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The mammalian Sec6/8 complex interacts with Ca2+ signaling complexes and regulates their activity

DC Field Value Language
dc.contributor.author신동민-
dc.date.accessioned2019-11-11T05:11:17Z-
dc.date.available2019-11-11T05:11:17Z-
dc.date.issued2000-
dc.identifier.issn0021-9525-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/171682-
dc.description.abstractThe localization of various Ca(2+) transport and signaling proteins in secretory cells is highly restricted, resulting in polarized agonist-stimulated Ca(2+) waves. In the present work, we examined the possible roles of the Sec6/8 complex or the exocyst in polarized Ca(2+) signaling in pancreatic acinar cells. Immunolocalization by confocal microscopy showed that the Sec6/8 complex is excluded from tight junctions and secretory granules in these cells. The Sec6/8 complex was found in at least two cellular compartments, part of the complex showed similar, but not identical, localization with the Golgi apparatus and part of the complex associated with Ca(2+) signaling proteins next to the plasma membrane at the apical pole. Accordingly, immunoprecipitation (IP) of Sec8 did not coimmunoprecipitate betaCOP, Golgi 58K protein, or mannosidase II, all Golgi-resident proteins. By contrast, IP of Sec8 coimmunoprecipitates Sec6, type 3 inositol 1,4,5-trisphosphate receptors (IP(3)R3), and the Gbetagamma subunit of G proteins from pancreatic acinar cell extracts. Furthermore, the anti-Sec8 antibodies coimmunoprecipitate actin, Sec6, the plasma membrane Ca(2+) pump, the G protein subunits Galphaq and Gbetagamma, the beta1 isoform of phospholipase C, and the ER resident IP(3)R1 from brain microsomal extracts. Antibodies against the various signaling and Ca(2+) transport proteins coimmunoprecipitate Sec8 and the other signaling proteins. Dissociation of actin filaments in the immunoprecipitate had no effect on the interaction between Sec6 and Sec8, but released the actin and dissociated the interaction between the Sec6/8 complex and Ca(2+) signaling proteins. Hence, the interaction between the Sec6/8 and Ca(2+) signaling complexes is likely mediated by the actin cytoskeleton. The anti-Sec6 and anti-Sec8 antibodies inhibited Ca(2+) signaling at a step upstream of Ca(2+) release by IP(3). Disruption of the actin cytoskeleton with latrunculin B in intact cells resulted in partial translocation of Sec6 and Sec8 from membranes to the cytosol and interfered with propagation of agonist-evoked Ca(2+) waves. Our results suggest that the Sec6/8 complex has multiple roles in secretory cells including governing the polarized expression of Ca(2+) signaling complexes and regulation of their activity.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherRockefeller University Press-
dc.relation.isPartOfJournal of Cell Biology-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHActins/physiology-
dc.subject.MESHAnimals-
dc.subject.MESHBrefeldin A/pharmacology-
dc.subject.MESHCalcium/metabolism*-
dc.subject.MESHCalcium Channels/isolation & purification-
dc.subject.MESHCalcium Channels/physiology-
dc.subject.MESHCalcium Signaling/drug effects-
dc.subject.MESHCalcium Signaling/physiology*-
dc.subject.MESHCarbachol/pharmacology-
dc.subject.MESHCarrier Proteins/analysis-
dc.subject.MESHCarrier Proteins/metabolism*-
dc.subject.MESHCell Membrane/physiology-
dc.subject.MESHCell Membrane/ultrastructure-
dc.subject.MESHCell Polarity-
dc.subject.MESHCells, Cultured-
dc.subject.MESHCytoskeleton/physiology-
dc.subject.MESHCytoskeleton/ultrastructure-
dc.subject.MESHGTP-Binding Proteins/isolation & purification-
dc.subject.MESHGTP-Binding Proteins/metabolism-
dc.subject.MESHGolgi Apparatus/physiology-
dc.subject.MESHGolgi Apparatus/ultrastructure-
dc.subject.MESHInositol 1,4,5-Trisphosphate Receptors-
dc.subject.MESHInositol Phosphates/pharmacology-
dc.subject.MESHMembrane Potentials/drug effects-
dc.subject.MESHMembrane Potentials/physiology-
dc.subject.MESHPancreas/cytology*-
dc.subject.MESHPancreas/physiology*-
dc.subject.MESHPatch-Clamp Techniques-
dc.subject.MESHRats-
dc.subject.MESHReceptors-
dc.subject.MESHCytoplasmic and Nuclear/isolation & purification-
dc.subject.MESHReceptors-
dc.subject.MESHCytoplasmic and Nuclear/physiology-
dc.titleThe mammalian Sec6/8 complex interacts with Ca2+ signaling complexes and regulates their activity-
dc.typeArticle-
dc.contributor.collegeCollege of Dentistry (치과대학)-
dc.contributor.departmentDept. of Oral Biology (구강생물학교실)-
dc.contributor.googleauthorDong Min Shin-
dc.contributor.googleauthorXiao-Song Zhao-
dc.contributor.googleauthorWeizhong Zeng-
dc.contributor.googleauthorMarina Mozhayeva-
dc.contributor.googleauthorShmuel Muallem-
dc.identifier.doi10.1083/jcb.150.5.1101-
dc.contributor.localIdA02091-
dc.relation.journalcodeJ01300-
dc.identifier.eissn1540-8140-
dc.identifier.pmid10973998-
dc.subject.keywordSec6/8 complex-
dc.subject.keywordCa2+ signaling proteins-
dc.subject.keywordassembly-
dc.subject.keywordactin cytoskeleton-
dc.subject.keywordCa2+ signaling-
dc.contributor.alternativeNameShin, Dong Min-
dc.contributor.affiliatedAuthor신동민-
dc.citation.volume150-
dc.citation.number5-
dc.citation.startPage1101-
dc.citation.endPage1112-
dc.identifier.bibliographicCitationJournal of Cell Biology, Vol.150(5) : 1101-1112, 2000-
Appears in Collections:
2. College of Dentistry (치과대학) > Dept. of Oral Biology (구강생물학교실) > 1. Journal Papers

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