Role of Reactive Oxygen Species in the Adipogenesis of Adipose-derived Stem Cells

지방유래줄기세포의 지방분화과정에서 활성산소가 미치는 영향

  • Chang, Hak (Research Institute of Plastic and Reconstructive Surgery, Department of Plastic and Reconstructive Surgery, Seoul National University College of Medicine) ;
  • Min, Kyung-Hee (Department of Plastic and Reconstructive Surgery, Eulji General Hospital) ;
  • Park, Young-In (Research Institute of Plastic and Reconstructive Surgery, Department of Plastic and Reconstructive Surgery, Seoul National University College of Medicine) ;
  • Kim, Yo-Han (Department of Plastic and Reconstructive Surgery, Eulji General Hospital) ;
  • Minn, Kyung-Won (Research Institute of Plastic and Reconstructive Surgery, Department of Plastic and Reconstructive Surgery, Seoul National University College of Medicine)
  • 장학 (서울대학교병원 성형외과학교실 성형재건연구소) ;
  • 민경희 (을지대학교 의과대학 을지병원 성형외과학교실) ;
  • 박영인 (서울대학교병원 성형외과학교실 성형재건연구소) ;
  • 김요한 (을지대학교 의과대학 을지병원 성형외과학교실) ;
  • 민경원 (서울대학교병원 성형외과학교실 성형재건연구소)
  • Received : 2010.10.21
  • Accepted : 2010.12.28
  • Published : 2011.03.10

Abstract

Purpose: Stem cells continue to receive research attention in the clinical fields, and adipose-derived stem cells (ADSCs) have been shown to be a good source raw material. Many plastic surgeons are researching the ADSC adipogenesis with a view of conducting clinical trials, and many attempts have been made to identify the factors that promote the adipogenesis of ADSCs, but comparatively few correlation studies have been undertaken to explore the relation between reactive oxygen species (ROS) and the ADSC adipogenesis. We undertook this study is to investigate the effects of ROS on ADSC adipogenesis. Methods: ADSCs were isolated and cultured from abdominal adipose tissue, and cultured in different media; 1) DMEM(control), 2) adipogenesis induction culture medium, 3) adipogenesis induction culture medium with ROS ($20{\mu}M/50{\mu}M\;H_2O_2$), 4) adipogenesis induction culture medium containing ROS ($20{\mu}M/50{\mu}M\;H_2O_2$) and antioxidant ($10{\mu}M/20{\mu}M$ Deferoxamine). We compared adipogenesis in these different media by taking absorbance measurements after Oil-Red O staining every 5 days. Results: After culturing for 20 days, significant differences were observed between these various culture groups. Absorbance results showed significantly more adipogenesis had occurred in media containing adipogenesis induction culture medium and $H_2O_2$ (in a $H_2O_2$ dose-dependently manner) than in media containing adipogenesis induction culture medium and no $H_2O_2$ (p<0.001). Furthermore, in media containing adipogenesis induction culture medium, $H_2O_2$, and antioxidant, absorbance results were significantly lower than in adipogenesis induction culture medium and $H_2O_2$ (p<0.001). Conclusion: These findings suggest that ROS promote the adipogenesis of ADSCs. We suggests that ROS could be used in the adipose tissue engineering to improve fat cell differentiation and implantable fat tissue organization.

Keywords

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