Rachel Waller
Metallothionein-I/II expression associates with the astrocyte DNA damage response and not Alzheimer-type pathology in the aging brain
Waller, Rachel; Murphy, Mark; Garwood, Claire J.; Jennings, Luke; Heath, Paul R.; Chambers, Annabelle; Matthews, Fiona E.; Brayne, Carol; Ince, Paul G.; Wharton, Stephen B.; Simpson, Julie E.
Authors
Mark Murphy
Claire J. Garwood
Luke Jennings
Paul R. Heath
Annabelle Chambers
Professor Fiona Matthews F.Matthews@hull.ac.uk
Pro-Vice-Chancellor Research and Enterprise
Carol Brayne
Paul G. Ince
Stephen B. Wharton
Julie E. Simpson
Abstract
Oxidative stress and oxidative DNA damage are early features of mild cognitive impairment and Alzheimer's disease (AD), occurring before the formation of classical AD neuropathology, and resulting from an imbalance between pro- and anti-oxidants. Astrocytes play a major neuroprotective role, producing high levels of anti-oxidants including metallothionein-I and -II (MT-I/II). In the present study we characterized the immunoreactive profile of MT-I/II in the temporal cortex of the Cognitive Function and Ageing Study (CFAS) aging population-representative neuropathology cohort, and examined H 2 O 2 -modulation of MT transcription by human astrocytes. MT-I/II is primarily expressed by astrocytes in the aging brain, but is also associated with pyramidal neurons in a small proportion of cases. Astrocyte expression of MT-I/II does not correlate with Alzheimer-type pathology (Aβ plaques and neurofibrillary tangles) but does relate to astrocyte oxidative DNA damage (r s =.312, p =.006) and the astrocyte response to oxidative DNA damage in vivo (r s =.238, p =.04), and MT gene expression is significantly induced in human astrocytes response to oxidative stress in vitro (p =.01). In contrast, neuronal MT-I/II does not relate to oxidative DNA damage or the neuronal DNA damage response, but is significantly higher in cases with high levels of local tangle pathology (p =.007). As MT-I/II is neuroprotective against oxidative stress, modulation of MT-I/II expression is a potential therapeutic target to treat the onset and progression of cognitive impairment.
Citation
Waller, R., Murphy, M., Garwood, C. J., Jennings, L., Heath, P. R., Chambers, A., Matthews, F. E., Brayne, C., Ince, P. G., Wharton, S. B., & Simpson, J. E. (2018). Metallothionein-I/II expression associates with the astrocyte DNA damage response and not Alzheimer-type pathology in the aging brain. Glia, 66(11), 2316-2323. https://doi.org/10.1002/glia.23465
Journal Article Type | Article |
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Publication Date | Nov 1, 2018 |
Deposit Date | Dec 8, 2023 |
Journal | GLIA |
Print ISSN | 0894-1491 |
Electronic ISSN | 1098-1136 |
Publisher | Wiley |
Volume | 66 |
Issue | 11 |
Pages | 2316-2323 |
DOI | https://doi.org/10.1002/glia.23465 |
Public URL | https://hull-repository.worktribe.com/output/4452584 |
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