The blood-brain barrier in systemic inflammation

被引:754
|
作者
Varatharaj, Aravinthan [1 ]
Galea, Ian [1 ]
机构
[1] Univ Southampton, Fac Med, Southampton Gen Hosp, Clin Neurosci,Clin & Expt Sci, Mailpoint 806,Tremona Rd, Southampton SO16 6YD, Hants, England
关键词
Blood-brain barrier; Systemic inflammation; Lipopolysaccharide; Sickness behaviour; Delirium; Septic encephalopathy; Multiple sclerosis; Alzheimer's disease; TUMOR-NECROSIS-FACTOR; IN-VITRO MODEL; CENTRAL-NERVOUS-SYSTEM; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; LIPOPOLYSACCHARIDE-INDUCED INFLAMMATION; EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS; ENHANCED TRANSCELLULAR TRANSPORT; MULTIPLE-SCLEROSIS; ENDOTHELIAL-CELLS; FACTOR-ALPHA;
D O I
10.1016/j.bbi.2016.03.010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The blood-brain barrier (BBB) plays a key role in maintaining the specialized microenvironment of the central nervous system (CNS), and enabling communication with the systemic compartment. BBB changes occur in several CNS pathologies. Here, we review disruptive and non-disruptive BBB changes in systemic infections and other forms of systemic inflammation, and how these changes may affect CNS function in health and disease. We first describe the structure and function of the BBB, and outline the techniques used to study the BBB in vitro, and in animal and human settings. We then summarise the evidence from a range of models linking BBB changes with systemic inflammation, and the underlying mechanisms. The clinical relevance of these BBB changes during systemic inflammation are discussed in the context of clinically-apparent syndromes such as sickness behaviour, delirium, and septic encephalopathy, as well as neurological conditions such as Alzheimer's disease and multiple sclerosis. We review emerging evidence for two novel concepts: (1) a heightened sensitivity of the diseased, versus healthy, BBB to systemic inflammation, and (2) the contribution of BBB changes induced by systemic inflammation to progression of the primary disease process. 2016 The Authors. Published by Elsevier Inc.
引用
收藏
页码:1 / 12
页数:12
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