Exosomes derived from Nr-CWS pretreated MSCs facilitate diabetic wound healing by promoting angiogenesis via the circIARS1/miR-4782-5p/VEGFA axis

Chin J Nat Med. 2023 Mar;21(3):172-184. doi: 10.1016/S1875-5364(23)60419-4.

Abstract

Mesenchymal stem cell (MSC)-derived exosomes (Exos) were reported to a prospective candidate in accelerating diabetic wound healing due to their pro-angiogenic effect. MSCs pretreated with chemistry or biology factors were reported to advance the biological activities of MSC-derived exosomes. Hence, this study was designed to explore whether exosomes derived from human umbilical cord MSCs (hucMSCs) preconditioned with Nocardia rubra cell wall skeleton (Nr-CWS) exhibited superior proangiogenic effect on diabetic wound repair and its underlying molecular mechanisms. The results showed that Nr-CWS-Exos facilitated the proliferation, migration and tube formation of endothelial cells in vitro. In vivo, Nr-CWS-Exos exerted great effect on advancing wound healing by facilitating the angiogenesis of wound tissues compared with Exos. Furthermore, the expression of circIARS1 increased after HUVECs were treated with Nr-CWS-Exos. CircIARS1 promoted the pro-angiogenic effects of Nr-CWS-Exos on endothelial cellsvia the miR-4782-5p/VEGFA axis. Taken together, those data reveal that exosomes derived from Nr-CWS-pretreated MSCs might serve as an underlying strategy for diabetic wound treatment through advancing the biological function of endothelial cells via the circIARS1/miR-4782-5p/VEGFA axis.

Keywords: Angiogenesis; Exosomes; Mesenchymal stromal cells; Nocardia rubra cell wall skeleton (Nr-CWS); circIARS1.

MeSH terms

  • Cell Wall Skeleton / metabolism
  • Diabetes Mellitus*
  • Endothelial Cells / metabolism
  • Exosomes* / chemistry
  • Exosomes* / metabolism
  • Humans
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • Neovascularization, Physiologic
  • Vascular Endothelial Growth Factor A / metabolism
  • Wound Healing* / physiology

Substances

  • Cell Wall Skeleton
  • MicroRNAs
  • Vascular Endothelial Growth Factor A
  • VEGFA protein, human