Enhancing effect of taurine on glucose response in
UCP2-overexpressing beta cells
- Author(s)
- Lee Sang-Hoon; Lee Hyun-Young; Kim So-Yeon; Lee In-Kyu; Song Dae-Kyu
- Keimyung Author(s)
- Song, Dae Kyu; Lee, In Kyu
- Department
- Dept. of Physiology (생리학)
Dept. of Internal Medicine (내과학)
- Journal Title
- Diabetes Research and Clinical Practice
- Issued Date
- 2004
- Volume
- 66
- Issue
- Supplement
- Abstract
- Uncoupling protein 2 (UCP2) is up-regulated in pancreatic beta cells when exposed to long-term high glucose or free fatty
acids, which results in impaired glucose-induced insulin secretion (GIIS). We have evaluated whether taurine pretreatment can
restore impaired GIIS of beta cells overexpressing UCP2 by adenovirus (Ad)-mediated transfection technique. In Ad-Null
control cells, externally applied glucose (10 mM) inhibited ATP-sensitive potassium (KATP) channel activity even in the
presence of 300 mMdiazoxide. In Ad-UCP2 cells, however, glucose failed to inhibit KATP channel activity; despite the response
of KATP channel itself to glibenclamide was normal. The glucose-stimulated increase of cytosolic Ca2+ concentration ([Ca2+]c)
and insulin secretion was also diminished (P < 0.05). When taurine (3 mM) was pretreated for 24 h, the glucose responses of
Ad-UCP2 cells were remarkably restored. The effect of taurine was, however, blocked by CCCP (carbonyl cyanide pchlorophenylhydrazone;
2 mM), a mitochondrial Ca2+ uniporter inhibitor. These results suggest that taurine restores impaired
GIIS in Ad-UCP2 cells, at least partially, by acting on the mechanism for Ca2+ sequestration into the mitochondrial matrix.
# 2004 Elsevier Ireland Ltd. All rights reserved.
Keywords: Uncoupling protein 2; Taurine; Glucose-induced insulin secretion; KATP channel; Ca2+ uniporter
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