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NFIA对棕色脂肪细胞分化和功能的转录调控:解读代谢疾病的最新观点

Transcriptional control of brown adipocyte differentiation and function by NFIA: recent perspectives on deciphering metabolic diseases.

作者信息

Hiraike Yuta

机构信息

Laboratory for Advanced Research on Pathophysiology of Metabolic Diseases, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan.

出版信息

J Biochem. 2025 Sep 3;178(3):147-159. doi: 10.1093/jb/mvaf038.

DOI:10.1093/jb/mvaf038
PMID:40581369
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12372464/
Abstract

Brown adipocytes dissipate chemical energy as heat and confer protection against type 2 diabetes and obesity. Nuclear factor I-A (NFIA) is a transcription factor that orchestrates the brown fat gene programme by activating cell type-specific enhancers and facilitating the genomic binding of PPARγ, the master regulator of adipogenesis, to these enhancers. NFIA promotes mitochondrial oxidative phosphorylation and thermogenesis, while reciprocally suppressing adipose tissue inflammation, thereby contributing to the maintenance of glucose and body weight homeostasis in mice. Here the author provides an overview of the identification of NFIA as a pivotal regulator of brown adipocyte biology, elucidates its underlying mechanisms of action, examines its implications for systemic metabolism and outlines future perspectives for research in this field.

摘要

棕色脂肪细胞将化学能以热量形式消耗,并对2型糖尿病和肥胖症起到保护作用。核因子I-A(NFIA)是一种转录因子,它通过激活细胞类型特异性增强子并促进脂肪生成的主要调节因子PPARγ与这些增强子的基因组结合,来协调棕色脂肪基因程序。NFIA促进线粒体氧化磷酸化和产热,同时相互抑制脂肪组织炎症,从而有助于维持小鼠体内的葡萄糖和体重稳态。在此,作者概述了NFIA作为棕色脂肪细胞生物学关键调节因子的鉴定过程,阐明了其潜在的作用机制,探讨了其对全身代谢的影响,并概述了该领域未来的研究前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1c9/12372464/55ddf680fa72/mvaf038f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1c9/12372464/f201e9e7e0c9/mvaf038ga.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1c9/12372464/55ddf680fa72/mvaf038f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1c9/12372464/f201e9e7e0c9/mvaf038ga.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1c9/12372464/c2acd4ba3ea7/mvaf038f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1c9/12372464/4852cba71aae/mvaf038f2.jpg
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本文引用的文献

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PCPE-1, a brown adipose tissue-derived cytokine, promotes obesity-induced liver fibrosis.PCPE-1,一种来源于棕色脂肪组织的细胞因子,可促进肥胖诱导的肝纤维化。
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Global burden and strength of evidence for 88 risk factors in 204 countries and 811 subnational locations, 1990-2021: a systematic analysis for the Global Burden of Disease Study 2021.
全球疾病负担研究 2021 年在 204 个国家和地区、811 个次国家级地点对 88 种风险因素的全球负担和证据强度:系统分析。
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Genetic evidence for involvement of β2-adrenergic receptor in brown adipose tissue thermogenesis in humans.β2-肾上腺素能受体参与人类棕色脂肪组织产热的遗传证据。
Int J Obes (Lond). 2024 Aug;48(8):1110-1117. doi: 10.1038/s41366-024-01522-6. Epub 2024 Apr 17.
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NFIA in adipocytes reciprocally regulates mitochondrial and inflammatory gene program to improve glucose homeostasis.NFIA 在脂肪细胞中相互调节线粒体和炎症基因程序,以改善葡萄糖稳态。
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