1. Unraveling the Impact of miR-146a in Pulmonary Arterial Hypertension Pathophysiology and Right Ventricular Function
- Author
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Joana Santos-Gomes, Pedro Mendes-Ferreira, Rui Adão, Carolina Maia-Rocha, Beatriz Rego, Manu Poels, Anaïs Saint-Martin Willer, Bastien Masson, Steeve Provencher, Sébastien Bonnet, David Montani, Frédéric Perros, Fabrice Antigny, Adelino F. Leite-Moreira, and Carmen Brás-Silva
- Subjects
miR-146a ,pulmonary arterial hypertension (PAH) ,right ventricular (RV) hypertrophy ,right ventricular (RV) failure ,Biology (General) ,QH301-705.5 ,Chemistry ,QD1-999 - Abstract
Pulmonary arterial hypertension (PAH) is a chronic disorder characterized by excessive pulmonary vascular remodeling, leading to elevated pulmonary vascular resistance and right ventricle (RV) overload and failure. MicroRNA-146a (miR-146a) promotes vascular smooth muscle cell proliferation and vascular neointimal hyperplasia, both hallmarks of PAH. This study aimed to investigate the effects of miR-146a through pharmacological or genetic inhibition on experimental PAH and RV pressure overload animal models. Additionally, we examined the overexpression of miR-146a on human pulmonary artery smooth muscle cells (hPASMCs). Here, we showed that miR-146a genic expression was increased in the lungs of patients with PAH and the plasma of monocrotaline (MCT) rats. Interestingly, genetic ablation of miR-146a improved RV hypertrophy and systolic pressures in Sugen 5415/hypoxia (SuHx) and pulmonary arterial banding (PAB) mice. Pharmacological inhibition of miR-146a improved RV remodeling in PAB-wild type mice and MCT rats, and enhanced exercise capacity in MCT rats. However, overexpression of miR-146a did not affect proliferation, migration, and apoptosis in control-hPASMCs. Our findings show that miR-146a may play a significant role in RV function and remodeling, representing a promising therapeutic target for RV hypertrophy and, consequently, PAH.
- Published
- 2024
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