期刊
BRAIN PATHOLOGY
卷 23, 期 3, 页码 303-310出版社
WILEY-BLACKWELL
DOI: 10.1111/bpa.12004
关键词
Alzheimer's disease; bloodbrain barrier; pericytes
资金
- National Institutes of Health [AG039452, AG23084, NS34467]
Neurovascular dysfunction contributes to Alzheimer's disease (AD). Cerebrovascular abnormalities and bloodbrain barrier (BBB) damage have been shown in AD. The BBB dysfunction can lead to leakage of potentially neurotoxic plasma components in brain that may contribute to neuronal injury. Pericytes are integral in maintaining the BBB integrity. Pericyte-deficient mice develop a chronic BBB damage preceding neuronal injury. Moreover, loss of pericytes was associated with BBB breakdown in patients with amyotrophic lateral sclerosis. Here, we demonstrate a decrease in mural vascular cells in AD, and show that pericyte number and coverage in the cortex and hippocampus of AD subjects compared with neurologically intact controls are reduced by 59% and 60% (P<0.01), and 32% and 33% (P<0.01), respectively. An increase in extravascular immunoglobulin G (IgG) and fibrin deposition correlated with reductions in pericyte coverage in AD cases compared with controls; the Pearson's correlation coefficient r for the magnitude of BBB breakdown to IgG and fibrin vs. reduction in pericyte coverage was 0.96 (P<0.01) and 0.81 (P<0.01) in the cortex, respectively, and 0.86 (P<0.01) and 0.98 (P<0.01) in the hippocampus, respectively. Thus, deficiency in mural vascular cells may contribute to disrupted vascular barrier properties and resultant neuronal dysfunction during AD pathogenesis.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据