| Literature DB >> 8739912 |
H Iwahashi1, T Hanafusa, Y Eguchi, H Nakajima, J Miyagawa, N Itoh, K Tomita, M Namba, M Kuwajima, T Noguchi, Y Tsujimoto, Y Matsuzawa.
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.Entities:
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Year: 1996 PMID: 8739912 DOI: 10.1007/bf00403299
Source DB: PubMed Journal: Diabetologia ISSN: 0012-186X Impact factor: 10.122