Mastroeni Diego, Khdour Omar M, Delvaux Elaine, Nolz Jennifer, Olsen Gary, Berchtold Nicole, Cotman Carl, Hecht Sidney M, Coleman Paul D
ASU-Banner Neurodegenerative Disease Research Center, Biodesign Institute and School of Life Sciences, Arizona State University, Tempe, AZ, USA; Banner Sun Health Research Institute, Sun City, AZ, USA.
Biodesign Institute, and Department of Chemistry and Biochemistry, Arizona State University, Tempe, AZ, USA.
Alzheimers Dement. 2017 May;13(5):510-519. doi: 10.1016/j.jalz.2016.09.003. Epub 2016 Oct 25.
We have comprehensively described the expression profiles of mitochondrial DNA and nuclear DNA genes that encode subunits of the respiratory oxidative phosphorylation (OXPHOS) complexes (I-V) in the hippocampus from young controls, age matched, mild cognitively impaired (MCI), and Alzheimer's disease (AD) subjects.
Hippocampal tissues from 44 non-AD controls (NC), 10 amnestic MCI, and 18 AD cases were analyzed on Affymetrix Hg-U133 plus 2.0 arrays.
The microarray data revealed significant down regulation in OXPHOS genes in AD, particularly those encoded in the nucleus. In contrast, there was up regulation of the same gene(s) in MCI subjects compared to AD and ND cases. No significant differences were observed in mtDNA genes identified in the array between AD, ND, and MCI subjects except one mt-ND6.
Our findings suggest that restoration of the expression of nuclear-encoded OXPHOS genes in aging could be a viable strategy for blunting AD progression.
我们全面描述了年轻对照组、年龄匹配的轻度认知障碍(MCI)和阿尔茨海默病(AD)受试者海马体中编码呼吸氧化磷酸化(OXPHOS)复合体(I-V)亚基的线粒体DNA和核DNA基因的表达谱。
在Affymetrix Hg-U133 plus 2.0芯片上分析了44名非AD对照组(NC)、10名遗忘型MCI和18例AD病例的海马组织。
微阵列数据显示AD中OXPHOS基因显著下调,尤其是那些由细胞核编码的基因。相比之下,与AD和ND病例相比,MCI受试者中相同基因上调。除了一个线粒体编码的NADH脱氢酶亚基6(mt-ND6)外,在AD、ND和MCI受试者阵列中鉴定的线粒体DNA基因未观察到显著差异。
我们的研究结果表明,恢复衰老过程中核编码的OXPHOS基因表达可能是减缓AD进展的可行策略。