The EMT/ITK/TSK (EMT) tyrosine kinase is activated during TCR signaling: LCK is required for optimal activation of EMT - PubMed (original) (raw)
. 1996 Apr 15;156(8):2716-22.
Affiliations
- PMID: 8609388
The EMT/ITK/TSK (EMT) tyrosine kinase is activated during TCR signaling: LCK is required for optimal activation of EMT
S Gibson et al. J Immunol. 1996.
Abstract
Functional T lymphocyte activation requires concurrent stimulation of the TCR complex and an accessory molecule, most frequently CD28. We have previously demonstrated that the TEC family tyrosine kinase EMT/ITK/TSK (EMT) is activated following cross-linking of CD28. We demonstrate herein that cross-linking of the CD3 component of the TCR complex also leads to EMT activation as indicated by a rapid and transient increase in EMT tyrosine phosphorylation and kinase activity in anti-EMT immunoprecipitates. However, although concurrent cross-linking of the TCR and CD28 results in a marked increase in production of the T cell growth factor IL-2, it does not result in a significant alteration in the magnitude or duration of EMT activation. Somatic cell mutants of the Jurkat T cell line, which lack the SRC family kinase LCK (JCaM1.6), fail to produce IL-2 when stimulated through the TCR complex. EMT activation, as evidenced by increased EMT tyrosine phosphorylation and EMT-associated kinase activity, was also greatly reduced following stimulation of the TCR in the JCaM1.6 Jurkat T cell mutants that lack LCK. In support of a role for LCK in EMT activation, reconstitution of the LCK-negative Jurkat T cell line by enforced expression of LCK restored TCR-mediated EMT activation. Taken together, the data indicate that the EMT tyrosine kinase is activated following cross-linking of the TCR, a process in which LCK likely plays an important role.
Similar articles
- Itk, a T cell-specific tyrosine kinase, is required for CD2-mediated interleukin-2 promoter activation in the human T cell line Jurkat.
Tanaka N, Abe H, Yagita H, Okumura K, Nakamura M, Sugamura K. Tanaka N, et al. Eur J Immunol. 1997 Apr;27(4):834-41. Eur J Immunol. 1997. PMID: 9130632 - Efficient CD28 signalling leads to increases in the kinase activities of the TEC family tyrosine kinase EMT/ITK/TSK and the SRC family tyrosine kinase LCK.
Gibson S, Truitt K, Lu Y, Lapushin R, Khan H, Imboden JB, Mills GB. Gibson S, et al. Biochem J. 1998 Mar 15;330 ( Pt 3)(Pt 3):1123-8. doi: 10.1042/bj3301123. Biochem J. 1998. PMID: 9494076 Free PMC article. - Signaling networks regulating beta1 integrin-mediated adhesion of T lymphocytes to extracellular matrix.
Woods ML, Shimizu Y. Woods ML, et al. J Leukoc Biol. 2001 Jun;69(6):874-80. J Leukoc Biol. 2001. PMID: 11404370 Review. - Tec family kinases in T lymphocyte development and function.
Berg LJ, Finkelstein LD, Lucas JA, Schwartzberg PL. Berg LJ, et al. Annu Rev Immunol. 2005;23:549-600. doi: 10.1146/annurev.immunol.22.012703.104743. Annu Rev Immunol. 2005. PMID: 15771581 Review.
Cited by
- TCR Signal Strength and Antigen Affinity Regulate CD8+ Memory T Cells.
Solouki S, Huang W, Elmore J, Limper C, Huang F, August A. Solouki S, et al. J Immunol. 2020 Sep 1;205(5):1217-1227. doi: 10.4049/jimmunol.1901167. Epub 2020 Aug 5. J Immunol. 2020. PMID: 32759295 Free PMC article. - Structural and diffusion weighted MRI demonstrates responses to ibrutinib in a mouse model of follicular helper (Tfh) T-cell lymphoma.
Allchin RL, Kelly ME, Mamand S, Doran AG, Keane T, Ahearne MJ, Wagner SD. Allchin RL, et al. PLoS One. 2019 Apr 23;14(4):e0215765. doi: 10.1371/journal.pone.0215765. eCollection 2019. PLoS One. 2019. PMID: 31013298 Free PMC article. - Comparison of interleukin-2-inducible kinase (ITK) inhibitors and potential for combination therapies for T-cell lymphoma.
Mamand S, Allchin RL, Ahearne MJ, Wagner SD. Mamand S, et al. Sci Rep. 2018 Sep 21;8(1):14216. doi: 10.1038/s41598-018-32634-5. Sci Rep. 2018. PMID: 30242208 Free PMC article. - Inhibition of BTK and ITK with Ibrutinib Is Effective in the Prevention of Chronic Graft-versus-Host Disease in Mice.
Schutt SD, Fu J, Nguyen H, Bastian D, Heinrichs J, Wu Y, Liu C, McDonald DG, Pidala J, Yu XZ. Schutt SD, et al. PLoS One. 2015 Sep 8;10(9):e0137641. doi: 10.1371/journal.pone.0137641. eCollection 2015. PLoS One. 2015. PMID: 26348529 Free PMC article. - People's instinctive travels and the paths to science.
August A. August A. Mol Biol Cell. 2014 Nov 1;25(21):3263-6. doi: 10.1091/mbc.E14-06-1120. Mol Biol Cell. 2014. PMID: 25360046 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Other Literature Sources
Miscellaneous