Mitochondrial Aging Defects Emerge in Directly Reprogrammed Human Neurons due to Their Metabolic Profile

Kim Y, Zheng X, Ansari Z, Bunnell MC, Herdy JR, Traxler L, Lee H, Paquola ACM, Blithikioti C, Ku M, Schlachetzki J, Winkler J, Edenhofer F, Glass CK, Paucar AA, Jaeger BN, Pham S, Boyer L, Campbell BC, Hunter T, Mertens J, Gage FH (2018)

Publication Type: Journal article

Publication year: 2018

Journal

Cell Reports Elsevier (Cell Press)

Book Volume: 23

Pages Range: 2550-2558

Journal Issue: 9

DOI: 10.1016/j.celrep.2018.04.105

Abstract

Mitochondria are a major target for aging and are instrumental in the age-dependent deterioration of the human brain, but studying mitochondria in aging human neurons has been challenging. Direct fibroblast-to-induced neuron (iN) conversion yields functional neurons that retain important signs of aging, in contrast to iPSC differentiation. Here, we analyzed mitochondrial features in iNs from individuals of different ages. iNs from old donors display decreased oxidative phosphorylation (OXPHOS)-related gene expression, impaired axonal mitochondrial morphologies, lower mitochondrial membrane potentials, reduced energy production, and increased oxidized proteins levels. In contrast, the fibroblasts from which iNs were generated show only mild age-dependent changes, consistent with a metabolic shift from glycolysis-dependent fibroblasts to OXPHOS-dependent iNs. Indeed, OXPHOS-induced old fibroblasts show increased mitochondrial aging features similar to iNs. Our data indicate that iNs are a valuable tool for studying mitochondrial aging and support a bioenergetic explanation for the high susceptibility of the brain to aging. Kim et al. compared mitochondrial features in aging human fibroblasts and directly induced neurons (iNs). They find that only iNs display severe signs of mitochondrial aging defects and show that the metabolic shift during fibroblast-to-neuron conversion renders iNs particularly vulnerable to mitochondrial aging.

Authors with CRIS profile

Johannes Schlachetzki Department of Molecular Neurology Jürgen Winkler Professur für Molekulare Neurologie

Involved external institutions

Salk Institute for Biological Studies US United States (USA) (US) Leopold-Franzens-Universität Innsbruck / University of Innsbruck AT Austria (AT) University of California, San Diego US United States (USA) (US)

How to cite

APA:

Kim, Y., Zheng, X., Ansari, Z., Bunnell, M.C., Herdy, J.R., Traxler, L.,... Gage, F.H. (2018). Mitochondrial Aging Defects Emerge in Directly Reprogrammed Human Neurons due to Their Metabolic Profile. Cell Reports, 23(9), 2550-2558. https://doi.org/10.1016/j.celrep.2018.04.105

MLA:

Kim, Yongsung, et al. "Mitochondrial Aging Defects Emerge in Directly Reprogrammed Human Neurons due to Their Metabolic Profile." Cell Reports 23.9 (2018): 2550-2558.

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