Elghazi L, Rachdi L, Weiss A J, Cras-Méneur C, Bernal-Mizrachi E
Department of Internal Medicine, Division of Endocrinology, Washington University School of Medicine, Metabolism & Lipid Research, St Louis, MO 63110, USA.
Diabetes Obes Metab. 2007 Nov;9 Suppl 2:147-57. doi: 10.1111/j.1463-1326.2007.00783.x.
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.
胰岛素受体底物-2/磷脂酰肌醇3-激酶(PI3K)通路在β细胞质量和功能的调节中起着关键作用,这在体外和体内均得到证实。丝氨酸苏氨酸激酶Akt是该通路中颇具前景的下游分子之一,已被确定为调节β细胞功能、诱导其增殖和存活的潜在靶点。在此,我们总结了一些由Akt调节β细胞质量和功能所涉及的分子机制、下游信号通路及关键组分。