Class IV semaphorin Sema4A enhances T-cell activation and interacts with Tim-2

被引:263
作者
Kumanogoh, A
Marukawa, S
Suzuki, K
Takegahara, N
Watanabe, C
Ch'ng, ES
Ishida, I
Fujimura, H
Sakoda, S
Yoshida, K
Kikutani, H
机构
[1] Osaka Univ, Microbial Dis Res Inst, Dept Mol Immunol, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Grad Sch Med, Dept Neurol, Suita, Osaka 5650871, Japan
[3] Osaka Univ, Grad Sch Med, Dept Internal Med & Mol Sci, Suita, Osaka 5650871, Japan
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nature01037
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Semaphorins are a family of phylogenetically conserved soluble and transmembrane proteins(1,2). Although many soluble semaphorins deliver guidance cues to migrating axons during neuronal development(3-5), some members are involved in immune responses(6-9). For example, CD100 (also known as Sema4D), a class IV transmembrane semaphorin, signals through CD72 to effect nonredundant roles in immune responses(7,10-13) in a ligand-receptor system that is distinct from any seen previously in the nervous system(14,15). Here we report that the class IV semaphorin Sema4A, which is expressed in dendritic cells and B cells, enhances the in vitro activation and differentiation of T cells and the in vivo generation of antigen-specific T cells. Treating mice with monoclonal antibodies against Sema4A blocks the development of an experimental autoimmune encephalomyelitis that is induced by an antigenic peptide derived from myelin oligodendrocyte glycoprotein. In addition, expression cloning shows that the Sema4A receptor is Tim-2, a member of the family of T-cell immunoglobulin domain and mucin domain (Tim) proteins that is expressed on activated T cells.
引用
收藏
页码:629 / 633
页数:6
相关论文
共 27 条
  • [1] Adachi T, 1998, J IMMUNOL, V160, P4662
  • [2] ALEXANDER BH, 2000, IMMUNITY, V13, P345
  • [3] Studies in B7-deficient mice reveal a critical role for B7 costimulation in both induction and effector phases of experimental autoimmune encephalomyelitis
    Chang, TT
    Jabs, C
    Sobel, RA
    Kuchroo, VK
    Sharpe, AH
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (05) : 733 - 740
  • [4] A poxvirus-encoded semaphorin induces cytokine production from monocytes and binds to a novel cellular semaphorin receptor, VESPR
    Comeau, MR
    Johnson, R
    DuBose, RF
    Petersen, M
    Gearing, P
    VandenBos, T
    Park, L
    Farrah, T
    Buller, RM
    Cohen, JI
    Strockbine, LD
    Rauch, C
    Spriggs, MK
    [J]. IMMUNITY, 1998, 8 (04) : 473 - 482
  • [5] CD100 is a leukocyte semaphorin
    Delaire, S
    Elhabazi, A
    Bensussan, A
    Boumsell, L
    [J]. CELLULAR AND MOLECULAR LIFE SCIENCES, 1998, 54 (11) : 1265 - 1276
  • [6] Dysregulation of T lymphocyte function in itchy mice:: a role for itch in TH2 differentiation
    Fang, DY
    Elly, C
    Gao, BX
    Fang, N
    Altman, Y
    Joazeiro, C
    Hunter, T
    Copeland, N
    Jenkins, N
    Liu, YC
    [J]. NATURE IMMUNOLOGY, 2002, 3 (03) : 281 - 287
  • [7] Unified nomenclature for the semaphorins collapsins
    Goodman, CS
    Kolodkin, AL
    Luo, Y
    Püschel, AW
    Raper, JA
    [J]. CELL, 1999, 97 (05) : 551 - 552
  • [8] GENERATION OF LARGE NUMBERS OF DENDRITIC CELLS FROM MOUSE BONE-MARROW CULTURES SUPPLEMENTED WITH GRANULOCYTE MACROPHAGE COLONY-STIMULATING FACTOR
    INABA, K
    INABA, M
    ROMANI, N
    AYA, H
    DEGUCHI, M
    IKEHARA, S
    MURAMATSU, S
    STEINMAN, RM
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 176 (06) : 1693 - 1702
  • [9] THE SEMAPHORIN GENES ENCODE A FAMILY OF TRANSMEMBRANE AND SECRETED GROWTH CONE GUIDANCE MOLECULES
    KOLODKIN, AL
    MATTHES, DJ
    GOODMAN, CS
    [J]. CELL, 1993, 75 (07) : 1389 - 1399
  • [10] Requirement for the lymphocyte semaphorin, CD100, in the induction of antigen-specific T cells and the maturation of dendritic cells
    Kumanogoh, A
    Suzuki, K
    Ch'ng, E
    Watanabe, C
    Marukawa, S
    Takegahara, N
    Ishida, I
    Sato, T
    Habu, S
    Yoshida, K
    Shi, W
    Kikutani, H
    [J]. JOURNAL OF IMMUNOLOGY, 2002, 169 (03) : 1175 - 1181