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International Journal of Bioprinting                       G40T60@WNT5A promotes osteoblast differentiation








































            Figure 10. Mechanism behind of the therapeutic effect of a degradable WNT5A-loaded scaffold fabricated using Masquelet technique on CTO&BD by
            virtue of the scaffold’s capacity in promoting osteogenic differentiation and angiogenesis.

            integrity to 3D-printed constructs.  Consistent with our   delivered promising outcomes, in terms of safety during
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            research  findings,  studies  have  found  that 3D-printed   in vivo surgery, biodegradation, and ability to induce bone
            scaffolds could direct the extracellular matrix/stromal   formation after membrane formation. 77,78
            stem cells for bone and cartilage defect regeneration. 23,32,75
            In addition, according to a previous report, 3D-printed   We extracted the rat’s induced membrane and co-
            bioresorbable hydrogel scaffolds, which have high flexibility   cultured it with BMSCs and UVECs. The results showed
            and adaptability and could be used for non-load-bearing   that the membrane induced by the G40T60@WNT5A
            bone regeneration, were successfully created. 31   scaffold significantly promoted osteogenic differentiation
                                                               and angiogenesis. The result indicated that 3D-printed
               We confirmed that the G40T60@WNT5A scaffold     degradable scaffolds could promote the formation of
            could  significantly  promote the  formation  of  induced   induced membrane in CTO&BD rat model, which
            membranes in a CTO&BD rat model we constructed, in   stimulates osteogenic differentiation and vascular
            which the scaffold was transplanted. The result indicated   neogenesis. Another study has attempted to analyze the
            that the WNT5A-loaded, degradable G40T60 scaffold   effects of a 3D-printed hydroxyapatite gel (HAP-GEL)
            fabricated by 3D printing could promote the formation
            of induced membrane in a CTO&BD rat, thus facilitating   scaffold combined with BMSCs and human umbilical
            osteogenic differentiation and angiogenesis. Our   vein endothelial cells (HUVECs) on repairing rabbit
            research  is  consistent  with  other  studies,  demonstrating   cranial defects, and found that the 3D-printed scaffold
            that  3D-printed  scaffolds  significantly  enhance  bone   and the combination of BMSCs and HUVECs exhibited
            regeneration in animal models.  Furthermore, 3D-printed   good osteogenic ability and biocompatibility and showed
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            biodegradable  scaffolds  have  been  demonstrated  to   excellent results in repairing rabbit cranial defects.  In a
            promote collagen synthesis and induce membrane     study regarding the synergistic effects of co-cultivation
            formation, vascularization, and osteogenesis, significantly   of endothelial cells and matrix cells on 3D-printed
            promoting maxillofacial regeneration.  In addition,   calcium silicate-doped β-TCP scaffolds, which promote
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            a few studies reported that 3D-printed degradable   vascularization and bone formation, significantly enhanced
            scaffolds in a rabbit femur cortical bone defect model   bone formation was noted in 3D-printed porous β-TCP


            Volume 10 Issue 2 (2024)                       244                                doi: 10.36922/ijb.1461
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