Surface modification techniques have been used to develop biomimetic scaffolds by incorporating cell adhesion
peptides. In our previous work, we have shown the tethering of laminin-332 α3 chain to
type I collagen scaffold using microbial
transglutaminase (mTGase), promotes cell adhesion, migration, and proliferation. In this study, we evaluated the wound healing properties of tailored laminin-332 α3 chain (
peptide A: PPFLMLLKGSTR) tethered to a
type I collagen scaffold using mTGase by incorporating
transglutaminase substrate
peptide sequences containing either
glutamine (
peptide B: PPFLMLLKGSTREAQQIVM) or
lysine (
peptide C: PPFLMLLKGSTRKKKKG) in rat full-thickness
wound model at two different time points (7 and 21 days). Histological evaluations were assessed for
wound closure, epithelialization, angiogenesis, inflammatory, fibroblastic cellular infiltrations, and quantified using stereological methods (p < 0.05).
Peptide A and B tethered to
collagen scaffold using mTGase stimulated neovascularization, decreased the inflammatory cell infiltration and prominently enhanced the fibroblast proliferation which significantly accelerated the wound healing process. We conclude that surface modification by incorporating motif of laminin-332 α3 chain (
peptide A: PPFLMLLK GSTR) domain and
transglutaminase substrate to the laminin-332 α3 chain (
peptide B: PPFLMLLKGSTREAQQIVM) using mTGase may be a potential candidate for tissue engineering applications and skin regeneration.