A novel functional interaction between Vav and PKCθ is required for TCR-induced T cell activation

被引:197
作者
Villalba, M
Coudronniere, N
Deckert, M
Teixeiro, E
Mas, P
Altman, A [1 ]
机构
[1] La Jolla Inst Allergy & Immunol, Div Cell Biol, San Diego, CA 92121 USA
[2] Univ Complutense Madrid, Fdn Jimenez Diaz, Dept Immunol, E-28040 Madrid, Spain
[3] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
关键词
D O I
10.1016/S1074-7613(00)80168-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Vav and PKC theta play an early and important role in the TCR/CD28-induced stimulation of MAP kinases and activation of the IL-2 gene. Vav is also essential for actin cytoskeleton reorganization and TCR capping. Here, we report that PKC theta function was selectively required in a Vav signaling pathway that mediates the TCR/CD28-induced activation of JNK and the IL-2 gene and the upregulation of CD69 expression. Vav also promoted PKC theta translocation from the cytosol to the membrane and cytoskeleton and induced its enzymatic activation in a CD3/CD28-initiated pathway that was dependent on Rac and on actin cytoskeleton reorganization. These findings reveal that the Vav/Rac pathway promotes the recruitment of PKC theta to the T cell synapse and its activation, essential processes for T cell activation and IL-2 production.
引用
收藏
页码:151 / 160
页数:10
相关论文
共 39 条
  • [11] Functional and physical interactions of Syk family kinases with the Vav proto-oncogene product
    Deckert, M
    TartareDeckert, S
    Couture, C
    Mustelin, T
    Altman, A
    [J]. IMMUNITY, 1996, 5 (06) : 591 - 604
  • [12] Vav is a regulator of cytoskeletal reorganization mediated by the T-cell receptor
    Fischer, KD
    Kong, YY
    Nishina, H
    Tedford, K
    Marengère, LEM
    Kozieradzki, I
    Sasaki, T
    Starr, M
    Chan, G
    Gardener, S
    Nghiem, MP
    Bouchard, D
    Barbacid, M
    Bernstein, A
    Penninger, JM
    [J]. CURRENT BIOLOGY, 1998, 8 (10) : 554 - 562
  • [13] DEFECTIVE T-CELL RECEPTOR SIGNALING AND POSITIVE SELECTION OF VAV-DEFICIENT CD4(+) CD8(+) THYMOCYTES
    FISCHER, KD
    ZMUIDZINAS, A
    GARDNER, S
    BARBACID, M
    BERNSTEIN, A
    GUIDOS, C
    [J]. NATURE, 1995, 374 (6521) : 474 - 477
  • [14] Ghaffari-Tabrizi N, 1999, EUR J IMMUNOL, V29, P132
  • [15] The Immunological Synapse: A Molecular Machine Controlling T Cell Activation
    Grakoui, Arash
    Bromley, Shannon K.
    Sumen, Cenk
    Davis, Mark M.
    Shaw, Andrey S.
    Allen, Paul M.
    Dustin, Michael L.
    [J]. JOURNAL OF IMMUNOLOGY, 2015, 194 (09) : 221 - 227
  • [16] MAJOR HISTOCOMPATIBILITY COMPLEX INDEPENDENT CLONAL T-CELL ANERGY BY DIRECT INTERACTION OF STAPHYLOCOCCUS-AUREUS ENTEROTOXIN-B WITH THE T-CELL ANTIGEN RECEPTOR
    HEWITT, CRA
    LAMB, JR
    HAYBALL, J
    HILL, M
    OWEN, MJ
    OHEHIR, RE
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (06) : 1493 - 1499
  • [17] Defects in actin-cap formation in Vav-deficient mice implicate an actin requirement for lymphocyte signal transduction
    Holsinger, LJ
    Graef, IA
    Swat, W
    Chi, T
    Bautista, DM
    Davidson, L
    Lewis, RS
    Alt, FW
    Crabtree, GR
    [J]. CURRENT BIOLOGY, 1998, 8 (10) : 563 - 572
  • [18] TRANSCRIPTIONAL REGULATION OF THE IL-2 GENE
    JAIN, J
    LOH, C
    RAO, A
    [J]. CURRENT OPINION IN IMMUNOLOGY, 1995, 7 (03) : 333 - 342
  • [19] Vav regulates peptide-specific apoptosis in thymocytes
    Kong, YY
    Fischer, KD
    Bachmann, MF
    Mariathasan, S
    Kozieradzki, I
    Nghiem, MP
    Bouchard, D
    Bernstein, A
    Ohashi, PS
    Penninger, JM
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (11) : 2099 - 2111
  • [20] Rac and Cdc42 induce actin polymerization and G1 cell cycle progression independently of p65(PAK) and the JNK/SAPK MAP kinase cascade
    Lamarche, N
    Tapon, N
    Stowers, L
    Burbelo, PD
    Aspenstrom, P
    Bridges, T
    Chant, J
    Hall, A
    [J]. CELL, 1996, 87 (03) : 519 - 529