このアイテムのアクセス数: 240

このアイテムのファイル:
ファイル 記述 サイズフォーマット 
eLife.76269.pdf4.56 MBAdobe PDF見る/開く
完全メタデータレコード
DCフィールド言語
dc.contributor.authorIchise, Hiroshien
dc.contributor.authorTsukamoto, Shokoen
dc.contributor.authorHirashima, Tsuyoshien
dc.contributor.authorKonishi, Yoshinobuen
dc.contributor.authorOki, Chojien
dc.contributor.authorTsukiji, Shinyaen
dc.contributor.authorIwano, Satoshien
dc.contributor.authorMiyawaki, Atsushien
dc.contributor.authorSumiyama, Kentaen
dc.contributor.authorTerai, Kentaen
dc.contributor.authorMatsuda, Michiyukien
dc.contributor.alternative一瀬, 大志ja
dc.contributor.alternative塚本, 祥子ja
dc.contributor.alternative平島, 剛志ja
dc.contributor.alternative小西, 義延ja
dc.contributor.alternative沖, 超二ja
dc.contributor.alternative築地, 真也ja
dc.contributor.alternative岩野, 智ja
dc.contributor.alternative宮脇, 敦史ja
dc.contributor.alternative隅山, 健太ja
dc.contributor.alternative寺井, 健太ja
dc.contributor.alternative松田, 道行ja
dc.date.accessioned2022-02-16T04:48:22Z-
dc.date.available2022-02-16T04:48:22Z-
dc.date.issued2022-
dc.identifier.urihttp://hdl.handle.net/2433/267925-
dc.descriptionナチュラルキラー(NK)細胞による転移がん細胞殺傷の可視化 --NK細胞とがん細胞の肺毛細血管上での戦いを実況中継する--. 京都大学プレスリリース. 2022-02-07.ja
dc.description.abstractNatural killer (NK) cells lyse invading tumor cells to limit metastatic growth in the lung, but how some cancers evade this host protective mechanism to establish a growing lesion is unknown. Here we have combined ultra-sensitive bioluminescence imaging with intravital two-photon microscopy involving genetically-encoded biosensors to examine this question. NK cells eliminated disseminated tumor cells from the lung within 24 hrs of arrival, but not thereafter. Intravital dynamic imaging revealed that 50% of NK-tumor cell encounters lead to tumor cell death in the first 4 hrs after tumor cell arrival, but after 24 hrs of arrival, nearly 100% of the interactions result in the survival of the tumor cell. During this 24 hrs period, the probability of ERK activation in NK cells upon encountering the tumor cells was decreased from 68% to 8%, which correlated with the loss of the activating ligand CD155/PVR/Necl5 from the tumor cell surface. Thus, by quantitatively visualizing the NK-tumor cell interaction at the early stage of metastasis, we have revealed the crucial parameters of NK cell immune surveillance in the lung.en
dc.language.isoeng-
dc.publishereLife Sciences Publications, Ltden
dc.rights© 2022, Ichise et al.en
dc.rightsThis article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/-
dc.subjectnatural killer cellsen
dc.subjecttumor immunologyen
dc.subjectlung metastasisen
dc.subjectcirculating tumor cellen
dc.subjectintravital imagingen
dc.subjectgenetically encoded biosensoren
dc.subjectthrombinen
dc.titleFunctional visualization of NK Cell-mediated killing of metastatic single tumor cellsen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleeLifeen
dc.identifier.volume11-
dc.relation.doi10.7554/eLife.76269-
dc.textversionpublisher-
dc.identifier.artnume76269-
dc.addressResearch Center for Dynamic Living Systems, Graduate School of Biostudies, Kyoto Universityen
dc.addressResearch Center for Dynamic Living Systems, Graduate School of Biostudies, Kyoto Universityen
dc.addressDepartment of Pathology and Biology of Diseases, Graduate School of Medicine, Kyoto Universityen
dc.addressResearch Center for Dynamic Living Systems, Graduate School of Biostudies, Kyoto Universityen
dc.addressDepartment of Nanopharmaceutical Sciences, Nagoya Institute of Technologyen
dc.addressDepartment of Nanopharmaceutical Sciences, Nagoya Institute of Technologyen
dc.addressBrain Science Institute, Center for Brain Science, RIKENen
dc.addressBrain Science Institute, Center for Brain Science, RIKENen
dc.addressLaboratory for Mouse Genetic Engineering, RIKEN Center for Biosystems Dynamics Researchen
dc.addressResearch Center for Dynamic Living Systems, Graduate School of Biostudies, Kyoto Universityen
dc.addressResearch Center for Dynamic Living Systems, Graduate School of Biostudies, Kyoto University; Department of Pathology and Biology of Diseases, Graduate School of Medicine, Kyoto University; Institute for Integrated Cell-Material Sciences, Kyoto Universityen
dc.identifier.pmid35113018-
dc.relation.urlhttps://www.kyoto-u.ac.jp/ja/research-news/2022-02-07-
dcterms.accessRightsopen access-
datacite.awardNumber18K15317-
datacite.awardNumber15H05949-
datacite.awardNumber16H06280-
datacite.awardNumber19H00993-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-18K15317/-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PLANNED-15H05949/-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-16H06280/-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-19H00993/-
dc.identifier.eissn2050-084X-
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.awardTitleNK細胞のがん細胞殺傷能を規定する分子メカニズムja
jpcoar.awardTitle細胞間コミュニケーションのライブイメージングja
jpcoar.awardTitle先端バイオイメージング支援プラットフォームja
jpcoar.awardTitle細胞増殖因子情報伝達系の活性波による細胞集団移動制御機構ja
出現コレクション:学術雑誌掲載論文等

アイテムの簡略レコードを表示する

Export to RefWorks


出力フォーマット 


このアイテムは次のライセンスが設定されています: クリエイティブ・コモンズ・ライセンス Creative Commons