Methods: In the experiment, inbred Ficher 344 rats were used for isogenous form of transplantation. Rats were seperated into 4 groups (n=10). Platelet rich plasma(PRP) was prepared from blood obtained from 4 donor rats. Inguinal fat pads were harvested. Adipose derived stem cells were isolated,expanded three passages and labeled with fluorescent DýI. Fat tissues were mixed with 0.2 ml Dulbecco’s modified Eagle Medium in group A, 0.2 ml PRP in Group B, 0.2 ml of 5x106DiI labeled adipose derived stem cell(ADSC) in group C,and a combination of PRP and ADSC in group D. All four types of fat preparations were injected subcutaneously into the scalp of the rats. After 3 months the fat grafts were extirpated and weighed. The volumes of the transplants were measured by the liquid overflow method
Tissue sections from the center of the dissected fat biopsy were stained with hematoxylin-eosin, triple and VEGF. The histologyc parameters evaluated included the number of capillary structures, cyst vacuoles, fibroblasts and intact adipocytes.The number of each parameter were counted on an area of 335076.3µm2 by Clemex Vision lite 3,5 visual analysing programme. In vitro growth factor (VEGF, TGFβ,FGF) levels of supernatant were compared between stem cell and stem cell plus platelet rich plasma group using the enzyme- linked immunosorbent assay method
Results: In group D there was more grafted fat retained 3 months later. The loss of graft mass was more significant in group A than the other groups. The number of capillary structures and intact adipocytes were significantly higher in group D. Less cyst formation and fibrosis was obtained in group D . Group C and D transplants exhibited the histological structure of normal fat tissue.
The level of growth factors were significantly higer in stem cell plus platelet rich plasma group.
Conclusion: the combined use of adipose derived stem cells and platelet rich plasma synergistically increase revascularization and fat graft survival.