논문 및 학회지

대한생식의학회지   제26권 제2호 2010년

생쥐배아의 냉동보존에 있어서 여러 조건의 평가 (저속 처리단계와 급속 처리단계, 배양액, 세포기)

전북대학교병원 산부인과 교실.

이승연, 권주택, 송희원, 조윤희, 이기숙, 김종덕,

The evaluation of various conditions in the cryopreservation of mouse embryos (Rapid and slow method of cryopreservation, culture media and cell stages)

Yi sy, K jt, Song hw, Cho yh, Lee ks, Kim jd

난외표제: 생쥐배아의 냉동보존에 있어서 여러 조건의 평가. = Abstract = Cryopreservation is able to store the surplus pre-embryos for freezing and furthermore thawing and transfer in a subsequent cycle. Cryopreserving cells which are maintaining their viability are the very complex process. This study has been carried out in order to find the effects of cryopreservation steps, freezing media and embryonic stages on the rates of viability and development of cryopreserved mouse embryos. Female ICR mice(6∼8 weeks old) were induced to superovulate by sequential intraperitoneal injection of 5 IU PMSG and 5 IU hCG 48h apart. Mouse embryos were collected according to its developmental stage after the injection of hCG. Embryos were cryopreserved not only by cryoprotectant step (1 step∼4 step) but also in a variety of media(HTF, IVF medium, D-PBS) and cell stage. The results were as follows : There is no clear advantage in these freezing media of rapid method, but 4 cell and 8 cell of slow method(2, 3, 4 step) have advantage in D-PBS. The development of embryos according to cell stage become greater in 8 cell stage. In the treatment steps of cryopreservation, the development of embryo to blastocyst was similar among rapid method, but the development of 4 cell and 8 cell embryos to blastocyst according to slow method was better than rapid method.

키워드 : Cryopreservation, Slow and rapid methods.

교신저자 :
전문 파일 :
 

최상단으로 이동