Imatinib mesylate (Gleevec) protects against streptozotocin-induced diabetes and islet cell death in vitro

被引:46
|
作者
Hagerkvist, Robert
Makeeva, Natalia
Elliman, Stephen
Welsh, Nils
机构
[1] Univ Uppsala, Biomedicum, Dept Med Cell Biol, S-75123 Uppsala, Sweden
[2] Novartis Inst BioMed Res, Diabet & Metab Dis Area, Cambridge, MA 02139 USA
关键词
imatinib; pancreatic islet; diabetes; JNK; apoptosis;
D O I
10.1016/j.cellbi.2006.08.006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The tyrosine kinase inhibitor imatinib mesylate (Gleevec) has been demonstrated to protect various cell types from death by inhibition of Abelson tyrosine kinase (c-Abl). The aim of the present study was to establish whether imatinib protects the insulin producing P-cell from the different apoptosis promoting agents it? vitro and whether imatinib counteracts streptozotocin-induced diabetes in NMRI mice. We observe that imatinib attenuated the actions of several different death promoting substances. In addition, mice injected with streptozotocin did not develop diabetes when given imatinib. The beneficial effects of imatinib may be related to inhibition of the pro-apoptotic MAP kinase JNK. We conclude that imatinib protects against beta-cell death and that this may contribute to the previously reported anti-diabetic actions of imatinib. (c) 2006 International Federation for Cell Biology. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1013 / 1017
页数:5
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