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β-淀粉样前体蛋白(APP)在人背根神经节中的表达。

Expression of beta-amyloid precursor protein (APP) in human dorsal root ganglia.

作者信息

Naves F J, Calzada B, Cabal A, Alonso-Cortina V, del Valle M E, Fernandez-Sanchez M T, Vega J A

机构信息

Departamento de Morfología y Biología Celular, Facultad de Medicina, Universidad de Oviedo, Spain.

出版信息

Neurosci Lett. 1994 Nov 7;181(1-2):73-7. doi: 10.1016/0304-3940(94)90563-0.

Abstract

The present study reports the occurrence and localization of beta-amyloid precursor protein (APP) immunoreactivity (IR) in human lumbar dorsal root ganglia of healthy adult subjects (age range 25-43 years). To ascertain that ganglionic cells displayed APP IR, neurofilament (NFP) and S-100 proteins (S100P) were studied in parallel. Immunoblotting revealed four or five major proteins with apparent molecular masses between 100-125 kDa, which corresponded with the different full-length APP isoforms. Moreover, an additional protein of approximately 55 kDa was detected. Selective APP IR was observed restricted to the satellite glial cell cytoplasms whereas neuron cell bodies resulted unlabeled. Moreover, some intraganglionic nerve fibers also displayed APP IR, apparently labelling Schwann cells. No individual differences among subjects were observed neither in the pattern of APP IR distribution, nor in the intensity of APP IR. Although it remains to be demonstrated whether or not human primary sensory neurons express APP, present results strongly suggest that supporting glial cells may be a primary source of APP or any related peptide, at least in adult healthy people. The functional and clinical relevance of these findings, if any, remain to be clarified.

摘要

本研究报告了健康成年受试者(年龄范围25 - 43岁)人腰段背根神经节中β-淀粉样前体蛋白(APP)免疫反应性(IR)的发生情况和定位。为确定神经节细胞显示APP IR,同时研究了神经丝(NFP)和S - 100蛋白(S100P)。免疫印迹显示有四或五种主要蛋白质,其表观分子量在100 - 125 kDa之间,这与不同的全长APP异构体相对应。此外,还检测到一种约55 kDa的额外蛋白质。观察到选择性APP IR局限于卫星神经胶质细胞的细胞质,而神经元细胞体未被标记。此外,一些神经节内神经纤维也显示APP IR,明显标记施万细胞。在受试者之间,无论是APP IR分布模式还是APP IR强度,均未观察到个体差异。虽然人类初级感觉神经元是否表达APP仍有待证实,但目前的结果强烈表明,至少在成年健康人中,支持性神经胶质细胞可能是APP或任何相关肽的主要来源。这些发现的功能和临床相关性(如果有的话)仍有待阐明。

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