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本文引用的文献

1
Meaningful respirometric measurements of UCP1-mediated thermogenesis.对UCP1介导的产热进行有意义的呼吸测定。
Biochimie. 2017 Mar;134:56-61. doi: 10.1016/j.biochi.2016.12.005. Epub 2016 Dec 14.
2
Human and Mouse Brown Adipose Tissue Mitochondria Have Comparable UCP1 Function.人类和小鼠棕色脂肪组织线粒体具有可比的解偶联蛋白1(UCP1)功能。
Cell Metab. 2016 Aug 9;24(2):246-55. doi: 10.1016/j.cmet.2016.07.004.
3
Underestimation of the Maximal Capacity of the Mitochondrial Electron Transport System in Oligomycin-Treated Cells.对寡霉素处理细胞中线粒体电子传递系统最大容量的低估。
PLoS One. 2016 Mar 7;11(3):e0150967. doi: 10.1371/journal.pone.0150967. eCollection 2016.
4
Severe Burn Injury Induces Thermogenically Functional Mitochondria in Murine White Adipose Tissue.严重烧伤会在小鼠白色脂肪组织中诱导产热功能的线粒体。
Shock. 2015 Sep;44(3):258-64. doi: 10.1097/SHK.0000000000000410.
5
Taking control over intracellular fatty acid levels is essential for the analysis of thermogenic function in cultured primary brown and brite/beige adipocytes.控制细胞内脂肪酸水平对于分析培养的原代棕色和米色脂肪细胞的产热功能至关重要。
EMBO Rep. 2014 Oct;15(10):1069-76. doi: 10.15252/embr.201438775. Epub 2014 Aug 18.
6
UCP1 in brite/beige adipose tissue mitochondria is functionally thermogenic.米色脂肪组织线粒体中的解偶联蛋白1具有产热功能。
Cell Rep. 2013 Dec 12;5(5):1196-203. doi: 10.1016/j.celrep.2013.10.044. Epub 2013 Nov 27.
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Methods for assessing mitochondrial function in diabetes.评估糖尿病中线粒体功能的方法。
Diabetes. 2013 Apr;62(4):1041-53. doi: 10.2337/db12-1219.
8
Mechanism of fatty-acid-dependent UCP1 uncoupling in brown fat mitochondria.褐色脂肪组织线粒体中脂肪酸依赖性 UCP1 解偶联的机制。
Cell. 2012 Oct 12;151(2):400-13. doi: 10.1016/j.cell.2012.09.010.
9
Uncoupling protein-1 is not leaky.解偶联蛋白-1并非渗漏性的。
Biochim Biophys Acta. 2010 Jun-Jul;1797(6-7):773-84. doi: 10.1016/j.bbabio.2010.04.007. Epub 2010 Apr 14.
10
Quantitative microplate-based respirometry with correction for oxygen diffusion.基于微量培养板的定量呼吸测量及其对氧气扩散的修正。
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人体棕色脂肪组织中解偶联蛋白1(UCP1)功能的定量分析。

Quantification of UCP1 function in human brown adipose tissue.

作者信息

Porter Craig

机构信息

a Department of Surgery , University of Texas Medical Branch , Galveston , TX , USA.

b Metabolism Unit, Shriners Hospitals for Children - Galveston , Galveston , TX , USA.

出版信息

Adipocyte. 2017 Apr 3;6(2):167-174. doi: 10.1080/21623945.2017.1319535. Epub 2017 Apr 14.

DOI:10.1080/21623945.2017.1319535
PMID:28453364
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5477712/
Abstract

Brown adipose tissue (BAT) mitochondria are distinct from their counterparts in other tissues in that ATP production is not their primary physiologic role. BAT mitochondria are equipped with a specialized protein known as uncoupling protein 1 (UCP1). UCP1 short-circuits the electron transport chain, allowing mitochondrial membrane potential to be transduced to heat, making BAT a tissue capable of altering energy expenditure and fuel metabolism in mammals without increasing physical activity. The recent discovery that adult humans have metabolically active BAT has rekindled an interest in this intriguing tissue, with the overarching aim of manipulating BAT function to augment energy expenditure as a countermeasure for obesity and the metabolic abnormalities it incurs. Subsequently, there has been heightened interest in quantifying BAT function and more specifically, determining UCP1-mediated thermogenesis in BAT specimens - including in those obtained from humans. In this article, BAT mitochondrial bioenergetics will be described and compared with more conventional mitochondria in other tissues. The biochemical methods typically used to quantify BAT mitochondrial function will also be discussed in terms of their specificity for assaying UCP1 mediated thermogenesis. Finally, recent data concerning BAT UCP1 function in humans will be described and discussed.

摘要

棕色脂肪组织(BAT)线粒体与其在其他组织中的对应物不同,因为产生ATP并非其主要生理功能。BAT线粒体配备有一种名为解偶联蛋白1(UCP1)的特殊蛋白质。UCP1使电子传递链短路,使线粒体膜电位转化为热量,使BAT成为一种能够在不增加体力活动的情况下改变哺乳动物能量消耗和燃料代谢的组织。最近发现成年人体内有代谢活跃的BAT,这重新引发了人们对这个有趣组织的兴趣,其总体目标是操纵BAT功能以增加能量消耗,作为对抗肥胖及其引发的代谢异常的一种对策。随后,人们对量化BAT功能,更具体地说,对确定BAT标本(包括从人类获取的标本)中UCP1介导的产热,兴趣日益浓厚。在本文中,将描述BAT线粒体生物能量学,并与其他组织中更传统的线粒体进行比较。还将讨论通常用于量化BAT线粒体功能的生化方法在检测UCP1介导的产热方面的特异性。最后,将描述和讨论有关人类BAT UCP1功能的最新数据。