Bta-miR-24-3p Controls the Myogenic Differentiation and Proliferation of Fetal, Bovine, Skeletal Muscle-Derived Progenitor Cells by Targeting <i>ACVR1B</i>

MicroRNAs modulate a variety of cellular events, including skeletal muscle development, but the molecular basis of their functions in fetal bovine skeletal muscle development is poorly understood. In this study, we report that bta-miR-24-3p promotes the myogenic differentiation of fetal bovine PDGFR...

Full description

Bibliographic Details
Main Authors: Xin Hu, Yishen Xing, Ling Ren, Yahui Wang, Qian Li, Xing Fu, Qiyuan Yang, Lingyang Xu, Luc Willems, Junya Li, Lupei Zhang
Format: Article
Language:English
Published: MDPI AG 2019-10-01
Series:Animals
Subjects:
Online Access:https://www.mdpi.com/2076-2615/9/11/859
Description
Summary:MicroRNAs modulate a variety of cellular events, including skeletal muscle development, but the molecular basis of their functions in fetal bovine skeletal muscle development is poorly understood. In this study, we report that bta-miR-24-3p promotes the myogenic differentiation of fetal bovine PDGFR&#945;<sup>-</sup> progenitor cells. The expression of bta-miR-24-3p increased during myogenic differentiation. Overexpression of bta-miR-24-3p significantly promoted myogenic differentiation, but inhibited proliferation. A dual-luciferase assay identified <i>ACVR1B</i> as a direct target of bta-miR-24-3p. Similarly, knocking down <i>ACVR1B</i> by RNA interference also significantly inhibited proliferation and promoted the differentiation of bovine PDGFR&#945;<sup>-</sup> progenitor cells. Thus, our study provides a mechanism in which bta-miR-24-3p regulates myogenesis by inhibiting <i>ACVR1B</i> expression.
ISSN:2076-2615