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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1994-10-18
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pubmed:abstractText |
Whether specific binding sites for endothelin-1 and endothelin-3 exist in mouse bone marrow-derived mast cells (BMMC) and if these endothelins are capable of stimulating chemical mediator release from the cells was investigated. A single component of binding sites for endothelin-1 was found in the cells, but no binding sites for endothelin-3 were observed. Endothelin-1 at 1-100 nM concentration dependently induced release of histamine and immunoreactive leukotriene C4 from BMMC, while endothelin-3 at up to 100 nM did not stimulate the release of either mediator. Time course experiments revealed that the release of histamine and immunoreactive leukotriene C4 induced by endothelin-1 occurred rapidly, reaching near maximal levels within 20 s and 2 min, respectively, after the stimulation, while histamine release induced by antigen, at the concentration which induced an extent of release similar to that induced by 100 nM endothelin-1, required comparatively prolonged incubation (approximately 10 min for submaximal levels). Cyclo(D-Asp-Pro-D-Val-Leu-D-Trp) (BQ-123), a selective antagonist of endothelin ETA receptors, not only dissociated [125I]endothelin-1 specifically bound to BMMC but also inhibited the release of both mediators from endothelin-1-induced cells. These results suggested strongly that BMMC have endothelin ETA receptors on their cell membrane, stimulation of which leads to chemical mediator release, probably via a mechanism different from that involved in the antigen-induced release.
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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/Calcimycin,
http://linkedlifedata.com/resource/pubmed/chemical/Endothelins,
http://linkedlifedata.com/resource/pubmed/chemical/Leukotriene C4,
http://linkedlifedata.com/resource/pubmed/chemical/Peptides, Cyclic,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Endothelin,
http://linkedlifedata.com/resource/pubmed/chemical/cyclo(Trp-Asp-Pro-Val-Leu)
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0014-2999
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
23
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pubmed:volume |
257
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
235-42
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pubmed:dateRevised |
2003-11-14
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pubmed:meshHeading |
pubmed-meshheading:7522171-Animals,
pubmed-meshheading:7522171-Binding Sites,
pubmed-meshheading:7522171-Bone Marrow,
pubmed-meshheading:7522171-Bone Marrow Cells,
pubmed-meshheading:7522171-Calcimycin,
pubmed-meshheading:7522171-Cells, Cultured,
pubmed-meshheading:7522171-Chromatography, High Pressure Liquid,
pubmed-meshheading:7522171-Endothelins,
pubmed-meshheading:7522171-Histamine Release,
pubmed-meshheading:7522171-Immunization, Passive,
pubmed-meshheading:7522171-Leukotriene C4,
pubmed-meshheading:7522171-Male,
pubmed-meshheading:7522171-Mast Cells,
pubmed-meshheading:7522171-Mice,
pubmed-meshheading:7522171-Mice, Inbred BALB C,
pubmed-meshheading:7522171-Peptides, Cyclic,
pubmed-meshheading:7522171-Receptors, Endothelin
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pubmed:year |
1994
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pubmed:articleTitle |
Endothelin-1 induces release of histamine and leukotriene C4 from mouse bone marrow-derived mast cells.
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pubmed:affiliation |
Department of Pharmacology, Kyoto Pharmaceutical University, Japan.
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pubmed:publicationType |
Journal Article
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