| pubmed-article:4610080 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:4610080 | lifeskim:mentions | umls-concept:C0085979 | lld:lifeskim |
| pubmed-article:4610080 | lifeskim:mentions | umls-concept:C0024297 | lld:lifeskim |
| pubmed-article:4610080 | lifeskim:mentions | umls-concept:C0597357 | lld:lifeskim |
| pubmed-article:4610080 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:4610080 | lifeskim:mentions | umls-concept:C1710082 | lld:lifeskim |
| pubmed-article:4610080 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:4610080 | lifeskim:mentions | umls-concept:C0205263 | lld:lifeskim |
| pubmed-article:4610080 | pubmed:issue | 6 | lld:pubmed |
| pubmed-article:4610080 | pubmed:dateCreated | 1975-2-18 | lld:pubmed |
| pubmed-article:4610080 | pubmed:abstractText | This study shows that bone marrow-derived lymphocytes of guinea pigs if appropriately activated produce a monocyte chemotactic factor (MNL CTX). Activation of B lymphocytes to produce a chemotactic lymphokine occurs subsequent to interactions with a variety of membrane-associated receptors. Polymeric B-cell mitogens with multiple binding sites, polymerized flagellin and lipopolysaccharide, initiated mediator synthesis. Furthermore, interaction of antigen-antibody complexes or aggregated gamma globulin with the Fc receptor and binding of antigen-antibody-complement complexes at the C3 receptor can effectively facilitate mediator production in the absence of a significant proliferative response. Additionally, intact anti-immunoglobulin but not its Fab fragments activated the B cells. An anti-Fab effectively converted the inactive Fab-bound B cells into producers of MNL CTX, suggesting that the basic mechanism of activation depended upon cross-linking of receptors. Thus, interaction of B-cell surface receptors such as Fc, Ig, and C3 sites with mitogenic as well as nonmitogenic molecules capable of bridging the receptors appears to trigger B-cell mediator production. | lld:pubmed |
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| pubmed-article:4610080 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:4610080 | pubmed:citationSubset | AIM | lld:pubmed |
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| pubmed-article:4610080 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:4610080 | pubmed:month | Dec | lld:pubmed |
| pubmed-article:4610080 | pubmed:issn | 0022-1007 | lld:pubmed |
| pubmed-article:4610080 | pubmed:author | pubmed-author:WahlS MSM | lld:pubmed |
| pubmed-article:4610080 | pubmed:author | pubmed-author:OppenheimJ... | lld:pubmed |
| pubmed-article:4610080 | pubmed:author | pubmed-author:IversonG MGM | lld:pubmed |
| pubmed-article:4610080 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:4610080 | pubmed:day | 1 | lld:pubmed |
| pubmed-article:4610080 | pubmed:volume | 140 | lld:pubmed |
| pubmed-article:4610080 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:4610080 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:4610080 | pubmed:pagination | 1631-45 | lld:pubmed |
| pubmed-article:4610080 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
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