. Eur Respir J. 2009, 34: 948-957. 10.1183/09031936.00143508.
Nishimura T, Vaszar LT, Faul JL, Zhao G, Berry GJ, Shi L, Qiu D, Benson G, Pearl RG, Kao PN: Simvastatin rescues rats from fatal pulmonary hypertension by inducing apoptosis of neointimal smooth muscle cells. Circulation. 2003, 108: 1640-1645. 10.1161/01.CIR.0000087592.47401.37.
Girgis RE, Mozammel S, Champion HC, Li D, Peng X, Shimoda L, Tuder RM, Johns RA, Hassoun PM: Regression of chronic hypoxic pulmonary hypertension by simvastatin. Am J Physiol Lung Cell Mol Physiol. 2007, 292: L1105-1110. 10.1152/ajplung.00411.2006.
Wilkins MR, Ali O, Bradlow W, Wharton J, Taegtmeyer A, Rhodes CJ, Ghofrani HA, Howard L, Nihoyannopoulos P, Mohiaddin RH, Gibbs JS: Simvastatin Pulmonary Hypertension Trial (SiPHT) Study Group: Simvastatin as a treatment for pulmonary hypertension trial. Am J Respir Crit Care Med. 2010, 181: 1106-1113.
Rakotoniaina Z, Guerard P, Lirussi F, Goirand F, Rochette L, Dumas M, Bardou M: The protective effect of HMG-CoA reductase inhibitors against monocrotaline-induced pulmonary hypertension in the rat might not be a class effect: comparison of pravastatin and atorvastatin. Naunyn Schmiedebergs Arch Pharmacol. 2006, 374: 195-206. 10.1007/s00210-006-0112-z.
McMurtry MS, Bonnet S, Michelakis ED, Bonnet S, Haromy A, Archer SL: Statin therapy, alone or with rapamycin, does not reverse monocrotaline pulmonary arterial hypertension: the rapamcyin-atorvastatin-simvastatin study. Am J Physiol Lung Cell Mol Physiol. 2007, 293: L933-940. 10.1152/ajplung.00310.2006.
Wharton J, Davie N, Upton PD, Yacoub MH, Polak JM, Morrell NW: Prostacyclin analogues differentially inhibit growth of distal and proximal human pulmonary artery smooth muscle cells. Circulation. 2000, 102: 3130-3136.
Davie N, Haleen SJ, Upton PD, Polak JM, Yacoub MH, Morrell NW, Wharton J: ET(A) and ET(B) receptors modulate the proliferation of human pulmonary artery smooth muscle cells. Am J Respir Crit Care Med. 2002, 165: 398-405.
Growcott EJ, Spink KG, Ren X, Afzal S, Banner KH, Wharton J: Phosphodiesterase type 4 expression and anti-proliferative effects in human pulmonary artery smooth muscle cells. Respir Res. 2006, 7: 9-10.1186/1465-9921-7-9.
Ongini E, Impagnatiello F, Bonazzi A, Guzzetta M, Govoni M, Monopoli A, Del Soldato P, Ignarro LJ: Nitric oxide (NO)-releasing statin derivatives, a class of drugs showing enhanced antiproliferative and antiinflammatory properties. Proc Natl Acad Sci USA. 2004, 101: 8497-8502. 10.1073/pnas.0401996101.
Wharton J, Strange JW, Moller GM, Growcott EJ, Ren X, Franklyn AP, Phillips SC, Wilkins MR: Antiproliferative effects of phosphodiesterase type 5 inhibition in human pulmonary artery cells. Am J Respir Crit Care Med. 2005, 172: 105-113. 10.1164/rccm.200411-1587OC.
Wort SJ, Woods M, Warner TD, Evans TW, Mitchell JA: Cyclooxygenase-2 acts as an endogenous brake on endothelin-1 release by human pulmonary artery smooth muscle cells: implications for pulmonary hypertension. Mol Pharmacol. 2002, 62: 1147-1153. 10.1124/mol.62.5.1147.
Takeda N, Kondo M, Ito S, Ito Y, Shimokata K, Kume H: Role of RhoA inactivation in reduced cell proliferation of human airway smooth muscle by simvastatin. Am J Respir Cell Mol Biol. 2006, 35: 722-729. 10.1165/rcmb.2006-0034OC.
Vigano T, Hernandez A, Corsini A, Granata A, Belloni P, Fumagalli R, Paoletti R, Folco G: Mevalonate pathway and isoprenoids regulate human bronchial myocyte proliferation. Eur J Pharmacol. 1995, 291: 201-203. 10.1016/0922-4106(95)90143-4.
Martinez-Gonzalez J, Vinals M, Vidal F, Llorente-Cortes V, Badimon L: Mevalonate deprivation impairs IGF-I/insulin signaling in human vascular smooth muscle cells. Atherosclerosis. 1997, 135: 213-223. 10.1016/S0021-9150(97)00164-0.
Kawut SM, Bagiella E, Lederer DJ, Shimbo D, Horn EM, Roberts KE, Hill NS, Barr RG, Rosenzweig EB, Post W, et al: Randomized Clinical Trial of Aspirin and Simvastatin for Pulmonary Arterial Hypertension: ASA-STAT. Circulation.
Sauzeau V, Rolli-Derkinderen M, Marionneau C, Loirand G, Pacaud P: RhoA expression is controlled by nitric oxide through cGMP-dependent protein kinase activation. J Biol Chem. 2003, 278: 9472-9480. 10.1074/jbc.M212776200.
Jurasz P, Courtman D, Babaie S, Stewart DJ: Role of apoptosis in pulmonary hypertension: from experimental models to clinical trials. Pharmacol Ther. 2010, 126: 1-8. 10.1016/j.pharmthera.2009.12.006.
Huang JB, Liu YL, Sun PW, Lv XD, Bo K, Fan XM: Novel strategy for treatment of pulmonary arterial hypertension: enhancement of apoptosis. Lung. 2010, 188: 179-189. 10.1007/s00408-010-9233-8.
Filippatos GS, Gangopadhyay N, Lalude O, Parameswaran N, Said SI, Spielman W, Uhal BD: Regulation of apoptosis by vasoactive peptides. Am J Physiol Lung Cell Mol Physiol. 2001, 281: L749-761.
Hernandez-Perera O, Perez-Sala D, Soria E, Lamas S: Involvement of Rho GTPases in the transcriptional inhibition of preproendothelin-1 gene expression by simvastatin in vascular endothelial cells. Circ Res. 2000, 87: 616-622.
Merklinger SL, Jones PL, Martinez EC, Rabinovitch M: Epidermal growth factor receptor blockade mediates smooth muscle cell apoptosis and improves survival in rats with pulmonary hypertension. Circulation. 2005, 112: 423-431. 10.1161/CIRCULATIONAHA.105.540542.
George J, D'Armiento J: Transgenic expression of human matrix metalloproteinase-9 augments monocrotaline-induced pulmonary arterial hypertension in mice. J Hypertens. 2010
Frisdal E, Gest V, Vieillard-Baron A, Levame M, Lepetit H, Eddahibi S, Lafuma C, Harf A, Adnot S, Dortho MP: Gelatinase expression in pulmonary arteries during experimental pulmonary hypertension. Eur Respir J. 2001, 18: 838-845. 10.1183/09031936.01.00084601.
Lepetit H, Eddahibi S, Fadel E, Frisdal E, Munaut C, Noel A, Humbert M, Adnot S, D'Ortho MP, Lafuma C: Smooth muscle cell matrix metalloproteinases in idiopathic pulmonary arterial hypertension. Eur Respir J. 2005, 25: 834-842. 10.1183/09031936.05.00072504.
Turner NA, O'Regan DJ, Ball SG, Porter KE: Simvastatin inhibits MMP-9 secretion from human saphenous vein smooth muscle cells by inhibiting the RhoA/ROCK pathway and reducing MMP-9 mRNA levels. Faseb J. 2005, 19: 804-806.
Shitara Y, Sugiyama Y: Pharmacokinetic and pharmacodynamic alterations of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors: drug-drug interactions and interindividual differences in transporter and metabolic enzyme functions. Pharmacol Ther. 2006, 112: 71-105. 10.1016/j.pharmthera.2006.03.003.
Ikeda T, Nakamura K, Akagi S, Kusano KF, Matsubara H, Fujio H, Ogawa A, Miura A, Miura D, Oto T, et al: Inhibitory effects of simvastatin on platelet-derived growth factor signaling in pulmonary artery smooth muscle cells from patients with idiopathic pulmonary arterial hypertension. J Cardiovasc Pharmacol. 2010, 55: 39-48. 10.1097/FJC.0b013e3181c0419c.
This work was supported by the British Heart Foundation.
This work was perofrmed at The Centre for Pharmacology and Therapeutics, Imperial College London, Hammersmith Campus, Du Cane Road, London W12 ONN, UK.
The authors declare that they have no competing interests.
OA carried out all the cell-based assays. EG participated in parts of the ET-1/MMP-9 experiments design and analysis. GB helped in the production of the manuscript. JW supervised the entire project and helped in the data analysis and manuscript preparation. All authors have read and approved the final manuscript.
Electronic supplementary material
Additional File 1: Pro-apoptotic effect of simvastatin, as assessed by Hoechst staining. (A) Simvastatin-treated PASMCs show characteristic nuclear condensation (arrows). (B-C) Pro-apoptotic effect of simvastatin in serum-deprived cells reversed by mevalonate (MVA, 100 μM), geranylgeranylpyrophosphate (GGPP; 10 μM) and the pan-caspase inhibitor Z-VAD-fmk (50 μM). Data are mean ± SEM from 3-4 distinct cell isolates. SF = serum-free untreated cells. (PPT 210 KB)
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
About this article
Cite this article
Ali, O.F., Growcott, E.J., Butrous, G.S. et al. Pleiotropic effects of statins in distal human pulmonary artery smooth muscle cells. Respir Res 12, 137 (2011). https://doi.org/10.1186/1465-9921-12-137
- Pulmonary Arterial Hypertension