SDF-1 liposomes promote sustained cell proliferation in mouse diabetic wounds

Wound Repair Regen. 2015 Sep;23(5):711-23. doi: 10.1111/wrr.12334. Epub 2015 Sep 8.

Abstract

Chronic skin wounds are a common complication of diabetes. When standard wound care fails to heal such wounds, a promising approach consists of using decellularized matrices and other porous scaffold materials to promote the restoration of skin. Proper revascularization is critical for the efficacy of such materials in regenerative medicine. Stromal cell-derived factor-1 (SDF-1) is a chemokine known to play a key role for angiogenesis in ischemic tissues. Herein we developed nanosized SDF-1 liposomes, which were then incorporated into decellularized dermis scaffolds used for skin wound healing applications. SDF-1 peptide associated with liposomes with an efficiency of 80%, and liposomes were easily dispersed throughout the acellular dermis. Acellular dermis spiked with SDF-1 liposomes exhibited more persistent cell proliferation in the dermis, especially in CD31(+) areas, compared to acellular dermis spiked with free SDF-1, which resulted in increased improved wound closure at day 21, and increased granulation tissue thickness at day 28. SDF-1 liposomes may increase the performance of a variety of decellularized matrices used in tissue engineering.

Keywords: Chemotaxis; Dermis; Diabetes; Growth factors; Liposome; Wound healing.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Acellular Dermis*
  • Animals
  • Cell Proliferation
  • Chemokine CXCL12 / administration & dosage*
  • Diabetes Mellitus, Experimental / complications*
  • Diabetes Mellitus, Experimental / metabolism
  • Diabetes Mellitus, Experimental / pathology
  • Humans
  • Liposomes
  • Mice
  • Skin / metabolism
  • Skin / pathology*
  • Tissue Engineering
  • Tissue Scaffolds*
  • Wound Healing / physiology*
  • Wounds and Injuries / etiology
  • Wounds and Injuries / metabolism
  • Wounds and Injuries / therapy*

Substances

  • Chemokine CXCL12
  • Liposomes