Ablation of insulin-producing neurons in flies: Growth and diabetic phenotypes

被引:829
作者
Rulifson, EJ [1 ]
Kim, SK
Nusse, R
机构
[1] Stanford Univ, Dept Dev Biol, Stanford, CA 94305 USA
[2] Stanford Univ, Beckman Ctr B300, Howard Hughes Med Inst, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Med, Div Oncol, Stanford, CA 94305 USA
关键词
D O I
10.1126/science.1070058
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In the fruit fly Drosophila, four insulin genes are coexpressed in small clusters of cells [insulin-producing cells (IPCs)] in the brain. Here, we show that ablation of these IPCs causes developmental delay, growth retardation, and elevated carbohydrate levels in larval hemolymph. All of the defects were reversed by ectopic expression of a Drosophila insulin transgene. On the basis of these functional data and the observation that IPCs release insulin into the circulatory system, we conclude that brain IPCs are the main systemic supply of insulin during larval growth. We propose that IPCs and pancreatic islet beta cells are functionally analogous and may have evolved from a common ancestral insulin-producing neuron. Interestingly, the phenotype of flies lacking IPCs includes certain features of diabetes mellitus.
引用
收藏
页码:1118 / 1120
页数:3
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