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少突胶质细胞环磷酸腺苷反应元件结合蛋白:转录因子CREB家族的一员。

Oligodendroglial cyclic AMP response element-binding protein: a member of the CREB family of transcription factors.

作者信息

Sato-Bigbee C, Chan E L, Yu R K

机构信息

Department of Biochemistry and Molecular Biophysics Medical College of Virginia, Virginia Commonwealth University, Richmond.

出版信息

J Neurosci Res. 1994 Aug 15;38(6):621-8. doi: 10.1002/jnr.490380604.

Abstract

Several laboratories have shown that cyclic AMP (cAMP) plays an important role in inducing oligodendrocyte differentiation and myelin synthesis. Our previous results have shown that oligodendrocytes contain a nuclear protein that binds to the DNA sequence TGACGTCA or cAMP response element (CRE) known to be involved in the transcriptional regulation of cAMP-responsive genes. In this report the oligodendroglial CRE-binding protein was further identified by using two different antibodies which specifically recognize the CRE-binding protein known as CREB. In DNA-shift assays CREB-1(X-12) antibody interacted with the CRE-protein complexes resulting in further retardation ("super shift") of the mobility of the bands in the gels. Immunoprecipitation of oligodendroglial nuclear extracts with CREB(240) antibody prior to the DNA binding assays resulted in a lack of formation of CRE-protein complexes. In addition immunoreaction with CREB(240) antibody identified the CRE-binding species as a 45 kDa phosphoprotein. Immunocytochemical staining with CREB(240) antibody in oligodendrocytes from 10-, 14-, and 18-day-old and adult rats indicated that this protein is expressed before the appearance of myelin basic protein (MBP) which was used as a marker of myelin synthesis. Collectively, these observations support our previous results and indicate that the oligodendroglial CRE-binding protein species is highly homologous to the CREB protein. The developmental expression of this CREB protein supports the idea of a possible role during the early stages of oligodendrocyte differentiation preceding the peak of myelin synthesis in rat CNS.

摘要

几个实验室已表明,环磷酸腺苷(cAMP)在诱导少突胶质细胞分化和髓鞘合成中起重要作用。我们之前的结果表明,少突胶质细胞含有一种核蛋白,它能与已知参与cAMP反应基因转录调控的DNA序列TGACGTCA或cAMP反应元件(CRE)结合。在本报告中,通过使用两种不同的抗体进一步鉴定了少突胶质细胞的CRE结合蛋白,这两种抗体能特异性识别被称为CREB的CRE结合蛋白。在DNA迁移率变动分析中,CREB - 1(X - 12)抗体与CRE - 蛋白复合物相互作用,导致凝胶中条带迁移率进一步减慢(“超迁移”)。在进行DNA结合分析之前,用CREB(240)抗体对少突胶质细胞核提取物进行免疫沉淀,导致CRE - 蛋白复合物无法形成。此外,与CREB(240)抗体的免疫反应确定CRE结合蛋白为一种45 kDa的磷蛋白。用CREB(240)抗体对10日龄、14日龄、18日龄和成年大鼠的少突胶质细胞进行免疫细胞化学染色,结果表明该蛋白在用作髓鞘合成标志物的髓鞘碱性蛋白(MBP)出现之前就已表达。总的来说,这些观察结果支持了我们之前的结果,并表明少突胶质细胞的CRE结合蛋白与CREB蛋白高度同源。这种CREB蛋白的发育性表达支持了其在大鼠中枢神经系统髓鞘合成高峰之前的少突胶质细胞分化早期可能发挥作用的观点。

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