Related Experiment Video
Updated: Oct 20, 2025

Isolation of Pulmonary Artery Smooth Muscle Cells from Neonatal Mice
Published on: October 19, 2013
MicroRNA-137 Inhibited Hypoxia-Induced Proliferation of Pulmonary Artery Smooth Muscle Cells by Targeting Calpain-2
Xiao-Yue Ge1, Tian-Tian Zhu2, Mao-Zhong Yao1
1Department of Pharmacology, Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, 410078 Hunan, China.
Abstract:
The proliferation of pulmonary artery smooth muscle cells (PASMCs) is an important cause of pulmonary vascular remodeling in pulmonary hypertension (PH). It has been reported that miR-137 inhibits the proliferation of tumor cells. However, whether miR-137 is involved in PH remains unclear. In this study, male Sprague-Dawley rats were subjected to 10% O2 for 3 weeks to establish PH, and rat primary PASMCs were treated with hypoxia (3% O2) for 48 h to induce cell proliferation. The effect of miR-137 on PASMC proliferation and calpain-2 expression was assessed by transfecting miR-137 mimic and inhibitor. The effect of calpain-2 on PASMC proliferation was assessed by transfecting calpain-2 siRNA. The present study found for the first time that miR-137 was downregulated in pulmonary arteries of hypoxic PH rats and in hypoxia-treated PASMCs. miR-137 mimic inhibited hypoxia-induced PASMC proliferation and upregulation of calpain-2 expression in PASMCs. Furthermore, miR-137 inhibitor induced the proliferation of PASMCs under normoxia, and knockdown of calpain-2 mRNA by siRNA significantly inhibited hypoxia-induced proliferation of PASMCs. Our study demonstrated that hypoxia-induced downregulation of miR-137 expression promoted the proliferation of PASMCs by targeting calpain-2, thereby potentially resulting in pulmonary vascular remodeling in hypoxic PH.
Insights
MicroRNA-137 (miR-137) is downregulated in pulmonary hypertension (PH), inhibiting pulmonary artery smooth muscle cell (PASMC) proliferation by targeting calpain-2. This finding reveals a new mechanism in PH development.
Area of Science:
- Cardiovascular Biology
- Molecular Medicine
- Cell Biology
Background:
- Pulmonary artery smooth muscle cell (PASMC) proliferation drives pulmonary vascular remodeling in pulmonary hypertension (PH).
- MicroRNA-137 (miR-137) is known to inhibit tumor cell proliferation, but its role in PH is unexplored.
Purpose of the Study:
- To investigate the role of miR-137 in hypoxia-induced PASMC proliferation and its potential mechanism involving calpain-2 in the context of pulmonary hypertension.
Main Methods:
- Established a rat model of PH using hypoxia (10% O2) and induced PASMC proliferation with hypoxia (3% O2).
- Utilized miR-137 mimic and inhibitor to assess miR-137's effect on PASMC proliferation and calpain-2 expression.
- Employed calpain-2 siRNA to evaluate the impact of calpain-2 on PASMC proliferation.
Main Results:
- Found miR-137 downregulated in pulmonary arteries of hypoxic PH rats and hypoxia-treated PASMCs.
- miR-137 mimic suppressed hypoxia-induced PASMC proliferation and calpain-2 upregulation.
- miR-137 inhibitor promoted PASMC proliferation under normoxia; calpain-2 knockdown inhibited hypoxia-induced PASMC proliferation.
Conclusions:
- Hypoxia-induced downregulation of miR-137 promotes PASMC proliferation by targeting calpain-2.
- This miR-137/calpain-2 pathway is a potential driver of pulmonary vascular remodeling in hypoxic PH.
More Related Videos
13:32Videomorphometric Analysis of Hypoxic Pulmonary Vasoconstriction of Intra-pulmonary Arteries Using Murine Precision Cut Lung Slices
Published on: January 14, 2014
09:45An In Vitro Protocol for Evaluating MicroRNA Levels, Functions, and Associated Target Genes in Tumor Cells
Published on: May 21, 2019
Related Concept Videos
MicroRNAs
Regulation of Angiogenesis and Blood Supply
Nitric Oxide Signaling Pathway