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Glial fibrillary acidic protein: from intermediate filament assembly and gliosis to neurobiomarker

机译:胶质纤维酸性蛋白:从中间丝组装和神经胶质变到神经生物标志物

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摘要

Glial fibrillary acidic protein (GFAP) is an intermediate filament (IF) III protein uniquely found in astrocytes in the central nervous system (CNS), non-myelinating Schwann cells in the peripheral nervous system (PNS), and enteric glial cells. GFAP mRNA expression is regulated by several nuclear-receptor hormones, growth factors, and lipopolysaccharides (LPSs). GFAP is also subject to numerous post-translational modifications (PTMs), while GFAP mutations result in protein deposits known as Rosenthal fibers in Alexander disease. GFAP gene activation and protein induction appear to play a critical role in astroglial cell activation (astrogliosis) following CNS injuries and neurodegeneration. Emerging evidence also suggests that, following traumatic brain and spinal cord injuries and stroke, GFAP and its breakdown products are rapidly released into biofluids, making them strong candidate biomarkers for such neurological disorders.
机译:胶质纤维酸性蛋白(GFAP)是一种中间丝(IF)III蛋白,独特地存在于中枢神经系统(CNS)的星形胶质细胞,外周神经系统(PNS)的非髓鞘雪旺细胞和肠神经胶质细胞中。 GFAP mRNA的表达受几种核受体激素,生长因子和脂多糖(LPS)的调节。 GFAP还需要进行大量的翻译后修饰(PTM),而GFAP突变会导致蛋白质沉积物,即亚历山大病中的Rosenthal纤维。在中枢神经系统损伤和神经退行性变之后,GFAP基因激活和蛋白诱导似乎在星形胶质细胞激活(星形胶质增生)中起关键作用。新兴证据还表明,在脑部和脊髓损伤和中风之后,GFAP及其分解产物迅速释放到生物流体中,使其成为此类神经系统疾病的强有力的候选生物标志物。

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