Page 489 - IJB-9-6
P. 489

International Journal of Bioprinting                              Bioprinting cell-laden protein-based hydrogel




                      GelMA (15% w/v)/  HUVECs and hBM-  Extrusion/chemical  •   Generated perfusable lumen   [150]
                      VEGF/silicate   SCs (2 × 10  cells/  crosslinking (pho-  possessing an endothelial lining
                                               6
                      nanoplatelets   mL)/-/bone        to-crosslinking)   at the construct’s center post-bi-
                                                                           oprinting
                                                                        •   Differentiation of hBMSCs in the
                                                                           inner gel to the smooth muscle
                                                                           cells, promoting the formation of
                                                                           vessels and enhancing the HU-
                                                                           VECs proliferation
                                                                        •   Promoted HUVEC’s survival and
                                                                           vasculogenesis, as well as formed
                                                                           mature bone niche by hBMSCs
                                                                           after 21 days
                      Alginate sulfate (1%  hBMSCs (20 × 10    Extrusion/chemical  •   Supported robust in vitro chon-  [151]
                                                   6
                      w/v)/GelMA (10%   cells/mL)/BALB/c   crosslinking (pho-  drogenesis due to the sustained
                      w/v)/ TGF-β     OlaHsd-Foxn1nu    to-crosslinking)   release of TGF-β , with little
                               3                                                       3
                                      nude mice/cartilage                  mineralization or hypertrophy
                                                                        •   Higher levels of sGAGs and
                                                                           collagen type II, as well as greater
                                                                           accumulation of matrix in groups
                                                                           treated with GF-loaded constructs

                      Decellularized   -/New Zealand White  Stereolithography/  •   Achieved constructs retaining   [139]
                      cartilage ECM (2%   rabbits/osteochondral  chemical crosslink-  exosomes, restoring chondro-
                      wt)/GelMA (10%                    ing (photo-cross-  cytes’ mitochondrial dysfunction,
                      w/v) containing                   linking)           improving cells migration, and
                      BMSCs-derived                                        polarizing the synovial macro-
                      exosomes                                             phage response towards an M2
                                                                           phenotype
                                                                        •   Formation of smooth tissues,
                                                                           regenerated fibrocartilage and
                                                                           hyaline-like cartilage, and more
                                                                           ossified tissues in ECM/GelMA/
                                                                           exosome-treated groups
                                                                        •   Higher score for animals treated
                                                                           with exosome-embedded struc-
                                                                           tures at 6 weeks after implantation
                      Atelocollagen type   hMSCs (5 × 10  cells/  Extrusion/-  •   Formation of a connective tissue   [154]
                                                 6
                      I (4% w/v) with (i)   mL) white male rats            capsule with multiple blood
                      hMSCs and with (ii)  (155–230 g; aged                vessels and detected cells with
                      decellularized ECM  1.5–2 months)/car-               cytoplasm including collagen type
                      granules (2.5% w/v)  tilage                          II in the first group
                      and hMSCs                                         •   Small islands of cartilaginous tis-
                                                                           sue with irregular shapes adjacent
                                                                           to the construct in the first group
              GFs and signaling molecules                               •   tiny isogenic groups, and the
                                                                        •
                                                                           Generation of a cartilage tissue
                                                                           with chondroblasts forming
                                                                           produced ECM having a great
                                                                           content of GAG in the second
                                                                           group
                                                                           Observed intense reaction to
                                                                           collagen type II by the tissue and
                                                                           signs of reduced proliferative
                                                                           activity in the second group

            bioprinting techniques [165,166] . It needs to be considered   weight,  an  essential  parameter  influencing  rheological
            that by extraction and purification procedures, proteins   properties [167] . To achieve the required purification degree
            can be degraded which negatively impacts their molecular   while  ensuring  the  best  quality,  selecting  the  proper



            Volume 9 Issue 6 (2023)                        481                          https://doi.org/10.36922/ijb.1089
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