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ファイル | 記述 | サイズ | フォーマット | |
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eLife.76269.pdf | 4.56 MB | Adobe PDF | 見る/開く |
完全メタデータレコード
DCフィールド | 値 | 言語 |
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dc.contributor.author | Ichise, Hiroshi | en |
dc.contributor.author | Tsukamoto, Shoko | en |
dc.contributor.author | Hirashima, Tsuyoshi | en |
dc.contributor.author | Konishi, Yoshinobu | en |
dc.contributor.author | Oki, Choji | en |
dc.contributor.author | Tsukiji, Shinya | en |
dc.contributor.author | Iwano, Satoshi | en |
dc.contributor.author | Miyawaki, Atsushi | en |
dc.contributor.author | Sumiyama, Kenta | en |
dc.contributor.author | Terai, Kenta | en |
dc.contributor.author | Matsuda, Michiyuki | en |
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.accessioned | 2022-02-16T04:48:22Z | - |
dc.date.available | 2022-02-16T04:48:22Z | - |
dc.date.issued | 2022 | - |
dc.identifier.uri | http://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.abstract | Natural 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.iso | eng | - |
dc.publisher | eLife Sciences Publications, Ltd | en |
dc.rights | © 2022, Ichise et al. | en |
dc.rights | This 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.uri | http://creativecommons.org/licenses/by/4.0/ | - |
dc.subject | natural killer cells | en |
dc.subject | tumor immunology | en |
dc.subject | lung metastasis | en |
dc.subject | circulating tumor cell | en |
dc.subject | intravital imaging | en |
dc.subject | genetically encoded biosensor | en |
dc.subject | thrombin | en |
dc.title | Functional visualization of NK Cell-mediated killing of metastatic single tumor cells | en |
dc.type | journal article | - |
dc.type.niitype | Journal Article | - |
dc.identifier.jtitle | eLife | en |
dc.identifier.volume | 11 | - |
dc.relation.doi | 10.7554/eLife.76269 | - |
dc.textversion | publisher | - |
dc.identifier.artnum | e76269 | - |
dc.address | Research Center for Dynamic Living Systems, Graduate School of Biostudies, Kyoto University | en |
dc.address | Research Center for Dynamic Living Systems, Graduate School of Biostudies, Kyoto University | en |
dc.address | Department of Pathology and Biology of Diseases, Graduate School of Medicine, Kyoto University | en |
dc.address | Research Center for Dynamic Living Systems, Graduate School of Biostudies, Kyoto University | en |
dc.address | Department of Nanopharmaceutical Sciences, Nagoya Institute of Technology | en |
dc.address | Department of Nanopharmaceutical Sciences, Nagoya Institute of Technology | en |
dc.address | Brain Science Institute, Center for Brain Science, RIKEN | en |
dc.address | Brain Science Institute, Center for Brain Science, RIKEN | en |
dc.address | Laboratory for Mouse Genetic Engineering, RIKEN Center for Biosystems Dynamics Research | en |
dc.address | Research Center for Dynamic Living Systems, Graduate School of Biostudies, Kyoto University | en |
dc.address | Research 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 University | en |
dc.identifier.pmid | 35113018 | - |
dc.relation.url | https://www.kyoto-u.ac.jp/ja/research-news/2022-02-07 | - |
dcterms.accessRights | open access | - |
datacite.awardNumber | 18K15317 | - |
datacite.awardNumber | 15H05949 | - |
datacite.awardNumber | 16H06280 | - |
datacite.awardNumber | 19H00993 | - |
datacite.awardNumber.uri | https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-18K15317/ | - |
datacite.awardNumber.uri | https://kaken.nii.ac.jp/grant/KAKENHI-PLANNED-15H05949/ | - |
datacite.awardNumber.uri | https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-16H06280/ | - |
datacite.awardNumber.uri | https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-19H00993/ | - |
dc.identifier.eissn | 2050-084X | - |
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.awardTitle | NK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 |

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