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机构地区:[1]西安交通大学第二附属医院(西北医院)老年神经科,西安710004 [2]陕西省人民医院医保办,西安710068
出 处:《神经解剖学杂志》2016年第5期647-652,共6页Chinese Journal of Neuroanatomy
摘 要:目的:探讨RANTES对MPP^+诱导的PC12细胞凋亡的保护作用及其机制。方法:利用MPP^+处理PC12细胞建立帕金森细胞模型,并分别转染RANTES siRNA和pcRANTES,MTT法检测细胞增殖,Annexin V-FITC/PI双染法检测细胞凋亡,Western Blot检测总Akt(t-Akt)、磷酸化-Akt(p-Akt)和cleaved caspase-3蛋白表达水平。结果:RANTES siRNA显著抑制RNATES的表达,而pc DNA RANTES成功使RNATES过表达;过表达RNATES可显著上调MPP^+处理的PC12细胞增殖(P<0.05),并抑制MPP^+诱导的PC12细胞凋亡(P<0.05),下调cleasved caspase-3蛋白表达水平(P<0.05)。此外,过表达RANTES可显著促进p-Akt/t-Akt蛋白表达水平(P<0.05),且PI3K/Akt通路抑制剂LY294002显著抑制RNATES对PC细胞增殖的促进作用和凋亡的抑制作用(P<0.05)。结论:RANTES可通过PI3K/Akt信号通路促进MPP^+处理的PC12细胞的增殖并抑制细胞的凋亡。Objective: To observe the protective effect and its mechanism of RANTES against PC12 cell apoptosis induced by 1-methyl-4-phenylpyridinium( MPP~+). Methods: Pakrkinson's disease( PD) cell model was built by addition of MPP~+into PC12 cell cultures,and RANTES and pc DNA3. 1-RANTES were transfected into PC12 cells. The cell proliferation was measured using MTT assay,cell apoptosis was detected by Annexin V-FITC / PI assay. The protein expression level of total-Akt( t-Akt),phosphorylated-Akt( p-Akt) and cleaved caspase-3 were measured using Western Blot assay. Results: RANTES siRNA significantly silenced the expression of RANTES,while pc DNA3 RANTES remarkably overexpressed RANTES. Overexpression of RANTES remarkably promoted cell proliferation that inhibited by MPP~+,inhibited cellular apoptosis induced by MPP~+( P〈0. 05) and downregulated the cleasved caspase-3 protein expression level( P〈0. 05). In addition,RANTES overexpression markedly up-regulated the ratio of p-Akt / t-Akt( P〈0. 05),and the PI3 K / Akt inhibitor LY294002 significantly suppressed the effect of RANTED on cellular proliferation and apoptosis. Conclusion: RANTES promotes cellular proliferation and inhibit apoptosis in PC12 cells treated with MPP~+partly through PI3 K / Akt signaling pathway.
关 键 词:帕金森 细胞凋亡 细胞增殖 RANTES PC12细胞
分 类 号:R742.5[医药卫生—神经病学与精神病学]
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