{"created":"2023-05-15T14:19:51.994534+00:00","id":4040,"links":{},"metadata":{"_buckets":{"deposit":"b0645b8d-2bde-4278-b460-8f92d8ad4444"},"_deposit":{"created_by":3,"id":"4040","owners":[3],"pid":{"revision_id":0,"type":"depid","value":"4040"},"status":"published"},"_oai":{"id":"oai:ohu-lib.repo.nii.ac.jp:00004040","sets":["90:246:255"]},"author_link":["13524","13523","13522"],"item_10002_biblio_info_7":{"attribute_name":"書誌情報","attribute_value_mlt":[{"bibliographicIssueDates":{"bibliographicIssueDate":"2014-12","bibliographicIssueDateType":"Issued"},"bibliographicIssueNumber":"3-4号","bibliographicPageStart":"99-105","bibliographicVolumeNumber":"41巻","bibliographic_titles":[{"bibliographic_title":"奥羽大学歯学誌"}]}]},"item_10002_description_5":{"attribute_name":"抄録","attribute_value_mlt":[{"subitem_description":"レチノイン酸はヒト歯肉上皮細胞からの抗歯ペプチド産生を誘導するか検討した。Ca9-22からのLL-37のmRNAはATRA添加濃度依存的に発現が促進された。LL-37のmRNAは時間依存的に促進され、24時間で最大となった。Ca9-22の培養上清中におけるLL-37の産生は、ATRA 1μM添加後1時間で促進された。ATRAの濃度10μMで有意なLL-37の産生促進を認めた。ATRA添加後24時間では2μMおよび5μMでRARαのmRNA発現が促進された。RARβではATRA添加後1時間では有意差は認められなかったが、24時間ではmRNAの発現が促進された。RXRαのmRNA発現に対し、ATRAは何ら影響を与えなかった。RXRβにおいてはATRA添加後24時間において、そのmRNA発現が有意に促進された。","subitem_description_type":"Abstract"}]},"item_10002_source_id_9":{"attribute_name":"ISSN","attribute_value_mlt":[{"subitem_source_identifier":"0916-2313","subitem_source_identifier_type":"ISSN"}]},"item_creator":{"attribute_name":"著者","attribute_type":"creator","attribute_value_mlt":[{"creatorNames":[{"creatorName":"渡辺, 敦"}],"nameIdentifiers":[{"nameIdentifier":"13522","nameIdentifierScheme":"WEKO"}]},{"creatorNames":[{"creatorName":"福井, 和徳"}],"nameIdentifiers":[{"nameIdentifier":"13523","nameIdentifierScheme":"WEKO"}]},{"creatorNames":[{"creatorName":"廣瀬, 公治"}],"nameIdentifiers":[{"nameIdentifier":"13524","nameIdentifierScheme":"WEKO"}]}]},"item_files":{"attribute_name":"ファイル情報","attribute_type":"file","attribute_value_mlt":[{"accessrole":"open_date","date":[{"dateType":"Available","dateValue":"2016-05-28"}],"displaytype":"detail","filename":"S41(3-4)99-105.pdf","filesize":[{"value":"1.3 MB"}],"format":"application/pdf","licensetype":"license_note","mimetype":"application/pdf","url":{"label":"S41(3-4)99-105.pdf","url":"https://ohu-lib.repo.nii.ac.jp/record/4040/files/S41(3-4)99-105.pdf"},"version_id":"64d2d66d-d69a-4edf-8ecf-a371851aab5b"}]},"item_keyword":{"attribute_name":"キーワード","attribute_value_mlt":[{"subitem_subject":"Glyceraldehyde-3-Phosphate Dehydrogenases; *Peptides; mRNA; *Tretinoin; *歯肉; 歯肉腫瘍; *上皮細胞; Retinoic Acid Receptors; 細胞質受容体と核内受容体; 時間因子; 抗菌性カチオンペプチド; 腫瘍細胞系; リアルタイムPCR法","subitem_subject_scheme":"Other"},{"subitem_subject":"CAP18 Lipopolysaccharide-Binding Protein","subitem_subject_scheme":"Other"},{"subitem_subject":"ヒト; 歯学","subitem_subject_scheme":"Other"}]},"item_resource_type":{"attribute_name":"資源タイプ","attribute_value_mlt":[{"resourcetype":"departmental bulletin paper","resourceuri":"http://purl.org/coar/resource_type/c_6501"}]},"item_title":"レチノイン酸はヒト歯肉上皮細胞からの抗菌ペプチド産生を誘導する","item_titles":{"attribute_name":"タイトル","attribute_value_mlt":[{"subitem_title":"レチノイン酸はヒト歯肉上皮細胞からの抗菌ペプチド産生を誘導する"}]},"item_type_id":"10002","owner":"3","path":["255"],"pubdate":{"attribute_name":"公開日","attribute_value":"2016-05-28"},"publish_date":"2016-05-28","publish_status":"0","recid":"4040","relation_version_is_last":true,"title":["レチノイン酸はヒト歯肉上皮細胞からの抗菌ペプチド産生を誘導する"],"weko_creator_id":"3","weko_shared_id":-1},"updated":"2023-05-15T14:59:47.848793+00:00"}