Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/113664
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dc.contributorDepartment of Biomedical Engineeringen_US
dc.creatorChen, Yen_US
dc.creatorXu, Yen_US
dc.creatorCai, Jen_US
dc.creatorLauwers, Men_US
dc.creatorXiang, Len_US
dc.creatorZheng, Yen_US
dc.creatorChu, Hen_US
dc.creatorChen, Xen_US
dc.creatorKer, DFEen_US
dc.creatorZhang, Cen_US
dc.date.accessioned2025-06-17T01:34:03Z-
dc.date.available2025-06-17T01:34:03Z-
dc.identifier.urihttp://hdl.handle.net/10397/113664-
dc.language.isoenen_US
dc.publisherAmerican Association for the Advancement of Science (AAAS)en_US
dc.rightsCopyright © 2025 Yanmei Chen et al. Exclusive licensee Korean Society for Biomaterials, Republic of Korea. No claim to original U.S. Government works. Distributed under a Creative Commons Attribution License (CC BY 4.0)(https://creativecommons.org/licenses/by/4.0/).en_US
dc.rightsThe following publication Chen Y, Xu Y, Cai J, Lauwers M, Xiang L, Zheng Y, Chu H, Chen X, Ker DFE, Zhang C, et al. Automated and Enclosed Three-Dimensional Biofabrication System for Mesenchymal Stem Cell Culture to Enhance Diabetic Wound Healing. Biomater. Res. 2025; 29: Article 0205 is available at https://doi.org/10.34133/bmr.0205.en_US
dc.titleAutomated and enclosed three-dimensional biofabrication system for mesenchymal stem cell culture to enhance diabetic wound healingen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.doi10.34133/bmr.0205en_US
dcterms.abstractThe industrialization of mesenchymal stem cells for regenerative medicine faces substantial challenges, particularly in large-scale production. Conventional 2-dimensional (2D) culture systems demonstrate limitations in meeting clinical requirements, such as inadequate cell yield, and poor cell–cell and cell–matrix interactions. These challenges can potentially be addressed by employing a 3D culture platform, which offers higher cell yields and enhanced efficacy. Moreover, it is essential to conduct a systematic and rigorous evaluation of cells produced in 3D culture systems to ensure their successful clinical translation. In this study, we cultured human umbilical cord mesenchymal stem cells (hUCMSCs) using an automated, scalable, and enclosed 3D microcarrier-bioreactor system, and comprehensively investigated their biological characteristics and potential therapeutic effects for diabetic wound repair. Our findings revealed that hUCMSCs harvested from this 3D microcarrier-bioreactor system are genetically stable and maintain the trilineage differentiation potential. Compared to hUCMSCs expanded under 2D conditions, those cultured in 3D exhibited reduced senescence and enhanced capabilities in migration, angiogenesis, and anti-inflammatory responses across different passages in vitro. RNA-sequencing analysis showed higher expression levels of genes related to angiogenesis and anti-inflammatory pathways in hUCMSCs cultured in 3D compared to those in 2D, which was further validated using quantitative real-time polymerase chain reaction and Western blot analysis. Additionally, 3D-cultured hUCMSCs demonstrated superior therapeutic effects for diabetic wound repair in mice, potentially due to their enhanced angiogenetic and anti-inflammatory effects. Collectively, our finding showcases the high quality of hUCMSCs cultured using an automated and enclosed 3D microcarrier-bioreactor system and their promising potential for diabetic wound repair.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationBiomaterials research, 2025, v.29, 0205en_US
dcterms.isPartOfBiomaterials researchen_US
dcterms.issued2025-
dc.identifier.eissn2055-7124en_US
dc.identifier.artn0205en_US
dc.description.validate202506 bcwhen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera3712-
dc.identifier.SubFormID50823-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextGuangdong Basic and Applied Basic Research Foundation; National Natural Science Foundation of China; The Innovation and Technology Communicationen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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