Please use this identifier to cite or link to this item: https://saber.ucv.ve/jspui/handle/10872/4624
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dc.contributor.authorColina, C-
dc.contributor.authorFlores, A-
dc.contributor.authorCastillo, M-
dc.contributor.authorRosario, M-
dc.contributor.authorIsrael, A-
dc.contributor.authorDiPolo, R-
dc.contributor.authorBenaím, Gustavo-
dc.date.accessioned2013-10-24T18:21:13Z-
dc.date.available2013-10-24T18:21:13Z-
dc.date.issued2005-
dc.identifier.citationVol. 336, pp.54–60es_VE
dc.identifier.issn0006-291X-
dc.identifier.otherdoi:10.1016/j.bbrc.2005.08.039-
dc.identifier.urihttp://hdl.handle.net/10872/4624-
dc.description.abstractSphingolipids comprise a very important class of second messengers involved in cell growth, differentiation, and apoptosis, among other different functions. Recently, these lipids have been implicated in calcium mobilization in different cell lines, including Jurkat T-lymphocytes. However, the effect of each particular sphingolipid appears to be cell-line specific. Among them, the least studied is ceramide-1-P (Cer-1-P). Here, we show that Cer-1-P increased the intracellular Ca2+ concentration in Jurkat T-cells. Furthermore, laser-scanning confocal microscopy indicated that Ca2+ is released from the endoplasmic reticulum. An effect on storeoperated Ca2+ channels was evidenced by whole-cell ‘‘patch clamp’’ measurements after Cer-1-P induced Ca2+ store depletion. The mechanism of action of Cer-1-P resembles that of the Jurkat anti-TCR antibody, but differs from that of ceramide, since Cer-1-P induced an increase in Ins(1,4,5)-P3.es_VE
dc.language.isoenes_VE
dc.publisherBiochemical and Biophysical Research Communicationses_VE
dc.subjectCeramide 1-Pes_VE
dc.subjectIns(1,4,5)-P3-
dc.subjectCapacitative calcium entry channel-
dc.subjectConfocal-
dc.subjectJurkat T-cells-
dc.subjectendoplasmic reticulum-
dc.titleCeramide-1-P induces Ca2+ mobilization in Jurkat T-cells by elevation of Ins(1,4,5)-P3 and activation of a store-operated calcium channeles_VE
dc.typeArticlees_VE
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