Three or more routes for leukocyte migration into the central nervous system

被引:768
作者
Ransohoff, RM
Kivisäkk, P
Kidd, G
机构
[1] Cleveland Clin Fdn, Mellen Ctr Multiple Sclerosis Treatment & Res, Dept Neurol, Cleveland, OH 44195 USA
[2] Cleveland Clin Fdn, Dept Neurosci, Lerner Res Inst, Cleveland, OH 44195 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nri1130
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Leukocyte migration into and through tissues is fundamental to normal physiology, immunopathology and host defence. Leukocyte entry into the central nervous system (CNS) is restricted, in part, because of the blood brain barrier (BBB). During the past decade, crucial components that are involved in the process of leukocyte migration have been identified and progress has been made in understanding the mechanisms of neuroinflammatory reactions. In this review, present knowledge of the trafficking determinants that guide the migration of leukocytes is superimposed onto the vascular and compartmental anatomy of the CNS. We discuss three distinct routes for leukocytes to enter the CNS and consider how different populations of leukocytes use trafficking signals to gain entry.
引用
收藏
页码:569 / 581
页数:13
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共 128 条
  • [1] CXCL13 is required for B1 cell homing, natural antibody production, and body cavity immunity
    Ansel, KM
    Harris, RBS
    Cyster, JG
    [J]. IMMUNITY, 2002, 16 (01) : 67 - 76
  • [2] CXC chemokines generate age-related increases in neutrophil-mediated brain inflammation and blood-brain barrier breakdown
    Anthony, D
    Dempster, R
    Fearn, S
    Clements, J
    Wells, G
    Perry, VH
    Walker, K
    [J]. CURRENT BIOLOGY, 1998, 8 (16) : 923 - 926
  • [3] INHIBITION OF EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS BY AN ANTIBODY TO THE INTERCELLULAR-ADHESION MOLECULE ICAM-1
    ARCHELOS, JJ
    JUNG, S
    MAURER, M
    SCHMIED, M
    LASSMANN, H
    TAMATANI, T
    MIYASAKA, M
    TOYKA, KV
    HARTUNG, HP
    [J]. ANNALS OF NEUROLOGY, 1993, 34 (02) : 145 - 154
  • [4] Clonal expansions of CD8+ T cells dominate the T cell infiltrate in active multiple sclerosis lesions as shown by micromanipulation and single cell polymerase chain reaction
    Babbe, H
    Roers, A
    Waisman, A
    Lassmann, H
    Goebels, N
    Hohlfeld, R
    Friese, M
    Schröder, R
    Deckert, M
    Schmidt, S
    Ravid, R
    Rajewsky, K
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (03) : 393 - 404
  • [5] SURFACE EXPRESSION OF ALPHA-4 INTEGRIN BY CD4 T-CELLS IS REQUIRED FOR THEIR ENTRY INTO BRAIN PARENCHYMA
    BARON, JL
    MADRI, JA
    RUDDLE, NH
    HASHIM, G
    JANEWAY, CA
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (01) : 57 - 68
  • [6] Recombinant human adenovirus with rat MIP-2 gene insertion causes prolonged PMN recruitment to the murine brain
    Bell, MD
    Taub, DD
    Kunkel, SJ
    Strieter, RM
    Foley, R
    Gauldie, J
    Perry, VH
    [J]. EUROPEAN JOURNAL OF NEUROSCIENCE, 1996, 8 (09) : 1803 - 1811
  • [7] ALPHA-4 INTEGRINS MEDIATE LYMPHOCYTE ATTACHMENT AND ROLLING UNDER PHYSIOLOGICAL FLOW
    BERLIN, C
    BARGATZE, RF
    CAMPBELL, JJ
    VONANDRIAN, UH
    SZABO, MC
    HASSLEN, SR
    NELSON, RD
    BERG, EL
    ERLANDSEN, SL
    BUTCHER, EC
    [J]. CELL, 1995, 80 (03) : 413 - 422
  • [8] DETECTION OF MHC CLASS-II ANTIGENS ON MACROPHAGES AND MICROGLIA, BUT NOT ON ASTROCYTES AND ENDOTHELIA IN ACTIVE MULTIPLE-SCLEROSIS LESIONS
    BO, L
    MORK, S
    KONG, PA
    NYLAND, H
    PARDO, CA
    TRAPP, BD
    [J]. JOURNAL OF NEUROIMMUNOLOGY, 1994, 51 (02) : 135 - 146
  • [9] Contribution of extracranial lymphatics and arachnoid villi to the clearance of a CSF tracer in the rat
    Boulton, M
    Flessner, M
    Armstrong, D
    Mohamed, R
    Hay, J
    Johnston, M
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1999, 276 (03) : R818 - R823
  • [10] In situ tolerance within the central nervous system as a mechanism for preventing autoimmunity
    Brabb, T
    von Dassow, P
    Ordonez, N
    Schnabel, B
    Duke, B
    Goverman, J
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (06) : 871 - 880