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本文引用的文献

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EBF2 regulates osteoblast-dependent differentiation of osteoclasts.EBF2调节破骨细胞的成骨细胞依赖性分化。
Dev Cell. 2005 Dec;9(6):757-67. doi: 10.1016/j.devcel.2005.10.009.
2
Gene expression analysis suggests that EBF-1 and PPARgamma2 induce adipogenesis of NIH-3T3 cells with similar efficiency and kinetics.基因表达分析表明,EBF-1和PPARγ2以相似的效率和动力学诱导NIH-3T3细胞的脂肪生成。
Physiol Genomics. 2005 Oct 17;23(2):206-16. doi: 10.1152/physiolgenomics.00015.2005. Epub 2005 Aug 16.
3
Krox20 stimulates adipogenesis via C/EBPbeta-dependent and -independent mechanisms.Krox20通过依赖C/EBPβ和不依赖C/EBPβ的机制刺激脂肪生成。
Cell Metab. 2005 Feb;1(2):93-106. doi: 10.1016/j.cmet.2004.12.009.
4
Krüppel-like transcription factor KLF5 is a key regulator of adipocyte differentiation.类Krüppel转录因子KLF5是脂肪细胞分化的关键调节因子。
Cell Metab. 2005 Jan;1(1):27-39. doi: 10.1016/j.cmet.2004.11.005.
5
Role of Krüppel-like factor 15 (KLF15) in transcriptional regulation of adipogenesis.Krüppel样因子15(KLF15)在脂肪生成转录调控中的作用。
J Biol Chem. 2005 Apr 1;280(13):12867-75. doi: 10.1074/jbc.M410515200. Epub 2005 Jan 20.
6
Interaction between GATA and the C/EBP family of transcription factors is critical in GATA-mediated suppression of adipocyte differentiation.GATA与转录因子C/EBP家族之间的相互作用在GATA介导的脂肪细胞分化抑制中至关重要。
Mol Cell Biol. 2005 Jan;25(2):706-15. doi: 10.1128/MCB.25.2.706-715.2005.
7
Abundance of two human preadipocyte subtypes with distinct capacities for replication, adipogenesis, and apoptosis varies among fat depots.两种人类前脂肪细胞亚型在复制、脂肪生成和凋亡能力上存在差异,其丰度在不同脂肪库中有所不同。
Am J Physiol Endocrinol Metab. 2005 Jan;288(1):E267-77. doi: 10.1152/ajpendo.00265.2004. Epub 2004 Sep 21.
8
The transcription factor CCAAT/enhancer-binding protein alpha is required for the intracellular retention of GLUT4.转录因子CCAAT/增强子结合蛋白α是GLUT4在细胞内滞留所必需的。
J Biol Chem. 2004 Oct 1;279(40):41468-76. doi: 10.1074/jbc.M405088200. Epub 2004 Jul 23.
9
Lipin expression preceding peroxisome proliferator-activated receptor-gamma is critical for adipogenesis in vivo and in vitro.在过氧化物酶体增殖物激活受体γ之前的脂素表达对于体内和体外的脂肪生成至关重要。
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10
Genetic disruptions of O/E2 and O/E3 genes reveal involvement in olfactory receptor neuron projection.O/E2和O/E3基因的遗传破坏显示其与嗅觉受体神经元投射有关。
Development. 2004 Mar;131(6):1377-88. doi: 10.1242/dev.01009.

Ebf1和Ebf2在脂肪生成转录级联反应中的关键作用。

Critical role for Ebf1 and Ebf2 in the adipogenic transcriptional cascade.

作者信息

Jimenez Maria A, Akerblad Peter, Sigvardsson Mikael, Rosen Evan D

机构信息

Division of Endocrinology, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.

出版信息

Mol Cell Biol. 2007 Jan;27(2):743-57. doi: 10.1128/MCB.01557-06. Epub 2006 Oct 23.

DOI:10.1128/MCB.01557-06
PMID:17060461
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1800806/
Abstract

The Ebf (O/E) family of helix-loop-helix transcription factors plays a significant role in B lymphocyte and neuronal development. The three primary members of this family, Ebf1, 2, and 3, are all expressed in adipocytes, and Ebf1 promotes adipogenesis when overexpressed in NIH 3T3 fibroblasts. Here we report that these three proteins have adipogenic potential in multiple cellular models and that peroxisome proliferator-activated receptor gamma (PPARgamma) is required for this effect, at least in part due to direct activation of the PPARgamma1 promoter by Ebf1. Ebf1 also directly binds to and activates the C/EBPalpha promoter, which exerts positive feedback on C/EBPdelta expression. Despite this, C/EBPalpha is dispensable for the adipogenic action of Ebf proteins. Ebf1 itself is induced by C/EBPbeta and delta, which bind and activate its promoter. Reduction of Ebf1 and Ebf2 proteins by specific short hairpin RNA blocks differentiation of 3T3-L1 cells, suggesting a critical role for these factors and the absence of functional redundancy between members of this family. Altogether, these data place Ebf1 within the known transcriptional cascade of adipogenesis and suggest critical roles for Ebf1 and Ebf2.

摘要

Ebf(O/E)家族的螺旋-环-螺旋转录因子在B淋巴细胞和神经元发育中发挥着重要作用。该家族的三个主要成员Ebf1、2和3均在脂肪细胞中表达,并且Ebf1在NIH 3T3成纤维细胞中过表达时可促进脂肪生成。在此我们报告,这三种蛋白在多种细胞模型中具有脂肪生成潜能,并且过氧化物酶体增殖物激活受体γ(PPARγ)对于此效应是必需的,至少部分原因是Ebf1直接激活了PPARγ1启动子。Ebf1还直接结合并激活C/EBPα启动子,后者对C/EBPδ表达发挥正反馈作用。尽管如此,C/EBPα对于Ebf蛋白的脂肪生成作用是可有可无的。Ebf1本身由C/EBPβ和δ诱导,它们结合并激活其启动子。通过特异性短发夹RNA降低Ebf1和Ebf2蛋白可阻断3T3-L1细胞的分化,提示这些因子具有关键作用且该家族成员之间不存在功能冗余。总之,这些数据将Ebf1置于已知的脂肪生成转录级联反应中,并提示Ebf1和Ebf2具有关键作用。