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Physiological effects of manipulating the level of insulin-degrading enzyme in insulin-producing cells of Drosophila

机译:操纵果蝇胰岛素产生细胞中胰岛素降解酶水平的生理效应

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摘要

Insulin-degrading enzyme (IDE) degrades insulin and other peptides, including the A beta peptide of Alzheimer's disease. However, the mechanism by which IDE acts on its substrates in vivo is unclear, and its role in pathogenesis of type 2 diabetes and Alzheimer's disease is controversial. Here, we show that in Drosophila knocking down IDE in insulin-producing cells (IPCs) of the brain results in increased body weight and fecundity, decreased circulating sugar levels and reduced lifespan. Moreover, knocking down and overexpressing IDE in IPCs have opposite physiological effects. As misregulated insulin signaling in peripheral tissues is known to cause similar phenotypes, our data suggest a role for Drosophila IDE in determining the level of insulin-like peptides made by IPCs that systemically activate insulin signaling.
机译:胰岛素降解酶(IDE)降解胰岛素和其他肽,包括阿尔茨海默氏病的Aβ肽。但是,IDE在体内作用于其底物的机制尚不清楚,其在2型糖尿病和阿尔茨海默氏病的发病机理中的作用还存在争议。在这里,我们显示了在果蝇中,击倒大脑胰岛素产生细胞(IPC)中的IDE会导致体重和生育力增加,循环糖水平降低和寿命缩短。此外,在IPC中取消和过分表达IDE具有相反的生理效应。由于已知外周组织中胰岛素信号调节失调会导致类似的表型,因此我们的数据表明果蝇IDE在确定由IPC全身性激活胰岛素信号转导的胰岛素样肽的水平中发挥作用。

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