Potential role of cartilage oligomeric matrix protein in the modulation of pulmonary arterial smooth muscle superoxide by hypoxia
Authors:
- 7 August 2019
- journal article
- research article
- Published by American Physiological Society in American Journal of Physiology-Lung Cellular and Molecular Physiology
- Vol. 317 (5) , L569-L577
Abstract
Changes in reactive oxygen species and extracellular matrix seem to participate in pulmonary hypertension development. Because we recently reported evidence for chronic hypoxia decreasing expression of cartilage oligomeric matrix protein (COMP) and evidence for this controlling loss of pulmonary arterial smooth muscle bone morphogenetic protein receptor-2 (BMPR2) and contractile phenotype proteins, we examined if changes in superoxide metabolism could be an important factor in a bovine pulmonary artery (BPA), organoid cultured under hypoxia for 48 h model. Hypoxia (3% O2) caused a depletion of COMP in BPA, but not in bovine coronary arteries. Knockdown of COMP by small-interfering RNA (siRNA) increased BPA levels of mitochondrial and extra-mitochondrial superoxide detected by MitoSOX and dihydroethidium (DHE) HPLC products. COMP siRNA-treated BPA showed reduced levels of SOD2 and SOD3 and increased levels of NADPH oxidases NOX2 and NOX4. Hypoxia increased BPA levels of MitoSOX-detected superoxide and caused changes in NOX2 and SOD2 expression similar to COMP siRNA, and exogenous COMP (0.5 μM) prevented the effects of hypoxia. In the presence of COMP, BMPR2 siRNA-treated BPA showed increases in superoxide detected by MitoSOX and depletion of SOD2. Superoxide scavengers (0.5 μM TEMPO or mitoTEMPO) maintained the expression of contractile phenotype proteins calponin and SM22α decreased by 48 h hypoxia (1% O2). Adenoviral delivery of BMPR2 to rat pulmonary artery smooth muscle cells prevented the depletion of calponin and SM22α by COMP siRNA. Thus, COMP regulation of BMPR2 appears to have an important role in controlling hypoxia-elicited changes in BPA superoxide and its potential regulation of contractile phenotype proteins.Keywords
Funding Information
- HHS | NIH | National Heart, Lung, and Blood Institute (HL115124, HL129797)
- National Natural Science Foundation of China (31400989)
- Natural Science Foundation of Heilongjiang Province (C2015069)
- Postdoctoral Science of Heilongjiang Provence (LBHQ15087)
This publication has 27 references indexed in Scilit:
- Hypoxia decrease expression of cartilage oligomeric matrix protein to promote phenotype switching of pulmonary arterial smooth muscle cellsThe International Journal of Biochemistry & Cell Biology, 2017
- Heme biosynthesis modulation via δ-aminolevulinic acid administration attenuates chronic hypoxia-induced pulmonary hypertensionAmerican Journal of Physiology-Lung Cellular and Molecular Physiology, 2015
- Dehydroepiandrosterone promotes pulmonary artery relaxation by NADPH oxidation-elicited subunit dimerization of protein kinase G 1αAmerican Journal of Physiology-Lung Cellular and Molecular Physiology, 2014
- Molecular pathogenesis of pulmonary arterial hypertensionJournal of Clinical Investigation, 2012
- Chronic hypoxia augments depolarization-induced Ca2+sensitization in pulmonary vascular smooth muscle through superoxide-dependent stimulation of RhoAAmerican Journal of Physiology-Lung Cellular and Molecular Physiology, 2010
- NADPH oxidases and reactive oxygen species at different stages of chronic hypoxia-induced pulmonary hypertension in newborn pigletsAmerican Journal of Physiology-Lung Cellular and Molecular Physiology, 2009
- HPLC study of oxidation products of hydroethidine in chemical and biological systems: ramifications in superoxide measurementsFree Radical Biology and Medicine, 2009
- Hypoxia-Dependent Regulation of Nonphagocytic NADPH Oxidase Subunit NOX4 in the Pulmonary VasculatureCirculation Research, 2007
- Cytosolic NADPH may regulate differences in basal Nox oxidase-derived superoxide generation in bovine coronary and pulmonary arteriesAmerican Journal of Physiology-Heart and Circulatory Physiology, 2005
- Extracellular matrix and pulmonary hypertension: control of vascular smooth muscle cell contractilityAmerican Journal of Physiology-Heart and Circulatory Physiology, 1998