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Detection of Calcium by a confocal laser scanning microscope in Na_2SeO_3-treated SW480 human colonic carcinoma cells

机译:Na_2SeO_3处理SW480人结肠癌细胞中共聚焦激光扫描显微镜检测钙

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A number of studies have demonstrated that perturbed cellular calcium homeostasis has been implicated in apoptosis. Some studies showed that selenium compounds were able to induce cell apoptosis. The main objective of this study is to evaluate effect of Na_2SeO_3 on intracellular Ca~(2+) levels in SW480 human colonic carcinoma cells. When SW480 cells were exposed to 25 to 100 μmol/L Na_2SeO_3, we also found that Na_2SeO_3 was able to induce [Ca~(2+)]_i, disruption of mitochondrial membrane potential (Δψm) in SW480 cells by using a confocal laser scanning microscope. Ca~(2+) channel inhibitor CoCl_2 and an intracellular Ca~(2+) chelator BAPTA completely inhibited [Ca~(2+)]_i increase. CoCl_2, BAPTA and ruthenium red also inhibited disruption of Δψm. The results suggest that Na_2SeO_3 is able to increase [Ca~(2+)]_i mitochondria permeability transition and Ca~(2+) is from extraceullar Ca~(2+).
机译:许多研究表明,扰动细胞钙稳态已经涉及细胞凋亡。一些研究表明,硒化合物能够诱导细胞凋亡。本研究的主要目的是评估Na_2SeO_3对SW480人结肠癌细胞中细胞内Ca〜(2+)水平的影响。当SW480细胞暴露于25至100μmol/ L Na_2 SEO_3时,我们还发现Na_2SeO_3能够诱导[Ca〜(2 +)] _ i,通过使用共聚焦激光扫描,在SW480细胞中破坏线粒体膜电位(Δψm)显微镜。 Ca〜(2+)通道抑制剂COCl_2和细胞内Ca〜(2+)螯合剂Bapta完全抑制[Ca〜(2 +)] _我增加。 Cocl_2,Bapta和钌红也抑制了Δψm的破坏。结果表明Na_2SeO_3能够增加[Ca〜(2 +)] _ i线粒体渗透率转换和Ca〜(2+)来自Ellardullar Ca〜(2+)。

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