Yu Minli, Wang Huan, Liu Zhen, Lu Yinglin, Yu Debing, Li Dongfeng, Du Wenxing
Department of Animal Genetics, Breeding and Reproduction, College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, Jiangsu Province, China.
Dev Growth Differ. 2017 Aug;59(6):540-551. doi: 10.1111/dgd.12380. Epub 2017 Jul 13.
Regulation of skeletal muscle development requires many of the regulatory networks that are fundamental to developmental myogenesis. ErbB3 binding protein-1 (Ebp1) is involved in the control of myoblasts development in chicken. However, the expression and biological functions of Ebp1 in the progress of myogenesis are unclear. This study focused on determining the effect of Ebp1 on myogenic proliferation and differentiation using a primary myoblasts culture model. Ebp1 was found to upregulate in proliferating myoblasts and decrease at the early stage of myogenic differentiation. The level of endogenous Ebp1 increased from E9 to E20 chicken leg muscles. Knockdown of Ebp1 had no effect on myoblasts proliferation. However, myogenic differentiation into multinucleated myotubes was significantly reduced. The mRNA and protein expression of MRFs was decreased when Ebp1 was knocked down. Downregulation of Ebp1, accompanied by elevated levels of pSMAD2/3, suggests that Ebp1 is involved in regulating myogenic differentiation via SMAD2/3 inhibition. The phosphorylation of SMAD2/3 was activated and the expression of MYOD and MYOG was reduced in Ebp1 knockdown myoblasts, but addition of LY2109761 (an inhibitor specified to SMAD2/3) blocked these effects. Collectively, these results indicate that Ebp1 promotes myoblast differentiation by inhibition of SMAD2/3 signaling pathway during chicken myogenesis. These data provide new insights into the biological role of Ebp1 in embryonic chicken skeletal muscle development.
骨骼肌发育的调控需要许多对发育性肌生成至关重要的调控网络。ErbB3结合蛋白1(Ebp1)参与鸡成肌细胞发育的控制。然而,Ebp1在肌生成过程中的表达和生物学功能尚不清楚。本研究利用原代成肌细胞培养模型,重点研究Ebp1对肌源性增殖和分化的影响。研究发现,Ebp1在增殖的成肌细胞中上调,在肌源性分化早期下降。从E9到E20鸡腿部肌肉,内源性Ebp1水平升高。敲低Ebp1对成肌细胞增殖没有影响。然而,向多核肌管的肌源性分化显著减少。敲低Ebp1时,MRFs的mRNA和蛋白表达降低。Ebp1的下调伴随着pSMAD2/3水平的升高,表明Ebp1通过抑制SMAD2/3参与调节肌源性分化。在敲低Ebp1的成肌细胞中,SMAD2/3的磷酸化被激活,MYOD和MYOG的表达降低,但添加LY2109761(一种针对SMAD2/3的抑制剂)可阻断这些作用。总体而言,这些结果表明,在鸡肌生成过程中,Ebp1通过抑制SMAD2/3信号通路促进成肌细胞分化。这些数据为Ebp1在胚胎鸡骨骼肌发育中的生物学作用提供了新的见解。