Journal
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY
Volume 42, Issue 6, Pages 2569-2581Publisher
KARGER
DOI: 10.1159/000480218
Keywords
Long non-coding RNAs; Pulmonary arterial hypertension; Proliferation; p53; Pulmonary artery smooth muscle cells
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Funding
- Natural Science Foundation of Jiangsu Province [BK20161297]
- Jiangsu Provincial Commission of Health and Family Planning [QNRC2016505]
- Social Fund for Development of Lianyungang Science and Technology Bureau [SH1612]
- Lianyungang First People's Hospital [BS15012]
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Background/Aims: Increasing evidence has demonstrated a significant role of long non coding RNAs (IncRNAs) in diverse biological processes, and many of which are likely to have functional roles in vascular remodeling. However, their functions in pulmonary arterial hypertension (PAH) remain largely unknown. Pulmonary vascular remodeling is an important pathological feature of PAH, leading to increased vascular resistance and reduced compliance. Pulmonary artery smooth muscle cells (PASMCs) dysfunction is involved in vascular remodeling. Long noncoding RNAs are potential regulators of PASMCs function. Herein, we determined whether long noncoding RNA maternally expressed gene 3 (MEG3) was involved in PAH-related vascular remodeling. Methods: The arterial wall thickness was examined by hematoxylin and eosin (H&E) staining in distal pulmonary arteries (PAs) isolated from lungs of healthy volunteers and PAH patients. The expression level of MEG3 was analyzed by qPCR. The effects of MEG3 on human PASMCs were assessed by cell counting Kit-8 assay, BrdU incorporation assay, flow cytometry, scratch-wound assay, immunofluorescence, and western blotting in human PASMCs. Results:We revealed that the expression of MEG3 was significantly downregulated in lung and PAs of patients with PAH. MEG3 knockdown affected PASMCs proliferation and migration in vitro. Moreover, inhibition of MEG3 regulated the cell cycle progression and made more smooth muscle cells from the G(0)/G(1), phase to the G(2)/M+S phase and the process could stimulate the expression of PCNA, Cyclin A and Cyclin E. In addition, we found that the p53 pathway was involved in MEG3 induced smooth muscle cell proliferation. Conclusions: This study identified MEG3 as a critical regulator in PAH and demonstrated the potential of gene therapy and drug development for treating PAH. (C) 2017 The Author(s) Published by S. Karger AG, Basel
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