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Suspension Culture-Mediated Tetraploid Formation in Mouse Embryonic Stem Cells

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  • 발행기관
    한국동물생명공학회(구 한국동물번식학회) 바로가기
  • 간행물
    Reproductive & developmental biology 바로가기
  • 통권
    Volume 36 No 1 (2012.03)바로가기
  • 페이지
    pp.21-26
  • 저자
    Jae Hee Lee, Seung Pyo Gong, Jeong Mook Lim, Seung Tae Lee
  • 언어
    영어(ENG)
  • URL
    https://www.earticle.net/Article/A172386

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초록

영어
Suspension culture is a useful tool for culturing embryonic stem (ES) cells in large-scale, but the stability of pluripotency and karyotype has to be maintained in vitro for clinical application. Therefore, we investigated whether the chromosomal abnormality of ES cells was induced in suspension culture or not. The ES cells were cultured in suspension as a form of aggregate with or without mouse embryonic fibroblasts (MEFs), and 0 or 1,000 U/ml leukemia inhibitory factor (LIF) was treated to suspended ES cells. After culturing ES cells in suspension, their karyotype, DNA content, and properties of pluripotency and differentiation were evaluated. As a result, the formation of tetraploid ES cell population was significantly increased in suspension culture in which ES cells were co-cultured with both MEFs and LIF. Tetraploid ES cell population was also generated when ES cells were cultured alone in suspension regardless of the existence of LIF. On the other hand, the formation of tetraploid ES cell population was not detected in LIF-free condition, in which MEFs were included. The origin of tetraploid ES cell population was turned out to be E14 ES cells and not MEFs by microsatellite analysis and the basic properties of them were still maintained despite ploidy-conversion to tetraploidy. Furthermore, we identified the ploidy shift from tetraploidy to near-triploidy as tetraploid ES cells were differentiated spontaneously. From these results, we demonstrated that suspension culture system could induce ploidy-conversion generating tetraploid ES cell population. Moreover, optimization of suspension culture system may make possible mass-production of ES cells.

목차

ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
  Animals
  Cell Preparation
  Suspension Culture by Aggregate Formation
  Adherent Culture of Aggregates after Suspension Culture
  Karyotyping
  Short-Tandom Repeat Microsatellite Analysis
  Characterization of ES Cells by Immunostaining
  Analysis of DNA Content by Propidium Iodide (PI) Staining
 RESULTS
  The Effects of Suspension Culture under Various Conditionson the Formation Of Tetraploid ES Cells
  Identification of Cell Origin
  Characterization and Ploidy Shift of Tetraploid Es Cells
 DISCUSSION
 REFERENCES

키워드

Embryonic stem cells Suspension culture Tetraploid)

저자

  • Jae Hee Lee [ Laboratory of Stem Cell and Bioevaluation, WCU Biomodulation Program, Seoul National University, Seoul 151-742, Korea, Department of Obstetrics, Gynecology & Reproductive Biology, Michigan State University College of Human Medicine, Grand Rapids, MI, USA ]
  • Seung Pyo Gong [ Department of Marine Biomaterials and Aquaculture, Pukyong National University, Busan 608-737, Korea ]
  • Jeong Mook Lim [ Laboratory of Stem Cell and Bioevaluation, WCU Biomodulation Program, Seoul National University, Seoul 151-742, Korea, Department of Agricultural Biotechnology, Seoul National University, Seoul 151-742, Korea, Cancer Research Institute, Seoul National University College of Medicine, Seoul 110-744, Korea ]
  • Seung Tae Lee [ Department of Animal Biotechnology, Kangwon National University, Chuncheon 200-701, 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 1

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