1년 이상 냉동 보관한 흡인 지방조직 내의 세포 생존

Viability of cells in aspirated fat tissue after 1 year cryopreservation

  • 손대구 (계명대학교 의과대학 성형외과학교실) ;
  • 오재훈 (가가성형외과) ;
  • 최태현 (계명대학교 의과대학 성형외과학교실) ;
  • 김준형 (계명대학교 의과대학 성형외과학교실) ;
  • 한기환 (계명대학교 의과대학 성형외과학교실)
  • Son, Daegu (Department of Plastic and Reconstructive Surgery, Keimyung University Dongsan Medical Center) ;
  • Oh, Jaehoon (Gaga Aesthetic Plastic Surgical Clinic) ;
  • Choi, Taehyun (Department of Plastic and Reconstructive Surgery, Keimyung University Dongsan Medical Center) ;
  • Kim, Junhyung (Department of Plastic and Reconstructive Surgery, Keimyung University Dongsan Medical Center) ;
  • Han, Kihwan (Department of Plastic and Reconstructive Surgery, Keimyung University Dongsan Medical Center)
  • 발행 : 2009.03.15

초록

Purpose: The use of an autogenous fat graft has become a common procedure in plastic surgery. However, questions remain concerning on the viability of fat cells and preservation method of aspirated fat. The purpose of this study was to examine the viability of fat cells stored at $-20^{\circ}C$ in the freeze for 1 year after harvest from abdominal liposuction. Methods: Eighteen adults (aged 24 to 65 years old, 16 female and 2 male) were recruited for this study. Harvested aspirated fat tissues were obtained by suction - assisted lipectomy and frozen at $-20^{\circ}C$ commercial refrigerator for one year (average 12.5 months). The viability off at cells in specimens were measured after thawing. The numbers of viable cells were measured on a fluorescence microscope after staining with fluorescein diacetate and propidium iodide. GPDH (Glycerol - 3 - phosphate dehydrogenase) activity was measured. Cell culture was done for 3 weeks. Results: There were no viable cells under the fluorescence microscope, no detectable GPDH activity, and no cultured cells. Conclusion: These findings suggest that aspirated fat after frozen storage for one year at $-20^{\circ}C$ freezer is inadequate to reuse.

키워드

참고문헌

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