돼지 단위생식란의 세포사멸 유전자 발현 양상에 관한 연구
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서지정보
ㆍ발행기관 : 한국수정란이식학회
ㆍ수록지정보 : Journal of Embryo Transfer / 30권 / 3호
ㆍ저자명 : 손종윤, 김상환, 정덕원, 류춘열, 윤종택
ㆍ저자명 : 손종윤, 김상환, 정덕원, 류춘열, 윤종택
목차
서 론재료 및 방법
1. 공시재료
2. 난자의 채란 및 체외 성숙
3. 단위생식 유도
4. 단위생식란의 전핵형성 및 핵성숙
5. Total RNA 분리
6. cDNA 합성
7. Real-Time PCR
8. Protein 분리
9. In-Direct ELISA
10. 통계처리
결 과
1. 돼지 난포란의 체외 성숙
2. 체외배양에 따른 단위생식란의 발달률
3. 생존신호 발현과 기저막분해 효소의 작용
4. 세포사멸 조절인자 첨가에 따른 세포사멸 관련 유전자의
5. 세포사멸 관련 단백질의 발현 양상
고 찰
결 론
REFERENCES
영어 초록
The nature of molecular mechanisms governing embryonic cell block is largely unknown, but recent reports have demonstrated that proper execution of programmed cell death is crucial for this process. The main objective of this study is to determine effects of programmed cell death on porcine oocytes development in vitro after parthenogenesis. Among the blastocysts matured in 3MA, MAP1LC3A and ATG5 RNA gene expression level increased in the order of Cyst < 3MA < RP. However, Casp-3 and TNF-r RNA gene expression level decreased in the order of RP < 3MA < Cyst. Expression of mTOR within the RP-cultured blastocyst was the most highly to the inner cell mass, while 3MA-cultured blastocyst showed very lowest expression in inner cell mass. The expression of mTOR showed a pattern opposite to that of MAP1LC3A. That is, its expression was the lowest in Cyst group. When the enzymatic activity of MMP-2 and MMP-9 was assessed in culture, the level of active MMP-9 was higher expression in the medium of each RP treatment group, with the level of another treatment group being relatively higher. Analyses of TIMP-2 and TIMP-3 revealed that their expression was higher in groups that did not receive RP treatment. More specifically, the level of TIMP-2 was not affected by Cyst treatment, while the level of TIMP-3 was higher in 3MA and RP treatment group. There was highly cell division activation efficiency of parthenogenesis on cultured system of RP supplement IVC medium. Therefore, these results suggest that embryo development was significantly increased in conditional culture medium with active autophagy as compared to common cultured condition. Further investigation of this distinction may enable the development of innovative improvements for the production of porcine somatic cell nuclear transfer.참고 자료
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