Myeloperoxidase aggravates pulmonary arterial hypertension by activation of vascular Rho-kinase
Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
P01 HL076491
NHLBI NIH HHS - United States
P20 HL113452
NHLBI NIH HHS - United States
P01 HL098055
NHLBI NIH HHS - United States
P01 HL103453
NHLBI NIH HHS - United States
K23 HL125697
NHLBI NIH HHS - United States
PubMed
29875311
PubMed Central
PMC6124430
DOI
10.1172/jci.insight.97530
PII: 97530
Knihovny.cz E-zdroje
- Klíčová slova
- Cardiology, Cardiovascular disease, Inflammation, Innate immunity, Microcirculation,
- MeSH
- amidy aplikace a dávkování MeSH
- arteria pulmonalis patologie patofyziologie MeSH
- dospělí MeSH
- hypoxie krev etiologie patologie MeSH
- intravenózní infuze MeSH
- Kaplanův-Meierův odhad MeSH
- kinázy asociované s Rho antagonisté a inhibitory metabolismus MeSH
- kohortové studie MeSH
- krysa rodu Rattus MeSH
- lidé středního věku MeSH
- lidé MeSH
- modely nemocí na zvířatech MeSH
- myši inbrední C57BL MeSH
- myši knockoutované MeSH
- myši MeSH
- peroxidasa aplikace a dávkování krev metabolismus MeSH
- plíce patologie MeSH
- plicní hypertenze krev mortalita patologie patofyziologie MeSH
- potkani Sprague-Dawley MeSH
- pyridiny aplikace a dávkování MeSH
- rekombinantní proteiny aplikace a dávkování krev metabolismus MeSH
- remodelace cév účinky léků fyziologie MeSH
- vazokonstrikce účinky léků fyziologie MeSH
- zvířata MeSH
- Check Tag
- dospělí MeSH
- krysa rodu Rattus MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- amidy MeSH
- kinázy asociované s Rho MeSH
- MPO protein, human MeSH Prohlížeč
- peroxidasa MeSH
- pyridiny MeSH
- rekombinantní proteiny MeSH
- Y 27632 MeSH Prohlížeč
Pulmonary arterial hypertension (PAH) remains a disease with limited therapeutic options and dismal prognosis. Despite its etiologic heterogeneity, the underlying unifying pathophysiology is characterized by increased vascular tone and adverse remodeling of the pulmonary circulation. Myeloperoxidase (MPO), an enzyme abundantly expressed in neutrophils, has potent vasoconstrictive and profibrotic properties, thus qualifying as a potential contributor to this disease. Here, we sought to investigate whether MPO is causally linked to the pathophysiology of PAH. Investigation of 2 independent clinical cohorts revealed that MPO plasma levels were elevated in subjects with PAH and predicted adverse outcome. Experimental analyses showed that, upon hypoxia, right ventricular pressure was less increased in Mpo-/- than in WT mice. The hypoxia-induced activation of the Rho-kinase pathway, a critical subcellular signaling pathway yielding vasoconstriction and structural vascular remodeling, was blunted in Mpo-/- mice. Mice subjected to i.v. infusion of MPO revealed activation of Rho-kinase and increased right ventricular pressure, which was prevented by coinfusion of the Rho-kinase inhibitor Y-27632. In the Sugen5416/hypoxia rat model, PAH was attenuated by the MPO inhibitor AZM198. The current data demonstrate a tight mechanistic link between MPO, the activation of Rho-kinase, and adverse pulmonary vascular function, thus pointing toward a potentially novel avenue of treatment.
Cardiovascular Institute Stanford University School of Medicine Stanford California USA
Center for Molecular Medicine Cologne CMMC University of Cologne Cologne Germany
Department of Cellular and Molecular Medicine Cleveland Clinic Cleveland Ohio USA
Department of Pneumology University Medical Center Hamburg Eppendorf Hamburg Germany
Heart Center Department of Cardiology
Institute of Biophysics Czech Academy of Sciences Brno Czech Republic
Pathobiology Lerner Research Institute Cleveland Clinic Cleveland Ohio USA
Pulmonary and Critical Care Medicine Respiratory Institute and
University Heart Center Hamburg University Medical Center Hamburg Eppendorf Hamburg Germany
Zobrazit více v PubMed
Simonneau G, et al. Updated clinical classification of pulmonary hypertension. J Am Coll Cardiol. 2013;62(25 Suppl):D34–D41. PubMed
Stenmark KR, Meyrick B, Galie N, Mooi WJ, McMurtry IF. Animal models of pulmonary arterial hypertension: the hope for etiological discovery and pharmacological cure. Am J Physiol Lung Cell Mol Physiol. 2009;297(6):L1013–L1032. doi: 10.1152/ajplung.00217.2009. PubMed DOI
O’Callaghan DS, et al. Treatment of pulmonary arterial hypertension with targeted therapies. Nat Rev Cardiol. 2011;8(9):526–538. doi: 10.1038/nrcardio.2011.104. PubMed DOI
Price LC, et al. Inflammation in pulmonary arterial hypertension. Chest. 2012;141(1):210–221. doi: 10.1378/chest.11-0793. PubMed DOI
Savai R, et al. Immune and inflammatory cell involvement in the pathology of idiopathic pulmonary arterial hypertension. Am J Respir Crit Care Med. 2012;186(9):897–908. doi: 10.1164/rccm.201202-0335OC. PubMed DOI
Lanza F. Clinical manifestation of myeloperoxidase deficiency. J Mol Med. 1998;76(10):676–681. doi: 10.1007/s001090050267. PubMed DOI
Exner M, et al. Myeloperoxidase predicts progression of carotid stenosis in states of low high-density lipoprotein cholesterol. J Am Coll Cardiol. 2006;47(11):2212–2218. doi: 10.1016/j.jacc.2006.01.067. PubMed DOI
Brevetti G, et al. Myeloperoxidase, but not C-reactive protein, predicts cardiovascular risk in peripheral arterial disease. Eur Heart J. 2008;29(2):224–230. PubMed
Baldus S, et al. Myeloperoxidase serum levels predict risk in patients with acute coronary syndromes. Circulation. 2003;108(12):1440–1445. doi: 10.1161/01.CIR.0000090690.67322.51. PubMed DOI
Brennan ML, et al. Prognostic value of myeloperoxidase in patients with chest pain. N Engl J Med. 2003;349(17):1595–1604. doi: 10.1056/NEJMoa035003. PubMed DOI
Lau D, Baldus S. Myeloperoxidase and its contributory role in inflammatory vascular disease. Pharmacol Ther. 2006;111(1):16–26. doi: 10.1016/j.pharmthera.2005.06.023. PubMed DOI
Eiserich JP, et al. Myeloperoxidase, a leukocyte-derived vascular NO oxidase. Science. 2002;296(5577):2391–2394. doi: 10.1126/science.1106830. PubMed DOI
Baldus S, et al. Endothelial transcytosis of myeloperoxidase confers specificity to vascular ECM proteins as targets of tyrosine nitration. J Clin Invest. 2001;108(12):1759–1770. doi: 10.1172/JCI12617. PubMed DOI PMC
Eiserich JP, et al. Formation of nitric oxide-derived inflammatory oxidants by myeloperoxidase in neutrophils. Nature. 1998;391(6665):393–397. doi: 10.1038/34923. PubMed DOI
Zhang C, et al. L-arginine chlorination products inhibit endothelial nitric oxide production. J Biol Chem. 2001;276(29):27159–27165. doi: 10.1074/jbc.M100191200. PubMed DOI
von Leitner EC, et al. Pathogenic cycle between the endogenous nitric oxide synthase inhibitor asymmetrical dimethylarginine and the leukocyte-derived hemoprotein myeloperoxidase. Circulation. 2011;124(24):2735–2745. doi: 10.1161/CIRCULATIONAHA.111.060541. PubMed DOI
Rudolph TK, et al. Myeloperoxidase deficiency preserves vasomotor function in humans. Eur Heart J. 2012;33(13):1625–1634. doi: 10.1093/eurheartj/ehr193. PubMed DOI PMC
Morimont P, et al. Effective arterial elastance as an index of pulmonary vascular load. Am J Physiol Heart Circ Physiol. 2008;294(6):H2736–H2742. doi: 10.1152/ajpheart.00796.2007. PubMed DOI
Wauthy P, Abdel Kafi S, Mooi WJ, Naeije R, Brimioulle S. Inhaled nitric oxide versus prostacyclin in chronic shunt-induced pulmonary hypertension. J Thorac Cardiovasc Surg. 2003;126(5):1434–1441. doi: 10.1016/S0022-5223(03)01183-8. PubMed DOI
Knock GA, Ward JP. Redox regulation of protein kinases as a modulator of vascular function. Antioxid Redox Signal. 2011;15(6):1531–1547. doi: 10.1089/ars.2010.3614. PubMed DOI
Rudolph V, et al. Myeloperoxidase acts as a profibrotic mediator of atrial fibrillation. Nat Med. 2010;16(4):470–474. doi: 10.1038/nm.2124. PubMed DOI PMC
Oka M, et al. Rho kinase-mediated vasoconstriction is important in severe occlusive pulmonary arterial hypertension in rats. Circ Res. 2007;100(6):923–929. doi: 10.1161/01.RES.0000261658.12024.18. PubMed DOI
Taraseviciene-Stewart L, et al. Inhibition of the VEGF receptor 2 combined with chronic hypoxia causes cell death-dependent pulmonary endothelial cell proliferation and severe pulmonary hypertension. FASEB J. 2001;15(2):427–438. doi: 10.1096/fj.00-0343com. PubMed DOI
Undurti A, Huang Y, Lupica JA, Smith JD, DiDonato JA, Hazen SL. Modification of high density lipoprotein by myeloperoxidase generates a pro-inflammatory particle. J Biol Chem. 2009;284(45):30825–30835. doi: 10.1074/jbc.M109.047605. PubMed DOI PMC
Klinke A, et al. Myeloperoxidase attracts neutrophils by physical forces. Blood. 2011;117(4):1350–1358. doi: 10.1182/blood-2010-05-284513. PubMed DOI
Fagan KA, et al. Upregulation of nitric oxide synthase in mice with severe hypoxia-induced pulmonary hypertension. Respir Res. 2001;2(5):306–313. doi: 10.1186/rr74. PubMed DOI PMC
Le Cras TD, Xue C, Rengasamy A, Johns RA. Chronic hypoxia upregulates endothelial and inducible NO synthase gene and protein expression in rat lung. Am J Physiol. 1996;270(1 Pt 1):L164–L170. PubMed
Gosgnach W, Messika-Zeitoun D, Gonzalez W, Philipe M, Michel JB. Shear stress induces iNOS expression in cultured smooth muscle cells: role of oxidative stress. Am J Physiol, Cell Physiol. 2000;279(6):C1880–C1888. doi: 10.1152/ajpcell.2000.279.6.C1880. PubMed DOI
Kristof AS, Marks-Konczalik J, Moss J. Mitogen-activated protein kinases mediate activator protein-1-dependent human inducible nitric-oxide synthase promoter activation. J Biol Chem. 2001;276(11):8445–8452. doi: 10.1074/jbc.M009563200. PubMed DOI
Schermuly RT, Ghofrani HA, Wilkins MR, Grimminger F. Mechanisms of disease: pulmonary arterial hypertension. Nat Rev Cardiol. 2011;8(8):443–455. doi: 10.1038/nrcardio.2011.87. PubMed DOI PMC
Nossaman BD, Kadowitz PJ. The role of the RhoA/rho-kinase pathway in pulmonary hypertension. Curr Drug Discov Technol. 2009;6(1):59–71. doi: 10.2174/157016309787581057. PubMed DOI
Shibata R, et al. Role of Rho-associated kinase in neointima formation after vascular injury. Circulation. 2001;103(2):284–289. doi: 10.1161/01.CIR.103.2.284. PubMed DOI
Seasholtz TM, Majumdar M, Kaplan DD, Brown JH. Rho and Rho kinase mediate thrombin-stimulated vascular smooth muscle cell DNA synthesis and migration. Circ Res. 1999;84(10):1186–1193. doi: 10.1161/01.RES.84.10.1186. PubMed DOI
Sommer N, et al. Regulation of hypoxic pulmonary vasoconstriction: basic mechanisms. Eur Respir J. 2008;32(6):1639–1651. doi: 10.1183/09031936.00013908. PubMed DOI
Björnsdottir H, et al. Neutrophil NET formation is regulated from the inside by myeloperoxidase-processed reactive oxygen species. Free Radic Biol Med. 2015;89:1024–1035. doi: 10.1016/j.freeradbiomed.2015.10.398. PubMed DOI
Schermuly RT, et al. Reversal of experimental pulmonary hypertension by PDGF inhibition. J Clin Invest. 2005;115(10):2811–2821. doi: 10.1172/JCI24838. PubMed DOI PMC