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胰岛素/叉头框 O 信号通路调节对生殖至关重要的卵巢前列腺素。

Insulin/FOXO signaling regulates ovarian prostaglandins critical for reproduction.

机构信息

Department of Cell Biology, University of Alabama at Birmingham, 35294, USA.

出版信息

Dev Cell. 2010 Dec 14;19(6):858-71. doi: 10.1016/j.devcel.2010.11.005.

Abstract

Abnormalities in insulin/IGF-1 signaling are associated with infertility, but the molecular mechanisms are not well understood. Here we use liquid chromatography with electrospray ionization tandem mass spectrometry to show that the C. elegans insulin/FOXO pathway regulates the metabolism of locally acting lipid hormones called prostaglandins. C. elegans prostaglandins are synthesized without prostaglandin G/H synthase homologs, the targets of nonsteroidal anti-inflammatory drugs. Our results support the model that insulin signaling promotes the conversion of oocyte polyunsaturated fatty acids (PUFAs) into F-series prostaglandins that guide sperm to the fertilization site. Reduction in insulin signaling activates DAF-16/FOXO, which represses the transcription of germline and intestinal genes required to deliver PUFAs to oocytes in lipoprotein complexes. Nutritional and neuroendocrine cues target this mechanism to control prostaglandin metabolism and reproductive output. Prostaglandins may be conserved sperm guidance factors and widespread downstream effectors of insulin actions that influence both reproductive and nonreproductive processes.

摘要

胰岛素/IGF-1 信号异常与不孕有关,但分子机制尚不清楚。在这里,我们使用液相色谱-电喷雾串联质谱联用技术表明,秀丽隐杆线虫胰岛素/FOXO 途径调节局部作用脂质激素(称为前列腺素)的代谢。秀丽隐杆线虫前列腺素的合成不需要前列腺素 G/H 合酶同源物,即非甾体抗炎药的靶标。我们的结果支持这样一种模型,即胰岛素信号促进卵母细胞多不饱和脂肪酸(PUFAs)转化为 F 系列前列腺素,引导精子到达受精部位。胰岛素信号的减少会激活 DAF-16/FOXO,从而抑制将 PUFAs 以脂蛋白复合物形式输送到卵母细胞所需的生殖系和肠道基因的转录。营养和神经内分泌线索靶向此机制以控制前列腺素代谢和生殖输出。前列腺素可能是保守的精子导向因子和胰岛素作用的广泛下游效应物,影响生殖和非生殖过程。

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