The blood-brain barrier: an overview - Structure, regulation, and clinical implications

被引:1661
作者
Ballabh, P
Braun, A
Nedergaard, M
机构
[1] Westchester Med Ctr, Neonatal Intens Care Unit, Valhalla, NY 10595 USA
[2] New York Med Coll, Dept Pediat, Valhalla, NY 10595 USA
[3] New York Med Coll, Dept Anat & Cell Biol, Valhalla, NY 10595 USA
[4] New York Med Coll, Dept Pathol, Valhalla, NY 10595 USA
关键词
blood-brain barrier; tight junction; germinal matrix; astrocyte; pericyte;
D O I
10.1016/j.nbd.2003.12.016
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The blood-brain barrier (BBB) is a diffusion barrier, which impedes influx of most compounds from blood to brain. Three cellular elements of the brain microvasculature compose the BBB-endothelial cells, astrocyte end-feet, and pericytes (PCs). Tight junctions (TJs), present between the cerebral endothelial cells, form a diffusion barrier, which selectively excludes most blood-borne substances from entering the brain. Astrocytic end-feet tightly ensheath the vessel wall and appear to be critical for the induction and maintenance of the TJ barrier, but astrocytes are not believed to have a barrier function in the mammalian brain. Dysfunction of the BBB, for example, impairment of the TJ seal, complicates a number of neurologic diseases including stroke and neuroinflammatory disorders. We review here the recent developments in our understanding of the BBB and the role of the BBB dysfunction in CNS disease. We have focused on intraventricular hemorrhage (IVH) in premature infants, which may involve dysfunction of the TJ seal as well as immaturity of the BBB in the germinal matrix (GM). A paucity of TJs or PCs, coupled with incomplete coverage of blood vessels by astrocyte end-feet, may account for the fragility of blood vessels in the GM of premature infants. Finally, this review describes the pathogenesis of increased BBB permeability in hypoxia-ischemia and inflammatory mechanisms involving the BRB in septic encephalopathy, HIV-induced dementia, multiple sclerosis, and Alzheimer disease. (C) 2004 Published by Elsevier Inc.
引用
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页码:1 / 13
页数:13
相关论文
共 136 条
  • [41] GhaziBirry HS, 1997, AM J NEURORADIOL, V18, P219
  • [42] SENILE PLAQUES STIMULATE MICROGLIA TO RELEASE A NEUROTOXIN FOUND IN ALZHEIMER BRAIN
    GIULIAN, D
    HAVERKAMP, LJ
    LI, J
    KARSHIN, WL
    YU, J
    TOM, D
    LI, X
    KIRKPATRICK, JB
    [J]. NEUROCHEMISTRY INTERNATIONAL, 1995, 27 (01) : 119 - 137
  • [43] AN IMMUNOHISTOCHEMICAL STUDY OF THE GERMINAL LAYER IN THE LATE GESTATION HUMAN-FETAL BRAIN
    GOULD, SJ
    HOWARD, S
    [J]. NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 1987, 13 (06) : 421 - 437
  • [44] O-2 EXCHANGE BETWEEN BLOOD AND BRAIN-TISSUES STUDIES WITH O-18(2) INDICATOR-DILUTION TECHNIQUE
    GRIEB, P
    FORSTER, RE
    STROME, D
    GOODWIN, CW
    PAPE, PC
    [J]. JOURNAL OF APPLIED PHYSIOLOGY, 1985, 58 (06) : 1929 - 1941
  • [45] QUANTITATIVE MEASUREMENTS OF CAPILLARY TRANSPORT IN HUMAN BRAIN-TUMORS BY COMPUTED-TOMOGRAPHY
    GROOTHUIS, DR
    VRIESENDORP, FJ
    KUPFER, B
    WARNKE, PC
    LAPIN, GD
    KURUVILLA, A
    VICK, NA
    MIKHAEL, MA
    PATLAK, CS
    [J]. ANNALS OF NEUROLOGY, 1991, 30 (04) : 581 - 588
  • [46] ORIGIN OF INTRAVENTRICULAR HEMORRHAGE IN PRETERM INFANT
    HAMBLETON, G
    WIGGLESWORTH, JS
    [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1976, 51 (09) : 651 - 659
  • [47] ZO-3, a novel member of the MAGUK protein family found at the tight junction, interacts with ZO-1 and occludin
    Haskins, J
    Gu, LJ
    Wittchen, ES
    Hibbard, J
    Stevenson, BR
    [J]. JOURNAL OF CELL BIOLOGY, 1998, 141 (01) : 199 - 208
  • [48] LOCALIZATION OF IMMUNOREACTIVE GLUTAMYL AMINOPEPTIDASE IN RAT-BRAIN .2. DISTRIBUTION AND CORRELATION WITH ANGIOTENSIN-II
    HEALY, DP
    WILK, S
    [J]. BRAIN RESEARCH, 1993, 606 (02) : 295 - 303
  • [49] VEGF induces hyperpermeability by a direct action on endothelial cells
    Hippenstiel, S
    Krüll, M
    Ikemann, A
    Risau, W
    Clauss, M
    Suttorp, N
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1998, 274 (05) : L678 - L684
  • [50] Hirase T, 1997, J CELL SCI, V110, P1603