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Protective Effect of BOEC Co-Culture System against Nitric Oxide on Development of Bovine IVM/IVF Embryos

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  • 발행기관
    한국동물생명공학회(구 한국동물번식학회) 바로가기
  • 간행물
    Reproductive & developmental biology 바로가기
  • 통권
    Volume 32 No 3 (2008.09)바로가기
  • 페이지
    pp.167-173
  • 저자
    Hyun-Yong Jang, Yu-Sung Jung, Zheng-Yi Li, Hyoung-Jong Yoon, Hee-Tae Cheong, Jong-Taek Kim, Choon-Keun Park, Boo-Keun Yang
  • 언어
    영어(ENG)
  • URL
    https://www.earticle.net/Article/A88587

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초록

영어
Somatic cells such as oviduct epithelial cell, uterine epithelial cell, cumulus-granulosa cell and buffalo rat river cell has been used to establish an effective culture system for bovine embryos produced in in vitro. But nitric oxide (NO) metabolites secreted from somatic cells were largely arrested the development of bovine in vitro matured/ in vitro fertilized (IVM/IVF) embryos, suggesting that NO was induced the embryonic toxic substance into culture medium. The objective of this study was to investigate whether BOEC co-culture system can ameliorate the NO-mediated oxidative stress in the culture of bovine IVM/IVF embryos. Therefore, we evaluated the developmental rate of bovine IVM/IVF embryos under BOEC co-culture system in the presence or absence of sodium nitroprusside (SNP), as a NO donor, and also detected the expression of growth factor (TGF-p , EGF and IGFBP) and apoptosis (Caspase-3, Bax and Bcl-2) genes. The supplement of SNP over 5 uM was strongly inhibited blastocyst development of bovine IVM/IVF embryos than in control and 1 uM SNP group (Table 2). The developmental rates beyond morulae stages of bovine IVM/IVF embryos co-cultured with BOEC regardless of SNP supplement (40.4% in 5 uM SNP+ BOEC group and 65.1% in BOEC group) were significantly increased than those of control (35.0%) and SNP single treatment group (23.3%, p<0.05: Table 3). The transcripts of Bax and Caspase-3 genes were detected in all experiment groups (1:Isolated fresh cell (IFC), 2:Primary culture cell (PCC), 3:PCC after using the embryo culture, 4: PCC containing 5 uM SNP and 5: PCC containing 5 uM SNP after using the embryo culture), but Bcl-2 gene was not detected in IFC and PCC (Fig. 1). In the expression of growth factor genes, TGF-p gene was found in all experimental groups, and EGF and IGFBP genes were not found in IFC and PCC (Fig. 2). These results indicate that BOEC co-culture system can increase the development beyond morula stages of bovine IVM/IVF embryos, possibly suggesting the alleviation of embryonic toxic substance like nitric oxide.

목차

ABSTRACT
 INTRODUCTION
 MATERIAL AND METHODS
  In Vitro Production of Bovine IVM/IVF Embryos
  Isolation and Primary Culture of Bovine Oviduct Epithelial Cell (BOEC)
  RNA Isolation of BOEC
  Reverse-transcription Poly merase Chain Reaction (RTPCR) Analysis
  Statistical Analysis
 RESULTS
 DISCUSSION
 ACKNOWLEDGEMENT
 REFERENCES

키워드

Bovine oviduct epithelial cell Bovine IVM/IVF embryo SNP Nitric oxide Crowth factor Apoptosis gene

저자

  • Hyun-Yong Jang [ College of Animal Life Science ]
  • Yu-Sung Jung [ College of Animal Life Science ]
  • Zheng-Yi Li [ College of PhAmAcy, Kangwon National University ]
  • Hyoung-Jong Yoon [ College of PhAmAcy, Kangwon National University ]
  • Hee-Tae Cheong [ School of Veterinary Medicine and College of Phamacy, Kangwon National University ]
  • Jong-Taek Kim [ School of Veterinary Medicine and College of Phamacy, Kangwon National University ]
  • Choon-Keun Park [ College of Animal Life Science ]
  • Boo-Keun Yang [ College of Animal Life Science ] Corresponding author

참고문헌

자료제공 : 네이버학술정보

간행물 정보

발행기관

  • 발행기관명
    한국동물생명공학회(구 한국동물번식학회) [The Korean Society of Animal Reproduction and Biotechnology]
  • 설립연도
    1976
  • 분야
    농수해양>축산학
  • 소개
    동물번식생리학, 동물생명공학, 수의학, 인공수정 및 수정란이식을 이용한 동물개량에 관한 이론과 기술의 발전을 통해 학계, 연구계, 산업계 및 양축가 상호간의 협력을 도모함으로써 동물과학발전 및 사회일반의 이익에 기여 한다는 목적을 위해 노력해 나가겠습니다.

간행물

  • 간행물명
    Reproductive & developmental biology
  • 간기
    계간
  • pISSN
    1738-2432
  • eISSN
    2288-0151
  • 수록기간
    1977~2018
  • 십진분류
    KDC 527 DDC 636

이 권호 내 다른 논문 / Reproductive & developmental biology Volume 32 No 3

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