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.

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.

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