Page 31 - manuscript_ijb05596
P. 31

ensuring that the new tissue had sufficient mechanical strength and provided space for

                   subsequent cell infiltration and angiogenesis. 96,97  However, chronic hyperglycemia in

                   diabetic patients directly damaged the function of fibroblasts by activating the polyol
                   pathway and the accumulation of advanced glycation end products (AGEs), which was

                   characterized  by  a  significant  decrease  in  migration  ability,  VEGF  secretion,  and

                   hypoxia-inducible factor 1α (HIF-1α) stability, leading to angiogenesis disorders. More

                   seriously, reactive aldehydes produced by lipid peroxidation could covalently modify

                   collagen  molecules  to  form  cross-linked  structures,  which  not  only  reduce  the

                   bioavailability  of  collagen,  but  also  disrupte  ECM  homeostasis  by  activating  the

                   overexpression of MMPs. This  double hit further impaired  the migration ability of

                                                                           98
                                                                                                99
                   keratinocytes and delayed the re-epithelialization process. Mujiao Liang et al. used
                   recombinant human collagen methacrylate (RHCMA) and HA to form a 3D network

                   by UV light cross-linking and loaded with AgNPs. The porous structure of the network

                   mimics ECM, promoted fibroblast adhesion and migration, and collagen components

                   directly induce collagen deposition. Combined with  its antibacterial properties,  this

                   hydrogel established a microenvironment conducive to healing and accelerates wound
                   repair. Feifei Huang et al. 100  constructed a bovine dermal type I collagen bionic scaffold

                   loaded  with  overexpressed  fibroblast  growth  factor  (bFGF-mscs).  This  biomimetic

                   scaffold activated the HIF-1 signaling pathway through continuous release of bFGF,

                   promoted endothelial tube formation and fibroblast migration, and accelerated diabetic

                   wound healing by enhancing AKT phosphorylation and collagen deposition. Although

                   the scaffolds involved in this article are similar to hydrogels in terms of their porous

                   structure, biocompatibility and controllable release characteristics. The gastrointestinal

                   surgical incision will be affected by the acidic environment to destroy blood clots and

                   delay the formation of granulation tissue. Therefore, fibroblast growth factor can be

                   added to the hydrogel for repairing the gastrointestinal surgical incision to significantly

                   accelerate angiogenesis. 101  Jie Wang et al. 102  showed the chemical ligation method of

                   Spy was used to efficiently integrate IFN-α, activate the migration ability of fibroblasts

                   and up-regulate the expression of extracellular matrix proteins such as COL-1α and α-


                                                            30
   26   27   28   29   30   31   32   33   34   35   36