3D bio-printed proteinaceous bioactive scaffold loaded with dual growth factor enhanced chondrogenesis and in situ cartilage regeneration

被引:2
作者
Shanto, Prayas Chakma [1 ]
Park, Seongsu [1 ]
Al Fahad, Md Abdullah [1 ]
Park, Myeongki [1 ]
Lee, Byong-Taek [1 ,2 ]
机构
[1] Soonchunhyang Univ, Coll Med, Dept Regenerat Med, Cheonan, South Korea
[2] Soonchunhyang Univ, Inst Tissue Regenerat, Cheonan, South Korea
基金
新加坡国家研究基金会;
关键词
3D bioprinting; dECM; TOCN; TGF-beta; 1/FGF-18; Cartilage regeneration; ARTICULAR-CARTILAGE; CELL VIABILITY; STEM-CELLS; HYDROGELS; ALGINATE; DIFFERENTIATION; OSTEOARTHRITIS; PROLIFERATION; CHONDROCYTES; TGF-BETA-1;
D O I
10.1016/j.bioactmat.2024.12.021
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Articular cartilage has a limited self-healing capacity, leading to joint degeneration and osteoarthritis over time. Therefore, bioactive scaffolds are gaining attention as a promising approach to regenerating and repairing damaged articular cartilage through tissue engineering. In this study, we reported on a novel 3D bio-printed proteinaceous bioactive scaffolds combined with natural porcine cancellous bone dECM, tempo-oxidized cellulose nanofiber (TOCN), and alginate carriers for TGF-beta 1, FGF-18, and ADSCs to repair cartilage defects. The characterization results demonstrate that the 3D scaffolds are physically stable and facilitate a controlled dual release of TGF-beta 1 and FGF-18. Moreover, the key biological proteins within the bioactive scaffold actively interact with the biological systems to create a favorable microenvironment for cartilage regeneration. Importantly, the in vitro, in vivo, and in silico simulation showed that the scaffolds promote stem cell recruitment, migration, proliferation, and ECM deposition, and synergistic effects of TGF-beta 1/FGF-18 with the bioactive scaffolds significantly regulate stem cell chondrogenesis by activating the PI3K/AKT and TGF beta 1/Smad4 signaling pathways. After implantation, the proteinaceous bioactive scaffold led to the regeneration of mechanically robust, full-thickness cartilage tissue that closely resembles native cartilage. Thus, these findings may provide a promising approach for regulating stem cell chondrogenesis and treating in situ cartilage regeneration.
引用
收藏
页码:365 / 385
页数:21
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