The Src, Syk, and Tec family kinases: distinct types of molecular switches
- PMID: 20206686
- DOI: 10.1016/j.cellsig.2010.03.001
The Src, Syk, and Tec family kinases: distinct types of molecular switches
Abstract
The Src, Syk, and Tec family kinases are three of the most well characterized tyrosine kinase families found in the human genome. Members of these kinase families function downstream of antigen and F(c) receptors in hematopoietic cells and transduce signals leading to calcium mobilization, altered gene expression, cytokine production, and cell proliferation. Over the last several years, structural and biochemical studies have begun to uncover the molecular mechanisms regulating activation of these kinases. It appears that each kinase family functions as a distinct type of molecular switch. This review discusses the activation of the Src, Syk, and Tec kinases from the perspective of structure, phosphorylation, allosteric regulation, and kinetics. The multiple factors that regulate the Src, Syk, and Tec families illustrate the important role played by each of these kinases in immune cell signaling.
Similar articles
-
Protein tyrosine kinases Syk and ZAP-70 display distinct requirements for Src family kinases in immune response receptor signal transduction.J Immunol. 1997 Feb 15;158(4):1650-9. J Immunol. 1997. PMID: 9029101
-
Signaling by adhesion in human neutrophils: activation of the p72syk tyrosine kinase and formation of protein complexes containing p72syk and Src family kinases in neutrophils spreading over fibrinogen.J Immunol. 1997 Feb 15;158(4):1902-10. J Immunol. 1997. PMID: 9029132
-
Nonredundant roles of Src-family kinases and Syk in the initiation of B-cell antigen receptor signaling.J Immunol. 2013 Feb 15;190(4):1807-18. doi: 10.4049/jimmunol.1202401. Epub 2013 Jan 18. J Immunol. 2013. PMID: 23335753
-
Src and Syk kinases: key regulators of phagocytic cell activation.Trends Immunol. 2005 Apr;26(4):208-14. doi: 10.1016/j.it.2005.02.002. Trends Immunol. 2005. PMID: 15797511 Review.
-
Src-family and Syk kinases in activating and inhibitory pathways in innate immune cells: signaling cross talk.Cold Spring Harb Perspect Biol. 2011 Mar 1;3(3):a002352. doi: 10.1101/cshperspect.a002352. Cold Spring Harb Perspect Biol. 2011. PMID: 21068150 Free PMC article. Review.
Cited by
-
Ibrutinib-Associated Cardiotoxicity: From the Pharmaceutical to the Clinical.Drug Des Devel Ther. 2022 Sep 20;16:3225-3239. doi: 10.2147/DDDT.S377697. eCollection 2022. Drug Des Devel Ther. 2022. PMID: 36164415 Free PMC article. Review.
-
PI3Kδ Sustains Keratinocyte Hyperproliferation and Epithelial Inflammation: Implications for a Topically Druggable Target in Psoriasis.Cells. 2021 Oct 2;10(10):2636. doi: 10.3390/cells10102636. Cells. 2021. PMID: 34685616 Free PMC article.
-
Multi-phased Kinetics and Interaction of Protein Kinase Signaling in Glycoprotein VI-Induced Platelet αIIbβ3 Integrin Activation and Degranulation.Thromb Haemost. 2025 May;125(5):470-483. doi: 10.1055/a-2311-0117. Epub 2024 Apr 23. Thromb Haemost. 2025. PMID: 38653482 Free PMC article.
-
Development of a Time-Resolved Fluorescence Resonance Energy Transfer ultra-high throughput screening assay for targeting SYK and FCER1G interaction.bioRxiv [Preprint]. 2024 Jun 13:2024.06.11.598473. doi: 10.1101/2024.06.11.598473. bioRxiv. 2024. Update in: SLAS Discov. 2024 Sep;29(6):100177. doi: 10.1016/j.slasd.2024.100177. PMID: 38915662 Free PMC article. Updated. Preprint.
-
Immunoreceptor signaling.Cold Spring Harb Perspect Biol. 2011 Dec 1;3(12):a011510. doi: 10.1101/cshperspect.a011510. Cold Spring Harb Perspect Biol. 2011. PMID: 22134888 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous