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International Journal of Bioprinting                    Peritoneal scaffolds for the peritoneal adhesion prevention











































            Figure 6. Peritoneal scaffolds directly participated in the repair of peritoneal damages revealed by in vivo tracking of GFP-labeled mesothelial cells. (A and
            B) Representative immunofluorescence staining of different groups on day 1 (A) and day 7 (B), postoperatively. (C) Quantification of the number of GFP   +
            peritoneal mesothelial cells per field of view (FOV) in IBM group or IBM + peritoneal scaffold group. n = 3/group. ****P < 0.0001.

            The peritoneal scaffold was based on the biodegradable   and  C). This suggests that the implanted peritoneal
            and biocompatible PCL materials, with the advantage of   scaffold was directly involved in the repair of the
            good mechanical strength and easy fixation. The peritoneal   damaged peritoneum.
            scaffold was fabricated based on the MEW technology,
            which  could  be  personalized  according  to  different   4. Conclusions
            applications. The in vivo experiments confirmed that the
            peritoneal scaffold had good biosafety, and prevented   Here, we reported an MEW-based peritoneal scaffold
            the formation of intraperitoneal adhesion and inhibited   application for the first time to prevent peritoneal
            fibrous tissue proliferation.                      adhesion and promote the repair of injured peritoneum.
                                                               The MEW-printed scaffold with the fibers crossed at
            3.6. Promotion of peritoneal repair by the peritoneal   30° was screened due to the improved flexibility and
            scaffolds in vivo                                  hydrophobic property. Such a fiber angle also facilitated
            To  confirm  whether  the  peritoneal scaffold  could   carriage of more mesothelial cells that grew in an
            participate in the repair of the damaged peritoneum   orderly manner on the scaffold. The resultant peritoneal
            as expected, mesothelial cell tracking by  GFP gene-  scaffolds inhibited migration of macrophages  in vitro
            contained lentivirus (Figure S5) was carried out.   and prevented peritoneal adhesions  in vivo. The use of
            We were able to assess the mesothelial cell survival   primary peritoneal mesothelial cells was a highlight in
            after implantation  in vivo,  and evaluate how  the  cells   the fabrication of cell-laden scaffolds because these cells
            affected the repair of damaged peritoneal tissues. To   were found to engage directly in the repair of injured
            our expectation, expression of GFP was seen at the   peritoneum. The peritoneal scaffold is a novel attempt to
            injured peritoneal site on the first day after peritoneal   solve the problem of peritoneal adhesions, and sets a good
            scaffold implantation (Figure 6A). On day 7, the injured   example of in situ repair based on cell-laden scaffolds for
            peritoneal site had higher GFP expression (Figure  6B    tissue engineering.

            Volume 9 Issue 3 (2023)                         61                          https://doi.org/10.18063/ijb.682
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