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Analysis of Changes of Ca Concentration and Mitochondrial Membrane Potential in HepG-2 Induced by CSBE by Laser Scanning Confocal Technology and Flow Cytometry

机译:激光扫描共谱技术和流式细胞术管CSBE诱导的HepG-2中Ca浓度和线粒体膜电位变化分析

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To discuss the mechanism of the apoptosis induced by n-butanol extract from Capparis spionosa L. (CSBE) in human heptocarcinoma cell Line HepG-2, Laser Scanning Confocal Technology and Flow Cytometry were used to investigat the changes of mitochondrial membrane potential and Ca~(2+) levels in HepG-2 cells. The changes of mitochondria membrane potential induced by CSBE on the HepG-2 cells were studied by flowcytometry. Intracellular Ca~(2+) levels of both the treated and untreated HepG-2 cells with CSBE were measured by laser confocal microscope. The mitochondria membrane potential of HepG-2 cells decreased in various degrees under CSBE. In addition, the intracellular Ca~(2+) level increased in the middle and high dose groups, resulting in an imbalance. CSBE can decrease the mitochondria membrane potential, open MPTP channel and cause the overload of intracellular Ca~(2+) level, which may induce the apoptosis of HepG-2 cell. These instructions give you basic guidelines for preparing camera-ready papers for conference proceedings.
机译:为了讨论由Capparis Spionosa L的凋亡诱导的凋亡的机制来自人体术术术细胞系Hepg-2,激光扫描共焦技术和流式细胞术用于调查线粒体膜电位和CA的变化〜 (2+)HepG-2细胞水平。通过流式细胞术研究CSBE在HepG-2细胞上诱导的线粒体膜电位的变化。通过激光共聚焦显微镜测量与CSBE的处理和未处理的HepG-2细胞的细胞内Ca〜(2+)水平。 HepG-2细胞的线粒体膜电位在CSBE下的各种程度下降。此外,中高剂量组的细胞内Ca〜(2+)水平增加,导致不平衡。 CSBE可以降低线粒体膜电位,打开MPTP通道并导致细胞内Ca〜(2+)水平的过载,这可能会诱导Hepg-2细胞的凋亡。这些说明为您提供了为会议程序准备相机准备论文的基本准则。

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