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

Cellular and Molecular Life Sciences - Tập 64 - Trang 1310-1316 - 2007
T. Jägerbrink1, H. Lexander2, C. Palmberg1, J. Shafqat1, V. Sharoyko3, P.-O. Berggren3, S. Efendic3, S. Zaitsev3,4, H. Jörnvall1
1Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden
2Department of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden
3The Rolf Luft Research Center for Diabetes and Endocrinology, Karolinska Institutet, Stockholm, Sweden
4Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow, Russia

Tóm tắt

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).