Literature DB >> 17919189

Regulation of beta-cell mass and function by the Akt/protein kinase B signalling pathway.

L Elghazi1, L Rachdi, A J Weiss, C Cras-Méneur, E Bernal-Mizrachi.   

Abstract

The insulin receptor substrate-2/phosphoinositide 3-kinase (PI3K) pathway plays a critical role in the regulation of beta-cell mass and function, demonstrated both in vitro and in vivo. The serine threonine kinase Akt is one of the promising downstream molecules of this pathway that has been identified as a potential target to regulate function and induce proliferation and survival of beta cells. Here we summarize some of the molecular mechanisms, downstream signalling pathways and critical components involved in the regulation of beta-cell mass and function by Akt.

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Year:  2007        PMID: 17919189     DOI: 10.1111/j.1463-1326.2007.00783.x

Source DB:  PubMed          Journal:  Diabetes Obes Metab        ISSN: 1462-8902            Impact factor:   6.577


  33 in total

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5.  Long-lived crowded-litter mice exhibit lasting effects on insulin sensitivity and energy homeostasis.

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6.  Impaired Store-Operated Calcium Entry and STIM1 Loss Lead to Reduced Insulin Secretion and Increased Endoplasmic Reticulum Stress in the Diabetic β-Cell.

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Review 7.  Growth factor control of pancreatic islet regeneration and function.

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8.  Ectopic expression of E2F1 stimulates beta-cell proliferation and function.

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10.  Differential effects of protein kinase B/Akt isoforms on glucose homeostasis and islet mass.

Authors:  Francesca Buzzi; Linhua Xu; Richard A Zuellig; Simone B Boller; Giatgen A Spinas; Debby Hynx; Zai Chang; Zhongzhou Yang; Brian A Hemmings; Oliver Tschopp; Markus Niessen
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