서창석 교수
Chang Suk Suh
서울대학교 산부인과 · 의학
연구실 소개
서창석 교수의 연구실은 생식 건강과 난소 조직의 극한 온도 보존 기술에 중점을 두고 있으며, 특히 난소 조직의 빠른 freezing(비결정성 냉각)과 동결 보존 기술의 최적화를 통해 생식능력 유지에 기여하고자 합니다. 다양한 동결 보존 조건, 첨가제 및 항결빙단백질의 영향을 분석하여 난소 난세포와 난포의 생존율을 높이는 데 초점을 맞추고 있으며, 이는 불임 치료 후 생식 기능 회복에 기여할 수 있습니다. 특히, 이식 전 혈관 형성 인자 도입을 통한 이소성 이식 후 조직 손상 완화 전략도 함께 개발하고 있습니다.
연구 현황
연구 성과 추이
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
주요 논문
15Different hormonal milieu, the reproductive health characteristics of infertile women such as distorted tubal function, technical issues of IVF procedures, and the estimated embryo implantation potential are possible risk factors. How each factor contributes to the risk of occurring ectopic pregnancy after assisted reproductive technology is uncertain and needs further investigation.
STUDY QUESTION: What is the optimal vitrification protocol according to the cryoprotective agent (CPA) for ovarian tissue (OT) cryopreservation? SUMMARY ANSWER: The two-step protocol with 7.5% ethylene glycol (EG) and 7.5% dimethyl sulfoxide (DMSO) for 10 min then 20% EG, 20% DMSO and 0.5 M sucrose for 5 min showed the best results in mouse OT vitrification. WHAT IS KNOWN ALREADY: Establishing the optimal cryopreservation protocol is one of the most important steps to improve OT survival. Howeve
Our results suggest that vitrification is a reliable and effective method for cryopreservation of HAMs.
Antifreeze proteins (AFPs) are a class of polypeptides that permit organismal survival in sub-freezing environments. The purpose of this study was to investigate the effect of AFP supplementation on immature mouse oocyte vitrification. Germinal vesicle-stage oocytes were vitrified using a two-step exposure to equilibrium and vitrification solution in the presence or absence of 500 ng/mL of AFP III. After warming, oocyte survival, in vitro maturation, fertilization, and embryonic development up t
AIM: In order to find the optimal exposure time of cryoprotectant, we performed a comparison of vitrification versus slow freezing according to the degree of normal morphology and apoptosis of human ovarian follicles. MATERIALS AND METHODS: Eleven patients aged 20-41 years who underwent operative laparoscopy for benign ovarian cysts or cesarean section were enrolled in this study. We carried out a prospective parallel comparison of survival and morphology of follicles after freezing (slow freezi
Cryopreservation and transplantation of ovarian tissue (OT) represents a method for fertility preservation. However, as the transplantation is performed without vessel anastomosis, unavoidable ischemic damage occurs. To reduce this ischemic damage and improve outcomes after transplantation, we used two kind of angiogenic factors, angiopoietin-2 (ang-2) and vascular endothelial growth factor (VEGF). Fresh or vitrified-warmed bovine OTs were prepared for xenotransplantation (XT). Fresh OTs were im
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