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International Journal of Bioprinting                          3D model of neurogenesis in Alzheimer’s disease




            bioprinted in the absence of Aβ oligomers increased up to   95% of AD cases are sporadic instead of familial, 98,99  and in
            eight days after bioprinting (p < 0.0001; day 8 vs. day 0   vitro models for this form of AD are scarce.
            [immediately after bioprinting]) (Figure 4A and B). This   The area of the neurospheres bioprinted in the hydrogel
            growth in the neurosphere area corresponded to increased   containing Aβ oligomers did not increase over time
            cell proliferation (379.8 ± 7.7%) on day 8 compared to day 0    (Figure 4B). Although there were smaller neurospheres on
            (p < 0.0001; immediately after bioprinting) (Figure 4C).   day 8 compared to day 0 (Figure 4A), the average size did
               Although a recent study has emphasized the great   not statistically change. A pronounced negative effect on
            potential of neurospheres from transgenic animals for   cell proliferation/viability was observed in neurospheres
            evaluating familial AD,  in this study, we prioritized the   bioprinted in the hydrogel containing Aβ oligomers
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            Aβ extracellular oligomers in the 3D model in the NSC   (52.7 ± 16.5% for day 3; 8.02 ± 3.1% for day 8; p < 0.0001,
            environment. This decision was based on the fact that over   compared with  constructs  bioprinted  in the  hydrogel























































            Figure 4. Amyloid β (Aβ) oligomers impact neurosphere area and proliferation in the 3D constructs. (A) Light microscope micrographs of constructs
            with neurospheres from the subventricular zone (SVZ) of six-week-old C57bl/6 mice, bioprinted with or without 1 µM Aβ oligomers. The black arrow
            indicates the well-delimited and spheroidal surface of the neurosphere, even eight days after bioprinting. The red arrow demonstrates the necrotic core and
            small neurospheres three days after bioprinting. Scale bars: 100 μm. (B) Area of neurospheres in constructs with and without Aβ oligomers ( p < 0.0001,
                                                                                                     ****
            compared with neurospheres area from day 0). (C) Cell proliferation in constructs with and without Aβ oligomers  (**** p < 0.0001; and ns: non-significant).

            Volume 10 Issue 5 (2024)                       515                                doi: 10.36922/ijb.3751
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