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dc.contributor.authorWu, Peizhengen
dc.contributor.authorYanagi, Kazuyaen
dc.contributor.authorYokota, Kazukien
dc.contributor.authorHakamada, Masatakaen
dc.contributor.authorMabuchi, Mamoruen
dc.contributor.alternative呉, 裴征ja
dc.contributor.alternative柳, 和弥ja
dc.contributor.alternative横田, 一樹ja
dc.contributor.alternative袴田, 昌高ja
dc.contributor.alternative馬渕, 守ja
dc.date.accessioned2023-10-31T08:48:11Z-
dc.date.available2023-10-31T08:48:11Z-
dc.date.issued2023-10-26-
dc.identifier.urihttp://hdl.handle.net/2433/285921-
dc.description.abstractA variety of cell behaviors, such as cell adhesion, motility, and fate, can be controlled by substrate characteristics such as surface topology and chemistry. In particular, the surface topology of substrates strongly affects cell behaviors, and the topological spacing is a critical factor in inducing cell responses. Various works have demonstrated that cell adhesion was enhanced with decreasing topological spacing although differentiation progressed slowly. However, there are exceptions, and thus, correlations between topological spacing and cell responses are still debated. We show that a nanoporous gold substrate affected cell adhesion while it neither affected osteogenic nor adipogenic differentiation. In addition, the cell adhesion was reduced with decreasing pore size. These do not agree with previous findings. A focal adhesion (FA) is an aggregate of modules comprising specific proteins such as FA kinase, talin, and vinculin. Therefore, it is suggested that because various extracellular signals can be independently branched off from the FA modules, the unusual effects of nanoporous gold substrates are related to the multi-branching of FAs.en
dc.language.isoeng-
dc.publisherSpringer Natureen
dc.rights© The Author(s) 2023en
dc.rightsThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/-
dc.subjectNanoporous golden
dc.subjectSurface topologyen
dc.subjectFocal adhesionen
dc.subjectCell adhesionen
dc.subjectDifferentiationen
dc.titleUnusual effects of a nanoporous gold substrate on cell adhesion and differentiation because of independent multi-branch signaling of focal adhesionsen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleJournal of Materials Science: Materials in Medicineen
dc.identifier.volume34-
dc.relation.doi10.1007/s10856-023-06760-0-
dc.textversionpublisher-
dc.identifier.artnum54-
dcterms.accessRightsopen access-
datacite.awardNumber20K20545-
datacite.awardNumber19H02458-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-20K20545/-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-19H02458/-
dc.identifier.eissn1573-4838-
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.awardTitleインテグリンシグナルの全原子解析に基づくナノ構造基板の細胞死誘導機構解明ja
jpcoar.awardTitleナノポーラス金による細胞接着制御ja
出現コレクション:学術雑誌掲載論文等

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