miR-210 has an antiapoptotic effect in pulmonary artery smooth muscle cells during hypoxia

• Published in: American journal of physiology. Lung cellular and molecular physiology 2012-10, Vol.303 (8), p.L682-L691
• Main Authors: Gou, Deming, Ramchandran, Ramaswamy, Peng, Xiao, Yao, Lijun, Kang, Kang, Sarkar, Joy, Wang, Zhixin, Zhou, Guofei, Zhou, Goufei, Raj, J Usha
• Format: Article
• Language: English
• Subjects: Animals; Apoptosis; Apoptosis - genetics; Chronic Disease; Disease Models, Animal; Down-Regulation - genetics; E2F3 Transcription Factor - genetics; E2F3 Transcription Factor - metabolism; Familial Primary Pulmonary Hypertension; Humans; Hypertension; Hypertension, Pulmonary - genetics; Hypertension, Pulmonary - pathology; Hypoxia; Hypoxia - genetics; Hypoxia - pathology; Hypoxia-Inducible Factor 1, alpha Subunit - genetics; Hypoxia-Inducible Factor 1, alpha Subunit - metabolism; Mice; MicroRNAs - genetics; Myocytes, Smooth Muscle - cytology; Myocytes, Smooth Muscle - physiology; Pathogenesis; Phenotype; Primary Cell Culture; Pulmonary Artery - cytology; Pulmonary Artery - physiology; Ribonucleic acid; RNA; RNA, Small Interfering - genetics; Rodents
• ISSN: 1040-0605; 1522-1504
• DOI: 10.1152/ajplung.00344.2011

MicroRNAs (miRNAs) were recently reported to play an important role in the pathogenesis of pulmonary arterial hypertension (PAH), but it is not clear which miRNAs are important or what pathways are involved in the process. Because hypoxia is an important stimulus for human pulmonary artery smooth muscle cell (HPASMC) proliferation and PAH, we performed miRNA microarray assays in hypoxia-treated and control HPASMC. We found that miR-210 is the predominant miRNA induced by hypoxia in HPASMC. Induction of miR-210 was also observed in whole lungs of mice with chronic hypoxia-induced PAH. We found that transcriptional induction of miR-210 in HPASMC is hypoxia-inducible factor-1α dependent. Inhibition of miR-210 in HPASMC caused a significant decrease in cell number due to increased apoptosis. We found that miR-210 appears to mediate its antiapoptotic effects via the regulation of transcription factor E2F3, a direct target of miR-210. Our results have identified miR-210 as a hypoxia-inducible miRNA both in vitro and in vivo, which inhibits pulmonary vascular smooth muscle cell apoptosis in hypoxia by specifically repressing E2F3 expression.