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

被引:91
作者
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
[1] OSAKA UNIV,SCH MED,BIOMED RES CTR,DEPT MED GENET,OSAKA 553,JAPAN
[2] OSAKA UNIV,SCH MED,DEPT PHYSIOL CHEM & NUTR,OSAKA 553,JAPAN
[3] UNIV TOKUSHIMA,SCH MED,DEPT LAB MED,TOKUSHIMA 770,JAPAN
[4] FUKUI MED SCH,DEPT BIOCHEM,FUKUI 91011,JAPAN
关键词
pancreatic beta cell; Bcl-2; apoptosis; cytokine; interleukin-1; tumour necrosis factor; interferon-gamma;
D O I
10.1007/BF00403299
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:530 / 536
页数:7
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