Tec family kinases in T lymphocyte development and function

被引:263
作者
Berg, LJ [1 ]
Finkelstein, LD
Lucas, JA
Schwartzberg, PL
机构
[1] Univ Massachusetts, Sch Med, Dept Pathol, Worcester, MA 01655 USA
[2] NHGRI, NIH, Bethesda, MD 20892 USA
关键词
Itk/Emt/Tsk; Rlk/Txk; Tec; phospholipase C-gamma; actin;
D O I
10.1146/annurev.immunol.22.012703.104743
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
The Tee family tyrosine kinases are now recognized as important mediators of antigen receptor signaling in lymphocytes. Three members of this family, Itk, Rlk, and Tee, are expressed in T cells and activated in response to T cell receptor (TCR) engagement. Although initial studies demonstrated a role for these proteins in TCR-mediated activation of phospholipase C-gamma, recent data indicate that Tee family kinases also regulate actin cytoskeletal reorganization and cellular adhesion following TCR stimulation. In addition, Tee family kinases are activated downstream of G protein-coupled chemokine receptors, where they play parallel roles in the regulation of Rho GTPases, cell polarization, adhesion, and migration. In all these systems, however, Tee family kinases are not essential signaling components, but instead function to modulate or amplify signaling pathways. Although they quantitatively reduce proximal signaling, mutations that eliminate Tee family kinases in T cells nonetheless qualitatively alter T cell development and differentiation.
引用
收藏
页码:549 / 600
页数:52
相关论文
共 222 条
[1]
p130Cas couples the tyrosine kinase Bmx/Etk with regulation of the actin cytoskeleton and cell migration [J].
Abassi, YA ;
Rehn, M ;
Ekman, N ;
Alitalo, K ;
Vuori, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (37) :35636-35643
[2]
Afar DEH, 1996, MOL CELL BIOL, V16, P3465
[3]
Induction of T helper type 2 immunity by a point mutation in the LAT adaptor [J].
Aguado, E ;
Richelme, S ;
Nuñez-Cruz, S ;
Miazek, A ;
Mura, AM ;
Richelme, M ;
Guo, XJ ;
Sainty, D ;
He, HT ;
Malissen, B ;
Malissen, M .
SCIENCE, 2002, 296 (5575) :2036-2040
[4]
Positive feedback regulation of PLCγ1/Ca2+ signaling by PKCθ in restimulated T cells via a Tec kinase-dependent pathway [J].
Altman, A ;
Kaminski, S ;
Busuttil, V ;
Droin, N ;
Hu, JR ;
Tadevosyan, Y ;
Hipskind, RA ;
Villalba, M .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2004, 34 (07) :2001-2011
[5]
Regulatory intramolecular association in a tyrosine kinase of the Tec family [J].
Andreotti, AH ;
Bunnell, SC ;
Feng, S ;
Berg, LJ ;
Schreiber, SL .
NATURE, 1997, 385 (6611) :93-97
[6]
The Tec family of tyrosine kinases in T cells, amplifiers of T cell receptor signals [J].
August, A ;
Fischer, A ;
Hao, S ;
Mueller, C ;
Ragin, M .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2002, 34 (10) :1184-1189
[7]
CD28 IS ASSOCIATED WITH AND INDUCES THE IMMEDIATE TYROSINE PHOSPHORYLATION AND ACTIVATION OF THE TEC FAMILY KINASE ITK/EMT IN THE HUMAN JURKAT LEUKEMIC T-CELL LINE [J].
AUGUST, A ;
GIBSON, S ;
KAWAKAMI, Y ;
KAWAKAMI, T ;
MILLS, GB ;
DUPONT, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (20) :9347-9351
[8]
Src-induced activation of inducible T cell kinase (ITK) requires phosphatidylinositol 3-kinase activity and the Pleckstrin homology domain of inducible T cell kinase [J].
August, A ;
Sadra, A ;
Dupont, B ;
Hanafusa, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (21) :11227-11232
[9]
Involvement of Wiskott-Aldrich syndrome protein in B-Cell cytoplasmic tyrosine kinase pathway [J].
Baba, Y ;
Nonoyama, S ;
Matsushita, M ;
Yamadori, T ;
Hashimoto, S ;
Imai, K ;
Arai, S ;
Kunikata, T ;
Kurimoto, M ;
Kurosaki, T ;
Ochs, HD ;
Yata, J ;
Kishimoto, T ;
Tsukada, S .
BLOOD, 1999, 93 (06) :2003-2012
[10]
Antiviral immune responses in Itk-deficient mice [J].
Bachmann, MF ;
Littman, DR ;
Liao, XC .
JOURNAL OF VIROLOGY, 1997, 71 (10) :7253-7257