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Lookup NU author(s): Holly Baines, Emeritus Professor Doug Turnbull, Professor Laura GreavesORCiD
This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).
A decline in the replicative and regenerative capacity of adult stem cell populations is a major contributor to the aging process. Mitochondrial DNA (mtDNA) mutations clonally expand with age in human stem cell compartments including the colon, small intestine, and stomach, and result in respiratory chain deficiency. Studies in a mouse model with high levels of mtDNA mutations due to a defect in the proofreading domain of the mtDNA polymerase (mtDNA mutator mice) have established causal relationships between the accumulation of mtDNA point mutations, stem cell dysfunction, and premature aging. These mtDNA mutator mice have also highlighted that the consequences of mtDNA mutations upon stem cells vary depending on the tissue. In this review, we present evidence that these studies in mice are relevant to normal human stem cell aging and we explore different hypotheses to explain the tissue-specific consequences of mtDNA mutations. In addition, we emphasize the need for a comprehensive analysis of mtDNA mutations and their effects on cellular function in different aging human stem cell populations.
Author(s): Baines HL, Turnbull DM, Greaves LC
Publication type: Review
Publication status: Published
Journal: Aging Cell
Year: 2014
Volume: 13
Issue: 2
Pages: 201-205
Print publication date: 01/04/2014
Online publication date: 28/01/2014
Acceptance date: 21/12/2013
ISSN (print): 1474-9718
ISSN (electronic): 1474-9726
Publisher: WILEY-BLACKWELL
URL: http://dx.doi.org/10.1111/acel.12199
DOI: 10.1111/acel.12199
