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Sphingoshine-1-Phosphate Enhances Meiotic Maturation and Further Embryonic Development in Pigs

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  • 발행기관
    한국동물생명공학회(구 한국동물번식학회) 바로가기
  • 간행물
    Reproductive & developmental biology 바로가기
  • 통권
    Volume 36 No 3 (2012.09)바로가기
  • 페이지
    pp.173-181
  • 저자
    Hyo-Sang Lee, Deog-Bon Koo
  • 언어
    영어(ENG)
  • URL
    https://www.earticle.net/Article/A186502

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초록

영어
Sphingosine-1-phosphate (S1P) has a many function involved proliferation, differentiation and survival of many cells. In this study, to investigate whether S1P improve the developmental competence of porcine embryos, 50 nM of S1P were supplemented during in vitro maturation (with EGF or without EGF) medium and/or in vitro culture (IVC) medium. Addition of S1P was significantly increased the rate of oocytes reaching metaphase II (MII) compared to the control (83.5 vs. 64.1%) in without EGF medium, but not with EGF medium (89.5 vs. 84.6%). When treated with 1 μM of N1N-dimethylsphingosine (DMS), a sphingosine kinase inhibitor which is blocked endogenous generation of S1P, the meiotic progression rates to MII stage (without EGF: 45.2 and with EGF: 66.7%) were significantly decreased and degeneration rates (without EGF: 51.2 and with EGF: 30.1%) were increased in both medium compared to control group during IVM periods. Also, the rates of blastocyst formation was significantly increased in the S1P treated group compared to control group (29.0 vs. 19.2%) of EGF supplemented medium, whereas there were no effect in the EGF free medium (9.0 vs. 10.5%). After 12 h IVM, the phosphorylation of ERK1 and ERK2, which is major signaling pathway of MAP kinase, were increased in the S1P group than that of control or DMS group. When supplemented of S1P during IVC, the rates of blastocyst formation and total cell number (30.2% and 40.6) were significantly increased in S1P-treated group compared with control (20.1% and 32.5), DMS (12.3% and 25.1), and S1P plus DMS group (24.7% and 33.6). The percentage of apoptosis nuclei in the S1P group was significantly decreased than other groups. Also, the rates of blastocyst formation (26.7 vs. 14%) and total cell number (42.8 vs. 32.5) were significantly increased in the S1P group than those of control group when S1P added during the entire IVM and IVC periods. Taken together, our results indicate that S1P supplementation in IVM and/or IVC medium affects beneficial effect of meiotic maturation and subsequent developmental competence of porcine embryos.

목차

ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
  Treatment of SlP and DMS
  In Vitro Maturation (IVM)
  In Vitro Fertilization (IVF) and Culture (IVC)
  Aceto-Orcein Staining
  Western Blot Analysis
  TUNEL and Cell Counting
  Statistical Analysis
 RESULTS
  Effect of S1P Treatment during IVM of Porcine Oocytes on Meiotic Maturation and Embryo Development
  S1P Induces MAP Kinase Phosphorylation in In Vitro Matured Porcine Oocytes
  Effect of S1P during IVC on Embryo Development and Apoptosis
  Effect of S1P during IVM and IVC Periods on Embryo Development
 DISCUSSION
 REFERENCES

키워드

Sphingoshine-1-phosphate Meiotic maturation Embryo development Pig

저자

  • Hyo-Sang Lee [ lDevelopment and Differentiation Research Center, Korea Research Institute of Bioscience and Biotechnology, Oregon National Primate Research Center, Oregon Health & Science University, 505 N. W. 185(th) Avenue, Beaverton, OR 97006, USA ]
  • Deog-Bon Koo [ Department of Biotechnology, College of Engineering, Daegu University, Gyeongsan 712-714, Korea ] 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 36 No 3

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