细胞色素c氧化酶
线粒体
生物
线粒体DNA
氧化应激
脂褐素
阿尔茨海默病
病理
免疫细胞化学
疾病
生物化学
医学
内分泌学
基因
作者
Keisuke Hirai,Gjumrakch Aliev,Akihiko Nunomura,Hisashi Fujioka,Robert L. Russell,Craig Atwood,Toby Johnson,Yvonne Kress,Harry V. Vinters,Massimo Tabaton,Shun Shimohama,Ayla Cash,Sandra L. Siedlak,Peggy L.R. Harris,Paul K. Jones,Robert B. Petersen,George Perry,Mark A. Smith
标识
DOI:10.1523/jneurosci.21-09-03017.2001
摘要
The finding that oxidative damage, including that to nucleic acids, in Alzheimer's disease is primarily limited to the cytoplasm of susceptible neuronal populations suggests that mitochondrial abnormalities might be part of the spectrum of chronic oxidative stress of Alzheimer's disease. In this study, we used in situ hybridization to mitochondrial DNA (mtDNA), immunocytochemistry of cytochrome oxidase, and morphometry of electron micrographs of biopsy specimens to determine whether there are mitochondrial abnormalities in Alzheimer's disease and their relationship to oxidative damage marked by 8-hydroxyguanosine and nitrotyrosine. We found that the same neurons showing increased oxidative damage in Alzheimer's disease have a striking and significant increase in mtDNA and cytochrome oxidase. Surprisingly, much of the mtDNA and cytochrome oxidase is found in the neuronal cytoplasm and in the case of mtDNA, the vacuoles associated with lipofuscin. Morphometric analysis showed that mitochondria are significantly reduced in Alzheimer's disease. The relationship shown here between the site and extent of mitochondrial abnormalities and oxidative damage suggests an intimate and early association between these features in Alzheimer's disease.
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