Stimulation of Fc gamma RIIIA results in phospholipase C-gamma 1 tyrosine phosphorylation and p56lck activation.
Open accessAbstract
Binding of ligand to the alpha subunit of Fc gamma RIIIA(CD16), expressed at the natural killer (NK) cell membrane in association with homo or heterodimers of proteins of the zeta family, results in phosphorylation of several proteins on tyrosine residues. We have analyzed the role of protein tyrosine phosphorylation in the regulation of molecular events induced upon stimulation of Fc gamma RIIIA in NK cells and in T cells expressing the Fc gamma RIII alpha chain in association with endogenous zeta 2 homodimers and devoid of other (CD3, CD2) transducing molecules. Our data indicate that treatment of these cells with protein tyrosine kinase inhibitors prevents not only Fc gamma RIIIA-induced protein tyrosine phosphorylation but also phosphatidylinositol 4,5 diphosphate hydrolysis and increased intracellular Ca2+ concentration, indicating a primary role of tyrosine kinase(s) in the induction of these early activation events. Occupancy of Fc gamma RIIIA by ligand results in phospholipase C (PLC)-gamma 1 tyrosine phosphorylation in NK cells and in Fc gamma RIIIA-transfected CD3-/CD2- T cells, and induces functional activation of p56lck in Fc gamma RIIIA alpha/zeta 2-transfected T cells, suggesting the possibility that the receptor-induced PLC-gamma 1 activation occurs upon phosphorylation of its tyrosine residues mediated by this kinase and is, at least in part, responsible for the signal transduction mediated via CD16 upon ligand binding.
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4,5-PIP2 is the primary substrate of PLCγ, which becomes activated upon engagement of FcγRs.
“In addition to its role as a direct docking site for skeletal proteins, 4,5-PIP2 is also the primary substrate of phospholipase Cγ (PLCγ), which was shown to become activated upon engagement of FcγRs (Azzoni et al. 1992; Liao et al. 1992).”
From Localized Biphasic Changes in Phosphatidylinositol-4,5-Bisphosphate at Sites of Phagocytosis (2000) · cites this paper as Azzoni et al. 1992
The discussion following Fig. 4 (p. 1748) says FcγRIIIA stimulation induces PLCγ1 tyrosine phosphorylation and strongly suggests that PLCγ1 activation may account for the observed PIP2 hydrolysis. This supports the proposed link, but the paper does not establish PLCγ1 activation directly or identify PIP2 as its primary substrate; its experiments concern FcγRIIIA rather than FcγRs generally. (LLM, conf=0.86)
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Phagocytosis and the actin cytoskeleton
May, R. C., & Machesky, L. M. (2001) · Journal of Cell Science · doi:10.1242/jcs.114.6.1061 · Cited by 715 · see citing works
Localized Biphasic Changes in Phosphatidylinositol-4,5-Bisphosphate at Sites of Phagocytosis
Botelho, R. J., Teruel, M., Dierckman, R., Anderson, R., Wells, A., York, J. D., Meyer, T., & Grinstein, S. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.151.7.1353 · Cited by 539 · see citing works
“PLCg Localizes to Phagocytic Cups Based on prior knowledge that PLCg undergoes tyrosine phosphorylation during FcgR cross-linking (Azzoni et al., 1992; Liao et al., 1992), we hypothesized that the phase of dissociation of PLCd-PH-GFP from phagosomes could be explained at least partly by…”
BackgroundPhospholipase C-γ2 Is a Critical Signaling Mediator for Murine NK Cell Activating Receptors
Tassi, I., Presti, R., Kim, S., Yokoyama, W. M., Gilfillan, S., & Colonna, M. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.2.749 · Cited by 121 · see citing works
- Authors
- Azzoni, L., Kamoun, M., Salcedo, T. W., Kanakaraj, P., & Perussia, B.
- Affiliations
- Thomas Jefferson University (US)
- Venue
- The Journal of experimental medicine
- Publisher
- Rockefeller University Press
- Published
- 1992-12-01
- Volume
- 176
- Issue
- 6
- Pages
- 1745-1750
- ISSN
- 0022-1007 (ISSN-L)
- 1540-9538
- PMC
- PMC2119466
- OpenAlex
- W2030655955
- Cited by
- 106
- References
- 0
- Citations by year
- 2023: 1 · 2022: 1 · 2021: 2 · 2019: 1 · 2018: 2 · 2016: 2 · 2014: 2 · 2013: 1 · 2012: 4
- FWCI
- 2.58
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- The Journal of Experimental Medicine (publishedVersion)
- PubMed Central (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- Funders
- Thomas Jefferson University
- National Institutes of Health (5r01ai020846-08, 5r01ca037155-13, 5r01ca045284-11)
- U.S. Public Health Service
- National Cancer Institute (CA 45284, CA37155)
- National Institute of Allergy and Infectious Diseases (AI 20846)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune Cell Function and Interaction
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Monoclonal and Polyclonal Antibodies Research
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Keywords
- CD16, phospholipase C-gamma1, Lck, tyrosine phosphorylation, protein tyrosine kinase inhibitors, phosphatidylinositol 4,5-bisphosphate hydrolysis, intracellular calcium, signal transduction, natural killer cells, T cells, zeta chain, receptor activation
- MeSH terms
- Antibodies, Monoclonal, Cell Membrane, Humans, Isoenzymes, Killer Cells, Natural, Type C Phospholipases, Phosphorylation, Protein-Tyrosine Kinases, Transfection, Tumor Cells, Cultured, Tyrosine, Receptors, IgG, Phosphotyrosine, Lymphocyte Specific Protein Tyrosine Kinase p56(lck), Macromolecular Substances
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