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小胶质细胞会吞噬阿尔茨海默病的β/A4-淀粉样老年斑核心吗?

Do microglial cells phagocyte the beta/A4-amyloid senile plaque core of Alzheimer disease?

作者信息

el Hachimi K H, Foncin J F

机构信息

EPHE Neurohistologie and INSERM U. 106, Hôpital de la Salpêtrière, Paris, France.

出版信息

C R Acad Sci III. 1994 May;317(5):445-51.

PMID:7994623
Abstract

We performed EM, immuno-EM and light microscope immunohistochemistry studies on the topographic and functional relationships between microglial cells and amyloid senile plaque core in Alzheimer's disease. Microglial cells with cytologic characteristics of phagocytic function were associated to amyloid fibrils and to other neuropathological degenerative processes. On the periphery of the amyloid plaque core, microglial cells contain intracytoplasmic bundles of membrane bound fibrils. These fibrils, like plaque core fibrils, are immunodecorated. Immunostaining was observed neither in secretory organelles nor in hyalaplasm. Preamyloid deposits in superficial layers were not associated to microglial cells. These data lead us to conclude that the microglial cells participate to phagocytosis of beta/A4 amyloid and do not secrete this substance in Alzheimer's disease.

摘要

我们对阿尔茨海默病中小胶质细胞与淀粉样老年斑核心之间的形态学和功能关系进行了电子显微镜、免疫电子显微镜和光学显微镜免疫组织化学研究。具有吞噬功能细胞学特征的小胶质细胞与淀粉样纤维以及其他神经病理退行性过程相关。在淀粉样斑块核心的周边,小胶质细胞含有胞浆内成束的膜结合纤维。这些纤维与斑块核心纤维一样,可被免疫染色。在分泌细胞器和透明质浆中均未观察到免疫染色。表层的淀粉样前体沉积物与小胶质细胞无关。这些数据使我们得出结论,在阿尔茨海默病中,小胶质细胞参与β/A4淀粉样蛋白的吞噬作用,而不分泌这种物质。

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