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[自噬抑制增强天花粉蛋白诱导HeLa细胞凋亡的机制]

[Mechanism of autophagy inhibition for sensitizing HeLa cell apoptosis induced by trichosanthin].

作者信息

Wang Hui, Li Ge, Li Ling-Yan, DU Yu-le, Lu Hua, Tang Qin-Cai, Liu Tao, Wang Xiao-Xing, You Cheng-Cheng, Huang Yi-Ling

机构信息

Hubei Key Laboratory of Tumor Microenvironment and Immunotherapy(China Three Gorges University) Yichang 443002, China Department of Pathology, College of Basic Medical Science, China Three Gorges University Yichang 443002,China Research Center of Basic and Clinical Pathology, China Three Gorges University Yichang 443002, China.

Hubei Key Laboratory of Tumor Microenvironment and Immunotherapy(China Three Gorges University) Yichang 443002, China Department of Pathology, College of Basic Medical Science, China Three Gorges University Yichang 443002,China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2024 Oct;49(19):5327-5334. doi: 10.19540/j.cnki.cjcmm.20240712.707.

Abstract

This research investigated the effect and mechanism of trichosanthin(TCS) in inducing autophagy and apoptosis of HeLa cells in cervical cancer. Two-step chromatography was used to prepare TCS. MTT assay was used to detect the inhibition effect of TCS on the proliferation of HeLa cells. The formation of autophagic vesicles and apoptotic bodies in HeLa cells treated with TCS was observed under transmission electron microscopy, and green fluorescent protein(GFP)-microtubule-associated protein 1 light chain beta 3(LC3B) fusion protein location was observed under laser confocal microscopy. The expression of autophagy and apoptosis-related proteins was detected by Western blot. It was found that the prepared TCS had high purity and biological activity. TCS could inhibit the proliferation of HeLa cells significantly in a concentration-dependent and time-dependent manner. Obvious autophagic vesicles were observed after HeLa cells were treated with TCS for 12 h, and typical apoptotic bodies were formed after 48 h. Under laser confocal microscopy, LC3B protein was observed to shift from a diffuse distribution to a spotted aggregation distribution in the cytoplasm. Western blot results showed that the expression of autophagy-activating protein LC3BⅡ began to increase in HeLa cells after being treated with TCS for 12 h and increased with the increase in drug concentration. Apoptosis-related protein poly ADP-ribose polymerase(PARP) began to activate as cleaved PARP after being treated with TCS for 24 h. The combination of TCS and 3-methyladenine(3-MA) further promoted the activation of cleaved PARP. The results showed that TCS could significantly inhibit the growth of HeLa cells in cervical cancer. Moreover, TCS induced autophagy in HeLa cells earlier than apoptosis, and inhibiting autophagy could sensitize apoptosis of HeLa cells induced by TCS. This indicated that autophagy induced by TCS was a protective cell response, and TCS combined with autophagy inhibitors could enhance the anti-cervical cancer effect of TCS.

摘要

本研究探讨了天花粉蛋白(TCS)诱导宫颈癌HeLa细胞自噬和凋亡的作用及机制。采用两步层析法制备TCS。采用MTT法检测TCS对HeLa细胞增殖的抑制作用。透射电子显微镜下观察TCS处理后HeLa细胞中自噬泡和凋亡小体的形成,激光共聚焦显微镜下观察绿色荧光蛋白(GFP)-微管相关蛋白1轻链3(LC3B)融合蛋白的定位。采用蛋白质免疫印迹法检测自噬和凋亡相关蛋白的表达。结果表明,所制备的TCS具有较高的纯度和生物学活性。TCS能以浓度和时间依赖性方式显著抑制HeLa细胞的增殖。TCS处理HeLa细胞12 h后可见明显的自噬泡,48 h后形成典型的凋亡小体。激光共聚焦显微镜下观察到,LC3B蛋白在细胞质中从弥漫分布转变为斑点状聚集分布。蛋白质免疫印迹结果显示,TCS处理HeLa细胞12 h后,自噬激活蛋白LC3BⅡ的表达开始增加,并随药物浓度的增加而升高。凋亡相关蛋白聚ADP核糖聚合酶(PARP)在TCS处理24 h后开始激活,表现为裂解的PARP。TCS与3-甲基腺嘌呤(3-MA)联合使用进一步促进了裂解PARP的激活。结果表明,TCS能显著抑制宫颈癌HeLa细胞的生长。此外,TCS诱导HeLa细胞自噬早于凋亡,抑制自噬可使TCS诱导的HeLa细胞凋亡敏感化。这表明TCS诱导的自噬是一种细胞保护反应,TCS与自噬抑制剂联合使用可增强TCS的抗宫颈癌作用。

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