| pubmed-article:6251879 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:6251879 | lifeskim:mentions | umls-concept:C0010737 | lld:lifeskim |
| pubmed-article:6251879 | lifeskim:mentions | umls-concept:C0441471 | lld:lifeskim |
| pubmed-article:6251879 | lifeskim:mentions | umls-concept:C0242599 | lld:lifeskim |
| pubmed-article:6251879 | lifeskim:mentions | umls-concept:C1524063 | lld:lifeskim |
| pubmed-article:6251879 | lifeskim:mentions | umls-concept:C0205087 | lld:lifeskim |
| pubmed-article:6251879 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:6251879 | pubmed:dateCreated | 1980-12-18 | lld:pubmed |
| pubmed-article:6251879 | pubmed:abstractText | Cytochalasin B greatly enhances secretion of beta-glucuronidase and generation of superoxide on stimulation of rabbit peritoneal neutrophils with the soluble chemotactic factor N-formylmethionylleucylphenylalanine (f-Met-Leu-Phe). There are smaller changes due to cytochalasin B on binding of f-Met-Leu-[(3)H]-Phe, stimulation of phosphatidylinositol turnover and the stimulated increase in the permeability of the cell membrane to Ca(2+). These latter changes are probably artefactual and arise as secondary consequences of cell stimulation. Our observations support the notion that changes in Ca(2+) permeability of membranes and stimulation of phosphatidylinositol turnover reflect early stages in the sequence of events initiated by f-Met-Leu-Phe binding to its receptor and which lead to cell activation phenomena such as secretion and superoxide production. | lld:pubmed |
| pubmed-article:6251879 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:6251879 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:6251879 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:6251879 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:6251879 | pubmed:issn | 0006-3002 | lld:pubmed |
| pubmed-article:6251879 | pubmed:author | pubmed-author:CockcroftSS | lld:pubmed |
| pubmed-article:6251879 | pubmed:author | pubmed-author:GompertsB DBD | lld:pubmed |
| pubmed-article:6251879 | pubmed:author | pubmed-author:BennettJ PJP | lld:pubmed |
| pubmed-article:6251879 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:6251879 | pubmed:day | 2 | lld:pubmed |
| pubmed-article:6251879 | pubmed:volume | 601 | lld:pubmed |
| pubmed-article:6251879 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:6251879 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:6251879 | pubmed:pagination | 584-91 | lld:pubmed |
| pubmed-article:6251879 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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| pubmed-article:6251879 | pubmed:year | 1980 | lld:pubmed |
| pubmed-article:6251879 | pubmed:articleTitle | Use of cytochalasin B to distinguish between early and late events in neutrophil activation. | lld:pubmed |
| pubmed-article:6251879 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:6251879 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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