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25-hexanedione induced apoptosis in mesenchymal stem cells from rat bonemarrow via mitochondria-dependent caspase-3 pathway

机译:25-己二酮诱导大鼠骨骼间充质干细胞凋亡经由线粒体依赖性caspase-3途径的骨髓

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摘要

2,5-hexanedione (HD) induces apoptosis of nerve cells. However,the mechanism of HD-induced apoptosis remains unknown. Mesenchymal stem cells (MSCs) are multipotential stem cells with the ability to differentiate into various cell types. This study is designed to investigate the apoptosis induced by HD in rat bone marrow MSCs (BMSCs) and the related underlying mechanisms. The fifth generation of MSCs was treated with 0, 10, 20 and 40 mM HD respectively. The viability of BMSCs was observed by MTT. Apoptosis were estimated by Hoechst 33342 staining and TUNEL assay. The disruption of mitochondrial transmembrane potential (MMP) was examined by JC-1 staining. Moreover, the expression of Bax and Bcl-2, cytochrome c release, and caspase-3 activity were determined by real-time RT-PCR, Western blot and Spectrophotometry. Our results showed that HD induced apoptosis in MSCs in a dose dependent manner. Moreover, HD downregulated the Bcl-2 expression,upregulated the Bax expression and the Bax/Bcl-2 ratio, promoted the disruption of MMP, induced the release of cytochrome c from mitochondria to cytosol, and increased the activity of caspase-3 in MSCs. These results indicate that HD induces apoptosis in MSCs and the activated mitochondria-dependent caspase-3 pathway may be involved in the HD-induced apoptosis.
机译:2,5-己二酮(HD)诱导神经细胞凋亡。然而,HD诱导细胞凋亡的机制仍然未知。间充质干细胞(MSC)是具有分化为多种细胞类型的能力的多能干细胞。本研究旨在研究HD诱导的大鼠骨髓MSC(BMSC)凋亡及其相关的潜在机制。第五代MSC分别用0、10、20和40μmMHD处理。通过MTT观察BMSCs的生存力。通过Hoechst 33342染色和TUNEL测定法估计细胞凋亡。通过JC-1染色检查线粒体跨膜电位(MMP)的破坏。此外,通过实时RT-PCR,蛋白质印迹和分光光度法测定Bax和Bcl-2的表达,细胞色素c的释放以及caspase-3的活性。我们的结果表明,HD以剂量依赖性方式诱导MSCs的凋亡。此外,HD下调了Bcl-2的表达,上调了Bax的表达和Bax / Bcl-2的比例,促进了MMP的破坏,诱导了细胞色素c从线粒体释放到细胞质中,并增加了MSC中caspase-3的活性。 。这些结果表明HD诱导MSCs凋亡,而激活的线粒体依赖性caspase-3途径可能参与HD诱导的凋亡。

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