Suppr超能文献

发育中大鼠少突胶质细胞中血栓素A2受体信号传导的特征:核受体定位及髓鞘碱性蛋白表达的刺激

Characterization of thromboxane A2 receptor signaling in developing rat oligodendrocytes: nuclear receptor localization and stimulation of myelin basic protein expression.

作者信息

Ramamurthy Santosh, Mir Fozia, Gould Robert M, Le Breton Guy C

机构信息

Department of Cellular and Molecular Pharmacology, University of Illinois at Chicago College of Medicine, Chicago, IL 60612-7343, USA.

出版信息

J Neurosci Res. 2006 Nov 15;84(7):1402-14. doi: 10.1002/jnr.21061.

Abstract

The present work investigates the role of thromboxane A(2) (TXA(2)) receptors in the development of oligodendrocytes (OLGs). The results demonstrate that the proteins of the TXA(2) signaling pathway, i.e., cyclooxygenase (COX-1), TXA(2) synthase (TS), and TXA(2) receptor (TPR) are expressed in the developing rat brain during myelination. Furthermore, culture of OLG progenitor cells (OPCs) revealed that the expression levels of these proteins as well as TXA(2) synthesis increase during OLG maturation. Separate studies established that activation of TPRs by the agonist U46619 increases intracellular calcium in both OPCs and OLGs as visualized by digital fluorescence imaging. Immunocytochemical staining demonstrated that TPRs are localized in the plasma membrane and perinuclear compartments in OPCs. However, during OLG differentiation, TPRs shift their localization pattern and also become associated with the nuclear compartment. This shift to nuclear localization was confirmed by biochemical analysis in cultured cells and by immunocytochemical analysis in developing rat brain. Finally, it was found that U46619 activation of TPRs in maturing OLGs resulted in enhanced myelin basic protein (MBP) expression. Alternatively, inhibition of endogenous TPR signaling led to reduced MBP expression. Furthermore, TPR-mediated MBP expression was found to be associated with increased transcription from the MBP promoter using a MBP-luciferase reporter. Collectively, these findings suggest a novel TPR signaling pathway in OLGs and a potential role for this signaling during OLG maturation and myelin production.

摘要

本研究探讨血栓素A(2)(TXA(2))受体在少突胶质细胞(OLGs)发育中的作用。结果表明,TXA(2)信号通路的蛋白,即环氧化酶(COX-1)、TXA(2)合酶(TS)和TXA(2)受体(TPR)在大鼠脑发育髓鞘形成过程中表达。此外,少突胶质前体细胞(OPCs)培养显示,在OLGs成熟过程中,这些蛋白的表达水平以及TXA(2)的合成均增加。单独的研究证实,激动剂U46619激活TPRs可增加OPCs和OLGs中的细胞内钙,这通过数字荧光成像得以可视化。免疫细胞化学染色表明,TPRs定位于OPCs的质膜和核周区室。然而,在OLGs分化过程中,TPRs的定位模式发生改变,并且还与核区室相关联。这种向核定位的转变在培养细胞的生化分析以及发育中大鼠脑的免疫细胞化学分析中得到证实。最后,发现U46619激活成熟OLGs中的TPRs会导致髓鞘碱性蛋白(MBP)表达增强。相反,抑制内源性TPR信号会导致MBP表达降低。此外,使用MBP-荧光素酶报告基因发现,TPR介导的MBP表达与MBP启动子转录增加相关。总的来说,这些发现提示了OLGs中一种新的TPR信号通路,以及该信号在OLGs成熟和髓鞘生成过程中的潜在作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验