Motaz M. Fadul
Transcriptomic analysis of age-associated periventricular lesions reveals dysregulation of the immune response
Fadul, Motaz M.; Heath, Paul R.; Cooper-Knock, Johnathan; Kurz, Julian M.; Al-Azzawi, Hayder A.; Ali, Zarki; Smith, Taylor; Matthews, Fiona E.; Brayne, Carol; Wharton, Stephen B.; Simpson, Julie E.
Authors
Paul R. Heath
Johnathan Cooper-Knock
Julian M. Kurz
Hayder A. Al-Azzawi
Zarki Ali
Taylor Smith
Professor Fiona Matthews F.Matthews@hull.ac.uk
Pro-Vice-Chancellor Research and Enterprise
Carol Brayne
Stephen B. Wharton
Julie E. Simpson
Abstract
White matter lesions (WML) are a common feature of the ageing brain associated with cognitive impairment. The gene expression profiles of periventricular lesions (PVL, n = 7) and radiologically-normal-appearing (control) periventricular white matter cases (n = 11) obtained from the Cognitive Function and Ageing Study (CFAS) neuropathology cohort were interrogated using microarray analysis and NanoString to identify novel mechanisms potentially underlying their formation. Histological characterisation of control white matter cases identified a subgroup (n = 4) which contained high levels of MHC-II immunoreactive microglia, and were classified as “pre-lesional.” Microarray analysis identified 2256 significantly differentially-expressed genes (p ≤ 0.05, FC ≥ 1.2) in PVL compared to non-lesional control white matter (1378 upregulated and 878 downregulated); 2649 significantly differentially-expressed genes in “pre-lesional” cases compared to PVL (1390 upregulated and 1259 downregulated); and 2398 significantly differentially-expressed genes in “pre-lesional” versus non-lesional control cases (1527 upregulated and 871 downregulated). Whilst histological evaluation of a single marker (MHC-II) implicates immune-activated microglia in lesion pathology, transcriptomic analysis indicates significant downregulation of a number of activated microglial markers and suggests established PVL are part of a continuous spectrum of white matter injury. The gene expression profile of “pre-lesional” periventricular white matter suggests upregulation of several signalling pathways may be a neuroprotective response to prevent the pathogenesis of PVL.
Citation
Fadul, M. M., Heath, P. R., Cooper-Knock, J., Kurz, J. M., Al-Azzawi, H. A., Ali, Z., Smith, T., Matthews, F. E., Brayne, C., Wharton, S. B., & Simpson, J. E. (2020). Transcriptomic analysis of age-associated periventricular lesions reveals dysregulation of the immune response. International Journal of Molecular Sciences, 21(21), Article 7924. https://doi.org/10.3390/ijms21217924
Journal Article Type | Article |
---|---|
Acceptance Date | Oct 23, 2020 |
Online Publication Date | Oct 25, 2020 |
Publication Date | Nov 1, 2020 |
Deposit Date | Sep 5, 2024 |
Publicly Available Date | Sep 6, 2024 |
Journal | International Journal of Molecular Sciences |
Electronic ISSN | 1422-0067 |
Publisher | MDPI |
Peer Reviewed | Peer Reviewed |
Volume | 21 |
Issue | 21 |
Article Number | 7924 |
DOI | https://doi.org/10.3390/ijms21217924 |
Keywords | Periventricular lesions; Transcriptomic profiling; Nanostring; Immune response |
Public URL | https://hull-repository.worktribe.com/output/4451617 |
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Copyright Statement
© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
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