Department of Pharmacology, Cell Death Disease Research Center, The Catholic University of Korea, Seoul, 137-701, Korea.
Neuroscience. 2011 Jul 14;186:170-8. doi: 10.1016/j.neuroscience.2011.02.046. Epub 2011 Mar 6.
Krüppel-like factor 6 (KLF6) is a transcriptional regulator involved in a broad range of cellular processes. To date, however, the expression of KLF6 in brains with pathophysiological conditions, such as epilepsy, has not been reported. Therefore, the present study investigated the temporal pattern of KLF6 expression in the mouse hippocampus and identified cell types expressing KLF6 after pilocarpine-induced status epilepticus (SE). Seizures were induced by administrating pilocarpine hydrochloride (280 mg/kg, i.p.) 30 min after an injection of atropine methyl nitrate (3 mg/kg, i.p.). Pilocarpine- and saline-injected animals were sacrificed 1, 3, 7, 14, or 28 days after the onset of SE. Immunohistochemistry showed that the proportion of KLF6-positive cells increased in the hippocampus 1 day after SE onset, peaked at 3 days after SE, and then gradually decreased until 28 days after SE, consistent with the results from our immunoblot analysis. Cells expressing increased levels of KLF6 following pilocarpine-induced SE also expressed GFAP and Ox-42, markers for astrocytes and microglia, respectively. Quantitative analysis revealed that astrocytes were the major type of KLF6-expressing glial cells. These cells also expressed heat shock protein 47 (HSP47), a collagen-specific molecular chaperone. This is the first report showing that KLF6 is inducible in the hippocampus and may be associated with glial responses, especially HSP47-related tissue remodeling after pilocarpine-induced SE.
Krüppel 样因子 6(KLF6)是一种参与广泛细胞过程的转录调节剂。然而,迄今为止,尚未有关于 KLF6 在具有生理病理条件的大脑中的表达的报道,例如癫痫。因此,本研究调查了 KLF6 在小鼠海马体中的表达时间模式,并确定了在匹鲁卡品诱导的癫痫持续状态(SE)后表达 KLF6 的细胞类型。通过在给予颠茄碱硝酸盐(3 mg/kg,i.p.)30 分钟后给予盐酸匹鲁卡品(280 mg/kg,i.p.)诱导癫痫发作。在 SE 发作后 1、3、7、14 或 28 天处死匹鲁卡品和盐水注射的动物。免疫组织化学显示,SE 发作后 1 天海马体中 KLF6 阳性细胞的比例增加,在 SE 发作后 3 天达到峰值,然后逐渐减少,直到 SE 发作后 28 天,与我们的免疫印迹分析结果一致。匹鲁卡品诱导的 SE 后表达水平升高的 KLF6 的细胞也表达 GFAP 和 Ox-42,分别为星形胶质细胞和小胶质细胞的标志物。定量分析显示,星形胶质细胞是表达 KLF6 的主要类型的神经胶质细胞。这些细胞还表达热休克蛋白 47(HSP47),一种胶原特异性分子伴侣。这是第一项表明 KLF6 在海马体中可诱导的报告,并且可能与神经胶质反应有关,特别是匹鲁卡品诱导的 SE 后与 HSP47 相关的组织重塑。