Ren Yuanyuan, Yang Jie, Wei Minxin, Su Chao
Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin 300070, China.
Division of Cardiac Surgery, Cardiovascular Medical Center, the University of Hong Kong-Shenzhen Hospital, Shenzhen 518057, China.
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2023 Aug;39(8):714-720.
Objective To establish a stable strain of H9c2 cardiomyocytes overexpressing Cx40 and preliminarily investigate the effect of lentiviral vector-mediated Cx40 protein overexpression on the proliferation of H9c2 cells and its related mechanisms. Methods The Cx40 gene fragment was cloned from H9c2 cells by PCR and linked with lentivirus vector pLVX-IRES-Puro to obtain the recombinant plasmid pLVX-Flag-Cx40. Recombinant lentiviral particles carrying Flag-Cx40 were obtained by cotransfection with packaging plasmids into HEK293T cells. A stable expression strain (H9c2-Flag-Cx40 cell) was screened from infected H9c2 cells by purinomycin. The expression of Cx40 protein was detected by Western blot analysis, and the effect of Cx40 on H9c2 cells proliferation was determined by CCK-8 assay; cell cycle changes were measured by flow cytometry; the expression of the cell cycle protein cyclin D1 was detected by qRT-PCR and Western blot analysis. Co-immunoprecipitation (Co-IP) immunoprecipitation and Western blot analysis were used to identify the binding of Cx40 and Yes associated protein (YAP) in H9c2 cells; cytoplasmic and cytosolic proteins were isolated to detect the effect of Cx40 on the localization of YAP using Western blot analysis. Results Sequencing results showed that the recombinant pLVX-Flag-Cx40 expression vector was successfully established. A stable transfected cell line containing recombinant Flag-Cx40 lentivirus (H9c2-Flag-Cx40 cell) was successfully constructed from H9c2 cells. Compared with the control group, overexpression of Cx40 significantly reduced the proliferation of H9c2 cells, arrested the cell cycle at G0/G1 and reduced cyclin D1 expression. A significant increase in YAP expression was observed in the cytoplasm of the H9c2-Flag-Cx40 stable cell line, while the expression in the nucleus was significantly reduced. Cx40 bound to YAP in the cytoplasm and prevented it from entering the nucleus to play the role of transcriptional coactivation. Conclusion Overexpression of Cx40 induces cell-cycle arrest at G0/G1 phase and inhibits the proliferation in H9c2 cells.
目的 构建稳定过表达Cx40的H9c2心肌细胞株,初步探讨慢病毒载体介导的Cx40蛋白过表达对H9c2细胞增殖的影响及其相关机制。方法 通过PCR从H9c2细胞中克隆Cx40基因片段,并与慢病毒载体pLVX-IRES-Puro连接,获得重组质粒pLVX-Flag-Cx40。将包装质粒共转染至HEK293T细胞中,获得携带Flag-Cx40的重组慢病毒颗粒。用嘌呤霉素从感染的H9c2细胞中筛选出稳定表达株(H9c2-Flag-Cx40细胞)。通过蛋白质免疫印迹法检测Cx40蛋白的表达,采用CCK-8法检测Cx40对H9c2细胞增殖的影响;通过流式细胞术检测细胞周期变化;采用实时定量聚合酶链反应和蛋白质免疫印迹法检测细胞周期蛋白cyclin D1的表达。采用免疫共沉淀和蛋白质免疫印迹法鉴定H9c2细胞中Cx40与Yes相关蛋白(YAP)的结合;分离细胞质和细胞核蛋白,用蛋白质免疫印迹法检测Cx40对YAP定位的影响。结果 测序结果表明,成功构建了重组pLVX-Flag-Cx40表达载体。从H9c2细胞中成功构建了含有重组Flag-Cx40慢病毒的稳定转染细胞系(H9c2-Flag-Cx40细胞)。与对照组相比,Cx40过表达显著降低了H9c2细胞的增殖,使细胞周期停滞在G0/G1期,并降低了cyclin D1的表达。在H9c2-Flag-Cx40稳定细胞系的细胞质中观察到YAP表达显著增加,而在细胞核中的表达显著降低。Cx40在细胞质中与YAP结合,阻止其进入细胞核发挥转录共激活作用。结论 Cx40过表达诱导H9c2细胞在G0/G1期发生细胞周期阻滞并抑制其增殖。