• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

表皮型脂氧合酶 3 调节脂肪细胞分化和过氧化物酶体增殖物激活受体 γ 的活性。

Epidermis-type lipoxygenase 3 regulates adipocyte differentiation and peroxisome proliferator-activated receptor gamma activity.

机构信息

Department of Biochemistry and Molecular Biology, University of Southern Denmark, Odense, Denmark.

出版信息

Mol Cell Biol. 2010 Aug;30(16):4077-91. doi: 10.1128/MCB.01806-08. Epub 2010 Jun 7.

DOI:10.1128/MCB.01806-08
PMID:20530198
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2916447/
Abstract

The nuclear receptor peroxisome proliferator-activated receptor gamma (PPAR gamma) is essential for adipogenesis. Although several fatty acids and their derivatives are known to bind and activate PPAR gamma, the nature of the endogenous ligand(s) promoting the early stages of adipocyte differentiation has remained enigmatic. Previously, we showed that lipoxygenase (LOX) activity is involved in activation of PPAR gamma during the early stages of adipocyte differentiation. Of the seven known murine LOXs, only the unconventional LOX epidermis-type lipoxygenase 3 (eLOX3) is expressed in 3T3-L1 preadipocytes. Here, we show that forced expression of eLOX3 or addition of eLOX3 products stimulated adipogenesis under conditions that normally require an exogenous PPAR gamma ligand for differentiation. Hepoxilins, a group of oxidized arachidonic acid derivatives produced by eLOX3, bound to and activated PPAR gamma. Production of hepoxilins was increased transiently during the initial stages of adipogenesis. Furthermore, small interfering RNA-mediated or retroviral short hairpin RNA-mediated knockdown of eLOX3 expression abolished differentiation of 3T3-L1 preadipocytes. Finally, we demonstrate that xanthine oxidoreductase (XOR) and eLOX3 synergistically enhanced PPAR gamma-mediated transactivation. Collectively, our results indicate that hepoxilins produced by the concerted action of XOR and eLOX3 may function as PPAR gamma activators capable of promoting the early PPAR gamma-dependent steps in the conversion of preadipocytes into adipocytes.

摘要

过氧化物酶体增殖物激活受体 γ(PPAR γ)是脂肪生成所必需的核受体。虽然已知几种脂肪酸及其衍生物可以结合并激活 PPAR γ,但促进脂肪细胞分化早期阶段的内源性配体的性质仍然是个谜。以前,我们表明脂氧合酶(LOX)活性参与脂肪细胞分化早期阶段的 PPAR γ激活。在已知的七种鼠 LOX 中,只有非常规 LOX 表皮型脂氧合酶 3(eLOX3)在 3T3-L1 前脂肪细胞中表达。在这里,我们表明,在通常需要外源性 PPAR γ配体进行分化的条件下,强制表达 eLOX3 或添加 eLOX3 产物可刺激脂肪生成。环氧合酶,一组由 eLOX3 产生的氧化花生四烯酸衍生物,与 PPAR γ结合并激活它。在脂肪生成的初始阶段,环氧合酶的产生短暂增加。此外,eLOX3 表达的小干扰 RNA 介导或逆转录病毒短发夹 RNA 介导的敲低消除了 3T3-L1 前脂肪细胞的分化。最后,我们证明黄嘌呤氧化还原酶(XOR)和 eLOX3 协同增强了 PPAR γ 介导的转录激活。总之,我们的结果表明,XOR 和 eLOX3 的协同作用产生的环氧合酶可能作为 PPAR γ 激活剂,能够促进前脂肪细胞向脂肪细胞转化过程中早期依赖 PPAR γ 的步骤。

相似文献

1
Epidermis-type lipoxygenase 3 regulates adipocyte differentiation and peroxisome proliferator-activated receptor gamma activity.表皮型脂氧合酶 3 调节脂肪细胞分化和过氧化物酶体增殖物激活受体 γ 的活性。
Mol Cell Biol. 2010 Aug;30(16):4077-91. doi: 10.1128/MCB.01806-08. Epub 2010 Jun 7.
2
Adipocyte differentiation of 3T3-L1 preadipocytes is dependent on lipoxygenase activity during the initial stages of the differentiation process.在分化过程的初始阶段,3T3-L1前脂肪细胞的脂肪细胞分化依赖于脂氧合酶活性。
Biochem J. 2003 Nov 1;375(Pt 3):539-49. doi: 10.1042/bj20030503.
3
Perfluorooctanoic acid binds to peroxisome proliferator-activated receptor γ and promotes adipocyte differentiation in 3T3-L1 adipocytes.全氟辛酸与过氧化物酶体增殖物激活受体γ结合,并促进3T3-L1脂肪细胞的脂肪生成。
Biosci Biotechnol Biochem. 2015;79(4):636-9. doi: 10.1080/09168451.2014.991683. Epub 2014 Dec 17.
4
Suppression of PPAR-gamma attenuates insulin-stimulated glucose uptake by affecting both GLUT1 and GLUT4 in 3T3-L1 adipocytes.在3T3-L1脂肪细胞中,过氧化物酶体增殖物激活受体γ(PPAR-γ)的抑制通过影响葡萄糖转运蛋白1(GLUT1)和葡萄糖转运蛋白4(GLUT4)来减弱胰岛素刺激的葡萄糖摄取。
Am J Physiol Endocrinol Metab. 2007 Jul;293(1):E219-27. doi: 10.1152/ajpendo.00695.2006. Epub 2007 Mar 27.
5
RNA interference of PPARgamma using fiber-modified adenovirus vector efficiently suppresses preadipocyte-to-adipocyte differentiation in 3T3-L1 cells.使用纤维修饰腺病毒载体对PPARγ进行RNA干扰可有效抑制3T3-L1细胞中前脂肪细胞向脂肪细胞的分化。
Gene. 2005 Mar 28;348:157-65. doi: 10.1016/j.gene.2005.01.005.
6
Knockdown of macrophage migration inhibitory factor disrupts adipogenesis in 3T3-L1 cells.巨噬细胞迁移抑制因子的敲低会破坏3T3-L1细胞的脂肪生成。
Endocrinology. 2008 Dec;149(12):6037-42. doi: 10.1210/en.2008-0158. Epub 2008 Aug 14.
7
Mechanisms of divergent effects of activated peroxisome proliferator-activated receptor-γ on mitochondrial citrate carrier expression in 3T3-L1 fibroblasts and mature adipocytes.激活的过氧化物酶体增殖物激活受体γ对3T3-L1成纤维细胞和成熟脂肪细胞中线粒体柠檬酸载体表达产生不同影响的机制。
Biochim Biophys Acta. 2013 Jun;1831(6):1027-36. doi: 10.1016/j.bbalip.2013.01.014. Epub 2013 Jan 28.
8
Tetrandrine has anti-adipogenic effect on 3T3-L1 preadipocytes through the reduced expression and/or phosphorylation levels of C/EBP-α, PPAR-γ, FAS, perilipin A, and STAT-3.汉防己甲素通过降低C/EBP-α、PPAR-γ、FAS、脂联素A和STAT-3的表达及/或磷酸化水平,对3T3-L1前脂肪细胞具有抗脂肪生成作用。
Biochem Biophys Res Commun. 2016 Aug 5;476(4):481-486. doi: 10.1016/j.bbrc.2016.05.150. Epub 2016 May 28.
9
Stearoyl-CoA desaturase 2 is required for peroxisome proliferator-activated receptor gamma expression and adipogenesis in cultured 3T3-L1 cells.硬脂酰辅酶A去饱和酶2是培养的3T3-L1细胞中过氧化物酶体增殖物激活受体γ表达和脂肪生成所必需的。
J Biol Chem. 2008 Feb 1;283(5):2906-16. doi: 10.1074/jbc.M705656200. Epub 2007 Nov 21.
10
Tob2 inhibits peroxisome proliferator-activated receptor γ2 expression by sequestering Smads and C/EBPα during adipocyte differentiation.Tob2 通过在脂肪细胞分化过程中隔离 Smads 和 C/EBPα 来抑制过氧化物酶体增殖物激活受体 γ2 的表达。
Mol Cell Biol. 2012 Dec;32(24):5067-77. doi: 10.1128/MCB.00610-12. Epub 2012 Oct 15.

引用本文的文献

1
Oxylipin Profiling of Airway Structural Cells Is Unique and Modified by Relevant Stimuli.气道结构细胞的氧化脂质谱具有独特性,并会受到相关刺激的影响而发生改变。
J Proteome Res. 2025 Feb 7;24(2):672-684. doi: 10.1021/acs.jproteome.4c00775. Epub 2025 Jan 3.
2
Multiple Roles of Apolipoprotein E4 in Oxidative Lipid Metabolism and Ferroptosis During the Pathogenesis of Alzheimer's Disease.载脂蛋白 E4 在阿尔茨海默病发病机制中的氧化脂质代谢和铁死亡中的多种作用。
J Mol Neurosci. 2024 Jul 3;74(3):62. doi: 10.1007/s12031-024-02224-4.
3
Functional Characterization of Transgenic Mice Overexpressing Human 15-Lipoxygenase-1 (ALOX15) under the Control of the aP2 Promoter.转染人 15-脂氧合酶-1(ALOX15)基因的 aP2 启动子调控的转基因小鼠的功能特征。
Int J Mol Sci. 2023 Mar 2;24(5):4815. doi: 10.3390/ijms24054815.
4
Transcriptome Analysis Identifies Key Metabolic Changes in the Brain of in Response to Chronic Hypoxia.转录组分析鉴定出慢性低氧应激下大脑中的关键代谢变化。
Genes (Basel). 2022 Jul 27;13(8):1347. doi: 10.3390/genes13081347.
5
Development of an In Vitro Screening Platform for the Identification of Partial PPARγ Agonists as a Source for Antidiabetic Lead Compounds.开发体外筛选平台鉴定部分过氧化物酶体增殖物激活受体γ激动剂作为抗糖尿病先导化合物的来源。
Molecules. 2018 Sep 22;23(10):2431. doi: 10.3390/molecules23102431.
6
Hepatocyte ALOXE3 is induced during adaptive fasting and enhances insulin sensitivity by activating hepatic PPARγ.肝细胞 ALOXE3 在适应性禁食期间被诱导,并通过激活肝 PPARγ 增强胰岛素敏感性。
JCI Insight. 2018 Aug 23;3(16). doi: 10.1172/jci.insight.120794.
7
Dietary Arachidonic Acid Has a Time-Dependent Differential Impact on Adipogenesis Modulated via COX and LOX Pathways in Grass Carp Ctenopharyngodon idellus.日粮花生四烯酸对草鱼(Ctenopharyngodon idellus)通过COX和LOX途径调节的脂肪生成具有时间依赖性差异影响。
Lipids. 2016 Dec;51(12):1325-1338. doi: 10.1007/s11745-016-4205-2. Epub 2016 Oct 17.
8
Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue.高脂饮食后脂联素表达降低与脂肪组织中醛脱氢酶1A1(ALDH1A1)的选择性上调及进一步的视黄酸受体信号传导有关。
FASEB J. 2017 Jan;31(1):203-211. doi: 10.1096/fj.201600263RR. Epub 2016 Oct 11.
9
Advances in Our Understanding of Oxylipins Derived from Dietary PUFAs.我们对源自膳食多不饱和脂肪酸的氧化脂质的认识进展
Adv Nutr. 2015 Sep 15;6(5):513-40. doi: 10.3945/an.114.007732. Print 2015 Sep.
10
Structural and functional biology of arachidonic acid 15-lipoxygenase-1 (ALOX15).花生四烯酸15-脂氧合酶-1(ALOX15)的结构与功能生物学
Gene. 2015 Nov 15;573(1):1-32. doi: 10.1016/j.gene.2015.07.073. Epub 2015 Jul 26.

本文引用的文献

1
Nuclear receptor-coregulator interaction profiling identifies TRIP3 as a novel peroxisome proliferator-activated receptor gamma cofactor.核受体共激活因子相互作用谱分析鉴定 TRIP3 为新型过氧化物酶体增殖物激活受体γ共激活因子。
Mol Cell Proteomics. 2009 Oct;8(10):2212-26. doi: 10.1074/mcp.M900209-MCP200. Epub 2009 Jul 10.
2
Reactive oxygen species facilitate adipocyte differentiation by accelerating mitotic clonal expansion.活性氧通过加速有丝分裂克隆扩增促进脂肪细胞分化。
J Biol Chem. 2009 Apr 17;284(16):10601-9. doi: 10.1074/jbc.M808742200. Epub 2009 Feb 23.
3
Structural basis for the activation of PPARgamma by oxidized fatty acids.氧化脂肪酸激活过氧化物酶体增殖物激活受体γ的结构基础。
Nat Struct Mol Biol. 2008 Sep;15(9):924-31. doi: 10.1038/nsmb.1474.
4
A functional peroxisome proliferator-activated receptor-gamma ligand-binding domain is not required for adipogenesis.脂肪生成并不需要一个功能性的过氧化物酶体增殖物激活受体γ配体结合结构域。
J Biol Chem. 2008 Sep 5;283(36):24290-4. doi: 10.1074/jbc.C800139200. Epub 2008 Jul 11.
5
Adipocyte differentiation of 3T3-L1 preadipocytes is dependent on lipoxygenase activity during the initial stages of the differentiation process.在分化过程的初始阶段,3T3-L1前脂肪细胞的脂肪细胞分化依赖于脂氧合酶活性。
Biochem J. 2003 Nov 1;375(Pt 3):539-49. doi: 10.1042/bj20030503.
6
Alternative mechanisms by which mediator subunit MED1/TRAP220 regulates peroxisome proliferator-activated receptor gamma-stimulated adipogenesis and target gene expression.介质亚基MED1/TRAP220调节过氧化物酶体增殖物激活受体γ刺激的脂肪生成和靶基因表达的替代机制。
Mol Cell Biol. 2008 Feb;28(3):1081-91. doi: 10.1128/MCB.00967-07. Epub 2007 Nov 26.
7
The hepoxilin connection in the epidermis.表皮中的肝氧素联系
FEBS J. 2007 Jul;274(14):3494-3502. doi: 10.1111/j.1742-4658.2007.05909.x. Epub 2007 Jul 2.
8
Control of oxygenation in lipoxygenase and cyclooxygenase catalysis.脂氧合酶和环氧化酶催化过程中的氧合作用控制。
Chem Biol. 2007 May;14(5):473-88. doi: 10.1016/j.chembiol.2007.04.007.
9
Epidermal lipoxygenase products of the hepoxilin pathway selectively activate the nuclear receptor PPARalpha.肝氧膦烯通路的表皮脂氧合酶产物选择性激活核受体PPARα。
Lipids. 2007 Jun;42(6):491-7. doi: 10.1007/s11745-007-3054-4. Epub 2007 Apr 14.
10
Xanthine oxidoreductase is a regulator of adipogenesis and PPARgamma activity.黄嘌呤氧化还原酶是脂肪生成和过氧化物酶体增殖物激活受体γ(PPARγ)活性的调节因子。
Cell Metab. 2007 Feb;5(2):115-28. doi: 10.1016/j.cmet.2007.01.005.