Volume 13, Issue 5 p. 510-519
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Nuclear but not mitochondrial-encoded oxidative phosphorylation genes are altered in aging, mild cognitive impairment, and Alzheimer's disease

Diego Mastroeni,

Corresponding Author

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

Corresponding author. Tel.: 602-369-6885.

E-mail address: diego.mastroeni@asu.edu

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Omar M. Khdour,

Biodesign Institute, and Department of Chemistry and Biochemistry, Arizona State University, Tempe, AZ, USA

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Elaine Delvaux,

ASU-Banner Neurodegenerative Disease Research Center, Biodesign Institute and School of Life Sciences, Arizona State University, Tempe, AZ, USA

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Jennifer Nolz,

ASU-Banner Neurodegenerative Disease Research Center, Biodesign Institute and School of Life Sciences, Arizona State University, Tempe, AZ, USA

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Gary Olsen,

Banner Sun Health Research Institute, Sun City, AZ, USA

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Nicole Berchtold,

Institute for Memory Impairments and Neurological Disorders, University of California, Irvine, CA, USA

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Carl Cotman,

Institute for Memory Impairments and Neurological Disorders, University of California, Irvine, CA, USA

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Sidney M. Hecht,

Biodesign Institute, and Department of Chemistry and Biochemistry, Arizona State University, Tempe, AZ, USA

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Paul D. Coleman,

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

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First published: 25 October 2016
Citations: 2

Abstract

Introduction

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.

Methods

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.

Results

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.

Discussion

Our findings suggest that restoration of the expression of nuclear-encoded OXPHOS genes in aging could be a viable strategy for blunting AD progression.