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控制白色脂肪细胞与棕色脂肪细胞分化的调控回路。

Regulatory circuits controlling white versus brown adipocyte differentiation.

作者信息

Hansen Jacob B, Kristiansen Karsten

机构信息

Department of Medical Biochemistry and Genetics, the Panum Institute, University of Copenhagen, DK-2200 Copenhagen N, Denmark.

出版信息

Biochem J. 2006 Sep 1;398(2):153-68. doi: 10.1042/BJ20060402.

DOI:10.1042/BJ20060402
PMID:16898874
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1550312/
Abstract

Adipose tissue is a major endocrine organ that exerts a profound influence on whole-body homoeostasis. Two types of adipose tissue exist in mammals: WAT (white adipose tissue) and BAT (brown adipose tissue). WAT stores energy and is the largest energy reserve in mammals, whereas BAT, expressing UCP1 (uncoupling protein 1), can dissipate energy through adaptive thermogenesis. In rodents, ample evidence supports BAT as an organ counteracting obesity, whereas less is known about the presence and significance of BAT in humans. Despite the different functions of white and brown adipocytes, knowledge of factors differentially influencing the formation of white and brown fat cells is sparse. Here we summarize recent progress in the molecular understanding of white versus brown adipocyte differentiation, including novel insights into transcriptional and signal transduction pathways. Since expression of UCP1 is the hallmark of BAT and a key factor determining energy expenditure, we also review conditions associated with enhanced energy expenditure and UCP1 expression in WAT that may provide information on processes involved in brown adipocyte differentiation.

摘要

脂肪组织是一个主要的内分泌器官,对全身的稳态有着深远影响。哺乳动物体内存在两种脂肪组织:白色脂肪组织(WAT)和棕色脂肪组织(BAT)。白色脂肪组织储存能量,是哺乳动物最大的能量储备,而表达解偶联蛋白1(UCP1)的棕色脂肪组织可通过适应性产热消耗能量。在啮齿动物中,有充分证据支持棕色脂肪组织是对抗肥胖的器官,而关于棕色脂肪组织在人类中的存在及意义了解较少。尽管白色和棕色脂肪细胞功能不同,但对差异影响白色和棕色脂肪细胞形成的因素的了解却很稀少。在此,我们总结了白色与棕色脂肪细胞分化分子理解方面的最新进展,包括对转录和信号转导途径的新见解。由于UCP1的表达是棕色脂肪组织的标志以及决定能量消耗的关键因素,我们还综述了与白色脂肪组织中能量消耗增加和UCP1表达相关的情况,这些情况可能提供有关棕色脂肪细胞分化过程的信息。

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Cell Metab. 2006 May;3(5):333-41. doi: 10.1016/j.cmet.2006.04.002.
2
Thermogenic mechanisms and their hormonal regulation.产热机制及其激素调节。
Physiol Rev. 2006 Apr;86(2):435-64. doi: 10.1152/physrev.00009.2005.
3
Thiazolidinediones and rexinoids induce peroxisome proliferator-activated receptor-coactivator (PGC)-1alpha gene transcription: an autoregulatory loop controls PGC-1alpha expression in adipocytes via peroxisome proliferator-activated receptor-gamma coactivation.噻唑烷二酮类药物和视黄酸X受体激动剂诱导过氧化物酶体增殖物激活受体辅激活因子(PGC)-1α基因转录:一种自调节环通过过氧化物酶体增殖物激活受体γ共激活作用控制脂肪细胞中PGC-1α的表达。
Endocrinology. 2006 Jun;147(6):2829-38. doi: 10.1210/en.2006-0070. Epub 2006 Mar 2.
4
Pocket proteins control white versus brown fat cell differentiation.口袋蛋白控制白色脂肪细胞与棕色脂肪细胞的分化。
Cell Cycle. 2006 Feb;5(4):341-2. doi: 10.4161/cc.5.4.2465. Epub 2006 Feb 15.
5
Critical roles of the p160 transcriptional coactivators p/CIP and SRC-1 in energy balance.p160转录共激活因子p/CIP和SRC-1在能量平衡中的关键作用。
Cell Metab. 2006 Feb;3(2):111-22. doi: 10.1016/j.cmet.2006.01.002.
6
Bile acids induce energy expenditure by promoting intracellular thyroid hormone activation.胆汁酸通过促进细胞内甲状腺激素激活来诱导能量消耗。
Nature. 2006 Jan 26;439(7075):484-9. doi: 10.1038/nature04330. Epub 2006 Jan 8.
7
Suppression of oxidative metabolism and mitochondrial biogenesis by the transcriptional corepressor RIP140 in mouse adipocytes.转录共抑制因子RIP140对小鼠脂肪细胞氧化代谢和线粒体生物合成的抑制作用。
J Clin Invest. 2006 Jan;116(1):125-36. doi: 10.1172/JCI26040. Epub 2005 Dec 22.
8
Transcriptional corepression by SHP: molecular mechanisms and physiological consequences.小异二聚体伴侣蛋白介导的转录共抑制:分子机制与生理后果
Trends Endocrinol Metab. 2005 Dec;16(10):478-88. doi: 10.1016/j.tem.2005.10.005. Epub 2005 Nov 4.
9
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Cell Metab. 2005 Nov;2(5):283-95. doi: 10.1016/j.cmet.2005.10.002.
10
RIP140-targeted repression of gene expression in adipocytes.脂肪细胞中RIP140靶向的基因表达抑制
Mol Cell Biol. 2005 Nov;25(21):9383-91. doi: 10.1128/MCB.25.21.9383-9391.2005.