Differential perivascular microglial activation in the deep white matter in vascular dementia developed post‐stroke

Hase, Y. et al. (2022) Differential perivascular microglial activation in the deep white matter in vascular dementia developed post‐stroke. Brain Pathology, 32(6), e13101. (doi: 10.1111/bpa.13101) (PMID:35748290) (PMCID:PMC9616090)

Abstract

With the hypothesis that perivascular microglia are involved as neuroinflammatory components of the gliovascular unit contributing to white matter hyperintensities on MRI and pathophysiology, we assessed their status in stroke survivors who develop dementia. Immunohistochemical and immunofluorescent methods were used to assess the distribution and quantification of total and perivascular microglial cell densities in 68 brains focusing on the frontal lobe WM and overlying neocortex in post‐stroke dementia (PSD), post‐stroke non‐dementia (PSND) and similar age control subjects. We primarily used CD68 as a marker of phagocytic microglia, as well as other markers of microglia including Iba‐1 and TMEM119, and the myeloid cell marker TREM2 to assess dementia‐specific changes. We first noted greater total densities of CD68+ and TREM2+ cells per mm2 in the frontal WM compared to the overlying cortex across the stroke cases and controls (p = 0.001). PSD subjects showed increased percentage of activated perivascular CD68+ cells distinct from ramified or primed microglia in the WM (p < 0.05). However, there was no apparent change in perivascular TREM2+ cells. Total densities of TREM2+ cells were only ~10% of CD68+ cells but there was high degree of overlap (>70%) between them in both the WM and the cortex. CD68 and Iba‐1 or CD68 and TMEM119 markers were colocalised by ~55%. Within the deep WM, ~30% of CD68+ cells were co‐localised with fragments of degraded myelin basic protein. Among fragmented CD68+ cells in adjacent WM of PSD subjects, >80% of the cells expressed cleaved caspase‐3. Our observations suggest although the overall repertoire of perivascular microglial cells is not changed in the parenchyma, PSD subjects accrue more perivascular‐activated CD68+ microglia rather than TREM2+ cells. This implies there is a subset of CD68+ cells, which are responsible for the differential response in perivascular inflammation within the gliovascular unit of the deep WM.

• Item Type: Articles
• Additional Information: This work was supported by a project grant from the Alzheimer's Society (AS-PG-17-007) and Alzheimer's Research UK (ARUK-PG2016B-6). Tissue for this study was collected by the Newcastle Brain Tissue Resource, which is funded in part by a grant from the UK MRC (G0400074), by the Newcastle NIHR Biomedical Research Centre in Ageing and Age-Related Diseases award to the Newcastle upon Tyne Hospitals NHS Foundation Trust, and by a grant from the Alzheimer's Society and ARUK as part of the Brains for Dementia Research Project.
• Status: Published
• Refereed: Yes
• Glasgow Author(s) Enlighten ID: Ameen-Ali, Dr Kamar
• Authors: Hase, Y., Ameen-Ali, K. E., Waller, R., Simpson, J. E., Stafford, C., Mahesh, A., Ryan, L., Pickering, L., Bodman, C., Hase, M., Boche, D., Horsburgh, K., Wharton, S. B., and Kalaria, R. N.
• College/School: College of Medical Veterinary and Life Sciences > School of Psychology & Neuroscience
• Journal Name: Brain Pathology
• Publisher: Wiley
• ISSN: 1015-6305
• ISSN (Online): 1750-3639
• Published Online: 24 June 2022
• Copyright Holders: Copyright © 2022 The Authors
• First Published: First published in Brain Pathology 32(6): e13101
• Publisher Policy: Reproduced under a Creative Commons License