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International Journal of Bioprinting                                Immunomodulatory bone repair by MBG/PCL

















































            Figure 3. Physicochemical characterization of MBG/PCL scaffolds. (A) FTIR spectra. (B) Thermogravimetric analysis graph. (C) Comparison of
            compressive strength between scaffolds. (D) Comparison of porosity between scaffolds. (E) Comparison of hydrophilicity between scaffolds, measured by
            contact angle.


            CD206 in MBG scaffolds was extremely low in all groups   of BMSCs, the  scaffolds in each group were added with
            except for the 10MBG/PCL group, but better than that of   corresponding MP-conditioned medium for  pro-BMSCs
            the 0MBG/PCL group. The expression of  Arg gene was   osteogenic differentiation. Basically, the  expression
            upregulated the most  significantly in  the 10MBG/PCL   of osteogenic genes in MBG-containing scaffolds was
            group, and the expression was the lowest in the 0MBG/  significantly higher than that in the pure PCL group, except
            PCL group, while there was no significant difference in   for the 0MBG/PCL and 30MBG/PCL groups, which
            the MBG scaffolds of the other three groups. Regarding   showed no significant difference in the expression of Col1
            the M1-type genes, the 10MBG/PCL group significantly   (Figure 5C). Compared with other groups, the expression
            inhibited the expression of  Tnfa and  Il1b, whereas the   of osteogenesis-related  genes  (Alp,  Runx2,  Opn,  Col1,
            0MBG/PCL group upregulated them most significantly.   Bmp2) was most significantly upregulated in the 10MBG/
            The 30MBG/PCL showed stronger inhibition on  Tnfa   PCL group. ALP staining and quantification, as displayed
            expression compared with than the 5MBG/PCL and     in Figure 5B-1 and B-2, showed that the ALP activity of
            20MBG/PCL groups. However, the inhibition of Il1b was   the composite scaffolds was significantly higher than
            more evident in the 20MBG/PCL and 5MBG/PCL groups   that of the pure PCL group, with the 10MBG/PCL group
            than in the 30MBG/PCL group.                       demonstrating the most pronounced ALP activity. The
               To evaluate the  potential of scaffold-mediated M2   ALP activity of the 20MBG/PCL group was higher than
            polarization of MPs to promote osteogenic differentiation   that of the 30MBG/PCL group, but none of them was
                                                               significantly different from that of 5MBG/PCL group.


            Volume 10 Issue 5 (2024)                       327                                doi: 10.36922/ijb.3551
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