Biphasic Mechanisms of Neurovascular Unit Injury and Protection in CNS Diseases

被引:85
作者
Maki, Takakuni
Hayakawa, Kazuhide
Pham, Loc-Duyen D.
Xing, Changhong
Lo, Eng H.
Arai, Ken
机构
[1] Massachusetts Gen Hosp, Dept Radiol & Neurol, Neuroprotect Res Lab, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Cambridge, MA 02138 USA
基金
日本学术振兴会; 美国国家卫生研究院;
关键词
Neurovascular unit; stroke; central nervous system injury; neuroprotection; remodeling; astrocyte; cerebral endothelial cell; microglia; BLOOD-BRAIN-BARRIER; ENDOTHELIAL GROWTH-FACTOR; AMYOTROPHIC-LATERAL-SCLEROSIS; AMYLOID-BETA CLEARANCE; MATRIX METALLOPROTEINASES; PARKINSONS-DISEASE; MOUSE MODEL; HIPPOCAMPAL NEUROGENESIS; NEUROBLAST MIGRATION; SUBVENTRICULAR ZONE;
D O I
10.2174/1871527311312030004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In the past decade, evidence has emerged that there is a variety of bidirectional cell-cell and/or cell-extracellular matrix interactions within the neurovascular unit (NVU), which is composed of neuronal, glial, and vascular cells along with extracellular matrix. Many central nervous system diseases, which lead to NVU dysfunction, have common features such as glial activation/transformation and vascular/blood-brain-barrier alteration. These phenomena show dual opposite roles, harmful at acute phase and beneficial at chronic phase. This diverse heterogeneity may induce biphasic clinical courses, i.e. degenerative and regenerative processes in the context of dynamically coordinated cell-cell/cell-matrix interactions in the NVU. A deeper understanding of the seemingly contradictory actions in cellular levels is essential for NVU protection or regeneration to suppress the deleterious inflammatory reactions and promote adaptive remodeling after central nervous system injury. This mini-review will present an overview of recent progress in the biphasic roles of the NVU and discuss the clinical relevance of NVU responses associated with central nervous system diseases, such as stroke and other chronic neurodegenerative diseases.
引用
收藏
页码:302 / 315
页数:14
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