rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
11
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pubmed:dateCreated |
1998-1-2
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pubmed:abstractText |
It is generally recognized that activation through membrane effector molecules such as CD40 or the B cell receptor (BCR) is mandatory to allow B cells to proliferate and differentiate into antibody (Ab)-secreting cells in response to cytokines. We show here that purified tonsillar B cells can be stimulated directly by a cytokine combination to proliferate and secrete immunoglobulins when cultures are performed at high cell density. The contact-mediated activation of B cells in this experimental system is strongly inhibited both by anti-very late antigen (VLA)-4 monoclonal Ab and by a peptide containing the LDV sequence specifically recognized by the alpha 4 integrin binding site. These reagents also significantly suppressed the B cell responses elicited by engagement of the BCR or CD40. Our data reveal that memory B cells but not virgin or germinal center B cells are sensitive to the direct stimulatory effect of cytokines in high-density cultures. Finally, we found that the dual expression of the alpha and beta chains of VLA-4 is a distinctive feature of the memory B cell population. Collectively, our findings support the notion that VLA-4-dependent homotypic B cell interactions can mediate a co-stimulatory signal to human memory B cells and might participate in the B cell activation triggered through the BCR and CD40.
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD40,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulins,
http://linkedlifedata.com/resource/pubmed/chemical/Integrin alpha4beta1,
http://linkedlifedata.com/resource/pubmed/chemical/Integrin beta Chains,
http://linkedlifedata.com/resource/pubmed/chemical/Integrins,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-10,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Lymphocyte Homing,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Very Late Antigen,
http://linkedlifedata.com/resource/pubmed/chemical/integrin beta7
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
|
pubmed:issn |
0014-2980
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pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
27
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
2757-64
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:9394796-Antigens, CD40,
pubmed-meshheading:9394796-B-Lymphocytes,
pubmed-meshheading:9394796-Cell Communication,
pubmed-meshheading:9394796-Cell Count,
pubmed-meshheading:9394796-Cell Differentiation,
pubmed-meshheading:9394796-Cells, Cultured,
pubmed-meshheading:9394796-Humans,
pubmed-meshheading:9394796-Immunoglobulins,
pubmed-meshheading:9394796-Immunologic Memory,
pubmed-meshheading:9394796-Integrin alpha4beta1,
pubmed-meshheading:9394796-Integrin beta Chains,
pubmed-meshheading:9394796-Integrins,
pubmed-meshheading:9394796-Interleukin-10,
pubmed-meshheading:9394796-Interleukin-2,
pubmed-meshheading:9394796-Lymphocyte Activation,
pubmed-meshheading:9394796-Receptors, Lymphocyte Homing,
pubmed-meshheading:9394796-Receptors, Very Late Antigen
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pubmed:year |
1997
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pubmed:articleTitle |
A role for the VLA-4 integrin in the activation of human memory B cells.
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pubmed:affiliation |
INSERM U 404, Immunité et Vaccination, Lyon, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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