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果蝇细胞因子非配对 2 通过远程控制胰岛素分泌来调节生理稳态。

Drosophila cytokine unpaired 2 regulates physiological homeostasis by remotely controlling insulin secretion.

机构信息

Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Cell. 2012 Sep 28;151(1):123-37. doi: 10.1016/j.cell.2012.08.019.

Abstract

In Drosophila, the fat body (FB), a functional analog of the vertebrate adipose tissue, is the nutrient sensor that conveys the nutrient status to the insulin-producing cells (IPCs) in the fly brain to release Drosophila insulin-like peptides (Dilps). Dilp secretion in turn regulates energy balance and promotes systemic growth. We identify Unpaired 2 (Upd2), a protein with similarities to type I cytokines, as a secreted factor produced by the FB in the fed state. When upd2 function is perturbed specifically in the FB, it results in a systemic reduction in growth and alters energy metabolism. Upd2 activates JAK/STAT signaling in a population of GABAergic neurons that project onto the IPCs. This activation relieves the inhibitory tone of the GABAergic neurons on the IPCs, resulting in the secretion of Dilps. Strikingly, we find that human Leptin can rescue the upd2 mutant phenotypes, suggesting that Upd2 is the functional homolog of Leptin.

摘要

在果蝇中,脂肪体(FB)是脊椎动物脂肪组织的功能类似物,它是向果蝇大脑中产生胰岛素的细胞(IPCs)传递营养状态的营养传感器,以释放果蝇胰岛素样肽(Dilps)。反过来,Dilp 的分泌调节能量平衡并促进全身生长。我们鉴定出 Unpaired 2(Upd2)是一种与 I 型细胞因子具有相似性的蛋白质,它是 FB 在进食状态下产生的一种分泌因子。当 upd2 功能在 FB 中被特异性破坏时,会导致全身生长减少并改变能量代谢。Upd2 在投射到 IPCs 的一群 GABA 能神经元中激活 JAK/STAT 信号。这种激活减轻了 GABA 能神经元对 IPCs 的抑制性影响,导致 Dilps 的分泌。引人注目的是,我们发现人类瘦素可以挽救 upd2 突变体的表型,这表明 Upd2 是瘦素的功能同源物。

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