Suppr超能文献

德尔塔睡眠诱导肽和糖皮质激素诱导亮氨酸拉链:昼夜节律机制与肥胖之间的潜在联系?

Delta sleep-inducing peptide and glucocorticoid-induced leucine zipper: potential links between circadian mechanisms and obesity?

机构信息

Stem Cell Biology Laboratory, Pennington Biomedical Research Center, Baton Rouge, LA 70808, USA.

出版信息

Obes Rev. 2009 Nov;10 Suppl 2:46-51. doi: 10.1111/j.1467-789X.2009.00661.x.

Abstract

As the obesity pandemic has accelerated, investigators have begun to explore alternative mechanisms linking circadian biology and sleep to adipose tissue metabolism and obesity. This manuscript reviews recent findings in murine and human models demonstrating the oscillatory expression of the mRNAs encoding the core circadian regulatory proteins in adipose tissue. Comparative transcriptomic analyses of circadian oscillating genes have been used to identify the 'delta sleep-inducing peptide immunoreactor', also known as 'glucocorticoid-induced leucine zipper (GILZ)', as a potential link in this chain. The GILZ gene has been found to differentially regulate stromal stem cell adipogenic and osteogenic differentiation in a reciprocal manner. In adipose and other metabolically active tissues, the circadian oscillation of GILZ expression is subject to entrainment by external stimuli. Together, these observations suggest that GILZ is an attractive candidate for future studies evaluating the role of circadian mechanisms in adipose tissue physiology and pathology.

摘要

随着肥胖症的流行加速,研究人员开始探索将生物钟生物学和睡眠与脂肪组织代谢和肥胖联系起来的其他机制。本文综述了最近在小鼠和人类模型中发现的核心生物钟调节蛋白的 mRNA 在脂肪组织中呈振荡表达的研究结果。对生物钟振荡基因的比较转录组分析已被用于鉴定“δ睡眠诱导肽反应蛋白”,也称为“糖皮质激素诱导亮氨酸拉链(GILZ)”,作为这一链条中的一个潜在联系。已经发现 GILZ 基因以一种相互的方式差异调节基质干细胞的脂肪生成和成骨分化。在脂肪和其他代谢活跃的组织中,GILZ 表达的昼夜节律振荡受到外部刺激的调节。综上所述,这些观察结果表明,GILZ 是未来研究生物钟机制在脂肪组织生理学和病理学中作用的一个有吸引力的候选者。

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