pubmed-article:7514872 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:7514872 | lifeskim:mentions | umls-concept:C0330390 | lld:lifeskim |
pubmed-article:7514872 | lifeskim:mentions | umls-concept:C0125090 | lld:lifeskim |
pubmed-article:7514872 | lifeskim:mentions | umls-concept:C0027950 | lld:lifeskim |
pubmed-article:7514872 | lifeskim:mentions | umls-concept:C0008013 | lld:lifeskim |
pubmed-article:7514872 | lifeskim:mentions | umls-concept:C0441471 | lld:lifeskim |
pubmed-article:7514872 | lifeskim:mentions | umls-concept:C0017262 | lld:lifeskim |
pubmed-article:7514872 | lifeskim:mentions | umls-concept:C1710082 | lld:lifeskim |
pubmed-article:7514872 | lifeskim:mentions | umls-concept:C0851285 | lld:lifeskim |
pubmed-article:7514872 | lifeskim:mentions | umls-concept:C2911684 | lld:lifeskim |
pubmed-article:7514872 | lifeskim:mentions | umls-concept:C0185117 | lld:lifeskim |
pubmed-article:7514872 | pubmed:dateCreated | 1994-6-17 | lld:pubmed |
pubmed-article:7514872 | pubmed:abstractText | Neutrophils express receptors for numerous phlogistons which, when occupied, trigger distinct signal-transduction pathways. Previous studies have shown that stimulation of neutrophils with chemoattractants induces shedding of the adhesive molecule L-selectin and increased expression of the beta 2-integrin CD11b/CD18. We determined the effect of ligation of classic, G-protein-linked chemoattractant receptors [C5a, interleukin-8 (IL-8), formylmethionyl-leucylphenylalanine (FMLP) and substance P], receptors for the Fc portion of IgG (Fc gamma receptors) and receptors for transforming growth factor beta (TGF beta) on expression of adhesive molecules by neutrophils and the stimulus-transduction mechanisms thought to mediate these changes. We were surprised to observe that occupancy of Fc gamma receptors by immunocomplexes (BSA-anti-BSA) stimulated increased expression by neutrophils of CD11b/CD18 at concentrations which did not affect L-selectin expression (EC50 9 micrograms/ml versus 350 micrograms/ml respectively, P < 0.00001, n = 5). In contrast, similar to previous studies, recombinant C5a, recombinant IL-8 and FMLP all stimulated increased expression of CD11b/CD18 (170-260% of basal, P < 0.001, n = 5) and shedding of L-selectin (56-75% reduction from basal, P < 0.001, n = 5) at similar concentrations and with similar potencies (EC50 = 2, 5, and 3 nM respectively). In contrast, neither TGF beta 1 nor, surprisingly, substance P affected expression of CD11b/CD18 or L-selectin. The regulation of expression of CD11b/CD18 or L-selectin in response to FMLP or immunocomplexes was unaffected by cytochalasin B (5 micrograms/ml) or the tyrosine kinase inhibitor tyrphostin-25 (25 microM). Although occupancy of both chemoattractant (FMLP) and Fc gamma receptors stimulated increments in the second messenger diacylglycerol, disruption of actin microfilaments by cytochalasin B enhanced diacylglycerol generation in response to FMLP but not in response to ligation of Fc gamma receptors. Moreover, both FMLP and immune aggregates provoked fluxes of intracellular Ca2+ concentration which differed with respect to both magnitude and kinetics and did not correlate well with regulation of adhesive-molecule expression. As upregulation of CD11b/CD18 is tightly linked to exocytosis of specific granules, these results suggest that shedding of L-selectin by activated neutrophils is not linked to exocytosis. These studies provide further evidence that receptors for chemoattractants and immunocomplexes on the neutrophil are linked to multiple signalling pathways. | lld:pubmed |
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pubmed-article:7514872 | pubmed:language | eng | lld:pubmed |
pubmed-article:7514872 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7514872 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:7514872 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7514872 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:7514872 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:7514872 | pubmed:month | May | lld:pubmed |
pubmed-article:7514872 | pubmed:issn | 0264-6021 | lld:pubmed |
pubmed-article:7514872 | pubmed:author | pubmed-author:AndersonD CDC | lld:pubmed |
pubmed-article:7514872 | pubmed:author | pubmed-author:CronsteinB... | lld:pubmed |
pubmed-article:7514872 | pubmed:author | pubmed-author:BuyonJ PJP | lld:pubmed |
pubmed-article:7514872 | pubmed:author | pubmed-author:HainesK AKA | lld:pubmed |
pubmed-article:7514872 | pubmed:author | pubmed-author:MoladYY | lld:pubmed |
pubmed-article:7514872 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:7514872 | pubmed:day | 1 | lld:pubmed |
pubmed-article:7514872 | pubmed:volume | 299 ( Pt 3) | lld:pubmed |
pubmed-article:7514872 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:7514872 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:7514872 | pubmed:pagination | 881-7 | lld:pubmed |
pubmed-article:7514872 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:7514872 | pubmed:year | 1994 | lld:pubmed |