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dc.contributor.author | Yoshimoto, Yu | en |
dc.contributor.author | Jo, Jun-ichiro | en |
dc.contributor.author | Tabata, Yasuhiko | en |
dc.contributor.alternative | 吉本, 雄 | ja |
dc.contributor.alternative | 城, 潤一郎 | ja |
dc.contributor.alternative | 田畑, 泰彦 | ja |
dc.date.accessioned | 2020-01-29T05:59:02Z | - |
dc.date.available | 2020-01-29T05:59:02Z | - |
dc.date.issued | 2020-06 | - |
dc.identifier.issn | 2352-3204 | - |
dc.identifier.uri | http://hdl.handle.net/2433/245476 | - |
dc.description.abstract | [Introduction]Inflammatory response plays an important role in the disease progress or therapeutic effect. In this context, it is highly required to develop a technology to visualize the inflammatory response. In this study, macrophages and their microRNA (miRNA) which are involved in the inflammatory response, were focused while a system of molecular beacon (MB) to detect the miRNA of macrophages was designed and prepared. [Methods]Gelatin nanospheres were prepared by the conventional coacervation method. An antibody with an affinity for the surface receptor of macrophages was immobilized onto the gelatin nanospheres by several methods. A nucleic acid-based MB for a pro-inflammatory miRNA 155–5p was designed and incorporated into the antibody-immobilized gelatin nanospheres (MB-gelatin NS). Macrophages before and after the polarization into pro-inflammatory or anti-inflammatory phenotypes were cultured with the MB-gelatin NS and change in the intracellular fluorescence was observed. [Results]The antibody-immobilized gelatin nanospheres prepared by a coupling between the amino groups of gelatin and the sugar chains of antibody with NaIO4 showed the highest affinity for cellular receptor. MB complexed with the cell-penetrating (CP) peptide was successfully incorporated into the antibody-immobilized gelatin nanospheres. When cultured with pro-inflammatory macrophages, MB-gelatin NS efficiently detected the miRNA 155–5p to emit fluorescence. [Conclusions]By the NaIO₄ method, the antibody was immobilized onto gelatin nanospheres with a high affinity remaining while the MB was incorporated into the antibody-immobilized gelatin nanospheres. The MB incorporated allowed mRNA to visualize the pro-inflammatory nature of macrophages. | en |
dc.format.mimetype | application/pdf | - |
dc.language.iso | eng | - |
dc.publisher | Elsevier B.V. | en |
dc.rights | ©2020, The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V. This is an open access article under the CC BY-NC-ND license(http://creativecommons.org/licenses/by-nc-nd/4.0/). | en |
dc.subject | Gelatin nanospheres | en |
dc.subject | Antibody immobilization | en |
dc.subject | Molecular beacon | en |
dc.subject | microRNA | en |
dc.subject | Macrophages | en |
dc.subject | Inflammatory response | en |
dc.title | Preparation of antibody-immobilized gelatin nanospheres incorporating a molecular beacon to visualize the biological function of macrophages | en |
dc.type | journal article | - |
dc.type.niitype | Journal Article | - |
dc.identifier.jtitle | Regenerative Therapy | en |
dc.identifier.volume | 14 | - |
dc.identifier.spage | 11 | - |
dc.identifier.epage | 18 | - |
dc.relation.doi | 10.1016/j.reth.2019.12.009 | - |
dc.textversion | publisher | - |
dc.address | Laboratory of Biomaterials, Institute for Frontier Life and Medical Sciences, Kyoto University | en |
dc.address | Laboratory of Biomaterials, Institute for Frontier Life and Medical Sciences, Kyoto University | en |
dc.address | Laboratory of Biomaterials, Institute for Frontier Life and Medical Sciences, Kyoto University | en |
dc.identifier.pmid | 31970268 | - |
dcterms.accessRights | open access | - |
datacite.awardNumber | 17H04736 | - |
dc.identifier.eissn | 2352-3204 | - |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName.alternative | Japan Society for the Promotion of Science (JSPS) | en |
出現コレクション: | 学術雑誌掲載論文等 |

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