Matsuda Toshio, Nagano Takayuki, Takemura Motohiko, Baba Akemichi
Laboratory of Medicinal Pharmacology, Graduate School of Pharmaceutical Sciences, Osaka University, Japan.
J Pharmacol Sci. 2006 Sep;102(1):22-6. doi: 10.1254/jphs.fmj06002x4. Epub 2006 Sep 8.
The Na(+)/Ca(2+) exchanger (NCX) plays a role in regulation of intracellular Ca(2+) levels, but little is known about the functional role of NCX in microglia. To clarify the role of NCX in microglia, we studied the responses of NCX to pathological conditions such as interferon-gamma or nitric oxide (NO) exposure. Treatment with interferon-gamma caused a biphasic increase in NCX activity. The delayed increase in NCX activity was accompanied by increases in the mRNA and protein levels. Pharmacological studies show that protein kinase C and tyrosine kinase are involved in the transient and delayed increases in NCX activity, and the extracellular signal-regulated protein kinase is involved in the delayed increase in NCX activity. On the other hand, NO causes apoptotic cell death in cultured microglia. We observed, using the specific NCX inhibitor SEA0400, that NO activates NCX activity and NCX is involved in NO-induced depletion of Ca(2+) in the endoplasmic reticulum (ER), leading to ER stress. These results suggest that NCX is involved in the regulation of Ca(2+) levels in the ER. The responses of NCX to interferon-gamma and NO implies that NCX plays a key role in microglial function.
钠/钙交换体(NCX)在调节细胞内钙离子水平方面发挥作用,但关于NCX在小胶质细胞中的功能作用知之甚少。为了阐明NCX在小胶质细胞中的作用,我们研究了NCX对诸如干扰素-γ或一氧化氮(NO)暴露等病理条件的反应。用干扰素-γ处理导致NCX活性呈双相增加。NCX活性的延迟增加伴随着mRNA和蛋白质水平的升高。药理学研究表明,蛋白激酶C和酪氨酸激酶参与了NCX活性的瞬时和延迟增加,而细胞外信号调节蛋白激酶参与了NCX活性的延迟增加。另一方面,NO在培养的小胶质细胞中导致凋亡性细胞死亡。我们使用特异性NCX抑制剂SEA0400观察到,NO激活NCX活性,并且NCX参与NO诱导的内质网(ER)中钙离子的消耗,导致内质网应激。这些结果表明,NCX参与内质网中钙离子水平的调节。NCX对干扰素-γ和NO的反应意味着NCX在小胶质细胞功能中起关键作用。