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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1994-8-4
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pubmed:abstractText |
We have developed a new model to study B cell activation induced by complex particulate Ag, immune complexes, and viruses. As the surrogate for such Ag, we have used 100-nm fluorescent latex beads bearing mAb to IgM and IgD. Anti-IgM- and anti-IgD-coated small latex beads bind readily to tonsil resting B cells and induce homotypic B cell aggregation. Aggregation induced by anti-IgM-coated beads but not by anti-IgD-coated beads was massively enhanced by IL-2 and IL-4. Anti-IgM- and anti-IgD-coated beads increased (4- to 12-fold) c-fos and c-myc mRNA levels in resting B cells in a dose-dependent manner; this increase was tyrosine kinase dependent. Anti-IgM- and anti-IgD-coated beads were mitogenic for resting B cells, but unlike other B cell activation models, mitogenesis was absolutely dependent on the presence of IL-2 or IL-4. Finally, anti-IgM-coated beads but not anti-IgD-coated beads were internalized as single beads into small, thin-walled endocytic vesicles; internalization was absolutely dependent on the presence of IL-4. Binding and internalization can be readily quantified because the beads are fluorescent. This model can also be used to study the functions of other cell surface molecules that modulate Ag-specific B cell immune responses. It will also be used for examining multiple aspects of T-B cell interactions during immune responses and Ag processing because of the dependence on T cell factors for B cell activation, coupled with the finding that the Ab-coated beads are internalized.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Anti-Idiotypic,
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2,
http://linkedlifedata.com/resource/pubmed/chemical/Latex,
http://linkedlifedata.com/resource/pubmed/chemical/anti-IgD,
http://linkedlifedata.com/resource/pubmed/chemical/anti-IgM
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
153
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
604-14
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:8021498-Animals,
pubmed-meshheading:8021498-Antibodies, Anti-Idiotypic,
pubmed-meshheading:8021498-Antibodies, Monoclonal,
pubmed-meshheading:8021498-B-Lymphocytes,
pubmed-meshheading:8021498-Base Sequence,
pubmed-meshheading:8021498-Endocytosis,
pubmed-meshheading:8021498-Genes, fos,
pubmed-meshheading:8021498-Genes, myc,
pubmed-meshheading:8021498-Humans,
pubmed-meshheading:8021498-Interleukin-2,
pubmed-meshheading:8021498-Latex,
pubmed-meshheading:8021498-Lymphocyte Activation,
pubmed-meshheading:8021498-Mice,
pubmed-meshheading:8021498-Molecular Sequence Data,
pubmed-meshheading:8021498-T-Lymphocytes
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pubmed:year |
1994
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pubmed:articleTitle |
T cell-dependent, B cell-activating properties of antibody-coated small latex beads. A new model for B cell activation.
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pubmed:affiliation |
Department of Immunology, Scripps Research Institute, La Jolla, CA 92037.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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