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International Journal of Bioprinting                       G40T60@WNT5A promotes osteoblast differentiation




            and calcium silicate scaffolds co-cultured with HUVECs   Funding
            and BMSCs. 80
                                                               This study was supported by Hebei Provincial Health and
            5. Conclusion                                      Health Commission Key Science and Technology Research
                                                               Program (20210120, 20221202), Hebei Provincial Department
            WNT5A is a positive regulatory factor in osteoblast   of Finance Funding for Prevention and Treatment of Geriatric
            differentiation and angiogenesis. In this study, the   Diseases, and 2022 Government-funded Clinical Medicine
            degradable G40T60 scaffolds loaded with WNT5A were   Excellence Training Program Leader Project.
            prepared based on Masquelet technique and using 3D
            printing, and we showed that they could promote the   Conflict of interest
            formation of induced membranes and thus facilitate   The authors declare no conflicts of interest.
            osteoblast differentiation and angiogenesis in CTO&BD
            rats (Figure 10). This study proposes a new method for   Author contributions
            treating CTO&BD. The degradable G40T60@WNT5A
            scaffold we constructed using 3D printing based on   Conceptualization: Tao Zhang
            the Masquelet technique successfully promoted the   Data curation: Tao Zhang
                                                               Formal analysis: Xinhui Wang
            differentiation of osteoblasts and neovascularization in   Investigation: Rongkang Guo
            rats. This research provides a new perspective for treating   Methodology: Tianhua Dong, Fan Liu
            chronic bone defects and has significant clinical relevance   Visualization: Rongkang Guo, Xinhui Wang
            by effectively improving the quality of life for patients.  Writing – original draft: Fan Liu, Chaohan Wu
               However, several limitations of this study should be   Writing – review & editing: Tao Zhang, Fan Liu
            acknowledged. Firstly, the experiments were conducted
            only in a rat model, and thus, further investigations   Ethics approval and consent to participate
            are required  for corroborating the clinical  application   Peripheral blood samples were collected with the approval
            of the scaffolds in humans. Secondly, due to cost and   of the Ethics Committee of the Third Hospital of Hebei
            technological limitations, a degradable scaffold was used in   Medical University (Ethics Committee number: Ke-2022-
            this study, and the degradation rate and biocompatibility   104-1). All animal experiments have been approved by
            of the material need further optimization. In addition,   the  Animal  Ethics  Committee  of  the  Third  Hospital  of
            CTO&BD is typically a chronic inflammatory process   Hebei Medical University (No. KSD2022-033-1), and all
            accompanied by bone destruction caused by bacterial   animal experiments in this study comply with the local
            infection; therefore, the  antimicrobial properties  of  the   principles for the management and use of experimental
            G40T60@WNT5A scaffold should also be evaluated.    animals. Subjects obtained their informed consent prior to
            Furthermore, this study requires further investigations   participation in this study.
            into the specific mechanisms behind the role of WNT5A
            gene in osteoblast differentiation and neovascularization,   Consent for publication
            as well as its interactions with other related factors. In   Consent for publication was obtained from the participants.
            future, it is necessary to further refine the treatment plan
            adopted in this study by optimizing degradation rate,   Availability of data
            improving biocompatibility of the scaffold material, and
            strengthening antimicrobial properties of the scaffold.   The data that support the findings of this study are available
            Additionally, more genes and molecular mechanisms   on request from the corresponding author.
            related to the development of CTO&BD, which have   References
            implications on the treatment, should be identified.

               In summary, this study offers new directions to improve   1.   Montanaro L, Speziale P, Campoccia D, et al. Scenery
            the treatment strategies for CTO&BD patients. Besides,   of Staphylococcus implant infections in orthopedics.
            the scaffolds we fabricated in this work will find broader      Future Microbiol. 2011;6(11):1329-1349.
                                                                  doi: 10.2217/fmb.11.117
            applications in the field of orthopedics.
                                                               2.   Claro T, Widaa A, O’Seaghdha M, et al.  Staphylococcus
            Acknowledgments                                       aureus protein A binds to osteoblasts and triggers signals that
                                                                  weaken bone in osteomyelitis. PLoS One. 2011;6(4):e18748.
            None.                                                 doi: 10.1371/journal.pone.0018748


            Volume 10 Issue 2 (2024)                       245                                doi: 10.36922/ijb.1461
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