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International Journal of Bioprinting                               Engineered 3D-printed PVA vascular grafts























































            Figure 14. Biocompatibility assessment of the modified vascular graft using the direct contact method for bEnd.3 endothelial cells, L929 fibroblasts, and
            U937 monocyte-like cells. (A) Viability of cells following a 24-h incubation with the vascular graft (via MTT assay). Data presented as mean ± standard
            deviation; **p < 0.01; ***p < 0.001. (B) Adenosine triphosphate (ATP) content in cells following a 24-h incubation with the vascular graft (via ATP assay).
            Data presented as mean ± standard deviation; **p < 0.01. (C) Levels of lactate dehydrogenase (LDH) released from cells following a 24-h incubation with
            the vascular graft (via LDH assay). Data presented as mean ± standard deviation; *p < 0.05. (D–I) Cell morphology following a 24-h incubation with the
            vascular graft: (D–F) negative controls (NC) and (G–I) graft samples; (D and G) bEnd.3 endothelial cells, (E and H) L929 fibroblasts, and (F and I) U937
            monocyte cells. Magnification: ×10.

            fibroblasts following incubation with the vascular graft for   For monocytes, activation of the mitochondrial activity
            24 h (0.101 ± 0.019% compared to negative control; p <   was noted following direct exposure to the modified
            0.05) (Figure 14C). There were no obvious changes in the   vascular graft, i.e., an increase in MTT metabolism
            morphology of fibroblasts for this time interval (i.e., 24 h)   compared to the control at 12.99 ± 3.46%; p < 0.01 (Figure
            (Figure 14E and H). A slight decrease in ATP concentration   14A). However, the production of ATP was slightly
            was noted following a 72-h incubation of fibroblasts in the   diminished compared to the  negative control  (84.03 ±
            presence of the vascular graft (15.87 ± 7.65% compared to   1.77% relative to the negative control;  p < 0.01) (Figure
            the negative control; p < 0.05) (Figure 15B). No obvious   14B). It has been reported that mitochondrial metabolism
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            changes in the morphology of the fibroblasts were noticed   affects immune cell activation.  Here, the increase in
                                                                                                           +
            compared to the negative control at 72 h as well, following   nicotinamide adenine dinucleotide phosphate (NADP ),
            direct contact with the vascular graft (Figure 16E and H).   directly measured through MTT  and ATP assays, suggests
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            Volume 10 Issue 3 (2024)                       551                                doi: 10.36922/ijb.2193
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