약령 마우스에서 분리한 난소의 기관배양에 관한 연구

Organ Culture of Ovary Isolated from Juvenile Mice

  • 이현주 (대구대학교 자연자원대학) ;
  • 김지철 (대구대학교 자연자원대학) ;
  • 김기동 (고려대학교 생명공학원) ;
  • 이상호 (고려대학교 생명공학원) ;
  • 송해범 (대구대학교 자연자원대학)
  • 발행 : 2002.12.01

초록

본 실험은 원시난포의 체외배양 체계를 확립할 수 있는 가능성을 검토하기 위해 0, 5, 10, 15 및 20일령 마우스에서 분리한 난소를 20, 15, 10, 5 및 0일동안 organ culture 하여 난소의 성장률, 난자의 회수율과 성장률 및 난자의 핵성숙 단계를 조사하여, 비교 ·검토하였다. 그 결과를 요약하면 다음과 같다. 1. Organ culture 전과 후의 각 일령에 따른 난소의 면적 차이는 0일령 35.9%, 5일령 8.7%, 10 일령 1.2% 및 15일령 14.4%로 15일령을 제외 하고는 배양일령이 증가할수록 면적 차이는 감소하였다. 2. Organ culture 후 난자의 회수율과 난자의 직경은 배양일령이 증가할수록 증대되었다. 3. GV기 이상의 핵성숙은 organ culture 후 배양 일령이 증가할수록 진행되는 단계에 있는 것으로 나타났다.

This study was to assess the developmental capacity of oocytes matured in vitro after 20, 15, 10, 5 and 0 days of organ culture when ovaries were isolated from juvenile mice at 0-, 5-, 10-,15- and 20-day old, respectively, and to develop in vitro culture system that observed a view to morphology of ovaries and nucleus maturation of oocytes. The size of ovaries decreased 35.9%, 8.7%, 1.2% and 14.4% after 20, 15, 10, 5 days of organ culture when the ovaries were isolated from 0-, 5-, 10 and 15-day old mice, respectively. After organ culture, the recovery rates, diameters of oocytes and the number of oocytes progressed from GV to MII were increased as increasing age of mice.

키워드

참고문헌

  1. Blandau R, Warrick E and Rumery RE. 1965. In vitro cultivation of fetal mouse ovaries. Fertil. Steril., 16;705-715 https://doi.org/10.1016/S0015-0282(16)35761-2
  2. Caroll J, Whittingham DG and Wood MJ. 1991. Effect of gonadotrophin environment on growth and development of isolated mouse primary ovarian follicles. J. Reprod. Fert., 93:71-79 https://doi.org/10.1530/jrf.0.0930071
  3. Chapeakar TN, Nayak GV and Ranadive KJ. 1996. Studies on the functional activity of organoty-pically cultured mouse ovary. J. Embr. Exp. Morph., 15:133-141
  4. Eppig JJ. 1992. Growth and development of mam-malian oocytes in vitro. Arch Pathol Lab. Med., 116:379-382
  5. Eppig JJ and O'Brien MJ. 1996. Development in vitro of mouse oocytes from primordial folli-cles. Biol. Reprod., 54:197-207 https://doi.org/10.1095/biolreprod54.1.197
  6. Eppig JJ and Schroeder AC. 1989. Capacity of mouse oocytes from preantral follicles to un-dergo embryogenesis and development to live young after growth, maturation and fertilization in vitro. Biol. Reprod., 41:268-276 https://doi.org/10.1095/biolreprod41.2.268
  7. Fainstat T. 1968. Organ culture of postnatal rat ovaries in chemically defined medium. Fertil Steril., 19:317-338
  8. Leibfried L and First NL. 1980. Follicular control of meiosis in the porcine oocyte. Biol. Reprod., 23:705-709 https://doi.org/10.1095/biolreprod23.4.705
  9. Ninomiya T, Hoshi M, Mizuno A, Nagao M and Yuki A. 1989. Selection of mouse preimplanta-tion embryos carrying exogenous DNA by polymerase chain reaction. Mol. Reprod. Dev., 1:242-248 https://doi.org/10.1002/mrd.1080010404
  10. Odor DL and Blandau RJ. 1971. Organ cultures of fetal mouse ovaries. I. Light microscopic struc-ture. Am. J. Anat., 131:387-414 https://doi.org/10.1002/aja.1001310402
  11. Racowsky C and Baldwin K.V. 1989. In vitro and in vivo studies reveal that hamster oocyte meiotic arrest is maintained only traiisiently by follicular fluid, but persistently by membrane/cumulus granulosa cell contact. Dev. Biol., 134:297-306 https://doi.org/10.1016/0012-1606(89)90102-4
  12. Tsafriri A and Channing CP. 1975. An inhibitory influence of granulosa cells and follicular fluid upon porcine oocyte meiosis in vitro. Endorcr-inology, 96:922-927
  13. Tsafriri A, Dekel N and Bar-Ami S. 1982. Role of oocyte maturation inhibitorin follicular regula-tion of oocyte maturation. J. Reprod. Fert., 64:541-551 https://doi.org/10.1530/jrf.0.0640541
  14. Whittingham DG. 1971. Culture of mouse ova. J Reprod. Fert. Suppl., 14:7-12