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培养的穆勒细胞中功能性受体和递质酶的表达。

Expression of functional receptors and transmitter enzymes in cultured Muller cells.

作者信息

Kubrusly Regina Celia Cussa, da Cunha Maria Cristina Caldas, Reis Ricardo Augusto de Melo, Soares Heline, Ventura Ana Lúcia Marques, Kurtenbach Eleonora, de Mello Maria Cristina Fialho, de Mello Fernando Garcia

机构信息

Laboratory of Neurochemistry, Program in Neurobiology IBCCF, Sala C1-031, CCS, UFRJ, Ilha do Fundao, 21949-900, Rio de Janeiro, Brazil.

出版信息

Brain Res. 2005 Mar 21;1038(2):141-9. doi: 10.1016/j.brainres.2005.01.031.

Abstract

Glia represents the most numerous group of nervous system cells and CNS development and function depend on glial cells. We developed a purified Muller glia culture to investigate the expression of several neurotransmitter markers on these cells, such as dopaminergic, cholinergic, GABAergic and peptidergic receptors or enzymes, based on functional assays measuring second messenger levels or Western blot for specific proteins. Purified Muller cell culture was obtained from 8-day-old (E8) embryonic chick. Glial cells cultured for 15 days (E8C15) expressed D1A and D1B receptors mRNAs, but not D1D, as detected by RT-PCR. The binding of [3H]-SCH 23390 revealed an amount of expressed receptors around 40 fmol/mg protein. Dopamine (100 microM), PACAP (50 nM) and forskolin (10 microM) induced a 50-, 30- and 40-fold cAMP accumulation on glial cells, respectively, but not ip3 production. The dopamine-promoted cAMP accumulation was blocked by 2 microM SCH 23390. Carbachol stimulated a 3-fold ip3 accumulation. Western blot analysis also revealed the expression of tyrosine hydroxylase, L-dopa decarboxylase, PAC1 receptor, GAD67 and beta2-nicotinic receptor subunit by these cells. These results indicate that several components of neurotransmitter signaling and metabolism are found in cultured Muller cells.

摘要

神经胶质细胞是神经系统中数量最多的细胞群,中枢神经系统的发育和功能依赖于神经胶质细胞。我们开发了一种纯化的穆勒胶质细胞培养物,以基于测量第二信使水平的功能测定或针对特定蛋白质的蛋白质印迹法,研究这些细胞上几种神经递质标志物的表达,如多巴胺能、胆碱能、γ-氨基丁酸能和肽能受体或酶。纯化的穆勒细胞培养物取自8日龄(E8)的胚胎鸡。通过逆转录-聚合酶链反应(RT-PCR)检测,培养15天的胶质细胞(E8C15)表达D1A和D1B受体的信使核糖核酸(mRNAs),但不表达D1D。[3H]-SCH 23390的结合显示表达的受体量约为40飞摩尔/毫克蛋白质。多巴胺(100微摩尔)、垂体腺苷酸环化酶激活肽(PACAP,50纳摩尔)和福斯高林(10微摩尔)分别在胶质细胞上诱导50倍、30倍和40倍的环磷酸腺苷(cAMP)积累,但不诱导肌醇三磷酸(ip3)产生。多巴胺促进的cAMP积累被2微摩尔的SCH 23390阻断。卡巴胆碱刺激ip3积累3倍。蛋白质印迹分析还显示这些细胞表达酪氨酸羟化酶(TH)、L-多巴脱羧酶(DDC)、PAC1受体、谷氨酸脱羧酶67(GAD67)和β2-烟碱受体亚基。这些结果表明,在培养的穆勒细胞中发现了神经递质信号传导和代谢的几个组成部分。

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