Uncoupling Protein 3 Promotes the Myogenic Differentiation of Type IIb Myotubes in C2C12 Cells

Author:

You Ziwei1ORCID,Wang Jieyu1,Li Faliang1,Hei Wei1,Li Meng1,Guo Xiaohong1,Gao Pengfei1,Cao Guoqing1,Cai Chunbo12,Li Bugao1

Affiliation:

1. College of Animal Science, Shanxi Agricultural University, 1 Mingxian Nanlu, Jinzhong 030801, China

2. Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, China

Abstract

Uncoupling protein 3 (Ucp3) is an important transporter within mitochondria and is mainly expressed in skeletal muscle, brown adipose tissue and the myocardium. However, the effects of Ucp3 on myogenic differentiation are still unclear. This study evaluated the effects of Ucp3 on myogenic differentiation, myofiber type and energy metabolism in C2C12 cells. Gain- and loss-of-function studies revealed that Ucp3 could increase the number of myotubes and promote the myogenic differentiation of C2C12 cells. Furthermore, Ucp3 promoted the expression of the type IIb myofiber marker gene myosin heavy chain 4 (Myh4) and decreased the expression of the type I myofiber marker gene myosin heavy chain 7 (Myh7). In addition, energy metabolism related to the expression of PPARG coactivator 1 alpha (Pgc1-α), ATP synthase, H+ transportation, mitochondrial F1 complex, alpha subunit 1 (Atp5a1), lactate dehydrogenase A (Ldha) and lactate dehydrogenase B (Ldhb) increased with Ucp3 overexpression. Ucp3 could promote the myogenic differentiation of type IIb myotubes and accelerate energy metabolism in C2C12 cells. This study can provide the theoretical basis for understanding the role of Ucp3 in energy metabolism.

Funder

National Natural Science Foundation of China

Key Research and Development Project of Shanxi Province

Special Fund for Science and Technology Innovation Teams of Shanxi Province

Shanxi Agricultural University Science and Technology Innovation and Promotion Project

Open Project of the Shanxi Provincial Key Laboratory for Exploration and Precision Breeding of Animal Genetic Resources

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

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