Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:9526008rdf:typepubmed:Citationlld:pubmed
pubmed-article:9526008lifeskim:mentionsumls-concept:C0036536lld:lifeskim
pubmed-article:9526008lifeskim:mentionsumls-concept:C0036537lld:lifeskim
pubmed-article:9526008lifeskim:mentionsumls-concept:C0597357lld:lifeskim
pubmed-article:9526008lifeskim:mentionsumls-concept:C0085862lld:lifeskim
pubmed-article:9526008lifeskim:mentionsumls-concept:C1280500lld:lifeskim
pubmed-article:9526008lifeskim:mentionsumls-concept:C1299583lld:lifeskim
pubmed-article:9526008lifeskim:mentionsumls-concept:C0439064lld:lifeskim
pubmed-article:9526008lifeskim:mentionsumls-concept:C0596235lld:lifeskim
pubmed-article:9526008lifeskim:mentionsumls-concept:C0086597lld:lifeskim
pubmed-article:9526008lifeskim:mentionsumls-concept:C1608386lld:lifeskim
pubmed-article:9526008lifeskim:mentionsumls-concept:C1549571lld:lifeskim
pubmed-article:9526008lifeskim:mentionsumls-concept:C0441712lld:lifeskim
pubmed-article:9526008lifeskim:mentionsumls-concept:C0051403lld:lifeskim
pubmed-article:9526008pubmed:issue8lld:pubmed
pubmed-article:9526008pubmed:dateCreated1998-4-20lld:pubmed
pubmed-article:9526008pubmed:abstractTextalpha-Latrotoxin (alpha-Ltx), a component of black widow spider venom, stimulates secretion from nerve terminals and from PC12 cells. In this study we examine the effects of expression of a newly cloned Ca2+-independent receptor for alpha-Ltx (CIRL) on secretion from bovine chromaffin cells. We first characterized the effect of alpha-Ltx on secretion from untransfected cells. alpha-Ltx, by binding in a Ca2+-independent manner to an endogenous receptor, causes subsequent Ca2+-dependent secretion from intact cells. The stimulation of secretion is correlated with Ca2+ influx caused by the toxin. In permeabilized cells in which the Ca2+ concentration is regulated by buffer, alpha-Ltx also enhances Ca2+-dependent secretion, indicating a direct role of the endogenous receptor in the secretory pathway. Expression of CIRL increased the sensitivity of intact and permeabilized cells to the effects of alpha-Ltx, demonstrating that this protein is functional in coupling to secretion. Importantly, in the absence of alpha-Ltx, the expression of CIRL specifically inhibited the ATP-dependent component of secretion in permeabilized cells without affecting the ATP-independent secretion. This suggests that this receptor modulates the normal function of the regulated secretory pathway and that alpha-Ltx may act by reversing the inhibitory effects of the receptor.lld:pubmed
pubmed-article:9526008pubmed:granthttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:9526008pubmed:granthttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:9526008pubmed:granthttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:9526008pubmed:languageenglld:pubmed
pubmed-article:9526008pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:9526008pubmed:citationSubsetIMlld:pubmed
pubmed-article:9526008pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:9526008pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:9526008pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:9526008pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:9526008pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:9526008pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:9526008pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:9526008pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:9526008pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:9526008pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:9526008pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:9526008pubmed:statusMEDLINElld:pubmed
pubmed-article:9526008pubmed:monthAprlld:pubmed
pubmed-article:9526008pubmed:issn0270-6474lld:pubmed
pubmed-article:9526008pubmed:authorpubmed-author:HolzR WRWlld:pubmed
pubmed-article:9526008pubmed:authorpubmed-author:PetrenkoA GAGlld:pubmed
pubmed-article:9526008pubmed:authorpubmed-author:BittnerM AMAlld:pubmed
pubmed-article:9526008pubmed:authorpubmed-author:StuenkelE LELlld:pubmed
pubmed-article:9526008pubmed:authorpubmed-author:KrasnoperovV...lld:pubmed
pubmed-article:9526008pubmed:issnTypePrintlld:pubmed
pubmed-article:9526008pubmed:day15lld:pubmed
pubmed-article:9526008pubmed:volume18lld:pubmed
pubmed-article:9526008pubmed:ownerNLMlld:pubmed
pubmed-article:9526008pubmed:authorsCompleteYlld:pubmed
pubmed-article:9526008pubmed:pagination2914-22lld:pubmed
pubmed-article:9526008pubmed:dateRevised2007-11-14lld:pubmed
pubmed-article:9526008pubmed:meshHeadingpubmed-meshheading:9526008-...lld:pubmed
pubmed-article:9526008pubmed:meshHeadingpubmed-meshheading:9526008-...lld:pubmed
pubmed-article:9526008pubmed:meshHeadingpubmed-meshheading:9526008-...lld:pubmed
pubmed-article:9526008pubmed:meshHeadingpubmed-meshheading:9526008-...lld:pubmed
pubmed-article:9526008pubmed:meshHeadingpubmed-meshheading:9526008-...lld:pubmed
pubmed-article:9526008pubmed:meshHeadingpubmed-meshheading:9526008-...lld:pubmed
pubmed-article:9526008pubmed:meshHeadingpubmed-meshheading:9526008-...lld:pubmed
pubmed-article:9526008pubmed:meshHeadingpubmed-meshheading:9526008-...lld:pubmed
pubmed-article:9526008pubmed:meshHeadingpubmed-meshheading:9526008-...lld:pubmed
pubmed-article:9526008pubmed:meshHeadingpubmed-meshheading:9526008-...lld:pubmed
pubmed-article:9526008pubmed:meshHeadingpubmed-meshheading:9526008-...lld:pubmed
pubmed-article:9526008pubmed:meshHeadingpubmed-meshheading:9526008-...lld:pubmed
pubmed-article:9526008pubmed:meshHeadingpubmed-meshheading:9526008-...lld:pubmed
pubmed-article:9526008pubmed:meshHeadingpubmed-meshheading:9526008-...lld:pubmed
pubmed-article:9526008pubmed:meshHeadingpubmed-meshheading:9526008-...lld:pubmed
pubmed-article:9526008pubmed:meshHeadingpubmed-meshheading:9526008-...lld:pubmed
pubmed-article:9526008pubmed:meshHeadingpubmed-meshheading:9526008-...lld:pubmed
pubmed-article:9526008pubmed:meshHeadingpubmed-meshheading:9526008-...lld:pubmed
pubmed-article:9526008pubmed:meshHeadingpubmed-meshheading:9526008-...lld:pubmed
pubmed-article:9526008pubmed:year1998lld:pubmed
pubmed-article:9526008pubmed:articleTitleA Ca2+-independent receptor for alpha-latrotoxin, CIRL, mediates effects on secretion via multiple mechanisms.lld:pubmed
pubmed-article:9526008pubmed:affiliationDepartment of Pharmacology, The University of Michigan Medical School, Ann Arbor, Michigan 48109, USA.lld:pubmed
pubmed-article:9526008pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:9526008pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
pubmed-article:9526008pubmed:publicationTypeResearch Support, U.S. Gov't, Non-P.H.S.lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:9526008lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:9526008lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:9526008lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:9526008lld:pubmed