pubmed-article:3259253 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:3259253 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
pubmed-article:3259253 | lifeskim:mentions | umls-concept:C0027950 | lld:lifeskim |
pubmed-article:3259253 | lifeskim:mentions | umls-concept:C0008013 | lld:lifeskim |
pubmed-article:3259253 | lifeskim:mentions | umls-concept:C0064833 | lld:lifeskim |
pubmed-article:3259253 | lifeskim:mentions | umls-concept:C0795657 | lld:lifeskim |
pubmed-article:3259253 | lifeskim:mentions | umls-concept:C0439855 | lld:lifeskim |
pubmed-article:3259253 | lifeskim:mentions | umls-concept:C0021469 | lld:lifeskim |
pubmed-article:3259253 | pubmed:issue | 5 | lld:pubmed |
pubmed-article:3259253 | pubmed:dateCreated | 1988-6-16 | lld:pubmed |
pubmed-article:3259253 | pubmed:abstractText | An inhibitor-proteinase complex consisting of human alpha 1-PI and human leukocyte elastase is chemotactic for human neutrophils. The chemotactic activity is optimal at 1 nM and is associated only with the alpha 1-PI portion of the complex. Neither HLE in the complex, free HLE, nor native alpha 1-PI possesses chemotactic activity for human neutrophils. alpha 1-PI in complex is hydrolyzed at the Met-358-Ser-359 bond. The chemotactic activity is associated with the Mr 4,200 fragment of alpha 1-PI that has Ser-359 as its NH2 terminus. The region of the HLE-alpha 1-PI complex that stimulates chemotaxis appears to be the same as that of the Mr 4,200 fragment generated by hydrolysis of the Pro-357-Met-358 bond during proteolytic inactivation of alpha 1-PI. The data suggest the presence of a neutrophil surface receptor bound by alpha 1-PI after the formation of a complex with HLE or after proteolytic degradation. This receptor may play a role in clearance of these modified alpha 1-PI molecules. | lld:pubmed |
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pubmed-article:3259253 | pubmed:language | eng | lld:pubmed |
pubmed-article:3259253 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:3259253 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:3259253 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:3259253 | pubmed:month | May | lld:pubmed |
pubmed-article:3259253 | pubmed:issn | 0022-1007 | lld:pubmed |
pubmed-article:3259253 | pubmed:author | pubmed-author:SeniorR MRM | lld:pubmed |
pubmed-article:3259253 | pubmed:author | pubmed-author:RiceA GAG | lld:pubmed |
pubmed-article:3259253 | pubmed:author | pubmed-author:GriffinG LGL | lld:pubmed |
pubmed-article:3259253 | pubmed:author | pubmed-author:BandaM JMJ | lld:pubmed |
pubmed-article:3259253 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:3259253 | pubmed:day | 1 | lld:pubmed |
pubmed-article:3259253 | pubmed:volume | 167 | lld:pubmed |
pubmed-article:3259253 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:3259253 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:3259253 | pubmed:pagination | 1608-15 | lld:pubmed |
pubmed-article:3259253 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:3259253 | pubmed:year | 1988 | lld:pubmed |
pubmed-article:3259253 | pubmed:articleTitle | The inhibitory complex of human alpha 1-proteinase inhibitor and human leukocyte elastase is a neutrophil chemoattractant. | lld:pubmed |
pubmed-article:3259253 | pubmed:affiliation | Laboratory of Radiobiology and Environmental Health, University of California, San Francisco 94143. | lld:pubmed |
pubmed-article:3259253 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:3259253 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:3259253 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
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