Self-assembling peptide hydrogel scaffold integrating stem cell-derived exosomes for infected bone defects

J Biomater Sci Polym Ed. 2024 Jul;35(10):1511-1522. doi: 10.1080/09205063.2024.2336316. Epub 2024 Apr 4.

Abstract

Infected bone defect (IBD) is a great challenge in orthopedics, which involves in bone loss and infection. Here, a self-assembling hydrogel scaffold (named AMP-RAD/EXO), integrating antimicrobial peptides(AMPs), RADA16 and BMSCs exosomes with an innovative strategy, is developed and applied in IBD treatment for sustained antimicrobial ability, accelerating osteoblasts proliferation and promoting bone regeneration. AMPs present an excellent ability to inhibit infection, RADA16 is a self-assembling peptide hydrogel for AMPs delivery, and BMSCs exosomes can promote the bone regeneration. The prepared AMP-RAD/EXO exhibited a polyporous 3D structure for imbibition of BMSCs exosomes and migration of osteoblasts. In vitro studies indicate AMP-RAD/EXO can inhibit the growth of Staphylococcus aureus, accelerate the proliferation and migration of BMSCs. More importantly, in vivo results also prove that AMP-RAD/EXO exhibit an excellent effect on IBD treatment. Thus, the prepared AMP-RAD/EXO provides a multifunctional scaffold concept for bone tissue engineering technology.

Keywords: AMPs; BMSCs exosomes; IBD; RADA16; Self-assembling hydrogel scaffold.

MeSH terms

  • Animals
  • Antimicrobial Peptides / chemistry
  • Antimicrobial Peptides / pharmacology
  • Bone Regeneration* / drug effects
  • Bone and Bones
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects
  • Exosomes* / chemistry
  • Hydrogels* / chemistry
  • Mesenchymal Stem Cells / cytology
  • Osteoblasts / cytology
  • Osteoblasts / drug effects
  • Staphylococcus aureus* / drug effects
  • Staphylococcus aureus* / physiology
  • Tissue Engineering
  • Tissue Scaffolds* / chemistry

Substances

  • Hydrogels
  • Antimicrobial Peptides