The MOH Key Laboratory of Geriatrics, Beijing Hospital, National Center of Gerontology, Beijing 100730, P.R. China.
Hebei Key Laboratory for Chronic Diseases, Tangshan Key Laboratory for Preclinical and Basic Research on Chronic Diseases, School of Basic Medical Sciences, North China University of Science and Technology, Tangshan, Hebei 063000, P.R. China.
Int J Oncol. 2018 Nov;53(5):2047-2055. doi: 10.3892/ijo.2018.4554. Epub 2018 Sep 5.
In a previous study, it was demonstrated that Rhein lysinate (RHL) inhibited HeLa cell proliferation via a specific mechanism. The aim of the present study was to clarify the mechanism of RHL by investigating its effect on mitochondrial damage and cell apoptosis. The results indicated that RHL inhibited cell growth and proliferation in HeLa cells. HeLa cells treated with RHL developed extensive vacuolization in a dose- and time-dependent manner. Ultrastructure analysis using transmission electron microscopy revealed that the vacuoles observed were damaged mitochondria and endoplasmic reticulum. The effects of RHL on mitochondria were further confirmed by a decrease in mitochondrial membrane potential and increased generation of reactive oxygen species. The mitochondrial proteome was analyzed, and the results demonstrated that the expression of the cytoskeletal protein keratin and dermal papilla derived protein 12 (associated with the oxidation-reduction process), which are associated with mitochondrial structure and function, were decreased compared with the untreated control group. Hoechst staining, flow cytometry and western blotting also revealed that apoptosis was induced at 24 h following RHL treatment. These results confirm that RHL toxicity in HeLa cells is a dynamic process. Vacuolar degeneration appeared in HeLa cells treated with 160 µmol/l RHL during the first 6 h and with the extension of RHL treatment, cell apoptosis was presented at ~24 h in HeLa cells.
在之前的研究中,已经证明赖诺普利赖氨酸盐(RHL)通过特定的机制抑制了 HeLa 细胞的增殖。本研究旨在通过研究其对线粒体损伤和细胞凋亡的影响来阐明 RHL 的作用机制。结果表明,RHL 抑制了 HeLa 细胞的生长和增殖。用 RHL 处理的 HeLa 细胞以剂量和时间依赖的方式发生广泛的空泡化。透射电子显微镜的超微结构分析显示,观察到的空泡是受损的线粒体和内质网。RHL 对线粒体的影响进一步通过降低线粒体膜电位和增加活性氧的产生得到证实。对线粒体蛋白质组进行了分析,结果表明,与线粒体结构和功能相关的细胞骨架蛋白角蛋白和真皮乳头衍生蛋白 12(与氧化还原过程相关)的表达与未处理的对照组相比降低。Hoechst 染色、流式细胞术和 Western blot 也显示,在用 RHL 处理 24 小时后诱导了细胞凋亡。这些结果证实 RHL 对 HeLa 细胞的毒性是一个动态过程。在 160µmol/l RHL 处理的 HeLa 细胞中,在最初的 6 小时内出现空泡变性,随着 RHL 处理的延长,约在 24 小时后 HeLa 细胞出现细胞凋亡。