B cell lymphoma 10 is essential for FcεR-mediated degranulation and IL-6 production in mast cells

被引:21
作者
Chen, Yuhong
Pappu, Bhanu P.
Zeng, Hu
Xue, Liquan
Morris, Stephan W.
Lin, Xin
Wen, Renren
Wang, Demin
机构
[1] Blood Ctr SE Wisconsin Inc, Blood Res Inst, Milwaukee, WI 53226 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Mol & Cellular Oncol, Houston, TX 77030 USA
[3] St Jude Childrens Hosp, Dept Pathol, Memphis, TN 38105 USA
[4] Med Coll Wisconsin, Dept Microbiol & Mol Genet, Milwaukee, WI 53226 USA
[5] Nanjing Univ, State Key Lab Pharmaceut Biotechnol, Nanjing 210008, Peoples R China
关键词
D O I
10.4049/jimmunol.178.1.49
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The adaptor protein B cell lymphoma 10 (Bcl10) plays an essential role in the functions of the AgRs in T and B cells. In this study, we report that Bcl10 also plays an important role in mast cells. Bcl10 is expressed in mast cells. Although Bcl10-deficient mast cells undergo normal development, we demonstrate that Bcl10 is essential for specific functions of Fc epsilon R. Although Bcl10-deficient mast cells have normal de novo synthesis and release of the lipid mediator arachidonic acid, the mutant cells possess impaired Fc epsilon R-mediated degranulation, indicated by decreased serotonin release, and impaired cytokine production, measured by release of IL-6. In addition, Bcl10-deficient mice display impaired IgE-mediated passive cutaneous anaphylaxis. Moreover, although Bc10-deficient mast cells have normal Fc epsilon R-mediated Ca2+ flux, activation of PI3K, and activation of the three types of MAPKs (ERKs, JNK, and p38), the mutant cells have markedly diminished Fc epsilon R-mediated activation of NF-kappa B and decreased activation of AP-1. Thus, Bcl10 is essential for Fc epsilon R-induced activation of AP-1, NF-kappa B, degranulation, and cytokine production in mast cells.
引用
收藏
页码:49 / 57
页数:9
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共 70 条
  • [1] v-Crk activates the phosphoinositide 3-kinase/AKT pathway in transformation
    Akagi, T
    Shishido, T
    Murata, K
    Hanafusa, H
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (13) : 7290 - 7295
  • [2] Mechanism of activation of protein kinase B by insulin and IGF-1
    Alessi, DR
    Andjelkovic, M
    Caudwell, B
    Cron, P
    Morrice, N
    Cohen, P
    Hemmings, BA
    [J]. EMBO JOURNAL, 1996, 15 (23) : 6541 - 6551
  • [3] BARANES D, 1991, BLOOD, V78, P2354
  • [4] BENHAMOU M, 1993, J BIOL CHEM, V268, P23318
  • [5] ERKS - A FAMILY OF PROTEIN-SERINE THREONINE KINASES THAT ARE ACTIVATED AND TYROSINE PHOSPHORYLATED IN RESPONSE TO INSULIN AND NGF
    BOULTON, TG
    NYE, SH
    ROBBINS, DJ
    IP, NY
    RADZIEJEWSKA, E
    MORGENBESSER, SD
    DEPINHO, RA
    PANAYOTATOS, N
    COBB, MH
    YANCOPOULOS, GD
    [J]. CELL, 1991, 65 (04) : 663 - 675
  • [6] Non-T cell activation linker (NTAL):: A transmembrane adaptor protein involved in immunoreceptor signaling
    Brdicka, T
    Imrich, M
    Angelisová, P
    Brdicková, N
    Horváth, O
    Spicka, J
    Hilgert, I
    Lusková, P
    Dráber, P
    Novák, P
    Engels, N
    Wienands, J
    Simeoni, L
    Österreicher, J
    Aguado, E
    Malissen, M
    Schraven, B
    Horejsí, V
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (12) : 1617 - 1626
  • [7] EPIDERMAL GROWTH-FACTOR REGULATES P21(RAS) THROUGH THE FORMATION OF A COMPLEX OF RECEPTOR, GRB2 ADAPTER PROTEIN, AND SOS NUCLEOTIDE EXCHANGE FACTOR
    BUDAY, L
    DOWNWARD, J
    [J]. CELL, 1993, 73 (03) : 611 - 620
  • [8] PROTEIN-KINASE-B (C-AKT) IN PHOSPHATIDYLINOSITOL-3-OH INASE SIGNAL-TRANSDUCTION
    BURGERING, BMT
    COFFER, PJ
    [J]. NATURE, 1995, 376 (6541) : 599 - 602
  • [9] Signal transduction from the B cell antigen-receptor
    Campbell, KS
    [J]. CURRENT OPINION IN IMMUNOLOGY, 1999, 11 (03) : 256 - 264
  • [10] CHAO TSO, 1994, J BIOL CHEM, V269, P7337