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细胞因子诱导小鼠胰腺β细胞系凋亡性细胞死亡:Bcl-2的抑制作用

Cytokine-induced apoptotic cell death in a mouse pancreatic beta-cell line: inhibition by Bcl-2.

作者信息

Iwahashi H, Hanafusa T, Eguchi Y, Nakajima H, Miyagawa J, Itoh N, Tomita K, Namba M, Kuwajima M, Noguchi T, Tsujimoto Y, Matsuzawa Y

机构信息

Second Department of Internal Medicine, Osaka University Medical School, Japan.

出版信息

Diabetologia. 1996 May;39(5):530-6. doi: 10.1007/BF00403299.

Abstract

Cytokines are thought to contribute to the induction of pancreatic beta-cell destruction in insulin-dependent diabetes mellitus. The molecular mechanisms that underlie beta-cell death were investigated by studying cytokine-induced cell death in beta-cell lines. A combination of three cytokines (interleukin-1 beta, tumour necrosis factor-alpha, and interferon-gamma) induced apoptotic cell death in the mouse pancreatic beta-cell line beta TC1, as judged from the appearance of cells with hypodiploid nuclei and oligonucleosomal DNA fragmentation. The same treatment also induced apoptosis in the mouse pancreatic alpha-cell line alpha TC1 and the NOD/Lt mouse beta-cell line NIT-1, although to a lesser extent than in beta TC1 cells. The abundance of endogenous Bcl-2 in beta TC1 cells was lower than that in the other two cell lines. Overexpression of human Bcl-2 in beta TC1 cells partially protected them from cytokine-induced cell death. These results suggest that apoptosis may be responsible, at least in part, for cytokine-induced beta-cell destruction and that Bcl-2 prevents apoptosis in pancreatic islet cells.

摘要

细胞因子被认为在胰岛素依赖型糖尿病中促成胰腺β细胞的破坏。通过研究细胞因子诱导β细胞系中的细胞死亡,对β细胞死亡的分子机制进行了研究。三种细胞因子(白细胞介素-1β、肿瘤坏死因子-α和干扰素-γ)的组合在小鼠胰腺β细胞系βTC1中诱导了凋亡性细胞死亡,这从具有亚二倍体核的细胞外观和寡核小体DNA片段化可以判断。相同的处理也在小鼠胰腺α细胞系αTC1和NOD/Lt小鼠β细胞系NIT-1中诱导了凋亡,尽管程度比在βTC1细胞中要小。βTC1细胞中内源性Bcl-2的丰度低于其他两个细胞系。人Bcl-2在βTC1细胞中的过表达部分保护它们免受细胞因子诱导的细胞死亡。这些结果表明,凋亡可能至少部分地是细胞因子诱导的β细胞破坏的原因,并且Bcl-2可防止胰岛细胞中的凋亡。

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