Inflammatory cell trafficking across the blood-brain barrier: chemokine regulation and in vitro models

被引:235
作者
Takeshita, Yukio [1 ,2 ,3 ]
Ransohoff, Richard M. [1 ]
机构
[1] Cleveland Clin, Neuroinflammat Res Ctr, Dept Neurosci, Lerner Res Inst, Cleveland, OH 44195 USA
[2] Yamaguchi Univ, Grad Sch Med, Dept Neurol & Clin Neurosci, Ube, Yamaguchi 755, Japan
[3] Yamaguchi Univ, Grad Sch Med, Dept Neurosci, Ube, Yamaguchi 755, Japan
基金
美国国家卫生研究院;
关键词
in vitro BBB model; BBB components; CNS chemokine; endothelial cell line; shear stress; CENTRAL-NERVOUS-SYSTEM; CAPILLARY ENDOTHELIAL-CELLS; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; MULTIPLE-SCLEROSIS; SHEAR-STRESS; FUNCTIONAL-CHARACTERIZATION; TIGHT JUNCTIONS; GROWTH-FACTOR; LYMPHOCYTE MIGRATION; VASCULAR ENDOTHELIUM;
D O I
10.1111/j.1600-065X.2012.01127.x
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 bloodbrain barrier (BBB) is the brain-specific capillary barrier that is critical for preventing toxic substances from entering the central nervous system (CNS). In contrast to vessels of peripheral organs, the BBB limits the exchange of inflammatory cells and mediators under physiological and pathological conditions. Clarifying these limitations and the role of chemokines in regulating the BBB would provide new insights into neuroprotective strategies in neuroinflammatory diseases. Because there is a paucity of in vitro BBB models, however, some mechanistic aspects of transmigration across the BBB still remain largely unknown. In this review, we summarize current knowledge of BBB cellular components, the multistep process of inflammatory cells crossing the BBB, functions of CNS-derived chemokines, and in vitro BBB models for transmigration, with a particular focus on new and recent findings.
引用
收藏
页码:228 / 239
页数:12
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