Literature DB >> 27245243

Blood-Brain Barrier Dysfunction as a Hallmark Pathology in Chronic Traumatic Encephalopathy.

Colin P Doherty1, Eoin O'Keefe1, Eugene Wallace1, Teresa Loftus1, James Keaney1, John Kealy1, Marian M Humphries1, Michael G Molloy1, James F Meaney1, Michael Farrell1, Matthew Campbell2.   

Abstract

Chronic traumatic encephalopathy (CTE) is a neurodegenerative condition associated with repetitive mild traumatic brain injury. In recent years, attention has focused on emerging evidence linking the development of CTE to concussive injuries in athletes and military personnel; however, the underlying molecular pathobiology of CTE remains unclear. Here, we provide evidence that the blood-brain barrier (BBB) is disrupted in regions of dense perivascular p-Tau accumulation in a case of CTE. Immunoreactivity patterns of the BBB-associated tight junction components claudin-5 and zonula occludens-1 were markedly discontinuous or absent in regions of perivascular p-Tau deposition; there was also immunohistochemical evidence of a BBB in these foci. Because the patient was diagnosed premortem clinically as having progressive supranuclear palsy (PSP), we also compromised that the CTE alterations appear to be distinct from those in the brain of a patient with PSP. This report represents the first description of BBB dysfunction in a pathologically proven CTE case and suggests a vascular component in the postconcussion cascade of events that may ultimately lead to development of a progressive degenerative disorder. BBB dysfunction may represent a correlate of neural dysfunction in live subjects suspected of being at risk for development of CTE.
© 2016 American Association of Neuropathologists, Inc. All rights reserved.

Entities:  

Keywords:  Blood–brain barrier; Chronic traumatic encephalopathy; Claudin-5; Tight junctions.

Mesh:

Year:  2016        PMID: 27245243      PMCID: PMC4913433          DOI: 10.1093/jnen/nlw036

Source DB:  PubMed          Journal:  J Neuropathol Exp Neurol        ISSN: 0022-3069            Impact factor:   3.685


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