Synergistic Effect of Adipose-Derived Stem Cells and Fat Graft on Wrinkles in Aged Mice

Plast Reconstr Surg. 2019 Jun;143(6):1637-1646. doi: 10.1097/PRS.0000000000005625.

Abstract

Background: The authors investigated the synergistic effects of adipose-derived stem cells and fat graft on skin wrinkles in a nude mouse model of chronologic aging.

Methods: After 50 weeks of chronologic aging, 44 female BALB/c nude mice were classified into four groups: (1) negative control, (2) mice injected subcutaneously with fat on the back skin (0.5 cm), (3) mice injected with adipose-derived stem cells (1 × 10 cells in 0.5 cm Hanks balanced salt solution), and (4) mice injected with both fat (0.5 cm) and adipose-derived stem cells (1 × 10 cells in 0.5 cm Hanks balanced salt solution). The degree of wrinkling was evaluated using replica analysis, and skin biopsies were performed after 4 weeks. The dermal thickness and density of collagen were determined. Type I procollagen and matrix metalloproteinase levels were determined using real-time polymerase chain reaction and Western blot analysis. Tropoelastin, fibrillin-1, and CD31 levels were evaluated using immunohistochemistry.

Results: Based on the total wrinkle area, there was significant wrinkle reduction in the fat-treated and adipose-derived stem cell with fat-treated groups. Type I procollagen mRNA and collagen levels were significantly higher in the adipose-derived stem cell with fat-treated group than in the adipose-derived stem cell-treated and the fat-treated groups. In addition, the adipose-derived stem cells with fat graft group exhibited significantly higher CD31 expression level than the adipose-derived stem cell-treated and the fat-treated groups.

Conclusion: Both adipose-derived stem cells and fat graft have a wrinkle-reducing effect and synergistically affect collagen synthesis and neovascularization.

Publication types

  • Comparative Study

MeSH terms

  • Adipocytes / transplantation*
  • Adipose Tissue / pathology
  • Adipose Tissue / transplantation*
  • Animals
  • Biopsy, Needle
  • Blotting, Western
  • Cell Proliferation
  • Collagen / metabolism*
  • Combined Modality Therapy
  • Disease Models, Animal
  • Female
  • Graft Survival
  • Humans
  • Immunohistochemistry
  • Injections, Intralesional
  • Mice
  • Mice, Inbred BALB C
  • Middle Aged
  • Random Allocation
  • Real-Time Polymerase Chain Reaction / methods
  • Sensitivity and Specificity
  • Skin Aging*
  • Stem Cell Transplantation / methods*

Substances

  • Collagen