The LIM-Only Protein FHL2 is Involved in Autophagy to Regulate the Development of Skeletal Muscle
Zihao LiuiD, Shunshun HaniD, Yan WangiD, Can CuiiD, Qing Chun ZhuiD, Xiaosong JiangiD, Chaowu YangiD, Huarui DuiD, Chunlin YuiD, Qingyun LiiD, Haorong HeiD, Xiaoxu SheniD, Yuqi CheniD, Yao ZhangiD, Lin YeiD, Zhichao ZhangiD, Diyan LiiD, Xiaoling ZhaoiD, Huadong YiniD
Abstract
Four and a half LIM domain protein 2 (FHL2) is a LIM domain protein expressed in muscle tissue whose deletion is causative of myopathies. Although FHL2 has a confirmed important role in muscle development, its autophagy-related function in muscle differentiation has not been fully determined. To explore the role of FHL2 in autophagy-related muscle regulation, FHL2-silenced and -overexpressing C2C12 mouse cells were examined. Immunofluorescence and co-immunoprecipitation assay findings showed that FHL2 silencing reduced LC3- protein expression and the amount of LC3 that co-immunoprecipitated with FHL2, indicating that FHL2 interacts with LC3- in the formation of autophagosomes. Moreover, the expression of muscle development marker genes such as MyoD1 and MyoG was lower in FHL2-silenced C2C12 cells but not in FHL2-overexpressing C2C12 cells. Electron microscopy analysis revealed large empty autophagosomes in FHL2-silenced myoblasts, while flow cytometry suggested that FHL2 silencing made cells more vulnerable to staurosporine-induced cell death. In conclusion, we propose that FHL2 interacts with LC3- in autophagosome formation to regulate the development of muscle cells.
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