Differential protein expression in pancreatic islets after treatment with an imidazoline compound

被引:13
|
作者
Jagerbrink, T.
Lexander, H.
Palmberg, C.
Shafqat, J.
Sharoyko, V.
Berggren, P-O
Efendic, S.
Zaitsev, S.
Jornvall, H. [1 ]
机构
[1] Karolinska Inst, Dept Med Biochem & Biophys, SE-17177 Stockholm, Sweden
[2] Karolinska Inst, Dept Oncol & Pathol, SE-17177 Stockholm, Sweden
[3] Karolinska Inst, Rolf Luft Res Ctr Diabet & Endocrinol, SE-17177 Stockholm, Sweden
[4] Moscow MV Lomonosov State Univ, Belozersky Inst Physicochem Biol, Moscow 119992, Russia
关键词
2-D gel electrophoresis; pancreatic islets; proteomics; type; 2; diabetes; imidazolines; BL11282;
D O I
10.1007/s00018-007-7136-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The effects of an imidazoline compound (BL11282) on protein expression in rat pancreatic islets were investigated with a proteomic approach. The compound increases insulin release selectively at high glucose concentrations and is therefore of interest in type 2 diabetes. Whole cell extracts from isolated drug-treated and native pancreatic rat islets were compared after separation by 2-D gel electrophoresis. Differentially expressed proteins were identified by mass spectrometry; 15 proteins were selectively up-regulated and 7 selectively down-regulated in drug-treated islets. Of special interest among the differentially expressed proteins are those involved in protein folding (Hsp60, protein disulfide isomerase, calreticulin), Ca2+ binding (calgizzarin, calcyclin and annexin I) and metabolism or signalling (pyruvate kinase, alpha enolase and protein kinase C inhibitor 1).
引用
收藏
页码:1310 / 1316
页数:7
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