Zhong Yuechun, Zou Liyi, Wang Zonggui, Pan Yaqiong, Dai Zhong, Liu Xinguang, Cui Liao, Zuo Changqing
Department of Pharmacology, Guangdong Medical University, Dongguan, Guangdong 523808, P.R. China.
Department of Biochemistry and Molecular Biology, Guangdong Medical University, Dongguan, Guangdong 523808, P.R. China.
Int J Mol Med. 2016 Nov;38(5):1411-1418. doi: 10.3892/ijmm.2016.2738. Epub 2016 Sep 15.
Many transcription factors and signaling molecules involved in the guidance of myogenic differentiation have been investigated in previous studies. However, the precise molecular mechanisms of myogenic differentiation remain largely unknown. In the present study, by performing a meta-analysis of C2C12 myogenic differentiation microarray data, we found that leucine-rich repeat-containing 75B (Lrrc75b), also known as AI646023, a molecule of unknown biological function, was downregulated during C2C12 myogenic differentiation. The knockdown of Lrrc75b using specific siRNA in C2C12 myoblasts markedly enhanced the expression of muscle-specific myogenin and increased myoblast fusion and the myotube diameter. By contrast, the adenovirus-mediated overexpression of Lrrc75b in C2C12 cells markedly inhibited myoblast differentiation accompanied by a decrease in myogenin expression. In addition, the phosphorylation of extracellular signal-regulated kinase 1/2 (Erk1/2) was suppressed in the cells in which Lrrc75b was silenced. Taken together, our results demonstrate that Lrrc75b is a novel suppressor of C2C12 myogenic differentiation by modulating myogenin and Erk1/2 signaling.
先前的研究已经对许多参与成肌分化导向的转录因子和信号分子进行了研究。然而,成肌分化的确切分子机制在很大程度上仍然未知。在本研究中,通过对C2C12成肌分化微阵列数据进行荟萃分析,我们发现富含亮氨酸重复序列的75B(Lrrc75b),也称为AI646023,一种生物学功能未知的分子,在C2C12成肌分化过程中表达下调。在C2C12成肌细胞中使用特异性siRNA敲低Lrrc75b可显著增强肌肉特异性肌细胞生成素的表达,并增加成肌细胞融合和肌管直径。相比之下,腺病毒介导的Lrrc75b在C2C12细胞中的过表达显著抑制成肌细胞分化,同时肌细胞生成素表达降低。此外,在Lrrc75b沉默的细胞中,细胞外信号调节激酶1/2(Erk1/2)的磷酸化受到抑制。综上所述,我们的结果表明,Lrrc75b是一种通过调节肌细胞生成素和Erk1/2信号通路来抑制C2C12成肌分化的新型抑制因子。