Doherty Colin P, O'Keefe Eoin, Wallace Eugene, Loftus Teresa, Keaney James, Kealy John, Humphries Marian M, Molloy Michael G, Meaney James F, Farrell Michael, Campbell Matthew
From the Department of Neurology, Health Care Centre, Hospital 5, St James's Hospital, Dublin, Ireland (CPD, EW); Smurfit Institute of Genetics, Trinity College Dublin, University of Dublin, Dublin, Ireland (EO, JK, JoK, MMH, MC); Department of Neuropathology, Beaumont Hospital, Dublin, Ireland (TL, MF); University School of Veterinary Medicine, Basseterre, St. Kitts, West Indies (JK); Department of Medicine, University College Cork, Cork, Ireland (MGM); and Department of Radiology, St James's Hospital, Dublin, Ireland (JFM).
J Neuropathol Exp Neurol. 2016 Jul;75(7):656-62. doi: 10.1093/jnen/nlw036. Epub 2016 May 31.
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.
慢性创伤性脑病(CTE)是一种与重复性轻度创伤性脑损伤相关的神经退行性疾病。近年来,人们的注意力集中在将CTE的发展与运动员和军事人员的脑震荡损伤联系起来的新证据上;然而,CTE潜在的分子病理生物学仍不清楚。在此,我们提供证据表明,在一例CTE病例中,血脑屏障(BBB)在血管周围p-Tau密集积聚的区域被破坏。在血管周围p-Tau沉积区域,与BBB相关的紧密连接成分claudin-5和闭锁小带蛋白-1的免疫反应模式明显不连续或缺失;在这些病灶中也有BBB的免疫组化证据。由于该患者生前临床诊断为进行性核上性麻痹(PSP),我们还认为CTE改变似乎与PSP患者大脑中的改变不同。本报告首次描述了经病理证实的CTE病例中的BBB功能障碍,并提示在可能最终导致进行性退行性疾病发展的脑震荡后事件级联中存在血管成分。BBB功能障碍可能代表疑似有CTE发展风险的活体受试者神经功能障碍的一个相关因素。