서창석 교수
Chang Suk Suh
서울대학교 · 의학
연구실 소개
서창석 교수의 연구실은 난소 기능 장애와 불임과 관련된 분자 기전을 규명하고, 특히 난세포의 성장 인자인 GDF-9과 BMP-15의 기능 이상이 다낭성 난소 증후군(PCOS)의 발달에 미치는 영향을 중심으로 연구를 진행하고 있습니다. 또한, 난세포 및 배아의 냉동 보존 기술, 특히 비동결법(vitrification)의 최적화와 항결빙단백질(AFP)의 활용을 통해 생식세포의 생존율과 발달 능력을 향상시키는 데 초점을 맞추고 있습니다. 이와 더불어 보조생식기술(ART) 후 발생할 수 있는 이포성 임신 등의 위험 요인 분석을 통해 임상적 응용가능성을 높이고자 합니다.
연구 현황
연구 성과 추이
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
주요 논문
15Polycystic ovary syndrome (PCOS) is a major cause of female infertility. Despite substantial effort, the etiology and pathogenesis of PCOS and polycystic ovaries (PCO) in women remain unknown. Recent studies in laboratory animals have documented a link between dysfunction of two oocyte growth factors, growth differentiation factor-9 (GDF-9) and bone morphogenetic factor-15 (BMP-15), and aberrant folliculogenesis. Because aberrant follicle development is a hallmark of PCOS, we wondered whether th
Different 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.
We compared eight vitrification protocols according to CPA composition and found the EDS protocol to be the optimal method among them. The data presented herein will help improve OT cryopreservation protocols for humans or other animals.
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
The 10-min exposure group for vitrification showed better results compared with other conditions and the slow-freezing group.
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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