• T. Jägerbrink
  • H. Lexander
  • C. Palmberg
  • J. Shafqat
  • V. Sharoyko
  • P. O. Berggren
  • S. Efendic
  • S. Zaitsev
  • H. Jörnvall

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).

Original languageEnglish
Pages (from-to)1310-1316
Number of pages7
JournalCellular and Molecular Life Sciences
Volume64
Issue number10
DOIs
StatePublished - May 2007

    Research areas

  • 2-D gel electrophoresis, BL11282, Imidazolines, Pancreatic islets, Proteomics, Type 2 diabetes

    Scopus subject areas

  • Molecular Medicine
  • Molecular Biology
  • Pharmacology
  • Cellular and Molecular Neuroscience
  • Cell Biology

ID: 5533079