Increased density of metallothionein I/II-immunopositive cortical glial cells in the early stages of Alzheimer's disease

Increased density of metallothionein I/II-immunopositive cortical glial cells in the early stages of Alzheimer's disease
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DOI:
10.1006/nbdi.1998.0203
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发表时间:
1998-11-01
影响因子:
6.1
通讯作者:
Vickers, JC
Vickers, JC
中科院分区:
医学1区
文献类型:
--
作者:
Adlard, PA;West, AK;Vickers, JC

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我们研究了金属硫蛋白VII(MT MR)在阿尔茨海默病(AD)中的可能作用,重点是MT MI相对于星形胶质细胞标记物胶质细胞酸性蛋白(GFAP)的细胞定位。在AD和临床前AD病例中,MT I/II免疫标记存在于神经胶质细胞中,并没有显示与P-淀粉样蛋白斑块或神经病理学的空间关系。有一个六至七倍的增加,NIT I/II-和GFAP-标记的细胞在灰质的AD病例,相对于非AD病例。然而,有三倍增加MT I/II-免疫反应细胞,但不是GFAP标记的细胞,在临床前AD病例的灰质相比,非AD病例。因此,MT I/II的特定增加与疾病过程的初始阶段相关,可能是由于氧化应激或重金属的代谢不良。(C)北京:科学出版社.
We have examined the possible role of metallothionein VII (MT mr) in Alzheimer's disease (AD), with a focus on the cellular localization of MT mi relative to the astrocyte marker, glial fibrillary acidic protein (GFAP). In AD and preclinical AD cases, MT I/II immunolabeling was present in glial cells and did not show a spatial relationship with P-amyloid plaques or neurofibrillary pathology. There was a six- to sevenfold increase in both NIT I/II- and GFAP-labeled cells in the gray matter of AD cases, relative to non-AD cases. However, there was a threefold increase in MT I/II-immunoreactive cells, but not GFAP-labeled cells, in the gray matter of preclinical AD cases compared to non-AD cases. Therefore, the specific increase in MT I/II is associated with the initial stages of the disease process, perhaps due to oxidative stress or the mismetabolism of heavy metals. (C) 1998 Academic Press.