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

被引:11
作者
Hyun, Joogyung [1 ]
Hashimoto, Carl [1 ]
机构
[1] Yale Univ, Sch Med, Dept Cell Biol, New Haven, CT 06510 USA
关键词
insulin proteolysis; signaling pathway; Drosophila; lifespan; beta cell; AMYLOID-BETA PEPTIDE; ALZHEIMERS-DISEASE; LIFE-SPAN; IN-VIVO; GROWTH; METABOLISM; EXPRESSION; ABLATION; SYSTEM; FLY;
D O I
10.4161/fly.5.1.14080
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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.
引用
收藏
页码:53 / 57
页数:5
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