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筛选药物以鉴定 GFAP 表达的抑制剂。

Drug screening to identify suppressors of GFAP expression.

机构信息

Waisman Center and Department of Comparative Biosciences, University of Wisconsin-Madison, 1500 Highland Avenue, Madison, WI 53705, USA.

出版信息

Hum Mol Genet. 2010 Aug 15;19(16):3169-78. doi: 10.1093/hmg/ddq227. Epub 2010 Jun 10.

Abstract

Glial fibrillary acidic protein (GFAP) is the major intermediate filament protein of astrocytes in the vertebrate central nervous system. Increased levels of GFAP are the hallmark feature of gliosis, a non-specific response of astrocytes to a wide variety of injuries and disorders of the CNS, and also occur in Alexander disease where the initial insult is a mutation within the coding region of GFAP itself. In both settings, excess GFAP may cause or exacerbate astrocyte dysfunction. With the goal of finding drugs that reduce the expression of GFAP, we have devised screens to detect changes in GFAP promoter activity or protein levels in primary cultures of mouse astrocytes in a 96-well format. We have applied these screens to libraries enriched in compounds that are already approved for human use by the FDA. We report that several compounds are active at micromolar levels in suppressing the expression of GFAP. Treatment of mice for 3 weeks with one of these drugs, clomipramine, causes nearly 50% reduction in the levels of GFAP protein in brain.

摘要

胶质纤维酸性蛋白(GFAP)是脊椎动物中枢神经系统中星形胶质细胞的主要中间丝蛋白。GFAP 水平的升高是神经胶质增生的标志特征,这是星形胶质细胞对中枢神经系统的各种损伤和疾病的非特异性反应,也发生在亚历山大病中,最初的损伤是 GFAP 自身编码区的突变。在这两种情况下,过多的 GFAP 可能导致或加剧星形胶质细胞功能障碍。为了寻找降低 GFAP 表达的药物,我们设计了筛选方法,以检测 96 孔板中小鼠星形胶质细胞原代培养物中 GFAP 启动子活性或蛋白水平的变化。我们已经将这些筛选方法应用于已经被 FDA 批准用于人类使用的化合物库中。我们报告说,有几种化合物在抑制 GFAP 表达方面具有微摩尔级的活性。用其中一种药物氯米帕明治疗小鼠 3 周,可使脑中 GFAP 蛋白水平降低近 50%。

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