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选择你的命运:借助COUP-TFII做出细胞命运决定。

Choose your destiny: Make a cell fate decision with COUP-TFII.

作者信息

Wu San-Pin, Yu Cheng-Tai, Tsai Sophia Y, Tsai Ming-Jer

机构信息

Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA; Adrienne Helis Malvin Medical Research Foundation, New Orleans, LA 70130, USA.

Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

J Steroid Biochem Mol Biol. 2016 Mar;157:7-12. doi: 10.1016/j.jsbmb.2015.11.011. Epub 2015 Dec 2.

DOI:10.1016/j.jsbmb.2015.11.011
PMID:26658017
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4724268/
Abstract

Cell fate specification is a critical process to generate cells with a wide range of characteristics from stem and progenitor cells. Emerging evidence demonstrates that the orphan nuclear receptor COUP-TFII serves as a key regulator in determining the cell identity during embryonic development. The present review summarizes our current knowledge on molecular mechanisms by which COUP-TFII employs to define the cell fates, with special emphasis on cardiovascular and renal systems. These novel insights pave the road for future studies of regenerative medicine.

摘要

细胞命运特化是一个从干细胞和祖细胞产生具有广泛特性细胞的关键过程。新出现的证据表明,孤儿核受体COUP-TFII在胚胎发育过程中作为决定细胞身份的关键调节因子。本综述总结了我们目前对COUP-TFII用于定义细胞命运的分子机制的认识,特别强调心血管和肾脏系统。这些新见解为再生医学的未来研究铺平了道路。

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1
Choose your destiny: Make a cell fate decision with COUP-TFII.选择你的命运:借助COUP-TFII做出细胞命运决定。
J Steroid Biochem Mol Biol. 2016 Mar;157:7-12. doi: 10.1016/j.jsbmb.2015.11.011. Epub 2015 Dec 2.
2
The orphan nuclear receptor COUP-TFII is required for angiogenesis and heart development.孤儿核受体COUP-TFII是血管生成和心脏发育所必需的。
Genes Dev. 1999 Apr 15;13(8):1037-49. doi: 10.1101/gad.13.8.1037.
3
A COUP-TFII Human Embryonic Stem Cell Reporter Line to Identify and Select Atrial Cardiomyocytes.A COUP-TFII 人胚胎干细胞报告系,用于鉴定和选择心房心肌细胞。
Stem Cell Reports. 2017 Dec 12;9(6):1765-1779. doi: 10.1016/j.stemcr.2017.10.024. Epub 2017 Nov 22.
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Regulatory potential of COUP-TFs in development: stem/progenitor cells.COUP-TFs 在发育中的调控潜能:干细胞/祖细胞。
Semin Cell Dev Biol. 2013 Dec;24(10-12):687-93. doi: 10.1016/j.semcdb.2013.08.005. Epub 2013 Aug 23.
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Nuclear receptor COUP-TFII-expressing neocortical interneurons are derived from the medial and lateral/caudal ganglionic eminence and define specific subsets of mature interneurons.核受体 COUP-TFII 表达的新皮层中间神经元来源于内侧和外侧/尾侧神经节隆起,并定义了成熟中间神经元的特定亚群。
J Comp Neurol. 2013 Feb 1;521(2):479-97. doi: 10.1002/cne.23186.
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The nuclear orphan receptor COUP-TFII is required for limb and skeletal muscle development.核孤儿受体COUP-TFII是肢体和骨骼肌发育所必需的。
Mol Cell Biol. 2004 Dec;24(24):10835-43. doi: 10.1128/MCB.24.24.10835-10843.2004.
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COUP-TFI and -TFII nuclear receptors are expressed in amacrine cells and play roles in regulating the differentiation of retinal progenitor cells.COUP-TFI 和 -TFII 核受体在无长突细胞中表达,并在调节视网膜祖细胞的分化中发挥作用。
Exp Eye Res. 2010 Jan;90(1):49-56. doi: 10.1016/j.exer.2009.09.009. Epub 2009 Sep 17.
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Dynamic expression of COUP-TFI and COUP-TFII during development and functional maturation of the mouse inner ear.COUP-TFI和COUP-TFII在小鼠内耳发育和功能成熟过程中的动态表达。
Gene Expr Patterns. 2005 Jun;5(5):587-92. doi: 10.1016/j.modgep.2005.03.012.
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Essential roles of COUP-TFII in Leydig cell differentiation and male fertility.COUP-TFII在睾丸间质细胞分化和雄性生育中的重要作用。
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Transcription factors COUP-TFI and COUP-TFII are required for the production of granule cells in the mouse olfactory bulb.转录因子COUP-TFI和COUP-TFII是小鼠嗅球中颗粒细胞产生所必需的。
Development. 2015 May 1;142(9):1593-605. doi: 10.1242/dev.115279.

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Front Endocrinol (Lausanne). 2023 Aug 18;14:1229033. doi: 10.3389/fendo.2023.1229033. eCollection 2023.
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Identification of novel genes and pathways regulated by the orphan nuclear receptor COUP-TFII in mouse MA-10 Leydig cells†.鉴定孤儿核受体 COUP-TFII 在小鼠 MA-10 间质细胞中调控的新基因和通路。
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NR2F2 Orphan Nuclear Receptor is Involved in Estrogen Receptor Alpha-Mediated Transcriptional Regulation in Luminal A Breast Cancer Cells.NR2F2 孤儿核受体参与腔 A 型乳腺癌细胞中雌激素受体 α 介导的转录调控。
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90 YEARS OF PROGESTERONE: New insights into progesterone receptor signaling in the endometrium required for embryo implantation.90 年的孕激素:胚胎着床所必需的子宫内膜孕激素受体信号转导的新见解。
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The Nuclear Receptor COUP-TFII Regulates Gene Transcription via a GC-Rich Promoter Element in Mouse Leydig Cells.核受体COUP-TFII通过富含GC的启动子元件调控小鼠睾丸间质细胞中的基因转录。
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COUP-TFII revisited: Its role in metabolic gene regulation.再探COUP-TFII:其在代谢基因调控中的作用
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Downregulation of COUP-TFII inhibits glioblastoma growth via targeting MPC1.COUP-TFII的下调通过靶向MPC1抑制胶质母细胞瘤的生长。
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本文引用的文献

1
MicroRNA-194 reciprocally stimulates osteogenesis and inhibits adipogenesis via regulating COUP-TFII expression.微小RNA-194通过调节COUP-TFII的表达相互刺激成骨作用并抑制脂肪生成。
Cell Death Dis. 2014 Nov 20;5(11):e1532. doi: 10.1038/cddis.2014.485.
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MicroRNA-302a stimulates osteoblastic differentiation by repressing COUP-TFII expression.MicroRNA-302a 通过抑制 COUP-TFII 表达来刺激成骨细胞分化。
J Cell Physiol. 2015 Apr;230(4):911-21. doi: 10.1002/jcp.24822.
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Cardiac cell lineages that form the heart.形成心脏的心脏细胞谱系。
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Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart Development.先天性心脏缺陷患者的染色体失衡:一项荟萃分析揭示了与心脏发育相关的新的潜在关键区域。
Congenit Heart Dis. 2015 May-Jun;10(3):193-208. doi: 10.1111/chd.12179. Epub 2014 Apr 11.
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Rare variants in NR2F2 cause congenital heart defects in humans.NR2F2 中的罕见变异可导致人类先天性心脏缺陷。
Am J Hum Genet. 2014 Apr 3;94(4):574-85. doi: 10.1016/j.ajhg.2014.03.007.
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SoxF factors and Notch regulate nr2f2 gene expression during venous differentiation in zebrafish.SoxF 因子和 Notch 在斑马鱼静脉分化过程中调节 nr2f2 基因的表达。
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Suppression of COUP-TFII by proinflammatory cytokines contributes to the pathogenesis of endometriosis.促卵泡激素转录因子 II 的抑制作用是由促炎细胞因子引起的,这有助于子宫内膜异位症的发病机制。
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Identification of dosage-sensitive genes in fetuses referred with severe isolated congenital diaphragmatic hernia.鉴定因严重孤立性先天性膈疝而转诊的胎儿中的剂量敏感基因。
Prenat Diagn. 2013 Dec;33(13):1283-92. doi: 10.1002/pd.4244. Epub 2013 Nov 14.
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Nkx genes are essential for maintenance of ventricular identity.Nkx 基因对于维持心室身份至关重要。
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Regulatory potential of COUP-TFs in development: stem/progenitor cells.COUP-TFs 在发育中的调控潜能:干细胞/祖细胞。
Semin Cell Dev Biol. 2013 Dec;24(10-12):687-93. doi: 10.1016/j.semcdb.2013.08.005. Epub 2013 Aug 23.