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本文引用的文献

1
Structural and functional roles of ether lipids.醚脂的结构和功能作用。
Protein Cell. 2018 Feb;9(2):196-206. doi: 10.1007/s13238-017-0423-5. Epub 2017 May 18.
2
Control of brown and beige fat development.棕色和米色脂肪发育的调控
Nat Rev Mol Cell Biol. 2016 Nov;17(11):691-702. doi: 10.1038/nrm.2016.96. Epub 2016 Aug 24.
3
Zfp423 Maintains White Adipocyte Identity through Suppression of the Beige Cell Thermogenic Gene Program.锌指蛋白423通过抑制米色细胞产热基因程序维持白色脂肪细胞特性。
Cell Metab. 2016 Jun 14;23(6):1167-1184. doi: 10.1016/j.cmet.2016.04.023. Epub 2016 May 26.
4
Myocardin-related transcription factor A regulates conversion of progenitors to beige adipocytes.心肌相关转录因子A调控祖细胞向米色脂肪细胞的转化。
Cell. 2015 Jan 15;160(1-2):105-18. doi: 10.1016/j.cell.2014.12.005. Epub 2015 Jan 8.
5
Cold-inducible Zfp516 activates UCP1 transcription to promote browning of white fat and development of brown fat.冷诱导的Zfp516激活UCP1转录以促进白色脂肪棕色化和棕色脂肪发育。
Mol Cell. 2015 Jan 22;57(2):235-46. doi: 10.1016/j.molcel.2014.12.005. Epub 2015 Jan 8.
6
Peroxisomal lipid synthesis regulates inflammation by sustaining neutrophil membrane phospholipid composition and viability.过氧化物酶体脂质合成通过维持中性粒细胞膜磷脂组成和活力来调节炎症。
Cell Metab. 2015 Jan 6;21(1):51-64. doi: 10.1016/j.cmet.2014.12.002.
7
Prdm16 is required for the maintenance of brown adipocyte identity and function in adult mice.Prdm16对于成年小鼠棕色脂肪细胞特性和功能的维持是必需的。
Cell Metab. 2014 Apr 1;19(4):593-604. doi: 10.1016/j.cmet.2014.03.007.
8
p107 is a crucial regulator for determining the adipocyte lineage fate choices of stem cells.p107是决定干细胞脂肪细胞谱系命运选择的关键调节因子。
Stem Cells. 2014 May;32(5):1323-36. doi: 10.1002/stem.1637.
9
Ablation of PRDM16 and beige adipose causes metabolic dysfunction and a subcutaneous to visceral fat switch.PRDM16 和米色脂肪细胞的消融会导致代谢功能障碍,并引起皮下脂肪向内脏脂肪的转变。
Cell. 2014 Jan 16;156(1-2):304-16. doi: 10.1016/j.cell.2013.12.021.
10
What we talk about when we talk about fat.我们谈论脂肪时在谈论什么。
Cell. 2014 Jan 16;156(1-2):20-44. doi: 10.1016/j.cell.2013.12.012.

pexrap 抑制 prdm16 介导的产热基因表达。

PexRAP Inhibits PRDM16-Mediated Thermogenic Gene Expression.

机构信息

Division of Endocrinology, Metabolism & Lipid Research, Washington University School of Medicine, Saint Louis, MO 63110, USA; Division of Biology and Biomedical Sciences, Washington University School of Medicine, Saint Louis, MO 63110, USA.

Division of Endocrinology, Metabolism & Lipid Research, Washington University School of Medicine, Saint Louis, MO 63110, USA; Division of Biology and Biomedical Sciences, Washington University School of Medicine, Saint Louis, MO 63110, USA.

出版信息

Cell Rep. 2017 Sep 19;20(12):2766-2774. doi: 10.1016/j.celrep.2017.08.077.

DOI:10.1016/j.celrep.2017.08.077
PMID:28930673
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5679740/
Abstract

How the nuclear receptor PPARγ regulates the development of two functionally distinct types of adipose tissue, brown and white fat, as well as the browning of white fat, remains unclear. Our previous studies suggest that PexRAP, a peroxisomal lipid synthetic enzyme, regulates PPARγ signaling and white adipogenesis. Here, we show that PexRAP is an inhibitor of brown adipocyte gene expression. PexRAP inactivation promoted adipocyte browning, increased energy expenditure, and decreased adiposity. Identification of PexRAP-interacting proteins suggests that PexRAP function extends beyond its role as a lipid synthetic enzyme. Notably, PexRAP interacts with importin-β1, a nuclear import factor, and knockdown of PexRAP in adipocytes reduced the levels of nuclear phospholipids. PexRAP also interacts with PPARγ, as well as PRDM16, a critical transcriptional regulator of thermogenesis, and disrupts the PRDM16-PPARγ complex, providing a potential mechanism for PexRAP-mediated inhibition of adipocyte browning. These results identify PexRAP as an important regulator of adipose tissue remodeling.

摘要

核受体 PPARγ 如何调节两种功能不同的脂肪组织(棕色脂肪和白色脂肪)的发育,以及白色脂肪的“棕色化”,目前尚不清楚。我们之前的研究表明,过氧化物酶体脂质合成酶 PexRAP 可调节 PPARγ 信号和白色脂肪生成。在这里,我们发现 PexRAP 是棕色脂肪细胞基因表达的抑制剂。PexRAP 失活促进脂肪细胞“棕色化”,增加能量消耗,减少脂肪堆积。鉴定 PexRAP 的互作蛋白表明,PexRAP 的功能超出了其作为脂质合成酶的作用。值得注意的是,PexRAP 与核输入因子 importin-β1 相互作用,而在脂肪细胞中敲低 PexRAP 会降低核磷脂的水平。PexRAP 还与 PPARγ 以及生热的关键转录调节因子 PRDM16 相互作用,并破坏 PRDM16-PPARγ 复合物,为 PexRAP 介导的脂肪细胞“棕色化”抑制提供了一种潜在的机制。这些结果表明 PexRAP 是脂肪组织重塑的重要调节因子。