Blood brain barrier leakage is not a consistent feature of white matter lesions in CADASIL

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http://hdl.handle.net/10138/309065

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Rajani , R M , Ratelade , J , Domenga-Denier , V , Hase , Y , Kalimo , H , Kalaria , R N & Joutel , A 2019 , ' Blood brain barrier leakage is not a consistent feature of white matter lesions in CADASIL ' , Acta Neuropathologica Communications , vol. 7 , no. 1 , 187 . https://doi.org/10.1186/s40478-019-0844-x

Title: Blood brain barrier leakage is not a consistent feature of white matter lesions in CADASIL
Author: Rajani, Rikesh M.; Ratelade, Julien; Domenga-Denier, Valerie; Hase, Yoshiki; Kalimo, Hannu; Kalaria, Raj N.; Joutel, Anne
Contributor: University of Helsinki, Medicum
Date: 2019-11-21
Language: eng
Number of pages: 14
Belongs to series: Acta Neuropathologica Communications
ISSN: 2051-5960
URI: http://hdl.handle.net/10138/309065
Abstract: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a genetic paradigm of small vessel disease (SVD) caused by NOTCH3 mutations that stereotypically lead to the vascular accumulation of NOTCH3 around smooth muscle cells and pericytes. White matter (WM) lesions (WMLs) are the earliest and most frequent abnormalities, and can be associated with lacunar infarcts and enlarged perivascular spaces (ePVS). The prevailing view is that blood brain barrier (BBB) leakage, possibly mediated by pericyte deficiency, plays a pivotal role in the formation of WMLs. Herein, we investigated the involvement of BBB leakage and pericyte loss in CADASIL WMLs. Using post-mortem brain tissue from 12 CADASIL patients and 10 age-matched controls, we found that WMLs are heterogeneous, and that BBB leakage reflects the heterogeneity. Specifically, while fibrinogen extravasation was significantly increased in WMLs surrounding ePVS and lacunes, levels of fibrinogen leakage were comparable in WMLs without other pathology ("pure" WMLs) to those seen in the normal appearing WM of patients and controls. In a mouse model of CADASIL, which develops WMLs but no lacunes or ePVS, we detected no extravasation of endogenous fibrinogen, nor of injected small or large tracers in WMLs. Moreover, there was no evidence of pericyte coverage modification in any type of WML in either CADASIL patients or mice. These data together indicate that WMLs in CADASIL encompass distinct classes of WM changes and argue against the prevailing hypothesis that pericyte coverage loss and BBB leakage are the primary drivers of WMLs. Our results also have important implications for the interpretation of studies on the BBB in living patients, which may misinterpret evidence of BBB leakage within WM hyperintensities as suggesting a BBB related mechanism for all WMLs, when in fact this may only apply to a subset of these lesions.
Subject: CADASIL
Small vessel disease
Blood brain barrier
White matter lesions
Pericytes
AUTOSOMAL-DOMINANT ARTERIOPATHY
SMALL VESSEL DISEASE
SUBCORTICAL INFARCTS
LEUKOENCEPHALOPATHY CADASIL
COGNITIVE IMPAIRMENT
PATHOGENESIS
PERICYTES
DYSFUNCTION
ECTODOMAIN
INTEGRITY
3112 Neurosciences
3124 Neurology and psychiatry
3111 Biomedicine
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