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An endoplasmic reticulum stress regulator, Tmbim6, modulates secretory stage of mice molar

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dc.contributor.author조성원-
dc.date.accessioned2020-02-11T06:30:31Z-
dc.date.available2020-02-11T06:30:31Z-
dc.date.issued2019-
dc.identifier.issn0021-9541-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/174703-
dc.description.abstractTo understand the role of endoplasmic reticulum (ER)-stress in mice molar development, we studied Tmbim6 that antagonizes the unfolded protein response, using Tmbim6 knockout (KO) mice and in vitro organ cultivation with knocking down using small interfering RNA. During molar development, Tmbim6 is expressed in developing tooth at E14-E16, postnatal0 (PN0), and PN6. Mineral content in Tmbim6 KO enamel was reduced while dentin was slightly increased revealing ultrastructural changes in pattern formation of both enamel and dentin. Moreover, odontoblast differentiation was altered with increased Dspp expression at PN0 followed by altered AMELX localizations at PN5. These results were confirmed by in vitro organ cultivation and showed altered Bmp signaling, proliferation, and actin rearrangement in the presumptive ameloblast and odontoblasts that followed the altered expression of differentiation and ER stress-related signaling molecules at E16.5. Overall, ER stress modulated by Tmbim6 would play important roles in patterned dental hard tissue formation in mice molar within a limited period of development.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherWiley-Liss-
dc.relation.isPartOfJOURNAL OF CELLULAR PHYSIOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleAn endoplasmic reticulum stress regulator, Tmbim6, modulates secretory stage of mice molar-
dc.typeArticle-
dc.contributor.collegeCollege of Dentistry (치과대학)-
dc.contributor.departmentDept. of Oral Biology (구강생물학교실)-
dc.contributor.googleauthorYam Prasad Aryal-
dc.contributor.googleauthorSanjiv Neupane-
dc.contributor.googleauthorNirpesh Adhikari-
dc.contributor.googleauthorChang‐Hyeon An-
dc.contributor.googleauthorJung‐Hong Ha-
dc.contributor.googleauthorTae‐Yub Kwon-
dc.contributor.googleauthorHitoshi Yamamoto-
dc.contributor.googleauthorJae‐Kwang Jung-
dc.contributor.googleauthorEui‐Kyun Park-
dc.contributor.googleauthorJi‐Youn Kim-
dc.contributor.googleauthorSung‐Won Cho-
dc.contributor.googleauthorWern‐Joo Sohn-
dc.contributor.googleauthorYoungkyun Lee-
dc.contributor.googleauthorHan‐Jung Chae-
dc.contributor.googleauthorHyung‐Ryong Kim-
dc.contributor.googleauthorJae‐Young Kim-
dc.identifier.doi10.1002/jcp.28635-
dc.contributor.localIdA03837-
dc.relation.journalcodeJ01304-
dc.identifier.eissn1097-4652-
dc.identifier.pmid30963569-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/full/10.1002/jcp.28635-
dc.subject.keywordER stress-
dc.subject.keywordTmbim6 knockout-
dc.subject.keywordamelogenesis-
dc.subject.keyworddentinogenesis-
dc.subject.keywordmolar development-
dc.contributor.alternativeNameCho, Sung Won-
dc.contributor.affiliatedAuthor조성원-
dc.citation.volume234-
dc.citation.number11-
dc.citation.startPage20354-
dc.citation.endPage20365-
dc.identifier.bibliographicCitationJOURNAL OF CELLULAR PHYSIOLOGY, Vol.234(11) : 20354-20365, 2019-
dc.identifier.rimsid63669-
dc.type.rimsART-
Appears in Collections:
2. College of Dentistry (치과대학) > Dept. of Oral Biology (구강생물학교실) > 1. Journal Papers

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