• 대한생식의학회:학술대회논문집
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• 2002.11a
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• pp.92.2-93
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• 2002

• 대한생식의학회:학술대회논문집
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• 2001.06a
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• pp.51-51
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• 2001

• Proceedings of the KSAR Conference
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• 2004.06a
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• pp.253-253
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• 2004

본 연구는 소를 이용한 체세포 핵이식에 있어서 탈핵전 demecolcine 처리 및 난자의 세포주기가 재구축배의 생산 및 발육에 미치는 영향을 검토하기 위하여 실시하였다. 도축장에서 회수한 난소로부터 채취한 미성숙란을 각 실험에 따라 성숙배양한 후 실험에 이용하였다. 난구세포 제거 후 일부 난자를 0.4 ㎍/㎖의 demecolcine이 함유된 배양액으로 40분간 처리하여 핵이식에 이용하였으며, 극체 미방출란 및 MI기 난자에 demecolcine을 처리하여 미성숙난자의 핵이식 이용 가능성을 검토하였다. (중략)

• Journal of Embryo Transfer
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• v.18 no.2
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• pp.109-113
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• 2003

The study was carried out to investigate the effects of morphology, preservation and reproductive cycle of oocytes in vitro maturation of cats oocytes and development of IVM embryos. The results were summarized as follows : 1. Nuclear status of GV and MI of in vitro cultured(24 h) oocytes with and whithout cumulus cells were 74.3% and 25.7%, 28.6% and 11.4%, 77.1% and 5.7%, respectively, The rate of oocytes with cumulus cells was higher than that of denuded oocytes. 2. Nuclear status of GV and MI of in vitro cultured(24 h) oocytes recovered from ovaries collected at different stages of the reproductive cycle(inactive, follicular and luteal) were 88.6% and 6.5%, 60.0% and 11.4%, 77.1% and 5.7%, respectively. 3. Nuclear status of fresh and salts-stored oocytes with and whithout cumulus cells were 74.3%, 25.7% and 37.1%, 11.4% and 57.1%, 13.3%, 17.1%, 3.3%, respectively. The rate of oocytes with cumulus cells(13.3%∼74.3%) was higher than that of denuded oocytes(3.3%∼57.1%).

• Journal of Embryo Transfer
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• v.21 no.1
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• pp.29-34
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• 2006

본 연구는 개 체외성숙 난자를 안정적으로 생산하기 위하여 채취시기, 난구세포 부착 여부 및 배양액에 EGF와 호르몬을 첨가 후 배양했을 때 체외성숙율에 미치는 영향을 조사하였다. 1. 미성숙 난포란을 TCM-199 배양액에서 24, 45시간 배양했을 때 체외성숙율은 각각 7.93%, 8.94%로서 48시간 배양했을 때 가장 높은 체외성숙율을 나타냈다. 2. 휴지기, 난포기, 황체기에 채취한 난소로부터 회수한 난자를 20 ng/ml의 EGF가 첨가된 TCM-199 배양액에서 배양했을 때 체외성숙율은 14.3%로서 0, 10 ng/ml의 EGF 첨가군(3.1%, 7.5%)에 비해 높은 체외성숙율을 나타냈다. 3. 난구세포 부착 및 미부착 난자를 48시간 배양했을 때 체외성숙율은 각각 18.8% 및 7.5%로서 난구세포 부착 난자가 미부착 난자보다 높은 체외성숙율을 나타냈다. 4. 난자의 체외성숙 배양 시 0.5 mg/ml FSH, 5 mg/ml LH, 1 mg/ml $E_2$와 FSH+LH, $FSH+LH+E_2$를 첨가한 TCM-199 배양액에서 배양했을 때 체외성숙율은 각각 1.2%, 10.0%, 2.0%와 10.0%, 31.2%로서 호르몬의 병용처리군이 높은 체외성숙율을 나타냈다. 5. 난자의 체외성숙 배양 시 EGF와 FSH, LH, $E_2$ 및 EGF와 FSH+LH, $FSH+LH+E_2$를 첨가한 TCM-199 배양액에서 배양했을 때 체외성숙율은 32.3%, 27.0%, 3.0%와 36.2%, 69.4%로서 EGF와 호르몬 병용 처리군이 높은 체외성숙율을 나타냈다.

• The Korean Journal of Zoology
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• v.37 no.1
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• pp.120-129
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• 1994

생쥐의 배우자간 인식과 수란관과 난자의 상호작용을 연구하기 위하여 수정 전후의 난자와 배아에 형광으로 표지된 5가지 렉틴(UEA-1. LCA, PNA RCA-1, GSL-1)을 처리하여 투명대, 위낭강 원형질 막에서 렉틴의 결합양상을 관찰하였다. 미수정난자 및 수정란의 투명 대에는 UIA-1을 제외한 4가지 렉틴이 결합하였다. PNA RCA-1, GSL-1은 투명대의 의총보다 내층에 강하게 결합되었고 UEA-1과 LCA는 투명대의 전층에서 미약하지만 고르게 결합하였다 배란된 난자의 위난강은 LCA와 PNA에 의해 결합되었으며 UEA-1은 수정 이후부터 GSL-1은 2-세포기 이후부터 위난강에 결합하였다. 난구세포를 제거하고 체외성숙을 일으킨 난자의 위난강에는 5가지 렉틴 모두 결합하지 않았다. 난자와 배아의 원형질막은 PNA. RCA-1, GSL-1에 의해 결합되었고, LCA 및 UEA기은 수정 이후부터 원형질막에 결합하였다. 이상의 결과에서 glucosamine, N-acetylgalactoamine 관기를 함유한 물질이 난구세포에서 생성되어 위난강에 축적되며 배란 후부터 난자의 위난강내 탄수화물관기는 수란관내액의 영향을 받는 것으로 사료된다. 난자 투명대의 탄수화물관기는 내층에 밀집되어 분포하는데 이는 정자의 투명대 관입 조절과 관련된 것으로 사료된다. 수정 후 난자의 원형질막 표면에 fucose와 mannose 등의 탄수화물 잔기가 새로이 노출되며 초기배아 발생동안 위난강에 존재하는 구조물의 렉틴 결합 특성이 유지되었다.

• Journal of Life Science
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• v.13 no.5
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• pp.732-739
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• 2003

The purpose of this study was to determine if the addition of spermatozoa into the culture medium could influence the nuclear maturation of denuded porcine germinal vesicle (GV) oocytes in vitro. Cumulus-oocyte complexes were collected from follicles of 3 to 5 mm in diameter, The cumulus and corona cells were removed from oocytes. Porcine denuded oocytes were cultured in tissue culture medium containing spermatozoa. After 48 h culture, oocytes were examined for the evidence of GV breakdown, metaphase I, anaphase-telophase I, and metaphase II (M II). The proportion of oocytes reaching M II stage was significantly (P<0.01) increased in the oocytes cultured in media containing spermatozoa compared to those in media without spermatozoa $(31.9\pm1.8%\; vs\; 14.9\pm1.0%)$.No differences in the rates of M II were observed among the different period of spermatozoa exposure nor among the spermatozoa from different species. The proportion of oocytes reaching M II stage was significantly different between high and low concentrations of spermatozoa. The present study suggests that mammalian spermatozoa contain a substance(s) that improves nuclear maturation in vitro of GV oocytes. Enhancing effect of spermatozoa for oocytes maturation in vitro is a highly dose-dependent.

• Korean Journal of Agricultural Science
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• v.23 no.2
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• pp.206-211
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• 1996

This study was conducted to investigate the effects of medium and cumulus cell on in vitro fertilization of porcine follicular oocytes. The results obtained are as follows ; 1. The normal fertilization rates of in vitro matured follicular oocytes cultured in 00, mT ALP and TCM-HEPES medium were 14.0~24.3%, 30.8~32.7% and 21.4~23.9%, respectively. These data indicated that the optimal medium for fertilization of porcine oocytes in vitro was the mTALP medium 2. The normal fertilization rates of epididymal sperm were 24.3%(80), 30.8%(mTALP) and 23.9%(TCM-HEPES), and those of ejaculated sperm were 14.0%(B0), 32.7%(mTALP) and 21.4%(TCM-HEPES). 3. The sperm penetration rates of cumulus-enclosed and cumulus-free oocytes on in vitro fertilization were 54.0% and 72.0%. The normal fertilization rates of cumulus-enclosed and cumulus-free oocytes were 11.9% and 21.5%. The normal fertilization rate of cumulus-enclosed oocytes was significantly(P<0.05) higher than that of cumulus-free oocytes.

• Korean Journal of Animal Reproduction
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• v.16 no.4
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• pp.289-299
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• 1993

The polypeptide patterns of cellular and follicular components were analysed by SDS-PAGE and two dimensional(2-D)electrophoresis combined with isoelectric focusing (IEF) to establish protein profiles in each of the components in porcine follicles. Oocyte-cumulus complexes were cultured in M16+FCS+Gn at 39 in an atmosphere of 5% CO$_2$, in air for 35 h. At the end of the culture, the zona-free oocyte, ZP alone and cumulus cells were prepared and analysed either on 10% SDS-PAGE for the protein profile at the first dimensional gel or 2-D protein pattern. The amounts of each samples were determined for the visualization with Coomasie brilliant blue (CBB) or silver staining, thus giving useful information for the identification of specific proteins in the components or appropriate amount of samples for proper visualization. Oocyte showed 25 and 114 kd major protein band. Other minor components were additionally visualized with CBB on the same gel after silver staining procedure. Cumulus cells also showed specific proteins which is not present in the oocytes. The number of cumulus cell was proper to give major bands with CBB and additional minor bands with silver staining. To establish the degree of contamination from the remnant of the corona radiata to the ZP, zonae were differently prepared or analysed by SDS-PAGE.The preparation of the ZP in this study did not showed any contamination judged by the protein profile of the components. Also follicular fluid showed its specific protein profile without any significant differences among the different sizes of follicles. The established protein profile of each follicular component should be helpful for the identification and elimination of contaminated components, i. e., antigen preparation or immunological studies. The results also suggest that the preparation of each components in the study was appropriate and can be used for a further sensitive biochemical analysis in mammalian oocytes and early embryos.

• Korean Journal of Agricultural Science
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• v.23 no.2
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• pp.212-218
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• 1996

This study was conducted to investigate the effects of coculture for the development rate to morula/blastocyst stages of early porcine embryos, derived from oocytes matured and fertilized In vitro, with porcine cumulus cell monolayers(PCM) in the two different media, respectively. The rates of embryos developed to 2-, 4-, 8~16-cell and morula/blastocyst stage were 48.7, 40.5, 34.8 and 17.0% in Ham's F-10 with PCM, and 48.3, 35.6, 22.1, and 13.4% in TCM-HEPES with PCM, respectively. The above development rates to morula/blastocyst stages were significantly higher than those of the embryos cultured in the Ham's F-10 and TCM-HEPES without PCM(P<0.05). The in vitro development rates to the morula/blastocyst stage of I-cell embryos cultured in Ham's F-10 and TCM-HEPES without PCM were 0.0~1.0%. Especially, most of embryos were observed to arrest the development beyond 4-cell stages. As shown in the above results, the coculture of in vitro fertilized porcine embryos with PCM in the two different media enhanced the development of fertilized eggs to morula/blastocyst stages in vitro. However, we didn't find out any difference for the in vitro development to morula/blastocyst stages between Ham's F-10 and TCM-HEPES media.