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Article: Bioactive Scaffold Fabricated by 3D Printing for Enhancing Osteoporotic Bone Regeneration

TitleBioactive Scaffold Fabricated by 3D Printing for Enhancing Osteoporotic Bone Regeneration
Authors
Keywordsadditive effect
focal adhesion signalling
icaritin
osteoporotic bone regeneration
PLGA/TCP
secretome
Issue Date2022
Citation
Bioengineering, 2022, v. 9, n. 10, article no. 525 How to Cite?
AbstractWe develop a poly (lactic-co-glycolic acid)/β-calcium phosphate (PLGA/TCP)-based scaffold through a three-dimensional (3D) printing technique incorporating icaritin (ICT), a unique phytomolecule, and secretome derived from human fetal mesenchymal stem cells (HFS), to provide mechanical support and biological cues for stimulating bone defect healing. With the sustained release of ICT and HFS from the composite scaffold, the cell-free scaffold efficiently facilitates the migration of MSCs and promotes bone regeneration at the femoral defect site in the ovariectomy (OVX)-induced osteoporotic rat model. Furthermore, mechanism study results indicate that the combination of ICT and HFS additively activates the Integrin–FAK (focal adhesion kinase)–ERK1/2 (extracellular signal-regulated kinase 1/2)–Runx2 (Runt-related transcription factor 2) axis, which could be linked to the beneficial recruitment of MSCs to the implant and subsequent osteogenesis enhancement. Collectively, the PLGA/TCP/ICT/HFS (P/T/I/S) bioactive scaffold is a promising biomaterial for repairing osteoporotic bone defects, which may have immense implications for their translation to clinical practice.
Persistent Identifierhttp://hdl.handle.net/10722/363492

 

DC FieldValueLanguage
dc.contributor.authorZhang, Xiaoting-
dc.contributor.authorWang, Xinluan-
dc.contributor.authorLee, Yuk Wai-
dc.contributor.authorFeng, Lu-
dc.contributor.authorWang, Bin-
dc.contributor.authorPan, Qi-
dc.contributor.authorMeng, Xiangbo-
dc.contributor.authorCao, Huijuan-
dc.contributor.authorLi, Linlong-
dc.contributor.authorWang, Haixing-
dc.contributor.authorBai, Shanshan-
dc.contributor.authorKong, Lingchi-
dc.contributor.authorChow, Dick Ho Kiu-
dc.contributor.authorQin, Ling-
dc.contributor.authorCui, Liao-
dc.contributor.authorLin, Sien-
dc.contributor.authorLi, Gang-
dc.date.accessioned2025-10-10T07:47:18Z-
dc.date.available2025-10-10T07:47:18Z-
dc.date.issued2022-
dc.identifier.citationBioengineering, 2022, v. 9, n. 10, article no. 525-
dc.identifier.urihttp://hdl.handle.net/10722/363492-
dc.description.abstractWe develop a poly (lactic-co-glycolic acid)/β-calcium phosphate (PLGA/TCP)-based scaffold through a three-dimensional (3D) printing technique incorporating icaritin (ICT), a unique phytomolecule, and secretome derived from human fetal mesenchymal stem cells (HFS), to provide mechanical support and biological cues for stimulating bone defect healing. With the sustained release of ICT and HFS from the composite scaffold, the cell-free scaffold efficiently facilitates the migration of MSCs and promotes bone regeneration at the femoral defect site in the ovariectomy (OVX)-induced osteoporotic rat model. Furthermore, mechanism study results indicate that the combination of ICT and HFS additively activates the Integrin–FAK (focal adhesion kinase)–ERK1/2 (extracellular signal-regulated kinase 1/2)–Runx2 (Runt-related transcription factor 2) axis, which could be linked to the beneficial recruitment of MSCs to the implant and subsequent osteogenesis enhancement. Collectively, the PLGA/TCP/ICT/HFS (P/T/I/S) bioactive scaffold is a promising biomaterial for repairing osteoporotic bone defects, which may have immense implications for their translation to clinical practice.-
dc.languageeng-
dc.relation.ispartofBioengineering-
dc.subjectadditive effect-
dc.subjectfocal adhesion signalling-
dc.subjecticaritin-
dc.subjectosteoporotic bone regeneration-
dc.subjectPLGA/TCP-
dc.subjectsecretome-
dc.titleBioactive Scaffold Fabricated by 3D Printing for Enhancing Osteoporotic Bone Regeneration-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.3390/bioengineering9100525-
dc.identifier.scopuseid_2-s2.0-85140458169-
dc.identifier.volume9-
dc.identifier.issue10-
dc.identifier.spagearticle no. 525-
dc.identifier.epagearticle no. 525-
dc.identifier.eissn2306-5354-

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