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载脂蛋白E和D在人脑β淀粉样蛋白沉积物中分布的免疫组织化学研究

Immunohistochemical study of distribution of apolipoproteins E and D in human cerebral beta amyloid deposits.

作者信息

Navarro Ana, Del Valle Eva, Astudillo Aurora, González del Rey Carmen, Tolivia Jorge

机构信息

Departamento de Morfología y Biología Celular, Facultad de Biología y Medicina, Universidad de Oviedo, Oviedo 33006, Spain.

出版信息

Exp Neurol. 2003 Dec;184(2):697-704. doi: 10.1016/S0014-4886(03)00315-7.

Abstract

Several molecules are known to be closely associated with amyloid deposits in human brain. Among these, apolipoproteins such as apolipoproteins E (apo E) and J (apo J) have been found in two neuropathological hallmarks of Alzheimer's disease (AD) and cerebral amyloid angiopathy (CAA): senile plaques (SPs) and cerebrovascular amyloid. These apolipoproteins may be implicated in amyloid fibrillogenesis. Apo D is a multiligand-multifunctional glycoprotein present in SPs, as we previously reported. The aim of this work is to study the link between immunolocalization of apo E and apo D in AD and CAA brains. Both apolipoproteins were found in all types of SPs, but apo E was observed more often than apo D in mature plaques. Whereas apo E is always located overlapping the amyloid core, apo D seems to situate preferably around and near the amyloid. Immunohistochemistry revealed that these apolipoproteins behave differently in cerebral vessels. Apo E labeling in vessels appears mainly linked to amyloid deposits, whereas apo D shows a distribution almost opposite to that of apo E. This could be an indication of the different roles that each apolipoprotein plays in the pathogenesis of amyloid deposition.

摘要

已知有几种分子与人类大脑中的淀粉样沉积物密切相关。其中,载脂蛋白如载脂蛋白E(apo E)和载脂蛋白J(apo J)已在阿尔茨海默病(AD)和脑淀粉样血管病(CAA)的两个神经病理学特征中被发现:老年斑(SPs)和脑血管淀粉样蛋白。这些载脂蛋白可能与淀粉样纤维形成有关。如我们之前报道的,载脂蛋白D是一种存在于老年斑中的多配体多功能糖蛋白。这项工作的目的是研究apo E和apo D在AD和CAA大脑中的免疫定位之间的联系。在所有类型的老年斑中都发现了这两种载脂蛋白,但在成熟斑块中观察到apo E比apo D更常见。虽然apo E总是位于与淀粉样核心重叠的位置,但apo D似乎更倾向于位于淀粉样物质周围和附近。免疫组织化学显示,这些载脂蛋白在脑血管中的表现不同。血管中的apo E标记主要与淀粉样沉积物相关,而apo D的分布几乎与apo E相反。这可能表明每种载脂蛋白在淀粉样沉积发病机制中发挥的不同作用。

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