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International Journal of Bioprinting                                      Bioprinted osteoarthritis scaffolds






























            Figure 7. H O  reduces the expression of type II collagen in the 3D-bioprinted cartilage senescence model. Immunofluorescence staining analysis (A)
                     2
                    2
            and summary of quantitative data (B) for type II collagen in the 3D-bioprinted cartilage senescence models. All statistical data are represented as mean ±
            standard deviation (n = 3; ***p < 0.001). Scale bar: 100 µm.
            senescence models were developed, and the optimal   and the Ganzhou Municipal Science and Technology
            H O  concentration and induction time for constructing   Project (2022-YB1396).
             2
               2
            the senescence models were determined to be 500 μM
            and 2 h, respectively. Compared to the 2D AC senescence   Conflict of interest
            models, the 3D-bioprinted cartilage senescence models   The authors declare no conflicts of interest.
            more closely resembled the natural aging state of human
            cartilage in terms of aging-related molecular expression.   Author contributions
            However, this study used SD rat ACs instead of humans
            and lacked comprehensive characterization of aging-  Conceptualization: Hanxiao Qin
            related markers, including inflammatory factors and   Formal analysis: Hanxiao Qin, Fanqing Xu
            senescence-related proteins. These limitations reduce   Investigation: Hanxiao Qin, Fanqing Xu
            the translational relevance of the model for elucidating   Methodology: All authors
            the mechanisms underlying OA development in        Writing–original draft: Hanxiao Qin
            humans. Future work should focus on developing more   Writing–review & editing: All authors
            human-compatible  in vitro OA models. Overall, the   All the authors have read and approved the final manuscript.
            3D-bioprinted cartilage senescence model may provide
            a valuable new experimental platform for research on   Ethics approval and consent to participate
            the prevention and treatment of aging-related OA
            and  the  mechanisms  underlying  its  development  and   The animal experiments were conducted in accordance
            progression. 70–72                                 with the “Regulations on the Management of Experimental
                                                               Animals” and were approved by the Experimental Animal
            Acknowledgments                                    Ethics Committee of Hangzhou Institute of Medicine
                                                               Chinese Academy of Sciences (approval no. 2023R0025).
            The authors are grateful to the Core Technology Platform
            of the Hangzhou Institute of Medicine Chinese Academy of   Consent for publication
            Sciences for providing the essential resources for this study.
                                                               Not applicable.
            Funding
            This  study  was  supported  by  the  Shenzhen     Availability of data
            Science  and  Technology  Innovation  Committee    Data  is  available  from  the  corresponding  author  upon
            (JCYJ20230807110259002 and JCYJ20240813150201003)   reasonable request.


            Volume 11 Issue 4 (2025)                       204                            doi: 10.36922/IJB025150136
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