{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["6(3)"],"submitter":["Sun X"],"funding":["National Natural Science Foundation of China","National Key Research and Development Program of China"],"pubmed_abstract":["Critical-sized bone defect repair in patients with diabetes mellitus remains a challenge in clinical treatment because of dysfunction of macrophage polarization and the inflammatory microenvironment in the bone defect region. Three-dimensional (3D) bioprinted scaffolds loaded with live cells and bioactive factors can improve cell viability and the inflammatory microenvironment and further accelerating bone repair. Here, we used modified bioinks comprising gelatin, gelatin methacryloyl (GelMA), and 4-arm poly (ethylene glycol) acrylate (PEG) to fabricate 3D bioprinted scaffolds containing BMSCs, RAW264.7 macrophages, and BMP-4-loaded mesoporous silica nanoparticles (MSNs). Addition of MSNs effectively improved the mechanical strength of GelMA/gelatin/PEG scaffolds. Moreover, MSNs sustainabl"],"journal":["Bioactive materials"],"pagination":["757-769"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC7522044"],"repository":["biostudies-literature"],"pubmed_title":["Three-dimensional bioprinting of multicell-laden scaffolds containing bone morphogenic protein-4 for promoting M2 macrophage polarization and accelerating bone defect repair in diabetes mellitus."],"pmcid":["PMC7522044"],"pubmed_authors":["Yang H","Jin W","Deng Q","Ma Z","Sun X","Zhou X","Wang J","Zhao X","Li T","Ma J","Wang W","Zhang C","Zhao J","Qiang L","Liang Q"],"additional_accession":[]},"is_claimable":false,"name":"Three-dimensional bioprinting of multicell-laden scaffolds containing bone morphogenic protein-4 for promoting M2 macrophage polarization and accelerating bone defect repair in diabetes mellitus.","description":"Critical-sized bone defect repair in patients with diabetes mellitus remains a challenge in clinical treatment because of dysfunction of macrophage polarization and the inflammatory microenvironment in the bone defect region. Three-dimensional (3D) bioprinted scaffolds loaded with live cells and bioactive factors can improve cell viability and the inflammatory microenvironment and further accelerating bone repair. Here, we used modified bioinks comprising gelatin, gelatin methacryloyl (GelMA), and 4-arm poly (ethylene glycol) acrylate (PEG) to fabricate 3D bioprinted scaffolds containing BMSCs, RAW264.7 macrophages, and BMP-4-loaded mesoporous silica nanoparticles (MSNs). Addition of MSNs effectively improved the mechanical strength of GelMA/gelatin/PEG scaffolds. Moreover, MSNs sustainabl","dates":{"release":"2021-01-01T00:00:00Z","publication":"2021 Mar","modification":"2025-05-29T21:27:24.216Z","creation":"2020-10-29T10:28:44Z"},"accession":"S-EPMC7522044","cross_references":{"pubmed":["33024897"],"doi":["10.1016/j.bioactmat.2020.08.030"]}}