0 543

Cited 18 times in

Orai1 and STIM1 in ER/PM junctions: roles in pancreatic cell function and dysfunction

DC Field Value Language
dc.contributor.author신동민-
dc.date.accessioned2017-02-24T08:10:16Z-
dc.date.available2017-02-24T08:10:16Z-
dc.date.issued2016-
dc.identifier.issn0363-6143-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/146571-
dc.description.abstractMembrane contact sites (MCS) are critical junctions that form between the endoplasmic reticulum (ER) and membranes of various organelles, including the plasma membrane (PM). Signaling complexes, including mediators of Ca(2+) signaling, are assembled within MCS, such as the ER/PM junction. This is most evident in polarized epithelial cells, such as pancreatic cells. Core Ca(2+) signaling proteins cluster at the apical pole, the site of inositol 1,4,5-trisphosphate-mediated Ca(2+) release and Orai1/transient receptor potential canonical-mediated store-dependent Ca(2+) entry. Recent advances have characterized the proteins that tether the membranes at MCS and the role of these proteins in modulating physiological and pathological intracellular signaling. This review discusses recent advances in the characterization of Ca(2+) signaling at ER/PM junctions and the relation of these junctions to physiological and pathological Ca(2+) signaling in pancreatic acini.-
dc.description.statementOfResponsibilityrestriction-
dc.format.extentC414~C422-
dc.publisherAmerican Physiological Society-
dc.relation.isPartOfAMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAnimals-
dc.subject.MESHCalcium/metabolism-
dc.subject.MESHCalcium Channels/metabolism-
dc.subject.MESHCalcium Signaling/physiology-
dc.subject.MESHCell Membrane/metabolism*-
dc.subject.MESHEndoplasmic Reticulum/metabolism*-
dc.subject.MESHMembrane Proteins/metabolism*-
dc.subject.MESHPancreas/metabolism*-
dc.titleOrai1 and STIM1 in ER/PM junctions: roles in pancreatic cell function and dysfunction-
dc.typeArticle-
dc.publisher.locationUnited States-
dc.contributor.collegeCollege of Dentistry-
dc.contributor.departmentDept. of Oral Biology-
dc.contributor.googleauthorAran Son-
dc.contributor.googleauthorSeonghee Park-
dc.contributor.googleauthorDong Min Shin-
dc.contributor.googleauthorShmuel Muallem-
dc.identifier.doi10.1152/ajpcell.00349.2015-
dc.contributor.localIdA02091-
dc.relation.journalcodeJ00102-
dc.identifier.eissn1522-1563-
dc.identifier.pmid26739495-
dc.identifier.urlhttp://ajpcell.physiology.org/content/310/6/C414-
dc.subject.keywordER-
dc.subject.keywordPM-
dc.subject.keywordjunctions-
dc.subject.keywordpancreas-
dc.subject.keywordsignaling-
dc.contributor.alternativeNameShin, Dong Min-
dc.contributor.affiliatedAuthorShin, Dong Min-
dc.citation.volume310-
dc.citation.number6-
dc.citation.startPage414-
dc.citation.endPage422-
dc.identifier.bibliographicCitationAMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, Vol.310(6) : 414-422, 2016-
dc.date.modified2017-02-24-
dc.identifier.rimsid46380-
dc.type.rimsART-
Appears in Collections:
2. College of Dentistry (치과대학) > Dept. of Oral Biology (구강생물학교실) > 1. Journal Papers

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.