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ファイル | 記述 | サイズ | フォーマット | |
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j.jmbbm.2023.105828.pdf | 5.65 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 | Yokoyama, Yuka | en |
dc.contributor.author | Kameo, Yoshitaka | en |
dc.contributor.author | Adachi, Taiji | en |
dc.contributor.alternative | 横山, 優花 | ja |
dc.contributor.alternative | 亀尾, 佳貴 | ja |
dc.contributor.alternative | 安達, 泰治 | ja |
dc.date.accessioned | 2023-05-18T05:39:39Z | - |
dc.date.available | 2023-05-18T05:39:39Z | - |
dc.date.issued | 2023-04 | - |
dc.identifier.uri | http://hdl.handle.net/2433/282142 | - |
dc.description.abstract | Biological tissues acquire various characteristic shapes through morphogenesis. Tissue shapes result from the spatiotemporally heterogeneous cellular activities influenced by mechanical and biochemical environments. To investigate multicellular tissue morphogenesis, this study aimed to develop a novel multiscale method that can connect each cellular activity to the mechanical behaviors of the whole tissue by constructing continuum-based particle models of cellular activities. This study proposed mechanical models of cell growth and proliferation that are expressed as volume expansion and cell division by extending the material point method. By simulating cell hypertrophy and proliferation under both free and constraint conditions, the proposed models demonstrated potential for evaluating the mechanical state and tracing cells throughout tissue morphogenesis. Moreover, the effect of a cell size checkpoint was incorporated into the cell proliferation model to investigate the mechanical behaviors of the whole tissue depending on the condition of cellular activities. Consequently, the accumulation of strain energy density was suppressed because of the influence of the checkpoint. In addition, the whole tissues acquired different shapes depending on the influence of the checkpoint. Thus, the models constructed herein enabled us to investigate the change in the mechanical behaviors of the whole tissue according to each cellular activity depending on the mechanical state of the cells during morphogenesis. | en |
dc.language.iso | eng | - |
dc.publisher | Elsevier BV | en |
dc.rights | © 2023 The Authors. Published by Elsevier Ltd. | en |
dc.rights | This is an open access article under the CC BY license. | en |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | - |
dc.subject | Morphogenesis | en |
dc.subject | Growth | en |
dc.subject | Proliferation | en |
dc.subject | Continuum-based particle modeling | en |
dc.subject | Material point method | en |
dc.subject | Computational biomechanics | en |
dc.title | Development of continuum-based particle models of cell growth and proliferation for simulating tissue morphogenesis | en |
dc.type | journal article | - |
dc.type.niitype | Journal Article | - |
dc.identifier.jtitle | Journal of the Mechanical Behavior of Biomedical Materials | en |
dc.identifier.volume | 142 | - |
dc.relation.doi | 10.1016/j.jmbbm.2023.105828 | - |
dc.textversion | publisher | - |
dc.identifier.artnum | 105828 | - |
dc.identifier.pmid | 37104898 | - |
dcterms.accessRights | open access | - |
datacite.awardNumber | 20H00659 | - |
datacite.awardNumber | 22K03827 | - |
datacite.awardNumber.uri | https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-20H00659/ | - |
datacite.awardNumber.uri | https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-22K03827/ | - |
dc.identifier.pissn | 1751-6161 | - |
dc.identifier.eissn | 1878-0180 | - |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.awardTitle | 骨のマイクロ損傷感知・修復メカニズムの多階層力学的理解と応用 | ja |
jpcoar.awardTitle | 骨代謝数理モデルに基づく皮質骨・海綿骨リモデリングの統合的理解 | ja |
出現コレクション: | 学術雑誌掲載論文等 |

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