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[雷公藤红素下调HL-60细胞中P-Akt和细胞周期蛋白D1的表达并诱导细胞凋亡]

[Celastrol down-regulates expression of P-Akt and cyclin D1 in HL-60 cells and induces apoptosis].

作者信息

Ma Yong-Lan, Yi Hong, Yang Fei-Lan, Zhang Yuan, Wang Ya, Wang Ying

机构信息

Department of Clinical Laboratorial Examination, Air Force 457 Hospital of PLA, Wuhan 430012, Hubei Province, China.

出版信息

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2010 Aug;18(4):898-902.

Abstract

The aim of this study was to investigate the effect of Celastrol on induction of HL-60 cell apoptosis and its possible mechanism. The proliferative activity of HL-60 cells treated with 0.25 - 8.0 μmol/L of Celastrol for 24 - 72 hours was assayed by MTT method, the effects of Celastrol on apoptosis and cell cycle of HL-60 were detected by TUNEL staining and flow cytometry with Annexin V-FITC/PI double labeling, the expression of pAkt and cyclin D1 at protein and gene level in HL-60 cells treated with Celastrol were measured by Western blot and RT-PCR. The results showed that the Celastrol could obviously inhibit the proliferation of HL-60 cells in concentration-and time-dependent manners, the IC₅₀ value of Celastrol for 24 hours was 6.21 ± 0.242 μmol/L. The Celastrol concentration-dependently induced the apoptosis of HL-60 cells, accompanying with morphological changes of apoptotic cells, which may be related with arrest of cells in G₀/G₁ phase. The Celastrol suppressed the expression of pAkt and Cyclin D1 in HL-60 cells to a varying degree which showed obvious concentration-and time-dependent manners. It is concluded that the Celastrol inhibits the proliferation and induced the apoptosis of HL-60 cells. Its mechanism may be related with down-regulation of p-Act and cyclin D1 expressions.

摘要

本研究旨在探讨雷公藤红素对HL-60细胞凋亡的诱导作用及其可能机制。采用MTT法检测0.25 - 8.0 μmol/L雷公藤红素处理HL-60细胞24 - 72小时后的增殖活性,通过TUNEL染色及Annexin V-FITC/PI双染流式细胞术检测雷公藤红素对HL-60细胞凋亡及细胞周期的影响,运用Western blot和RT-PCR检测雷公藤红素处理后HL-60细胞中pAkt和细胞周期蛋白D1在蛋白及基因水平的表达。结果显示,雷公藤红素能明显以浓度和时间依赖性方式抑制HL-60细胞增殖,雷公藤红素作用24小时的IC₅₀值为6.21 ± 0.242 μmol/L。雷公藤红素呈浓度依赖性诱导HL-60细胞凋亡,并伴有凋亡细胞的形态学变化,这可能与细胞阻滞于G₀/G₁期有关。雷公藤红素不同程度地抑制HL-60细胞中pAkt和细胞周期蛋白D1的表达,呈明显的浓度和时间依赖性。结论:雷公藤红素抑制HL-60细胞增殖并诱导其凋亡,其机制可能与下调p-Akt和细胞周期蛋白D1的表达有关。

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