Differential contributions of graft-derived and host-derived cells in tissue regeneration/remodeling after fat grafting

Plast Reconstr Surg. 2015 Jun;135(6):1607-1617. doi: 10.1097/PRS.0000000000001292.

Abstract

Background: Recent research indicates that the adipose tissue of nonvascularized grafts is completely remodeled within 3 months, although origins of next-generation cells are unclear.

Methods: Inguinal fat pads of green fluorescent protein mice and wild-type mice were cross-transplanted beneath the scalp. At 1, 2, 4, and 12 weeks after transplantation, grafted fat was harvested, weighed, and analyzed through immunohistochemistry, whole-mount staining, and flow cytometry of cell isolates. Bone marrow of green fluorescent protein mice was transplanted to wild-type mice (after irradiation). Eight weeks later, these mice also received fat grafts, which were analyzed as well.

Results: The majority of host-derived cells detected during remodeling of grafted fat were macrophages (>90 percent at the early stage; 60 percent at 12 weeks). Cell origins were analyzed at 12 weeks (i.e., when completely regenerated). At this point, mature adipocytes were largely derived from adipose-derived stem/stromal cells of grafts. Although vascular wall constituents were chiefly graft derived, vascular endothelial cells originated equally from graft and host bone marrow. Adipose-derived stem/stromal cells of regenerated fat were an admixture of grafted, host nonbone marrow, and host bone marrow cells.

Conclusions: The above findings underscore the importance of adipose stem/stromal cells in the grafted fat for adipocyte regeneration. Host bone marrow and local tissues contributed substantially to capillary networks and provided new adipose-derived stem/stromal cells. An appreciation of mechanisms that are operant in this setting stands to improve clinical outcomes of fat grafting and cell-based therapies.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / transplantation*
  • Adipose Tissue / transplantation*
  • Animals
  • Bone Marrow Transplantation / methods*
  • Cell Survival
  • Chimera / physiology
  • Disease Models, Animal
  • Female
  • Flow Cytometry
  • Graft Survival
  • Immunohistochemistry
  • Mice
  • Mice, Inbred C57BL
  • Random Allocation
  • Regeneration / physiology*
  • Statistics, Nonparametric
  • Tissue Transplantation / adverse effects
  • Tissue Transplantation / methods
  • Tissue and Organ Harvesting