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作 者:覃超群 黄斌 阳芳 王昌明 肖影 黄汉灿 李丽英 高枫 QIN Chaoqun;HUANG Bin;YANG Fang;WANG Changming;XIAO Ying;HUANG Hancan;LI Liying;GAO Feng(Department of Respiratory and Critical Care Medicine,Guilin People's Hospital,Guilin 541002,Guangxi,China)
机构地区:[1]桂林市人民医院呼吸与危重医学科,广西桂林541002
出 处:《山东大学学报(医学版)》2022年第5期8-15,共8页Journal of Shandong University:Health Sciences
基 金:广西壮族自治区卫生健康委员会项目(Z20190330)
摘 要:目的探讨糖原合成酶激酶3β(GSK3β)/真核延伸因子2激酶(eEF2K)在肺成纤维细胞转化为肌成纤维细胞过程中的表达,以及对细胞自噬和纤维化的影响。方法将L-929细胞(对照组)于适宜条件下培养48 h,加入5 ng/mL TGF-β1诱导其表型转化为肌成纤维细胞(TGF-β1组)。将空质粒、si-eEF2K及si-GSK3β转染肌成纤维细胞,培养48 h后采用免疫荧光染色法检测p-eEF2K和α-SMA蛋白表达情况,蛋白质印迹法检测各组eEF2K、p-eEF2K、GSK3β、P62及LC3-Ⅱ/Ⅰ蛋白表达情况。结果与对照组相比,TGF-β1组细胞p-eEF2K、GSK3β蛋白和α-SMA蛋白表达显著增加(P<0.05);转染si-eEF2K及si-GSK3β后,L-929细胞p-eEF2K/eEF2K表达下降(P<0.05),P62和LC3-Ⅱ/Ⅰ表达水平增加(P<0.05),α-SMA蛋白表达降低(P<0.05)。结论GSK3β/eEF2K信号可能通过降低自噬活性促进肺成纤维细胞向肌纤维细胞的表型转化,促进细胞纤维化进程。Objective To explore the expression of glycogen syntheses kinases 3β(GSK3β)/eukaryotic elongation factor 2 kinases(eEF2 K)during the conversion of lung fibroblasts into myofibroblasts,and to investigate its effects on cellular fibrosis and autophagy.Methods L-929 cells(control group)were cultured under appropriate conditions for 48 h,and transformed into myofibroblasts(TGF-β1 group)by 5 ng/mL TGF-β1.Myofibroblasts were transfected with empty plasmid,si-eEF2 K and si-GSK3β.The protein expressions of p-eEF2 K andα-SMA were detected with immunofluorescence staining after 48 hours of culture,and the protein expressions of eEF2 K,p-eEF2 K,GSK3β,P62 and LC3-Ⅱ/Ⅰwere detected with Western blotting.Results Compared with the control group,the TGF-β1 group had increased expression of p-eEF2 K,GSK3βandα-SMA(P<0.05).After transfection with si-eEF2 K and si-GSK3β,the expressions of p-eEF2 K andα-SMA decreased,while the expressions of P62 and LC3-Ⅱ/Ⅰincreased(P<0.05).Conclusion GSK3β/eEF2 K signalling may promote the phenotypic transformation of lung fibroblasts to myofibroblasts by reducing autophagic activity and facilitating the process of cellular fibrosis.
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