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钙离子(Ca2+)和环磷酸腺苷(cAMP)对海马神经元中由MEF2D(肌细胞增强因子2D)和环磷酸腺苷反应元件结合蛋白介导的转录的不同影响。

Differential effects of Ca2+ and cAMP on transcription mediated by MEF2D and cAMP-response element-binding protein in hippocampal neurons.

作者信息

Belfield Johanna L, Whittaker Chris, Cader M Zaeem, Chawla Sangeeta

机构信息

Department of Pharmacology, University of Cambridge, Tennis Court Road, Cambridge CB2 1PD, United Kingdom.

出版信息

J Biol Chem. 2006 Sep 22;281(38):27724-32. doi: 10.1074/jbc.M601485200. Epub 2006 Jul 26.

Abstract

In neurons, the second messengers Ca(2+) and cAMP are mediators of transcriptional responses that are important for the development and function of the nervous system. The pro-survival neuronal transcription factors cAMP-response elementbinding protein (CREB) and myocyte enhancer factor-2 (MEF2) both stimulate gene expression in response to activity-dependent increases in the concentration of intracellular Ca(2+) ions. CREB is also activated by increases in intracellular cAMP. Here we have investigated whether the MEF2 family member MEF2D, similar to CREB, is also activated by cAMP in hippocampal neurons. We have shown that, unlike CREB, MEF2D is not activated by agents that increase intracellular cAMP. Moreover, increases in cAMP inhibit Ca(2+)-activated MEF2D-mediated gene expression. We have also shown that cAMP inhibits Ca(2+)-induced nuclear export of the MEF2 co-repressor HDAC5 and prevents Ca(2+)-stimulated nuclear import of the MEF2 co-activator NFAT3/c4. Our results suggest that cAMP interferes with MEF2D-mediated gene expression at multiple levels by antagonizing the derepression of MEF2D by HDAC5 and by inhibiting recruitment of the co-activator NFAT.

摘要

在神经元中,第二信使Ca(2+)和环磷酸腺苷(cAMP)是转录反应的介质,对神经系统的发育和功能至关重要。促生存神经元转录因子环磷酸腺苷反应元件结合蛋白(CREB)和肌细胞增强因子2(MEF2)均会响应细胞内Ca(2+)离子浓度的活性依赖性增加而刺激基因表达。CREB也会因细胞内cAMP的增加而被激活。在此,我们研究了MEF2家族成员MEF2D是否与CREB类似,也会在海马神经元中被cAMP激活。我们发现,与CREB不同,MEF2D不会被增加细胞内cAMP的试剂激活。此外,cAMP的增加会抑制Ca(2+)激活的MEF2D介导的基因表达。我们还表明,cAMP会抑制Ca(2+)诱导的MEF2共抑制因子HDAC5的核输出,并阻止Ca(2+)刺激的MEF2共激活因子NFAT3/c4的核输入。我们的结果表明,cAMP通过拮抗HDAC5对MEF2D的去抑制作用以及抑制共激活因子NFAT的募集,在多个水平上干扰MEF2D介导的基因表达。

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