연구는 갈치 Trichiurus lepturus의 성 성숙과 생식생물학적 기초 정보를 제공하기 위해 수행하 였다. 난자형성과정 동안 난모세포와 핵의 크기는 증가하였으나 핵에 대한 인의 비율은 감소 하였다. H-E 염색 결과, 세포질의 염색성은 호염기성에서 호산성으로 변하였다. 난황형성개시 기 난모세포의 난경은 약 63.2 (±12.7) μm였다. 세포질에서는 호산성의 난황핵이 관찰되었다. 성숙기 난모세포의 난경은 216.6 (±24.7) μm였으며, GVBD (germinal vesicle breakdown)가 관 찰되었다. 완숙기 난모세포의 난경은 317.9 (±80.9) μm였으며, 방사대의 두께는 4.2 (±1.7) μm 였다. 난모세포의 발달형태는 난군동기발달형에 속하며, 난황 축적은 대부분의 경골어류와 마 찬가지로 외재적 방법과 내재적 방법에 의한 것으로 판단되었다.

This study was performed to investigate the effect of types of oil (OVOIL vs. OIL) on B6D2F1 mice oogenesis. In this study, B6D2F1 F1 mice were used in order to maximize oogenesis. The expansion rate of cumulus cells (82.0%±0.2 vs. 78.0%±0.1), in vitro fertilization rate (92.0%±0.1 vs. 88.0%±0.1), developmental rate (91.0%±0.1 vs. 87.0%±0.2), blastocysts formation rate (56.0%±0.1 vs. 57.0%±0.1), and zona hatched rate(41.4%±0.2 vs. 24.0%±0.1) were not different between groups (NS; P>0.05). However, there was a significant difference in maturation rate; the OVOIL group showed higher maturation rate compared to that of the OIL group (96.0%±0.1 vs. 87.0%±0.1; P<0.05). In the blastocysts cell numbers, the total cell numbers (83.9±26.1 vs. 56.9±23.9), ICM cell numbers (15.7±8.8 vs. 6.3±3.5), TE cell numbers (68.3±25.7 vs. 50.7±24.1), % ICM (21.6%±0.1 vs. 12.7%±0.1), and the ratio of ICM:TE (1:6.2±6.5 vs. 1:10.3±7.0) were significantly higher in the OVOIL group than the OIL group (P<0.05). These results suggested that it is expected to achieve the more developmental ability of B6D2F1 mice depending on the type of oil (OVOIL vs. OIL). In addition, the results can provide essential information for culture condition on B6D2F1 mice. Henceforth, thus, it is expected that these results herein might be used for in vitro culture of human embryos.

This study was conducted to evaluate the effects of different volume (100 μl vs. 2 ml) of microdrop culture on B6D2F1 mice oogenesis. In the present study, B6D2F1/CrljOri F1 mice were utilized in order to maximize oogenesis. Also we used TCM-199, Dulbecco's medified Eagle's medium (DMEM), embryo culture medium (Fertilization medium, Cleavage medium, Blastocyst medium), G series medium and One step medium. Blastulation rate was not different between groups (58.4±2.9% vs. 61.2±4.8%). Zona hatched rate (38±15.4% vs. 27±3.4%) and attached rate (55±13.9% vs. 46±3.9%) did not differ by the volume of culture media. Total cell numbers (59.8±9.7 vs. 70.3±8.7), ICM cell numbers (15.8±0.6 vs. 16.8±1.5), TE cell numbers (44.0±9.7 vs. 53.6±7.3), % ICM (26.4±2.9% vs. 23.8±3.3%) and ICM:TE ratio (1: 2.8±0.4 vs. 1: 3.2±0.6) were not different between groups (i.e., 100 μl vs. 2 ml). These results show that the capacity of the culture medium did not effect the cell numbers of B6D2F1 mice blastocysts. In summary, these results can provide fundamental data to maximize culture condition for in vitro fertilization on B6D2F1 mice.

This study was conducted to evaluate the effects of type of culture media (BM, G2, OS, TCM, and MEM) on B6D2F1 mice oogenesis. In the present study, B6D2F1/CrljOri F1 mice were utilized in order to maximize oogenesis. Also we used TCM-199, Dulbecco's medified Eagle's medium (DMEM), embryo culture medium (Fertilization medium, Cleavage medium, Blastocyst medium), G series medium and One step medium. In vitro maturation was highest in BM followed by the order of OS, MEM, TCM and G2 (90±2.8% > 88±3.2% > 85±4.9% > 78±10.2% > 64±7.7%, respectively). To note, the G2 group was statistically different compared to other groups (p<0.05). On the other hand the fertilization rate was highest in the G2 group followed by BM, OS, TCM, and MEM (87±7.2% > 85±6.9% > 74±14.0% > 71±13.8% > 2±1.4%, respectively). The MEM group was significantly lower compared to other groups (p<0.05). The developmental rate was highest in the OS group followed by the G2 group and the BM group albeit no statistical significance was noted (73±11.6% > 71±9.2% > 66±10.4%). Of note, all cells of the TCM and MEM groups were died during embryonic development. The zona hatched rate (51±9.8% vs. 50±9.1% vs. 47±7.2% for BM, G2, and OS respectively) and attached rate (45±12.3% vs. 38±16.1% vs. 37±11.5% for BM, G2, and OS respectively) were not different amongst groups. No difference was found in total cell numbers (74±13.9 vs. 64±9.2 vs. 76±6.7 for BM, G2, and OS respectively), ICM cell numbers (20±1.9 vs. 14±1.8 vs. 15±2.1), TE cell numbers (55±12.5 vs. 49±10.7 vs. 61±5.9), % ICM (30±2.8% vs. 24±7.0% vs. 22.8±2.2%) and ICM:TE ratio (1:2±0.5 vs. 1:3.1±0.8 vs. 1:3.1 ±0.5) amongst groups. In summary, these results can provide fundamental data to maximize culture condition for in vitro fertilization on B6D2F1 mice.

1998년 3월부터 1999년 2월까지 전라남도 대흑산도 연안에서 채집한 비단가리비를 대상으로 생식소중량지수, 생식세포 분화 및 난소주기를 조직, 세포학적 관찰에 의해 조사하였다. 초기 난황형성 난모세포에서, 골지체, 미토콘드리아 및 조면소포체들은 지방적 형성에 관여하였다. 후기난황형성난모세포에서 생식상피상에 존재하는 외인성 물질들 즉, 글리코겐 입자들 및 지방 과립상 물질들이 난황막의 미세융모를 통해서 난모세포의 난질로 통과해 들어갔다. 후기난황형성난

한국 곰소만산 암컷 바지락(Ruditapes philippinarum)의 난모세포의 발달 및 퇴화과정 중 일어나는 미세구조적 변화에 관해 기술하였다. 난소소낭은 영양성분을 저장하는 포상결체조직세포(VCT cell)들의 기질에 의해 둘러싸여 있다. 난 형성과정 초기에 초기난황형성난모세포와 보조세포(follicle cell)들 사이에 desmosome-like gap junction들이 나타났다. 난황형성과정은 골지체, 미토톤드리아, 조면소포체가 결합되어

갈색띠매물고둥, Neptunea (Barbitonia) arthritica cumingii의 난자 형성과정 중 난황 형성, 생식주기 및 군성숙도를 광학 및 전자현미경적 관찰에 의해서 조사하였다. 초기 난황 형성 단계의 난모세포에서 골지복합체와 미토콘드리아가 지방적 및 난황 과립의 형성에 관여되었다. 후기 난황 형성 단계의 난모세포에서는 조면소포체와 다포체가 세포질 내에서 단백질성 난황 과립 형성에 관여되었다. 성숙 단계 난모세포에서 성숙 난황 과립은 주

R. Philippinarum is dioecious and oviparous. In the early vitellogenic oocyte, the Golgi apparatus and mitochondria present in the perinuclear region are involved in the formation of lipid droplets and in lipid granule formation. In the late vitellogenic oocyte, the endoplasmic reticulum, mitochondria in the cytoplasm are involved in the formation of proteid yolk granules. At this time, exogenous lipid granular substance and glycogen particles in the germinal epithelium are passed into the ooplasm of oocyte through the microvilli of the vitelline envelope. Ripe oocytes are about 55-60 m in diameter. The spawning period was once a year between early June and early October, and the main spawning occurred between July and August when seawater temperature was approximately 20 C. The reproductive cycle of this species can be categorized into five successive stages: early active stage (February to March), late active stage (April to May), ripe stage (April to August), partially spawned stage (June to October), and spent/inactive stage (August to March). Gonad developmental phases by histological qualitative analysis showed similar results with those of quantitative image analysis.

강화인자 검출법을 이용 X염색체에 P[1ArB]이 형질전환되어 극세포 및 경게세포에서 표시유전자 lacZ를 발현하는 노랑초파리 (EDL 149)를 이용하여 난자형성과정 동안의 경계새포의 분화 및 이동을 조사하였다. 경계세포는 9기 난포의 선단에 위치한 난포 세포로부터 분화하여 9기와 10기에 이동하는 것을 확인하였다. 난소내 \beta -galactosidase의 활성은 우화 후 처음 4일간 급격히 증가하는 것을 확인하였으며 이 시기는 난포 내에서 경계