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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
1989-10-20
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pubmed:abstractText |
The murine B cell FcR for IgG (Fc gamma RII) is a membrane glycoprotein reported to mediate inhibition of B cell activation and differentiation. We show that IL-4 inhibits the enhanced expression of Fc gamma RII by LPS-stimulated B cells. This activity is completely reversed by anti-IL-4 mAb and is specific, in that multiple other lymphokines tested do not exert a similar effect. This effect of IL-4 is apparent by day 1 of culture, although maximal inhibition occurs on day 4 at a concentration of 500 U/ml. The IL-4-induced inhibition of enhanced Fc gamma RII expression by LPS stimulation observed on day 4 of culture is associated with a significant reduction in the steady state level of Fc gamma RII beta gene-specific mRNA. IFN-gamma which inhibits many of the effects of IL-4 on B cells, does not reverse the IL-4-induced inhibition of Fc gamma RII membrane expression nor the levels of beta gene-specific mRNA. Fc gamma RII expression is significantly increased in B cells stimulated with antigen-specific, CD4+ T cell clones of the Th1 type (i.e., IL-2 and IFN-gamma-producing). By contrast, three different Th2 clones (i.e., IL-4-producing) fail to stimulate an increase in Fc gamma RII levels. Anti-IL-4 mAb significantly enhanced Fc gamma RII expression by Th2-stimulated B cells indicating that IL-4 was the active, inhibitory, substance produced by the Th2 cells. Supernatants from stimulated Th2 clones inhibited the enhanced expression of Fc gamma RII by LPS-stimulated B cells and this activity was completely reversed by anti-IL-4 mAb. By contrast, supernatants from stimulated Th1 clones further enhanced Fc gamma RII expression by LPS-stimulated B cells. The differential regulation of B cell Fc gamma RII expression by Th subsets may play an important role in the regulation of humoral immunity by altering the sensitivity of B cells to IgG immune complex-mediated inhibition of B cell activation and differentiation in vivo.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Differentiation,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Differentiation...,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin G,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-4,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukins,
http://linkedlifedata.com/resource/pubmed/chemical/Lipopolysaccharides,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Fc,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, IgG
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
143
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2133-41
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:2528589-Animals,
pubmed-meshheading:2528589-Antigens, Differentiation,
pubmed-meshheading:2528589-Antigens, Differentiation, T-Lymphocyte,
pubmed-meshheading:2528589-B-Lymphocytes,
pubmed-meshheading:2528589-Binding, Competitive,
pubmed-meshheading:2528589-Cell Line,
pubmed-meshheading:2528589-Female,
pubmed-meshheading:2528589-Genes, Immunoglobulin,
pubmed-meshheading:2528589-Immunoglobulin G,
pubmed-meshheading:2528589-Interferon-gamma,
pubmed-meshheading:2528589-Interleukin-4,
pubmed-meshheading:2528589-Interleukins,
pubmed-meshheading:2528589-Kinetics,
pubmed-meshheading:2528589-Lipopolysaccharides,
pubmed-meshheading:2528589-Lymphocyte Activation,
pubmed-meshheading:2528589-Membrane Proteins,
pubmed-meshheading:2528589-Mice,
pubmed-meshheading:2528589-Mice, Inbred C3H,
pubmed-meshheading:2528589-Mice, Inbred DBA,
pubmed-meshheading:2528589-Phenotype,
pubmed-meshheading:2528589-RNA, Messenger,
pubmed-meshheading:2528589-Receptors, Fc,
pubmed-meshheading:2528589-Receptors, IgG,
pubmed-meshheading:2528589-T-Lymphocytes, Helper-Inducer
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pubmed:year |
1989
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pubmed:articleTitle |
Differential regulation of murine B cell Fc gamma RII expression by CD4+ T helper subsets.
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pubmed:affiliation |
Department of Pathology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.
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