Suppr超能文献

类固醇激素20-羟基蜕皮酮通过促进脂肪动激素途径,经由脑-脂肪组织轴诱导脂肪自噬。

The steroid hormone 20-hydroxyecdysone induces lipophagy via the brain-adipose tissue axis by promoting the adipokinetic hormone pathway.

作者信息

Li Yan-Xue, Li Yan-Li, Wang Xiao-Pei, Liu Tian-Wen, Dong Du-Juan, Wang Jin-Xing, Zhao Xiao-Fan

机构信息

Shandong Provincial Key Laboratory of Animal Cells and Developmental Biology, School of Life Sciences, Shandong University, Qingdao, China.

Shandong Provincial Key Laboratory of Animal Cells and Developmental Biology, School of Life Sciences, Shandong University, Qingdao, China.

出版信息

J Biol Chem. 2025 Feb;301(2):108179. doi: 10.1016/j.jbc.2025.108179. Epub 2025 Jan 10.

Abstract

Lipophagy is a way to degrade lipids; however, the molecular mechanisms are not fully understood. Using the holometabolous lepidopteran insect Helicoverpa armigera, cotton bollworm, as a model, we revealed that the larval fat body undergoes lipophagy during metamorphosis, and lipophagy is essential for metamorphosis. The steroid hormone 20-hydroxyecdysone (20E) induced lipophagy by promoting the expression of the peptide hormone adipokinetic hormone (AKH, the insect analog of glucagon) and the adipokinetic hormone receptor (AKHR). Akh was highly expressed in the brain and Akhr was expressed in various tissues. The 20E upregulated the expression of Akh and Akhr by its nuclear receptor EcR during metamorphosis. AKH and AKHR increased glucose levels via gluconeogenesis and promoted lipophagy. The high glucose level induced acetylation of FOXO and nuclear localization to promote the expression of lipases and autophagy genes. Thus, the steroid hormone 20E induced lipophagy via the brain-adipose tissue axis by promoting the AKH pathway, which presented nutrients and energy to pupal and adult development during insect metamorphosis after feeding stops.

摘要

脂质自噬是一种降解脂质的方式;然而,其分子机制尚未完全明确。我们以全变态鳞翅目昆虫棉铃虫作为模型,揭示了幼虫脂肪体在变态过程中会发生脂质自噬,且脂质自噬对变态至关重要。类固醇激素20-羟基蜕皮酮(20E)通过促进肽激素促脂动激素(AKH,昆虫体内类似胰高血糖素的物质)及其受体促脂动激素受体(AKHR)的表达来诱导脂质自噬。Akh在脑中高表达,Akhr在多种组织中表达。在变态过程中,20E通过其核受体EcR上调Akh和Akhr的表达。AKH和AKHR通过糖异生作用提高血糖水平并促进脂质自噬。高血糖水平诱导FOXO乙酰化并使其定位于细胞核,从而促进脂肪酶和自噬基因的表达。因此,类固醇激素20E通过促进AKH途径,经由脑-脂肪组织轴诱导脂质自噬,在昆虫停止取食后的变态过程中为蛹期和成虫发育提供营养和能量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2a8/11835591/c80e0cf2f0ac/gr1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验