| Literature DB >> 30475765 |
Sabrina Strobel1,2, Edna Grünblatt3,4,5, Helmut Heinsen6,7, Peter Riederer8,9, Thomas Espach10, Michael Meder1,2, Camelia-Maria Monoranu10,2.
Abstract
Oxidative stress is implicated in the pathogenesis of neurodegenerative diseases, including sporadic Alzheimer's disease (AD). Mitochondrial DNA (mtDNA) deletions are markers of oxidative damage with an age-dependent accumulation. In a previous study, we analyzed mtDNA levels in diverse neuronal cell types in order to unravel the impact of oxidative stress in brains of AD patients. The aim of this study was to identify possible correlations between mtDNA deletion levels of selected astrocytes and microglia from three brain regions with different vulnerability to AD pathology and different stages of disease compared to controls. Our results reflect a higher vulnerability of hippocampal astrocytes and microglia to oxidative stress compared to other brain regions, such as cerebellum and brainstem.Entities:
Keywords: Alzheimer’s disease; astrocytes; brainstem; cerebellum; hippocampus; microglia; mitochondrial DNA; oxidative stress; selective vulnerability
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Year: 2019 PMID: 30475765 DOI: 10.3233/JAD-180661
Source DB: PubMed Journal: J Alzheimers Dis ISSN: 1387-2877 Impact factor: 4.472