Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:3755432rdf:typepubmed:Citationlld:pubmed
pubmed-article:3755432lifeskim:mentionsumls-concept:C0086418lld:lifeskim
pubmed-article:3755432lifeskim:mentionsumls-concept:C0027950lld:lifeskim
pubmed-article:3755432lifeskim:mentionsumls-concept:C0521449lld:lifeskim
pubmed-article:3755432lifeskim:mentionsumls-concept:C0025251lld:lifeskim
pubmed-article:3755432lifeskim:mentionsumls-concept:C0242485lld:lifeskim
pubmed-article:3755432lifeskim:mentionsumls-concept:C0392747lld:lifeskim
pubmed-article:3755432lifeskim:mentionsumls-concept:C0596235lld:lifeskim
pubmed-article:3755432lifeskim:mentionsumls-concept:C0443172lld:lifeskim
pubmed-article:3755432lifeskim:mentionsumls-concept:C0521115lld:lifeskim
pubmed-article:3755432pubmed:issue21lld:pubmed
pubmed-article:3755432pubmed:dateCreated1986-9-17lld:pubmed
pubmed-article:3755432pubmed:abstractTextThe activation of human neutrophils by chemotactic peptides evokes a rapid change in membrane potential and an increase in cytoplasmic Ca2+ levels. These events are followed up to a minute later by detectable levels of microbicidal agents formed by the oxidative burst. Except for the latter, the sequence of events has remained unclear. We report here that a new fluorescent Ca2+ indicator developed by R. Tsien, Indo-1, has allowed us to resolve the temporal relationship between the rapid and transient cytoplasmic Ca2+ rise and the membrane potential change and to do so on very small samples by using a fluorescence-activated cell sorter. We have adapted a FACS 440 for simultaneous single cell membrane depolarization and cytoplasmic [Ca2+] detection in human neutrophils upon stimulation with formyl-methionyl-leucyl-phenylalanine (fMLP). A membrane potential probe, dipentyloxacarbocyanine, allows us to determine that the membrane potential change is fMLP dose-dependent and apparently biphasic. The depolarization is maximal 40 s after stimulation. In contrast, cytosolic [Ca2+], while fMLP-dose dependent, is maximal at 10 s and already decreasing rapidly when the cell has reached its lowest potential. It can be measured with Indo-1 which has a fluorescence emission (lambda ex = 357 nm) maximum at 485 nm when Ca2+-free and 405 nm when Ca2+-liganded. The ratio of these fluorescences may then be calibrated in terms of cytoplasmic Ca2+ levels. Thus, Ca2+ release into the cytoplasm becomes the earliest evidence of neutrophil stimulation by fMLP and occurs in close association with an apparent membrane hyperpolarization.lld:pubmed
pubmed-article:3755432pubmed:granthttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:3755432pubmed:granthttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:3755432pubmed:granthttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:3755432pubmed:languageenglld:pubmed
pubmed-article:3755432pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:3755432pubmed:citationSubsetIMlld:pubmed
pubmed-article:3755432pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:3755432pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:3755432pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:3755432pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:3755432pubmed:statusMEDLINElld:pubmed
pubmed-article:3755432pubmed:monthJullld:pubmed
pubmed-article:3755432pubmed:issn0021-9258lld:pubmed
pubmed-article:3755432pubmed:authorpubmed-author:SimonsE RERlld:pubmed
pubmed-article:3755432pubmed:authorpubmed-author:LazzariK GKGlld:pubmed
pubmed-article:3755432pubmed:authorpubmed-author:ProtoP JPJlld:pubmed
pubmed-article:3755432pubmed:issnTypePrintlld:pubmed
pubmed-article:3755432pubmed:day25lld:pubmed
pubmed-article:3755432pubmed:volume261lld:pubmed
pubmed-article:3755432pubmed:ownerNLMlld:pubmed
pubmed-article:3755432pubmed:authorsCompleteYlld:pubmed
pubmed-article:3755432pubmed:pagination9710-3lld:pubmed
pubmed-article:3755432pubmed:dateRevised2007-11-14lld:pubmed
pubmed-article:3755432pubmed:meshHeadingpubmed-meshheading:3755432-...lld:pubmed
pubmed-article:3755432pubmed:meshHeadingpubmed-meshheading:3755432-...lld:pubmed
pubmed-article:3755432pubmed:meshHeadingpubmed-meshheading:3755432-...lld:pubmed
pubmed-article:3755432pubmed:meshHeadingpubmed-meshheading:3755432-...lld:pubmed
pubmed-article:3755432pubmed:meshHeadingpubmed-meshheading:3755432-...lld:pubmed
pubmed-article:3755432pubmed:meshHeadingpubmed-meshheading:3755432-...lld:pubmed
pubmed-article:3755432pubmed:meshHeadingpubmed-meshheading:3755432-...lld:pubmed
pubmed-article:3755432pubmed:meshHeadingpubmed-meshheading:3755432-...lld:pubmed
pubmed-article:3755432pubmed:meshHeadingpubmed-meshheading:3755432-...lld:pubmed
pubmed-article:3755432pubmed:year1986lld:pubmed
pubmed-article:3755432pubmed:articleTitleSimultaneous measurement of stimulus-induced changes in cytoplasmic Ca2+ and in membrane potential of human neutrophils.lld:pubmed
pubmed-article:3755432pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:3755432pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:3755432lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:3755432lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:3755432lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:3755432lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:3755432lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:3755432lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:3755432lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:3755432lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:3755432lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:3755432lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:3755432lld:pubmed