Allogenic Grafting of Cryopreserved Fat Cell.
- Author:
Jong Hoon LEE
1
;
Hong Hyeuk CHOI
Author Information
1. Department of Plastic and Reconstructive Surgery, College of Medicine, Eulji University, Daejoen, Korea. joaljh@eulji.ac.kr
- Publication Type:Original Article
- Keywords:
Allograft;
Cryopreservation;
Adipocyte
- MeSH:
Adipocytes;
Animals;
Centrifugation;
Collagenases;
Cryopreservation;
Eosine Yellowish-(YS);
Freezing;
Graft Survival;
Handling (Psychology);
Hematoxylin;
Intra-Abdominal Fat;
Lymphocyte Culture Test, Mixed;
Lymphocytes;
Mice;
Rejection (Psychology);
Transplantation, Homologous;
Transplants;
Weight Loss
- From:Journal of the Korean Society of Plastic and Reconstructive Surgeons
2008;35(4):385-392
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: The most effective methods of harvesting, preparing, and injecting autologous fat grafts have been inconsistent and conflicting. With its limitation as resorption in fat grafting, handling various techniques affect adipocyte survival, and is crucial to optimizing its long-term survival. To improve graft survival, re-implantation of cryopreserved adipocytes was developed. In addition, adipocytes do not induce immune rejection in response to non-self lymphocytes in a mixed lymphocyte reaction. The purpose of this study is to analyze the changes in cryopreserved adipocytes so as to determine the most efficient long-term storage period, and to analyze the changes in cryopreserved allografted adipocytes so as to determine the efficacy of cryopreserved adipocytes allografting. METHODS: Fat tissues were harvested from the inguinal and retroperitoneal fat pad of mice. After the centrifugation of the harvested fat tissues, they were disintegrated with collagenase. The adipocytes were obtained by centrifugation of the disintegrated fat tissues. The adipocytes were treated as follows: (1) They were examined for weight and then frozen at -20degrees C (n=25). For four months, each five frozen samples were taken and examined for weight and histologic changes in the 1st week, the 1st month, the 2nd month, the 3rd month, and the 4th month, respectively. (2) The adipocytes were immediately frozen at -20degrees C (n=125). For four months, five frozen samples were taken, and allografted in the same time period as above. Finally, for four months, five cryopreserved allografted adipocytes were taken and examined for histologic changes in the same time period as above. RESULTS: (1) Significant weight changes and histologic findings with inflammatory and destructive changes were observed in the cryopreserved adipocytes in three months. (2) Significant fat necrotic changes in the histologic changes with Hematoxylin and eosin stain were observed in the cryopreserved allografted adipocytes since the first week, independent of the freezing period. CONCLUSION: The study results show that the adipocytes that were cryopreserved for more than three months underwent obvious weight reductions and necrotic changes, and the adipocytes that were allografted without freezing were viable for four months, but the cryopreserved allografted adipocytes had obvious necrotic changes since the first week regardless of the freezing period.
