Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:8864571rdf:typepubmed:Citationlld:pubmed
pubmed-article:8864571lifeskim:mentionsumls-concept:C0225336lld:lifeskim
pubmed-article:8864571lifeskim:mentionsumls-concept:C1383501lld:lifeskim
pubmed-article:8864571lifeskim:mentionsumls-concept:C0026237lld:lifeskim
pubmed-article:8864571lifeskim:mentionsumls-concept:C0037083lld:lifeskim
pubmed-article:8864571lifeskim:mentionsumls-concept:C0006100lld:lifeskim
pubmed-article:8864571lifeskim:mentionsumls-concept:C0242485lld:lifeskim
pubmed-article:8864571lifeskim:mentionsumls-concept:C1710082lld:lifeskim
pubmed-article:8864571lifeskim:mentionsumls-concept:C1948023lld:lifeskim
pubmed-article:8864571lifeskim:mentionsumls-concept:C0596235lld:lifeskim
pubmed-article:8864571lifeskim:mentionsumls-concept:C0242842lld:lifeskim
pubmed-article:8864571pubmed:issue1lld:pubmed
pubmed-article:8864571pubmed:dateCreated1996-12-16lld:pubmed
pubmed-article:8864571pubmed:abstractTextIn this study we have monitored the change of intracellular Ca2+ concentrations in the cytosol ([Ca2+]c) and the mitochondria ([Ca2+]m) of single bovine endothelial cells following treatment with bradykinin (BK). Using laser scanning confocal microscopy, we have found that the Ca2+ indicator, Fluo-3, is compartmentalized in the mitochondria of endothelial cells loaded with Fluo-3/AM. After BK stimulation, the pattern of Ca2+ increase in the cytosol is different from that in the mitochondria. The amplitude of the Ca2+ rise in the mitochondria is higher than that in the cytosol. Further analysis using rapid scanning measurements indicates that the [Ca2+]c increase is very fast after BK addition and reaches a maxima level within 400 ms. In contrast, the [Ca2+]m increase appears to be biphasic with an initial rapid increase (concomitant with the [Ca2+]c increase) followed by a slower [Ca2+]m increase before reaching a maximal level (within 5 s of BK treatment). The differential Ca2+ signaling pattern between the cytosol and the mitochondria suggests that the intracellular Ca2+ concentrations needed to regulate various Ca(2+)-dependent enzymes located in these two compartments are different during BK-induced endothelial cell activation.lld:pubmed
pubmed-article:8864571pubmed:granthttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8864571pubmed:granthttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8864571pubmed:languageenglld:pubmed
pubmed-article:8864571pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8864571pubmed:citationSubsetIMlld:pubmed
pubmed-article:8864571pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8864571pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8864571pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8864571pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8864571pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8864571pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:8864571pubmed:statusMEDLINElld:pubmed
pubmed-article:8864571pubmed:monthJullld:pubmed
pubmed-article:8864571pubmed:issn0143-4160lld:pubmed
pubmed-article:8864571pubmed:authorpubmed-author:BourguignonL...lld:pubmed
pubmed-article:8864571pubmed:authorpubmed-author:DonnadieuEElld:pubmed
pubmed-article:8864571pubmed:issnTypePrintlld:pubmed
pubmed-article:8864571pubmed:volume20lld:pubmed
pubmed-article:8864571pubmed:ownerNLMlld:pubmed
pubmed-article:8864571pubmed:authorsCompleteYlld:pubmed
pubmed-article:8864571pubmed:pagination53-61lld:pubmed
pubmed-article:8864571pubmed:dateRevised2007-11-14lld:pubmed
pubmed-article:8864571pubmed:meshHeadingpubmed-meshheading:8864571-...lld:pubmed
pubmed-article:8864571pubmed:meshHeadingpubmed-meshheading:8864571-...lld:pubmed
pubmed-article:8864571pubmed:meshHeadingpubmed-meshheading:8864571-...lld:pubmed
pubmed-article:8864571pubmed:meshHeadingpubmed-meshheading:8864571-...lld:pubmed
pubmed-article:8864571pubmed:meshHeadingpubmed-meshheading:8864571-...lld:pubmed
pubmed-article:8864571pubmed:meshHeadingpubmed-meshheading:8864571-...lld:pubmed
pubmed-article:8864571pubmed:meshHeadingpubmed-meshheading:8864571-...lld:pubmed
pubmed-article:8864571pubmed:meshHeadingpubmed-meshheading:8864571-...lld:pubmed
pubmed-article:8864571pubmed:meshHeadingpubmed-meshheading:8864571-...lld:pubmed
pubmed-article:8864571pubmed:meshHeadingpubmed-meshheading:8864571-...lld:pubmed
pubmed-article:8864571pubmed:meshHeadingpubmed-meshheading:8864571-...lld:pubmed
pubmed-article:8864571pubmed:meshHeadingpubmed-meshheading:8864571-...lld:pubmed
pubmed-article:8864571pubmed:meshHeadingpubmed-meshheading:8864571-...lld:pubmed
pubmed-article:8864571pubmed:meshHeadingpubmed-meshheading:8864571-...lld:pubmed
pubmed-article:8864571pubmed:year1996lld:pubmed
pubmed-article:8864571pubmed:articleTitleCa2+ signaling in endothelial cells stimulated by bradykinin: Ca2+ measurement in the mitochondria and the cytosol by confocal microscopy.lld:pubmed
pubmed-article:8864571pubmed:affiliationDepartment of Cell Biology and Anatomy, University of Miami Medical School, Florida 33101, USA.lld:pubmed
pubmed-article:8864571pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8864571pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
pubmed-article:8864571pubmed:publicationTypeResearch Support, U.S. Gov't, Non-P.H.S.lld:pubmed
pubmed-article:8864571pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:8864571lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:8864571lld:pubmed