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The LIM-Only Protein FHL2 is involved in Autophagy to Regulate the Development of Skeletal Muscle Cell

机译:仅LIM蛋白FHL2参与自噬以调节骨骼肌细胞的发育

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Scope: 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. Methods: C2C12 cells were treated with FHL2-konwdown or FHL2-overexpression. The morphology of C2C12 cells was observed by transmission electron microscopy. The mRNA and protein abundances of muscle related genes and autophagy related genes were measured by RT-PCR and western blot. Immunofluorescence and co-immunoprecipitation assay were used to verify the interaction between FHL2 and LC3 protein. Results: FHL2 silencing reduced LC3-Ⅱ protein expression and the amount of LC3 that co-immunoprecipitated with FHL2, indicating that FHL2 interacts with LC3-Ⅱ 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. Conclusion: These results suggest that FHL2 interacts with LC3-Ⅱ in autophagosome formation to regulate the development of muscle cells.
机译:范围:四个半LIM域蛋白2(FHL2)是在肌肉组织中表达的LIM域蛋白,其缺失是肌病的病因。尽管FHL2在肌肉发育中具有重要作用,但其自噬相关功能在肌肉分化中的作用尚未完全确定。方法:用FHL2-konwdown或FHL2-过表达处理C2C12细胞。通过透射电子显微镜观察C2C12细胞的形态。通过RT-PCR和western blot检测肌肉相关基因和自噬相关基因的mRNA和蛋白质丰度。免疫荧光和免疫共沉淀法用于验证FHL2和LC3蛋白之间的相互作用。结果:FHL2沉默降低了LC3-Ⅱ蛋白的表达以及与FHL2共同免疫沉淀的LC3的量,表明FHL2与LC3-Ⅱ相互作用形成自噬体。此外,肌肉发育标记基因如MyoD1和MyoG的表达在FHL2沉默的C2C12细胞中较低,而在FHL2过表达的C2C12细胞中则没有。电子显微镜分析显示,FHL2沉默的成肌细胞中有大量空的自噬体,而流式细胞仪表明FHL2沉默使细胞更容易受到星形孢菌素诱导的细胞死亡的影响。结论:这些结果表明FHL2与LC3-Ⅱ在自噬小体形成中相互作用,以调节肌肉细胞的发育。

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