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首页> 外文期刊>Biotechnology & Biotechnological Equipment >Chlamydia trachomatis pORF5 plasmid-encoded protein regulates autophagy and apoptosis of HeLa cells
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Chlamydia trachomatis pORF5 plasmid-encoded protein regulates autophagy and apoptosis of HeLa cells

机译:Chlamydia Thachomatis porf5质粒编码蛋白调节Hela细胞的自噬和凋亡

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Chlamydia trachomatis is an important human pathogen responsible for a variety of important diseases. pORF5, a plasmid protein in C. trachomatis , has been reported to contribute to chlamydial pathogenesis. Apoptosis and autophagy are two important cellular processes, which also participate in the pathological and the physiological processes in C. trachomatis infection. The present study aimed to explore the effects of pORF5 protein on autophagy and apoptosis in HeLa cells. Stable pORF5-HeLa and vector-HeLa cell lines that were transduced with pORF5 recombination lentivirus and control lentivirus, respectively, were constructed. Immunofluorescence was used to observe the cells. Western blotting was carried out to detect expression of target proteins. Real-time polymerase chain reaction was used to determine the mRNA expression. Flow cytometry, TUNEL assay and Hoechst staining were employed to detect apoptosis. pORF5 sensitized HeLa cells to autophagy that was induced by nutrient deprivation. In addition, pORF5 increased the ratio of LC3-II/LC3-I and Beclin-1 expression, down-regulated the expression of Bax and Caspase-3 and up-regulated Bcl-2 expression to suppress apoptosis induced by TNF-α. Autophagy inhibitor 3-MA elevated apoptotic rate significantly in pORF5-HeLa cells. The study preliminarily confirms that plasmid protein pORF5 mediates the crosstalk between autophagy and apoptosis, which may contribute to persistent C. trachomatis infection in host cells.
机译:Chlamydia Thachomatis是负责各种重要疾病的重要人体病原体。据报道,Porf5,C. Thachomatis中的质粒蛋白质促进了曲底发病机制。细胞凋亡和自噬是两个重要的细胞过程,也参与C. Thachomatis感染的病理和生理过程。本研究旨在探讨PORF5蛋白对HeLa细胞的自噬和细胞凋亡的影响。构建了用Porf5重组慢病毒和对照慢病毒转导的稳定PORF5-HELA和载体-Hela细胞系。免疫荧光用于观察细胞。进行蛋白质印迹以检测靶蛋白的表达。实时聚合酶链反应用于确定mRNA表达。流式细胞术,TUNEL测定和HOECHST染色用于检测细胞凋亡。 Porf5敏化Hela细胞对营养剥夺诱导的自噬。此外,PORF5增加了LC3-II / LC3-I和BECLIN-1的比例,下调了BAX和Caspase-3和上调的BCL-2表达的表达,以抑制TNF-α诱导的细胞凋亡。在PORF5-HELA细胞中,自噬抑制剂3-MA显着提高凋亡率。该研究初步证实,质粒蛋白PORF5介导自噬和凋亡之间的串扰,这可能有助于宿主细胞中的持久性C. Thachomatis感染。

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