Connexins protect mouse pancreatic β cells against apoptosis.


Autoria(s): Klee P.; Allagnat F.; Pontes H.; Cederroth M.; Charollais A.; Caille D.; Britan A.; Haefliger J.A.; Meda P.
Data(s)

2011

Resumo

Type 1 diabetes develops when most insulin-producing β cells of the pancreas are killed by an autoimmune attack. The in vivo conditions modulating the sensitivity and resistance of β cells to this attack remain largely obscure. Here, we show that connexin 36 (Cx36), a trans-membrane protein that forms gap junctions between β cells in the pancreatic islets, protects mouse β cells against both cytotoxic drugs and cytokines that prevail in the islet environment at the onset of type 1 diabetes. We documented that this protection was at least partially dependent on intercellular communication, which Cx36 and other types of connexin channels establish within pancreatic islets. We further found that proinflammatory cytokines decreased expression of Cx36 and that experimental reduction or augmentation of Cx36 levels increased or decreased β cell apoptosis, respectively. Thus, we conclude that Cx36 is central to β cell protection from toxic insults.

Identificador

http://serval.unil.ch/?id=serval:BIB_D563A9D1CAC6

isbn:1558-8238 (Electronic)

pmid:22056383

doi:10.1172/JCI40509

isiid:000297599500034

Idioma(s)

en

Fonte

Journal of Clinical Investigation, vol. 121, no. 12, pp. 4870-4879

Tipo

info:eu-repo/semantics/article

article