Cited by 106Immune Cell Function and InteractionMonoclonal and Polyclonal Antibodies ResearchT-cell and B-cell Immunology

Stimulation of Fc gamma RIIIA results in phospholipase C-gamma 1 tyrosine phosphorylation and p56lck activation.

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Azzoni, L, Kamoun, M, Salcedo, T W, Kanakaraj, P, Perussia, B·1992·The Journal of experimental medicine

Abstract

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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Crossref · 10.1084/jem.176.6.1745

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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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Authors
Azzoni, L., Kamoun, M., Salcedo, T. W., Kanakaraj, P., & Perussia, B.
Affiliations
Thomas Jefferson University (US)
Venue
The Journal of experimental medicine
Published
1992-12-01
Volume
176
Issue
6
Pages
1745-1750
ISSN
  • 0022-1007 (ISSN-L)
  • 1540-9538
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
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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