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A Versatile Murine Model of Subcortical White Matter Stroke for the Study of Axonal Degeneration and White Matter Neurobiology
Published on: March 17, 2016
Pathological correlates of white matter hyperintensities in a case of progranulin mutation associated frontotemporal
Ione O C Woollacott1, Martina Bocchetta1, Carole H Sudre1,2
1a Dementia Research Centre, Department of Neurodegenerative Disease , UCL Institute of Neurology , London , UK.
Abstract:
White matter hyperintensities (WMH) are often seen on MRI brain scans in frontotemporal dementia (FTD) due to progranulin (GRN) mutations, but their pathological correlates are unknown. We examined the histological changes underlying WMH in a patient with GRN mutation associated behavioral variant FTD. In vivo and cadaveric MRI showed progressive, asymmetric frontotemporal and parietal atrophy, and asymmetrical WMH predominantly affecting frontal mid-zones. We first performed segmentation and localization analyses of WMH present on cadaveric MRI FLAIR images, then selected five different brain regions directly matched to differing severities of WMH for histological analysis. We used immunohistochemistry to assess vascular pathology, degree of spongiosis, neuronal and axonal loss, TDP-43, demyelination and astrogliosis, and microglial burden and morphology. Brain regions with significant WMH displayed severe cortical and white matter pathology, and prominent white matter microglial activation and microglial dystrophy, but only mild axonal loss and minimal vascular pathology. Our study suggests that WMH in GRN mutation carriers are not secondary to vascular pathology. Whilst cortical pathology induced axonal degeneration could contribute to white matter damage, individuals with GRN mutations could develop selective white matter vulnerability and myelin loss due to chronic, regional microglial dysfunction arising from GRN haploinsufficiency.
Insights
White matter hyperintensities in progranulin (GRN) mutation frontotemporal dementia are not vascular. Chronic microglial dysfunction may cause selective white matter vulnerability and myelin loss.
Area of Science:
- Neurology
- Neuroscience
- Pathology
Background:
- White matter hyperintensities (WMH) are common in progranulin (GRN) mutation-associated frontotemporal dementia (FTD).
- The underlying pathological basis of WMH in this context remains unclear.
Observation:
- This study investigated WMH pathology in a patient with GRN mutation-associated behavioral variant FTD.
- In vivo and cadaveric MRI revealed progressive atrophy and asymmetrical WMH, predominantly in frontal regions.
- Histological analysis focused on regions with varying WMH severity, examining vascular pathology, spongiosis, neuronal/axonal loss, TDP-43, demyelination, astrogliosis, and microglial changes.
Findings:
- WMH regions showed severe cortical and white matter pathology.
- Prominent white matter microglial activation and dystrophy were observed.
- Minimal axonal loss and vascular pathology were noted, suggesting WMH are not primarily vascular-related.
Implications:
- WMH in GRN mutation carriers are unlikely secondary to vascular issues.
- Chronic microglial dysfunction due to GRN haploinsufficiency may lead to selective white matter vulnerability and myelin loss.
- This offers new insights into FTD pathogenesis and potential therapeutic targets.
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