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International Journal of Bioprinting                                DNA-functionalized hyaluronic acid bioink




















































            Figure 8. DNA-functionalized hydrogels for construction of tissue in vitro. (a) BMSCs recognition and binding by Apt19S-FAM, analysis of fluorescence
            microscopy, and quantitative assessment. Reprinted with permission from ref.  Copyright © 2022 American Chemical Society. (b) Aptamer-bilayer
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            scaffold in osteochondral defect repair. Reprinted with permission from ref.  Copyright © 2017 Wiley. (c) Aptamer-based 3D-bioprinted scaffolds for
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            enhanced cartilage regeneration. Reprinted with permission from ref.  Copyright © 2021 American Chemical Society. (d) In vivo macroscopic and
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            confocal images of endogenous stem cell migration. Reprinted with permission from ref.  Copyright © 2021 American Chemical Society. (e) Polymer
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            crosslinking scheme using a library of crosslinker splints to prevent intramolecular bond formation. Reprinted with permission from ref.  Copyright ©
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            2023 Nature. (f) Confocal microscopy images of hiPSC cysts in DyNAtrix [+RGD] vs. Matrigel at day 7, and images of a trophoblast organoid in DyNAtrix
            [+RGD] stained for TEAD4, E-cadherin, GCM1, and DAPI (nuclei) at day 7. Reprinted with permission from ref.  Copyright © 2023 Nature.
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            creates structures with viable cells and normal functions.   can bind with DNA crosslinkers composed of two splints,
            By mixing peptide–DNA conjugates (bioink A) and    forming a dynamic supramolecular network. By changing
            covalent DNA linkers (bioink B) in specific ratios, the   the sequence information of the overlap domain between
            hydrogel forms rapidly and possesses self-healing and   the splints in the DNA crosslinkers, the mechanical,
            high mechanical strength properties. It also responds to   thermodynamic, and kinetic properties of the hydrogel
            proteases and nucleases, allowing selective removal of   can be systematically regulated to suit different cell and
            hydrogel sections in the presence of cells. This advancement   organoid culture needs. For instance, stress relaxation
            opens doors to fabricating precise 3D tissue structures with   time from less than 1 s to several hours can be achieved by
            diverse cell arrangements.  Recently, Peng et al. developed   choosing different lengths of overlap domain. Thermally
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            a hydrogel named DyNAtrix, which consists of ultra-high-  activated crosslinking at 37°C can be achieved by adding
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            molecular-weight polymers and DNA crosslinkers.  The   blocking  strand.  Controlled degradation  of the  hydrogel
            polymers are connected with DNA anchor chains, which   can be achieved by adding DNase I. Since the non-covalent

            Volume 10 Issue 2 (2024)                        38                                doi: 10.36922/ijb.1814
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