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Cripto-1 induces apoptosis in HC-11 mouse mammary epithelial cells.

机译:Cripto-1诱导HC-11小鼠乳腺上皮细胞凋亡。

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摘要

Cripto-1 (CR-1) is an epidermal growth factor (EGF)-related protein. CR-1 can inhibit beta-casein and whey acidic protein expression in mouse mammary epithelial cells. The present study demonstrates that CR-1 can induce apoptosis in HC-11 mouse mammary epithelial cells, as measured by bis-benzimide stained nuclei, TUNEL assay and cell death ELISA. Apoptosis could be observed after 2 days of exposure of confluent HC-11 cells to CR-1 in the absence of the survival factors EGF and insulin, with maximum apoptosis occurring at 3 days. A reduction in poly(ADP-ribose) polymerase (PARP) expression and an increase in beta-catenin cleavage was found after 18 h of exposure to CR-1 suggesting that apoptosis was preceded by the induction of a caspase activity since the caspase inhibitor ZFAD.FMK could block the CR-1-induced reduction in PARP expression and CR-1-induced apoptosis. CR-1 was found to increase the expression of caspase-3-like protease. Although, the levels of p27kip1 and p21Bax did not change after exposure to CR-1 for 18 h, the levels of Bcl-xL became undetectable. These studies suggest that CR-1 promotes apoptosis by mediating the induction of caspase-3-like protease and downregulating the expression of Bcl-xL.
机译:Cripto-1(CR-1)是一种表皮生长因子(EGF)相关蛋白。 CR-1可以抑制小鼠乳腺上皮细胞中的β-酪蛋白和乳清酸性蛋白表达。本研究表明,通过双苯甲酰亚胺染色的核,TUNEL分析和细胞死亡ELISA检测,CR-1可以诱导HC-11小鼠乳腺上皮细胞凋亡。在没有生存因子EGF和胰岛素的情况下,将融合的HC-11细胞暴露于CR-1 2天后,可以观察到细胞凋亡,最大凋亡发生在3天。暴露于CR-1 18小时后,发现聚(ADP-核糖)聚合酶(PARP)表达减少,β-catenin裂解增加,这表明自胱天蛋白酶抑制剂ZFAD诱导凋亡发生在胱天蛋白酶活性的诱导之前.FMK可以阻止CR-1诱导的PARP表达减少和CR-1诱导的凋亡。发现CR-1增加caspase-3样蛋白酶的表达。尽管在暴露于CR-1 18小时后p27kip1和p21Bax的水平没有变化,但是Bcl-xL的水平却变得不可检测。这些研究表明,CR-1通过介导caspase-3-like蛋白酶的诱导并下调Bcl-xL的表达来促进细胞凋亡。

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