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PMID: 1387672 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Induction of tumor necrosis factor-alpha production by mast cells via Fc gamma R. Role of the Fc gamma RIII gamma subunit.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 149 ·No. 6 ·1992-09-15 ·Pages 2155-62

Latour S, Bonnerot C, Fridman WH, Daëron M

Abstract

Murine mast cells produce cytokines in response to cross-linking of high affinity receptors for IgE (Fc epsilon RI). Murine mast cells also express the two types of low-affinity receptors for IgG, murine (m)Fc gamma RII, and mFc gamma RIII. We examined the ability of mFc gamma R to trigger a cytokine response such as TNF-alpha production by mast cells. We found that the mFc gamma RII- and mFc gamma RIII-positive mouse mastocytoma cells MMC-1 released TNF-alpha when challenged with F(ab')2 fragments of the rat anti-mFc gamma RII/III 2.4G2 mAb and mouse anti-rat IgG F(ab')2. The release of TNF-alpha was preceded by an increase in TNF-alpha transcripts. mFc gamma RII and mFc gamma RIII have 95% homologous extracellular domains but unrelated transmembrane and intracytoplasmic (IC) domains. mFc gamma RII are single chain receptors whereas mFc gamma RIII associate with a homodimeric gamma-chain that also associates with Fc epsilon RI and TCR. In order to analyze the ability of mFc gamma RII and III to trigger the synthesis of TNF-alpha, we studied RBL-2H3 cells transfected with corresponding cDNA. Rat basophilic leukemia (RBL) transfectants expressing mFc gamma RIII produced TNF-alpha in response to 2.4G2 F(ab')2, but not transfectants expressing mFc gamma RII. Non-transfected RBL cells and mFc gamma RII- or mFc gamma RIII-expressing transfectants, however, released TNF-alpha in response to a rat IgG2a mAb. The respective roles of the alpha and gamma subunits of mFc gamma RIII were examined by studying the production of TNF-alpha by RBL cells expressing deletant and chimeric mFc gamma R. The deletion of intracellular amino acids of the Fc gamma RIII alpha subunit did not prevent 2.4G2 F(ab')2 from triggering the synthesis of TNF-alpha. The substitution of the IC domain of mFc gamma RII for that of mFc gamma RIII gamma, but not that of Fc gamma RIII alpha, enabled 2.4G2 F(ab')2 to trigger the release of TNF-alpha by RBL transfectants. A cytokine response can therefore be induced in mouse and rat mast cells through Fc gamma R. This response is triggered upon cross-linking of mFc gamma RIII but not mFc gamma RII. It depends on the IC sequences of the gamma but not of the alpha subunit of mFc gamma RIII.

MeSH Terms
Animals Antigens, Differentiation/physiology Base Sequence DNA Mutational Analysis Gene Expression In Vitro Techniques L Cells Mast Cells/metabolism Mice Molecular Sequence Data Oligodeoxyribonucleotides/chemistry RNA, Messenger/genetics Rats Receptors, Fc/physiology Receptors, IgG Structure-Activity Relationship Tumor Cells, Cultured Tumor Necrosis Factor-alpha/biosynthesis,genetics
Chemicals
Antigens, Differentiation Oligodeoxyribonucleotides RNA, Messenger Receptors, Fc Receptors, IgG Tumor Necrosis Factor-alpha
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Latour S
Laboratoire d'Immunologie Cellulaire et Clinique, INSERM U. 255, Institut Curie, Paris, France.
Bonnerot C
Fridman W H
Daëron M
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1992-09-15
Pages
2155-62
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
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