The role of the transcription factor ETV5 in insulin exocytosis

转录因子ETV5在胰岛素外排中的作用

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作者:Ruth Gutierrez-Aguilar, Dong-Hoon Kim, Marina Casimir, Xiao-Qing Dai, Paul T Pfluger, Jongsun Park, April Haller, Elizabeth Donelan, Jisoo Park, David D'Alessio, Stephen C Woods, Patrick E MacDonald, Randy J Seeley

Methods

Etv5 knockout (KO) mice were monitored weekly for body weight (BW) and food intake. Body composition was measured at 8 and 16 weeks of age. Glucose metabolism was studied, and glucose-stimulated insulin secretion was measured in vivo and in vitro.

Results

Etv5 KO mice are smaller and leaner, and have a reduced BW and lower fat mass than their wild-type controls on a chow diet. When exposed to a high-fat diet, KO mice are resistant to diet-induced BW gain. Despite a greater insulin sensitivity, KO mice have profoundly impaired glucose tolerance associated with impaired insulin secretion. Morphometric analysis revealed smaller islets and a reduced beta cell size in the pancreatic islets of Etv5 KO mice. Knockdown of ETV5 in an insulin-secreting cell line or beta cells from human donors revealed intact mitochondrial and Ca(2+) channel activity, but reduced insulin exocytosis.

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