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发育中大鼠大脑小胶质细胞中血小板反应蛋白的免疫组织化学检测。

Immunohistochemical detection of thrombospondin in microglia in the developing rat brain.

作者信息

Chamak B, Dobbertin A, Mallat M

机构信息

INSERM U114, Collège de France, Paris, France.

出版信息

Neuroscience. 1995 Nov;69(1):177-87. doi: 10.1016/0306-4522(95)00236-c.

Abstract

The development of microglia involves the expression of a phenotype displaying phagocytic behaviour termed brain macrophage or amoeboid microglial cell. We have previously shown that rat brain macrophages purified in vitro secrete thrombospondin, an extracellular matrix protein, which acts on cultured neuronal cells by promoting neurite growth. In the present study, the expression of thrombospondin was investigated in tissue sections of the developing rat forebrain in relation to the distribution of microglia. These cells were identified using anti-macrophage antibodies and the isolectin B4 from Bandeiraea simplicifolia. Immunocytochemical detection of thrombospondin clearly outlined a cell population displaying the morphologies and distribution of brain macrophages, from the 17th day of embryonic life up to the end of the second postnatal week. These cells were most numerous in cortical and subcortical regions of developing fibre tracts such as the corpus callosum or the internal capsule. The localization of thrombospondin in brain macrophages was confirmed by double immunostaining using ED1 monoclonal anti-macrophage antibodies. Ramified microglial cells were also labelled transiently by anti-thrombospondin antibodies during early postnatal life. These results provide in situ evidence supporting the notion that microglial cells could favour axonal growth by producing thrombospondin during development.

摘要

小胶质细胞的发育涉及一种表现出吞噬行为的表型的表达,这种表型被称为脑巨噬细胞或阿米巴样小胶质细胞。我们之前已经表明,体外纯化的大鼠脑巨噬细胞会分泌血小板反应蛋白,这是一种细胞外基质蛋白,它通过促进神经突生长作用于培养的神经元细胞。在本研究中,我们研究了发育中的大鼠前脑组织切片中血小板反应蛋白的表达与小胶质细胞分布的关系。使用抗巨噬细胞抗体和来自单叶豆的异凝集素B4来鉴定这些细胞。血小板反应蛋白的免疫细胞化学检测清楚地勾勒出一群细胞,它们呈现出脑巨噬细胞的形态和分布,从胚胎期第17天到出生后第二周结束。这些细胞在发育中的纤维束(如胼胝体或内囊)的皮质和皮质下区域最为丰富。使用ED1单克隆抗巨噬细胞抗体进行双重免疫染色证实了血小板反应蛋白在脑巨噬细胞中的定位。在出生后早期,分支状小胶质细胞也会被抗血小板反应蛋白抗体短暂标记。这些结果提供了原位证据,支持小胶质细胞在发育过程中通过产生血小板反应蛋白促进轴突生长这一观点。

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