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环磷酸腺苷反应元件结合蛋白/活化转录因子1的缺失抑制了异位表达CCAAT/增强子结合蛋白(C/EBP)α、C/EBPβ或过氧化物酶体增殖物激活受体γ2的3T3-L1细胞的脂肪生成转化。

Depletion of cAMP-response element-binding protein/ATF1 inhibits adipogenic conversion of 3T3-L1 cells ectopically expressing CCAAT/enhancer-binding protein (C/EBP) alpha, C/EBP beta, or PPAR gamma 2.

作者信息

Fox Keith E, Fankell Dana M, Erickson Paul F, Majka Susan M, Crossno Joseph T, Klemm Dwight J

机构信息

Research Service, Veterans Affairs Medical Center, University of Colorado Health Sciences Center, Denver, Colorado 80220, USA.

出版信息

J Biol Chem. 2006 Dec 29;281(52):40341-53. doi: 10.1074/jbc.M605077200. Epub 2006 Oct 27.

Abstract

The differentiation of preadipocytes to adipocytes is orchestrated by the expression of the "master adipogenic regulators," CCAAT/enhancer-binding protein (C/EBP) beta, peroxisome proliferator-activated receptor gamma (PPARgamma), and C/EBP alpha. In addition, activation of the cAMP-response element-binding protein (CREB) is necessary and sufficient to promote adipogenic conversion and prevent apoptosis of mature adipocytes. In this report we used small interfering RNA to deplete CREB and the closely related factor ATF1 to explore the ability of the master adipogenic regulators to promote adipogenesis in the absence of CREB and probe the function of CREB in late stages of adipogenesis. Loss of CREB/ATF1 blocked adipogenic conversion of 3T3-L1 cells in culture or 3T3-F442A cells implanted into athymic mice. Loss of CREB/ATF1 prevented the expression of PPARgamma, C/EBP alpha, and adiponectin and inhibited the loss of Pref-1. Loss of CREB/ATF1 inhibited adipogenic conversion even in cells ectopically expressing C/EBP alpha, C/EBP beta, or PPARgamma2 individually. CREB/ATF1 depletion did not attenuate lipid accumulation in cells expressing both PPARgamma2 and C/EBP alpha, but adiponectin expression was severely diminished. Conversely ectopic expression of constitutively active CREB overcame the blockade of adipogenesis due to depletion of C/EBP beta but not due to loss of PPARgamma2 or C/EBP alpha. Depletion of CREB/ATF1 did not suppress the expression of C/EBP beta as we had previously observed using dominant negative forms of CREB. Finally results are presented showing that CREB promotes PPARgamma2 gene transcription. The results indicate that CREB and ATF1 play a central role in adipogenesis because expression of individual master adipogenic regulators is unable to compensate for their loss. The data also indicate that CREB not only functions during the initiation of adipogenic conversion but also at later stages.

摘要

前脂肪细胞向脂肪细胞的分化由“主要成脂调节因子”CCAAT/增强子结合蛋白(C/EBP)β、过氧化物酶体增殖物激活受体γ(PPARγ)和C/EBPα的表达所调控。此外,环磷酸腺苷反应元件结合蛋白(CREB)的激活对于促进成脂转化和防止成熟脂肪细胞凋亡是必要且充分的。在本报告中,我们使用小干扰RNA来耗尽CREB以及与之密切相关的因子ATF1,以探究主要成脂调节因子在缺乏CREB的情况下促进脂肪生成的能力,并探究CREB在脂肪生成后期的功能。CREB/ATF1的缺失阻断了培养的3T3-L1细胞或植入无胸腺小鼠体内的3T3-F442A细胞的成脂转化。CREB/ATF1的缺失阻止了PPARγ、C/EBPα和脂联素的表达,并抑制了Pref-1的减少。即使在分别异位表达C/EBPα、C/EBPβ或PPARγ2的细胞中,CREB/ATF1的缺失也会抑制成脂转化。CREB/ATF1的缺失并未减弱同时表达PPARγ2和C/EBPα的细胞中的脂质积累,但脂联素的表达却严重减少。相反,组成型活性CREB的异位表达克服了由于C/EBPβ耗尽而非PPARγ2或C/EBPα缺失导致的脂肪生成障碍。与我们之前使用CREB的显性负性形式所观察到的情况不同,CREB/ATF1的缺失并未抑制C/EBPβ的表达。最后,展示的结果表明CREB促进PPARγ2基因转录。这些结果表明,CREB和ATF1在脂肪生成中起核心作用,因为单个主要成脂调节因子的表达无法弥补它们的缺失。数据还表明,CREB不仅在成脂转化起始阶段发挥作用,在后期阶段也发挥作用。

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