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本文引用的文献

1
Prdm16 determines the thermogenic program of subcutaneous white adipose tissue in mice.PRDM16 决定了小鼠皮下白色脂肪组织的产热程序。
J Clin Invest. 2011 Jan;121(1):96-105. doi: 10.1172/JCI44271. Epub 2010 Dec 1.
2
Transcriptional control of brown fat development.棕色脂肪发育的转录控制。
Cell Metab. 2010 Apr 7;11(4):257-62. doi: 10.1016/j.cmet.2010.03.005.
3
Human brown adipose tissue.人体棕色脂肪组织。
Cell Metab. 2010 Apr 7;11(4):248-52. doi: 10.1016/j.cmet.2010.03.008.
4
Chronic peroxisome proliferator-activated receptor gamma (PPARgamma) activation of epididymally derived white adipocyte cultures reveals a population of thermogenically competent, UCP1-containing adipocytes molecularly distinct from classic brown adipocytes.慢性过氧化物酶体增殖物激活受体 γ (PPARγ) 激活附睾衍生的白色脂肪细胞培养物揭示了一群具有产热能力、含有 UCP1 的脂肪细胞,它们在分子上与经典的棕色脂肪细胞不同。
J Biol Chem. 2010 Mar 5;285(10):7153-64. doi: 10.1074/jbc.M109.053942. Epub 2009 Dec 22.
5
Multiple roles of PPARalpha in brown adipose tissue under constitutive and cold conditions.PPARα 在组成型和冷刺激条件下棕色脂肪组织中的多重作用。
Genes Cells. 2010 Feb;15(2):91-100. doi: 10.1111/j.1365-2443.2009.01368.x. Epub 2009 Dec 9.
6
Peroxisome proliferator-activated receptor-alpha control of lipid and glucose metabolism in human white adipocytes.过氧化物酶体增殖物激活受体-α对人白色脂肪细胞中脂质和葡萄糖代谢的调控。
Endocrinology. 2010 Jan;151(1):123-33. doi: 10.1210/en.2009-0726. Epub 2009 Nov 3.
7
Functional brown adipose tissue in healthy adults.健康成年人中的功能性棕色脂肪组织。
N Engl J Med. 2009 Apr 9;360(15):1518-25. doi: 10.1056/NEJMoa0808949.
8
Identification and importance of brown adipose tissue in adult humans.成人棕色脂肪组织的识别及其重要性。
N Engl J Med. 2009 Apr 9;360(15):1509-17. doi: 10.1056/NEJMoa0810780.
9
Cold-activated brown adipose tissue in healthy men.健康男性体内的冷激活棕色脂肪组织
N Engl J Med. 2009 Apr 9;360(15):1500-8. doi: 10.1056/NEJMoa0808718.
10
Mutual dependence of Foxo3a and PGC-1alpha in the induction of oxidative stress genes.Foxo3a与PGC-1α在氧化应激基因诱导中的相互依赖性。
J Biol Chem. 2009 May 22;284(21):14476-84. doi: 10.1074/jbc.M807397200. Epub 2009 Mar 26.

过氧化物酶体增殖物激活受体 α(PPARα)诱导过氧化物酶体增殖物激活受体 γ 共激活因子 1α(PGC-1α)基因表达,并有助于棕色脂肪的产热激活:涉及 PRDM16。

Peroxisome proliferator-activated receptor α (PPARα) induces PPARγ coactivator 1α (PGC-1α) gene expression and contributes to thermogenic activation of brown fat: involvement of PRDM16.

机构信息

Department of Biochemistry and Molecular Biology and Institute of Biomedicine, University of Barcelona, and CIBER Fisiopatología de la Obesidad y Nutrición, Barcelona, Catalonia, Spain.

出版信息

J Biol Chem. 2011 Dec 16;286(50):43112-22. doi: 10.1074/jbc.M111.252775. Epub 2011 Oct 27.

DOI:10.1074/jbc.M111.252775
PMID:22033933
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3234861/
Abstract

Peroxisome proliferator activated receptor α (PPARα) is a distinctive marker of the brown fat phenotype that has been proposed to coordinate the transcriptional activation of genes for lipid oxidation and for thermogenic uncoupling protein 1 in brown adipose tissue. Here, we investigated the involvement of PPARα in the transcriptional control of the PPARγ coactivator (PGC)-1α gene. Treatment with PPARα agonists induced PGC-1α mRNA expression in brown fat in vivo and in primary brown adipocytes. This enhancement of PGC-1α transcription was mediated by PPARα binding to a PPAR-responsive element in the distal PGC-1α gene promoter. PGC-1α gene expression was decreased in PPARα-null brown fat, both under basal conditions and in response to thermogenic activation. Moreover, PPARα- and cAMP-mediated pathways interacted to control PGC-1α transcription. PRDM16 (PRD1-BF1-RIZ1 homologous domain-containing 16) promoted PPARα induction of PGC-1α gene transcription, especially under conditions in which protein kinase A pathways were activated. This enhancement was associated with the interaction of PRDM16 with the PGC-1α promoter at the PPARα-binding site. In addition, PPARα promoted the expression of the PRDM16 gene in brown adipocytes, and activation of PPARα in human white adipocytes led to the appearance of a brown adipocyte pattern of gene expression, including induction of PGC-1α and PRDM16. Collectively, these results suggest that PPARα acts as a key component of brown fat thermogenesis by coordinately regulating lipid catabolism and thermogenic gene expression via induction of PGC-1α and PRDM16.

摘要

过氧化物酶体增殖物激活受体α(PPARα)是棕色脂肪表型的独特标志物,它被提议协调棕色脂肪组织中脂质氧化和解偶联蛋白 1 的热生成基因的转录激活。在这里,我们研究了 PPARα 在过氧化物酶体增殖物激活受体γ共激活因子(PGC)-1α基因转录调控中的作用。PPARα 激动剂处理在体内和原代棕色脂肪细胞中诱导 PGC-1αmRNA 的表达。这种 PGC-1α 转录的增强是由 PPARα 与 PGC-1α 基因启动子远端的 PPAR 反应元件结合介导的。在基础条件下和对热激活的反应中,PPARα 缺失的棕色脂肪中的 PGC-1α 基因表达均降低。此外,PPARα 和 cAMP 介导的途径相互作用以控制 PGC-1α 转录。PRDM16(PRD1-BF1-RIZ1 同源结构域包含 16)促进 PPARα 诱导 PGC-1α 基因转录,尤其是在蛋白激酶 A 途径被激活的情况下。这种增强与 PRDM16 在 PPARα 结合位点与 PGC-1α 启动子的相互作用有关。此外,PPARα 在棕色脂肪细胞中促进 PRDM16 基因的表达,并且 PPARα 在人白色脂肪细胞中的激活导致出现一种棕色脂肪细胞的基因表达模式,包括 PGC-1α 和 PRDM16 的诱导。总的来说,这些结果表明 PPARα 通过诱导 PGC-1α 和 PRDM16 协调调节脂质分解代谢和热生成基因表达,从而作为棕色脂肪产热的关键组成部分发挥作用。