CNS dendritic cells: Critical participants in CNS inflammation?

被引:67
作者
McMahon, Eileen J.
Bailey, Samantha L.
Miller, Stephen D.
机构
[1] Northwestern Univ, Sch Med, Dept Immunol Microbiol, Chicago, IL 60611 USA
[2] Northwestern Univ, Sch Med, Interdept Immunobiol Ctr, Chicago, IL 60611 USA
[3] Westmont Coll, Dept Biol, Santa Barbara, CA 93108 USA
基金
美国国家卫生研究院;
关键词
dendritic cells; CNS inflammation; CNS autoimmunity;
D O I
10.1016/j.neuint.2006.04.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dendritic cells (DCs) are a heterogeneous population of migratory cells specialized for the uptake, processing, and presentation of antigen to T cells. They consist of a variety of mature subpopulations, classically divided into "lymphoid" and "myeloid" subsets. Although there likely exists significant plasticity and redundancy between DC subpopulations, unique differences have been noted in their abilities for T cell stimulation, tolerance induction, T helper cell polarization, cytokine secretion, and anatomic localization. Although DCs are conspicuously absent from the healthy CNS parenchyma, their presence in the vascular-rich regions of the healthy CNS has been well established and suggests they may have a role in immune surveillance. DCs do accumulate in the CNS parenchyma in a wide range of inflammatory responses including parasite, viral, or bacterial infection and CNS autoimmune disease. They also are present in CNS immune responses without overt T cell involvement, such as the inflammation accompanying CNS injury or neurodegeneration. Controversy remains on the role of CNS DCs during inflammation and whether they differentiate from CNS-resident microglia or infiltrate from a blood-borne population. This review will summarize DC subsets and function, overview the current research on DCs in the healthy and inflamed CNS, and address discrepancies between experimental studies. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:195 / 203
页数:9
相关论文
共 90 条
  • [1] Central nervous system involvement in experimental infection with Leishmania (Leishmania) amazonensis
    Abreu-Silva, AL
    Calabrese, KS
    Tedesco, RC
    Mortara, RA
    De Costa, SCG
    [J]. AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2003, 68 (06) : 661 - 665
  • [2] Defining antigen-dependent stages of T cell migration from the blood to the central nervous system parenchyma
    Archambault, AS
    Sim, J
    Gimenez, MAT
    Russell, JH
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 2005, 35 (04) : 1076 - 1085
  • [3] MOUSE THYMIC DENDRITIC CELL SUBPOPULATIONS
    ARDAVIN, C
    WU, L
    FERRERO, I
    SHORTMAN, K
    [J]. IMMUNOLOGY LETTERS, 1993, 38 (01) : 19 - 25
  • [4] Mouse type IIFN-producing cells are immature APCs with plasmacytoid morphology
    Asselin-Paturel, C
    Boonstra, A
    Dalod, M
    Durand, I
    Yessaad, N
    Dezutter-Dambuyant, C
    Vicari, A
    O'Garra, A
    Biron, C
    Brière, F
    Trinchieri, G
    [J]. NATURE IMMUNOLOGY, 2001, 2 (12) : 1144 - 1150
  • [5] Infected splenic dendritic cells are sufficient for prion transmission to the CNS in mouse scrapie
    Aucouturier, P
    Geissmann, F
    Damotte, D
    Saborio, GP
    Meeker, HC
    Kascsak, R
    Kascsak, R
    Carp, RI
    Wisniewski, T
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2001, 108 (05) : 703 - 708
  • [6] Dendritic cells and the control of immunity
    Banchereau, J
    Steinman, RM
    [J]. NATURE, 1998, 392 (6673) : 245 - 252
  • [7] Becher B, 2000, GLIA, V29, P293
  • [8] Begley CG, 1996, EXP HEMATOL, V24, P1247
  • [9] Mucosal CD8α+ DC, with a plasmacytoid phenotype, induce differentiation and support function of T cells with regulatory properties
    Bilsborough, J
    George, TC
    Norment, A
    Viney, JL
    [J]. IMMUNOLOGY, 2003, 108 (04) : 481 - 492
  • [10] Flexibility of mouse classical and plasmacytoid-derived dendritic cells in directing T helper type 1 and 2 cell development: Dependency on antigen dose and differential toll-like receptor ligation
    Boonstra, A
    Asselin-Paturel, C
    Gilliet, M
    Crain, C
    Trinchieri, G
    Liu, YJ
    O'Garra, A
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (01) : 101 - 109