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首页> 外文期刊>Glia >Calcium/calcineurin signaling in primary cortical astrocyte cultures: Rcan1-4 and cyclooxygenase-2 as NFAT target genes
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Calcium/calcineurin signaling in primary cortical astrocyte cultures: Rcan1-4 and cyclooxygenase-2 as NFAT target genes

机译:钙/钙调神经磷酸信号在初级皮质星形胶质细胞培养中:Rcan1-4和环氧合酶2作为NFAT靶基因

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The calcineurinuclear factor of activated T cells (NFAT) signaling pathway mediates important cell responses to calcium, but its activity and function in astrocytes have remained unclear. We show that primary cortical astrocyte cultures express the regulatory and catalytic subunits of the phosphatase calcineurin as well as the calcium-regulated NFAT family members (NFATe1, c2, c3, and c4). NFATs are activated by calcium-mobilizing agents in astrocytes, and this activation is blocked by the calcineurin inhibitor cyclosporine A. Microarray screening identified cyclooxygenase-2 (Cox-2), which is implicated in brain injury, and Rcan 1-4, an endogenous calcineurin inhibitor, as genes up-regulated by calcineurin-dependent calcium signals in astrocytes. Mobilization of intracellular calcium with ionophore potently augments the promoter activity and mRNA and protein expression of Rcan 1-4 and Cox-2 induced by combined treatment with phorbol esters. Moreover, Rcan 1-4 expression is efficiently induced by calcium mobilization alone. For both the genes, the calcium signal component is dependent on calcineurin and is replicated by exogenous expression of a constitutively active NFAT, strongly suggesting that the calcium-induced gene activation is mediated by NFATs. Finally, we report that calcineurin-dependent expression of Cox-2 and Rcan 1-4 is induced by physiological calcium mobilizing agents, such as thrombin, agonists of purinergic and glutamate receptors, and L-type voltage-gated calcium channels. These findings provide insights into calcium-initiated gene transcription in astrocytes, and have implications for the regulation of calcium responses in astrocytes. (c) 2008 Wiley-Liss, Inc.
机译:钙调神经磷酸酶/激活的T细胞(NFAT)信号通路的核因子介导重要的细胞对钙的反应,但其在星形胶质细胞中的活性和功能仍不清楚。我们表明,初级皮质星形胶质细胞培养物表达磷酸酶钙调磷酸酶以及钙调节的NFAT家族成员(NFATe1,c2,c3和c4)的调节和催化亚基。 NFAT被星形胶质细胞中的钙动员剂激活,而这种激活被钙调神经磷酸酶抑制剂环孢菌素A阻断。微阵列筛选鉴定出与脑损伤有关的环氧合酶2(Cox-2)和内源性Rcan 1-4。钙调磷酸酶抑制剂,是星形胶质细胞中钙调磷酸酶依赖性钙信号上调的基因。用离子载体动员细胞内钙有效地增强了佛波酯的联合处理诱导的Rcan 1-4和Cox-2的启动子活性以及mRNA和蛋白表达。此外,仅通过钙动员就可以有效地诱导Rcan 1-4的表达。对于这两个基因,钙信号成分均依赖于钙调神经磷酸酶,并通过组成型活性NFAT的外源表达得以复制,这强烈表明钙诱导的基因激活是由NFAT介导的。最后,我们报告了钙钙调磷酸酶依赖性的Cox-2和Rcan 1-4的表达是由生理钙动员剂引起的,例如凝血酶,嘌呤能和谷氨酸受体激动剂以及L型电压门控钙通道。这些发现为星形胶质细胞中钙启动的基因转录提供了见识,并且对星形胶质细胞中钙反应的调节有影响。 (c)2008 Wiley-Liss,Inc.

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