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PMID: 315845 Published · ppublish English Journal Article

Receptors for IgM on human lymphocytes. II. Mitogen-induced modulation of receptor expression.

Clinical and experimental immunology ·Vol. 37 ·No. 3 ·1979-09-00 ·Pages 486-94

Lydyard PM, Fanger MW

Abstract

Human peripheral lymphocytes undergoing blastogenesis induced by phytohaemagglutinin (PHA) or concanavalin A did not express receptors for the Fc portion of IgM (RFcmu). Furthermore, treatment of lymphocytes with PHA produced a dose-dependent loss of RFcmu which began as early as 5 hr after exposure to the mitogen. Within 24 hr after the addition of PHA, the percentage of lymphocytes expressing RFcmu had decreased from 65% to 4%. Under the same conditions of treatment, the expression of the receptor for sheep erythrocytes (E) was unchanged. These findings seemed inconsistent with a direct blocking effect of PHA but suggested that PHA induced a time-dependent modulation (switch off) of expression of RFcmu. Pronase cleavage of surface proteins on cells incubated with PHA for 24 hr followed by overnight incubation showed an almost complete irreversibility of RFcmu modulation up to 72 hr later. Studies using T cells isolated by E-rosetting showed that RFcmu modulation predominantly occurred on T cells. The modulation of RFcmu expression is discussed in terms of its possible role in the immune response.

MeSH Terms
Humans Immunoglobulin G/immunology Immunoglobulin M/immunology Lymphocyte Activation Lymphocytes/immunology Mitogens/pharmacology Phytohemagglutinins/pharmacology Pronase/pharmacology Receptors, Fc/immunology Rosette Formation T-Lymphocytes/immunology Time Factors
Chemicals
Immunoglobulin G Immunoglobulin M Mitogens Phytohemagglutinins Receptors, Fc Pronase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Lydyard P M
Fanger M W
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14 references, click to expand
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Article Info
Journal
Clinical and experimental immunology
Abbr.
Clin Exp Immunol
ISSN
0009-9104
Published
1979-09-00
Pages
486-94
Language
English
Region
England
NLM ID
0057202
PMCID
PMC1537787
Subset
IM
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