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人类胚胎早期大脑皮质中神经祖细胞的免疫组化标志物

Immunohistochemical markers of neural progenitor cells in the early embryonic human cerebral cortex.

作者信息

Vinci L, Ravarino A, Fanos V, Naccarato A G, Senes G, Gerosa C, Bevilacqua G, Faa G, Ambu R

机构信息

University of Cagliari.

出版信息

Eur J Histochem. 2016 Feb 1;60(1):2563. doi: 10.4081/ejh.2016.2563.

Abstract

The development of the human central nervous system represents a delicate moment of embryogenesis. The purpose of this study was to analyze the expression of multiple immunohistochemical markers in the stem/progenitor cells in the human cerebral cortex during the early phases of development.  To this end, samples from cerebral cortex were obtained from 4 human embryos of 11 weeks of gestation. Each sample was formalin-fixed, paraffin embedded and immunostained with several markers including GFAP, WT1, Nestin, Vimentin, CD117, S100B, Sox2, PAX2, PAX5, Tβ4, Neurofilament, CD44, CD133, Synaptophysin and Cyclin D1. Our study shows the ability of the different immunohistochemical markers to evidence different zones of the developing human cerebral cortex, allowing the identification of the multiple stages of differentiation of neuronal and glial precursors. Three important markers of radial glial cells are evidenced in this early gestational age: Vimentin, Nestin and WT1. Sox2 was expressed by the stem/progenitor cells of the ventricular zone, whereas the postmitotic neurons of the cortical plate were immunostained by PAX2 and NSE. Future studies are needed to test other important stem/progenitor cells markers and to better analyze differences in the immunohistochemical expression of these markers during gestation.

摘要

人类中枢神经系统的发育是胚胎发生过程中的一个微妙阶段。本研究的目的是分析人类大脑皮质发育早期阶段干/祖细胞中多种免疫组化标志物的表达情况。为此,从4例妊娠11周的人类胚胎获取大脑皮质样本。每个样本用福尔马林固定、石蜡包埋,并用包括GFAP、WT1、巢蛋白、波形蛋白、CD117、S100B、Sox2、PAX2、PAX5、Tβ4、神经丝、CD44、CD133、突触素和细胞周期蛋白D1在内的多种标志物进行免疫染色。我们的研究显示了不同免疫组化标志物在显示发育中的人类大脑皮质不同区域方面的能力,从而能够识别神经元和神经胶质前体细胞分化的多个阶段。在这个妊娠早期阶段证实了三种重要的放射状胶质细胞标志物:波形蛋白、巢蛋白和WT1。Sox2由脑室区的干/祖细胞表达,而皮质板的有丝分裂后神经元则被PAX2和神经元特异性烯醇化酶免疫染色。未来的研究需要检测其他重要的干/祖细胞标志物,并更好地分析这些标志物在妊娠期间免疫组化表达的差异。

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