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胰岛素信号转导在 CoA 活化水平调节脂肪酸分解代谢。

Insulin signaling regulates fatty acid catabolism at the level of CoA activation.

机构信息

German Cancer Research Center (DKFZ), Heidelberg, Germany.

出版信息

PLoS Genet. 2012 Jan;8(1):e1002478. doi: 10.1371/journal.pgen.1002478. Epub 2012 Jan 19.

DOI:10.1371/journal.pgen.1002478
PMID:22275878
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3261918/
Abstract

The insulin/IGF signaling pathway is a highly conserved regulator of metabolism in flies and mammals, regulating multiple physiological functions including lipid metabolism. Although insulin signaling is known to regulate the activity of a number of enzymes in metabolic pathways, a comprehensive understanding of how the insulin signaling pathway regulates metabolic pathways is still lacking. Accepted knowledge suggests the key regulated step in triglyceride (TAG) catabolism is the release of fatty acids from TAG via the action of lipases. We show here that an additional, important regulated step is the activation of fatty acids for beta-oxidation via Acyl Co-A synthetases (ACS). We identify pudgy as an ACS that is transcriptionally regulated by direct FOXO action in Drosophila. Increasing or reducing pudgy expression in vivo causes a decrease or increase in organismal TAG levels respectively, indicating that pudgy expression levels are important for proper lipid homeostasis. We show that multiple ACSs are also transcriptionally regulated by insulin signaling in mammalian cells. In sum, we identify fatty acid activation onto CoA as an important, regulated step in triglyceride catabolism, and we identify a mechanistic link through which insulin regulates lipid homeostasis.

摘要

胰岛素/IGF 信号通路是调节代谢的高度保守的调控因子,在果蝇和哺乳动物中调节多种生理功能,包括脂质代谢。尽管已知胰岛素信号调节代谢途径中许多酶的活性,但对胰岛素信号通路如何调节代谢途径仍缺乏全面的了解。公认的知识表明,甘油三酯 (TAG) 分解代谢的关键调节步骤是通过脂肪酶作用从 TAG 释放脂肪酸。我们在这里表明,一个额外的重要调节步骤是通过酰基辅酶 A 合成酶 (ACS) 激活脂肪酸进行β氧化。我们鉴定出 pudge 是一种 ACS,它在果蝇中受 FOXO 的直接转录调控。体内增加或减少 pudge 的表达分别导致生物体 TAG 水平的降低或增加,表明 pudge 的表达水平对脂质的适当动态平衡至关重要。我们表明,在哺乳动物细胞中,许多 ACS 也受到胰岛素信号的转录调控。总之,我们确定脂肪酸向 CoA 的激活是甘油三酯分解代谢的一个重要调节步骤,并且我们确定了胰岛素调节脂质动态平衡的机制联系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84cd/3261918/700e55f22f19/pgen.1002478.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84cd/3261918/f1c617652f17/pgen.1002478.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84cd/3261918/f33d3836d54f/pgen.1002478.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84cd/3261918/138f3eb90d7e/pgen.1002478.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84cd/3261918/4ec1df9812e9/pgen.1002478.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84cd/3261918/40b1903b3b51/pgen.1002478.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84cd/3261918/700e55f22f19/pgen.1002478.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84cd/3261918/f1c617652f17/pgen.1002478.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84cd/3261918/f33d3836d54f/pgen.1002478.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84cd/3261918/138f3eb90d7e/pgen.1002478.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84cd/3261918/4ec1df9812e9/pgen.1002478.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84cd/3261918/40b1903b3b51/pgen.1002478.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84cd/3261918/700e55f22f19/pgen.1002478.g006.jpg

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