The impact of microglial activation on blood-brain barrier in brain diseases

被引:430
作者
Carvalho da Fonseca, Anna Carolina [1 ]
Matias, Diana [1 ]
Garcia, Celina [1 ]
Amaral, Rackele [1 ]
Geraldo, Luiz Henrique [1 ]
Freitas, Catarina [1 ]
Souza Lima, Flavia Regina [1 ]
机构
[1] Univ Fed Rio de Janeiro, Lab Morfogenese Celular, Inst Ciencias Biomed, Ctr Ciencias Saude, BR-21949590 Rio De Janeiro, RJ, Brazil
关键词
microglia; endothelium; blood-brain barrier; neuroinflammation; brain diseases; microglial activation; TUMOR-NECROSIS-FACTOR; FOCAL CEREBRAL-ISCHEMIA; TIGHT JUNCTION PROTEINS; MONOCYTE CHEMOATTRACTANT PROTEIN-1; IMMUNODEFICIENCY-VIRUS-INFECTION; FACTOR-ALPHA; ALZHEIMERS-DISEASE; OXIDATIVE STRESS; TNF-ALPHA; MATRIX METALLOPROTEINASES;
D O I
10.3389/fncel.2014.00362
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The blood-brain barrier (BBB), constituted by an extensive network of endothelial cells(ECs) together with neurons and glial cells, including microglia, forms the neurovascular unit (NVU). The crosstalk between these cells guarantees a proper environment for brain function. In this context, changes in the endothelium-microglia interactions are associated with a variety of inflammation-related diseases in brain, where BBB permeability is compromised. Increasing evidences indicate that activated microglia modulate expression of tight junctions, which are essential for BBB integrity and function. On the other hand, the endothelium can regulate the state of microglial activation. Here, we review recent advances that provide insights into interactions between the microglia and the vascular system in brain diseases such as infectious/inflammatory diseases, epilepsy, ischemic stroke and neurodegenerative disorders.
引用
收藏
页码:1 / 13
页数:13
相关论文
共 185 条
[1]  
Adibhatla RM, 2006, AAPS J, V8, pE314
[2]   Microglia derive from progenitors, originating from the yolk sac, and which proliferate in the brain [J].
Alliot, F ;
Godin, I ;
Pessac, B .
DEVELOPMENTAL BRAIN RESEARCH, 1999, 117 (02) :145-152
[3]  
Andjelkovic AV, 1999, GLIA, V28, P225, DOI 10.1002/(SICI)1098-1136(199912)28:3<225::AID-GLIA6>3.3.CO
[4]  
2-Y
[5]   Characterization of binding sites for chemokines MCP-1 and MIP-1α on human brain microvessels [J].
Andjelkovic, AV ;
Pachter, JS .
JOURNAL OF NEUROCHEMISTRY, 2000, 75 (05) :1898-1906
[6]   Cellular Mechanisms of Neurovascular Damage and Repair After Stroke [J].
Arai, Ken ;
Lok, Josephine ;
Guo, Shuzhen ;
Hayakawa, Kazuhide ;
Xing, Changhong ;
Lo, Eng H. .
JOURNAL OF CHILD NEUROLOGY, 2011, 26 (09) :1193-1198
[7]   Pericytes regulate the blood-brain barrier [J].
Armulik, Annika ;
Genove, Guillem ;
Mae, Maarja ;
Nisancioglu, Maya H. ;
Wallgard, Elisabet ;
Niaudet, Colin ;
He, Liqun ;
Norlin, Jenny ;
Lindblom, Per ;
Strittmatter, Karin ;
Johansson, Bengt R. ;
Betsholtz, Christer .
NATURE, 2010, 468 (7323) :557-U231
[8]   Expression pattern of miR-146a, an inflammation-associated microRNA, in experimental and human temporal lobe epilepsy [J].
Aronica, E. ;
Fluiter, K. ;
Iyer, A. ;
Zurolo, E. ;
Vreijling, J. ;
van Vliet, E. A. ;
Baayen, J. C. ;
Gorter, J. A. .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2010, 31 (06) :1100-1107
[9]   Astrocyte immune responses in epilepsy [J].
Aronica, Eleonora ;
Ravizza, Teresa ;
Zurolo, Emanuele ;
Vezzani, Annamaria .
GLIA, 2012, 60 (08) :1258-1268
[10]   Effects of matrix metalloproteinase-9 gene knock-out on the proteolysis of blood-brain barrier and white matter components after cerebral ischemia [J].
Asahi, M ;
Wang, XY ;
Mori, T ;
Sumii, T ;
Jung, JC ;
Moskowitz, MA ;
Fini, ME ;
Lo, EH .
JOURNAL OF NEUROSCIENCE, 2001, 21 (19) :7724-7732