Connexin-36 contributes to control function of insulin-producing cells

被引:50
作者
Le Gurun, S
Martin, D
Formenton, A
Maechler, P
Caille, D
Waeber, G
Meda, P
Haefliger, JA
机构
[1] Univ Lausanne Hosp, Dept Internal Med, Lausanne 1011, Switzerland
[2] Univ Geneva, Dept Med, Geneva 1211 4, Switzerland
[3] Univ Geneva, Dept Morphol, Geneva 1211 4, Switzerland
关键词
D O I
10.1074/jbc.M212382200
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
Connexin-36 (Cx36) is a gap junction protein expressed by the insulin-producing beta-cells. We investigated the contribution of this protein in normal beta-cell function by using a viral gene transfer approach to alter Cx36 content in the insulin-producing line of INS-1E cells and rat pancreatic islets. Transcripts for Cx43, Cx45, and Cx36 were detected by reverse transcriptase-PCR in freshly isolated pancreatic islets, whereas only a transcript for Cx36 was detected in INS-1E cells. After infection with a sense viral vector, which induced de novo Cx36 expression in the Cx-defective HeLa cells we used to control the transgene expression, Western blot, immunofluorescence, and freeze-fracture analysis showed a large increase of Cx36 within INS-1E cell membranes. In contrast, after infection with an antisense vector, Cx36 content was decreased by 80%. Glucose-induced insulin release and insulin content were decreased, whether infected INS-1E cells expressed Cx36 levels that were largely higher or lower than those observed in wild-type control cells. In both cases, basal insulin secretion was unaffected. Comparable observations on basal secretion and insulin content were made in freshly isolated rat pancreatic islets. The data indicate that large changes in Cx36 alter insulin content and, at least in INS-1E cells, also affect glucose-induced insulin release.
引用
收藏
页码:37690 / 37697
页数:8
相关论文
共 46 条
[31]   The pancreatic beta-cell as a fuel sensor: An electrophysiologist's viewpoint [J].
Rorsman, P .
DIABETOLOGIA, 1997, 40 (05) :487-495
[32]   Adenovirus-mediated overexpression of liver carnitine palmitoyltransferase I in INS1E cells:: effects on cell metabolism and insulin secretion [J].
Rubí, B ;
Antinozzi, PA ;
Herrero, L ;
Ishihara, H ;
Asins, G ;
Serra, D ;
Wollheim, CB ;
Maechler, P ;
Hegardt, FG .
BIOCHEMICAL JOURNAL, 2002, 364 (01) :219-226
[33]   GAD65-mediated glutamate decarboxylation reduces glucose-stimulated insulin secretion in pancreatic beta cells [J].
Rubi, B ;
Ishihara, H ;
Hegardt, FG ;
Wollheim, CB ;
Maechler, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (39) :36391-36396
[34]   EFFICIENT SELECTION OF RECOMBINANT ADENOVIRUSES BY VECTORS THAT EXPRESS BETA-GALACTOSIDASE [J].
SCHAACK, J ;
LANGER, S ;
GUO, XL .
JOURNAL OF VIROLOGY, 1995, 69 (06) :3920-3923
[35]   Glucose sensing in pancreatic β-cells -: A model for the study of other glucose-regulated cells in gut, pancreas, and hypothalamus [J].
Schuit, FC ;
Huypens, P ;
Heimberg, H ;
Pipeleers, DG .
DIABETES, 2001, 50 (01) :1-11
[36]   Diverse roles of KATP channels learned from Kir6.2 genetically engineered mice [J].
Seino, S ;
Iwanaga, T ;
Nagashima, K ;
Miki, T .
DIABETES, 2000, 49 (03) :311-318
[37]   Cx36 preferentially connects β-cells within pancreatic islets [J].
Serre-Beinier, V ;
Le Gurun, S ;
Belluardo, N ;
Trovato-Salinaro, A ;
Charollais, A ;
Haefliger, JA ;
Condorelli, DF ;
Meda, P .
DIABETES, 2000, 49 (05) :727-734
[38]   The murine gap junction gene connexin36 is highly expressed in mouse retina and regulated during brain development [J].
Söhl, G ;
Degen, J ;
Teubner, B ;
Willecke, K .
FEBS LETTERS, 1998, 428 (1-2) :27-31
[39]   Gap junction proteins - Where they live and how they die [J].
Spray, DC .
CIRCULATION RESEARCH, 1998, 83 (06) :679-681
[40]  
Tawadros T, 2002, J CELL SCI, V115, P385