• 제목/요약/키워드: Yolk vesicle

검색결과 30건 처리시간 0.028초

Reduction of Twin Pregnancy by Transvaginal Ultrasound-guided Aspiration in a Mare

  • Lee, Eun-bee;Song, Mingeun;Park, Chull-gyu;Hwang, Jun-seok;Chun, Yong-woo;Lee, Seung-hwan;Cheong, Jongtae;Lee, Joomyoung;Kang, Tae-Young;Seo, Jong-pil
    • 한국임상수의학회지
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    • 제34권4호
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    • pp.304-306
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    • 2017
  • A 3-year-old Thoroughbred mare was referred to J&C Equine Hospital with gestation day 30 twin pregnancy. On transrectal ultrasonographic examination, two similar sized (28 mm) embryonic vesicles, unilaterally fixed in the uterine horn, were detected. Transvaginal ultrasound-guided aspiration (TUGA) was performed for reduction of one embryonic vesicle. Yolk sac and allantoic cavity fluids from one embryonic vesicle were aspirated by a needle guided by using transvaginal ultrasound. The mare continued normal singleton pregnancy after twin reduction and delivered a foal successfully. This is the first case described the clinical use of TUGA in Korea. Clinical use of TUGA in twin reduction after embryonic fixation is recommended for equine clinicians.

Developmental Changes of the Oocyte and Its Enveloping Layers, in Micropercops swinhonis (Pisces: Perciformes)

  • Park, Jong-Young;Richardson, Ken-C.Richardson;Kim, Ik-Soo
    • Animal cells and systems
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    • 제2권4호
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    • pp.501-506
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    • 1998
  • In the goby Micropercops swinhonis, the development of its egg's enveloping layers could be divided into 4 stages. In the earliest developmental period, stage I, there is a simple oocyte surrounded by a layer of squamous follicular cells. Stage II corresponds to the yolk vesicle stage of vitellogenesis. Here the initial follicular layer has become bilaminar with the retention of its outer squamous cell layer and the acquisition of an inner cuboidal cell layer just over the zona radiata. The number and size of the cuboidal cells increases throughout this stage. Stage III corresponds to the yolk granule stage of true vitellogenesis. Here the cuboidal cells begin to be replaced by columnar cells. As the oocyte grows, the columnar cells increase in size. The columnar cells produce cytoplasmic neutral mucins and by the end of this stage their cytoplasm has been filled with this mucin. In stage IV a single layer of squamous cells still remained as the outer follicular layer of the oocyte. The secretory activity of the inner follicular layers' columnar cells has ceased and they had lost their cell wall integrity and ended as a series of bullet-shaped, neutral mucin deposits.

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Egg Development and Morphology of Larva and Juvenile of the Oryzias latipes

  • Lee, Sung-Hun;Kim, Chun-Cheol;Koh, Soo-Jin;Shin, Lim-Soo;Cho, Jae-Kwon;Han, Kyeong-Ho
    • 한국발생생물학회지:발생과생식
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    • 제18권3호
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    • pp.173-178
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    • 2014
  • In order to monitor the developmental features of embryos, larvae, and juveniles of Oryzias latipes (Temminck and Schlegel), Oryzias latipes was caught in river of Shinduck-dong, Yeosu-si, Jeollanam-do, on May 2011, and experiments were carried out in Ichthyology laboratory at Chonnam National University. The blastodisc step was the first level for natural spawning. The optic vesicle, Kupffer's vesicle, myotome began to appear 75 hours 57 minutes later. After blastodisc development, the pectoral fins were made at 143 hours 37 minutes and the tail was separated started at the same time. Hatching was observed at 167 hours 27 minutes after blastodisc. The total length of the hatched larvae was 4.95~5.10 mm (mean, 5.01 mm), the mouth and anus were opened. Larvae used yolk completely after 3 days after hatching. The total length larvae was 5.45~5.56 mm (mean, 5.52 mm) after 8 days after hatching, and appeared the stems for tail. The stems pectoral, anal fin were showed after 14 days and the stems dorsal, ventral fin were appeared after 19 days. For 35 days after hatching, the total length of larvae 13.95~15.30 mm (mean, 14.64 mm), and at this time, fins and body were transferred like the adult Oryzias latipes.

노랑초파리의 난자형성과정에 대한 연구. I. 노랑초파리의 난자형성과정에서 Egg Chamber 내에서의 물질이동에 따른 미세구조적 변화

  • 이양림;박성순
    • 한국동물학회지
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    • 제31권4호
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    • pp.318-326
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    • 1988
  • 여포세포에서 합성된 난황단백질이 난모세포로 이동하는 동안에 난황체가 이 두 종류의 세포사이에 형성되었다가 결국은 난황막으로 전환한다. 단계7까지는 뚜렷하게 보이던 난모세포막과 여포세포막이 소멸되고 그 자리에 전자 밀도가 높은 난황체 물질이 산만하게 축적된다. 난황체는 단계9에서 막성 구조의 일종인 linkage bridge로 둘러싸여 단계11까지는 두께가 5∼7um가 되리 만큼 성숙한다. 단계13에서 난황체는 비로소 난황막으로 전환되는데, 이때 난황막의 두께는 겨우 1 U m에 지나지 않는다. 이러한 두깨의 감소는 난황체 물질이 다량 난모세포 쪽으로 이동한 것으로 생각 되었다. coated vesicle을 포함한 다양한 종류의 과립이 난황체 양쪽에서 관찰되었는데, 난모세포쪽에 출현한 과립은 난황체 물질이 난모세포로 이동되는 구조로 해석되었고 여포 세포쪽에서 관찰된 과립은 주로 난황체의 전자밀도와 동일한 점으로보아 여포세포에서 합성되어 난황체를 형성하는 물질로 이루어진 구조로 해석되었다. As yolk proteins are transported from !he follicle cells into oocvtes, vitelline body forms and changes into a vitelline membrane between the ko celt types during the vitellogenic period. Cell membranes of oocyte and follicle cells surrounding the oocyte disappear at stage 7 and high electron-dense substance of vitelline body simultaneously accumulates sporadically between the cell types. The vitelline body becomes surrounded by linkage bridge, a membranous structure, at stage 9 and greatly increases in thickness to be 5-7 U m thick at stage 11. At stage 13 the vitelline body becomes vitelline membrane, which is now only 1 U m thick, suggesting that much of the substance of the vitelline body has been transported into oocyte. Various types of vesicles including coated vesicles were observed at both sides of th vitelline body. The vesicles occurred at the side of oocyte were interpreted to be structures transported from the vitelline body into oocyte, whereas those found at the side of the follicle cells were thought to be structures made in the follicle cells and fused into the vitelline body.

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좀구굴치 Micropercops swinhonis의 난여포층 (Follicular Layer of Oocytes of Micropercops swinhonis (Pisces: Perciformes))

  • 박종영;김익수;이용주
    • 한국어류학회지
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    • 제13권4호
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    • pp.254-260
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    • 2001
  • 좀구굴치 성숙란의 난여포층은 외층인 theca cell과 내층인 granulosa cell로 구분되며 특히 원주형인 granulosa cell은 분비활동으로 인하여 세포질에 분비물이 축적되면서 난모세포를 둘러싸게 된다. 이러한 granulosa cell은 난황형성 초기인 난황포 시기에 입방형태를 보이지만 난황구시기에는 원주상세포로 바뀌면서 점액을 분비하는 특징을 보여 주고 있다. 이러한 부착물질은 형태가 없으며 전자밀도가 높다. 또한 이러한 분비물을 가지는 난막은 난황형성이 더욱 진행됨에 따라 동물극 부근이 식물극보다 더욱 두꺼워지고 커지게 된다. 이러한 점막여포층 아래에는 약 $7.8{\sim}11.5\;{\mu}m$ 두께의 방사대가 존재한다. 방사대는 전자밀도가 낮은 외층과 3~5층의 여러 전자밀도층을 가지는 내층으로 구성되어 있다. 한편 점막여포층은 방사대에 존재하지 않고 있기 때문에 이 물질은 난세포질이 여포상피로부터 기원된 것으로 생각된다.

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한국 남해에 서식하는 물가자미, Eopsetta grigorjewi (Herzenstein)의 재생산 연구 (Reproduction of the Shotted halibut in the southern Korean waters)

  • 차형기;강수경;최정화;오택윤;서영일
    • 수산해양기술연구
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    • 제47권3호
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    • pp.194-202
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    • 2011
  • Maturation and spawning of the Shotted halibut, Eopsetta grigorjewi was investigated based on the samples captured in South Korean waters from January 2008 to December 2009. Gonadosomatic index began to increase in December, and reached maximum between January to March. After spawning it began to decrease from May. Reproductive season was estimated to January-April, with peak in February. Fecundity was proportional to the size of the female, with the clutch size varying from 170,000 eggs in the smallest female (total length, 28.9cm) to 1,300,000 eggs in the largest (total length, 41.5cm). Size at 50% sexual maturity (TL50), determined from mature females, was 28.8cm. Annual reproductive cycles of this species could be divided into six successive stages; immature stage (May-October), nucleolus stage (November-January), yolk vesicle stage (January-February), vitellogenic and ripe stage (January-April) and spent stage (April-May).

Gametogenesis and Reproductive Cycle of the Rock Shell, Reishia (Thais) clavigera (Neogastropoda: Muricidae), on the West Coast of Korea

  • Lee, Ju-Ha
    • Animal cells and systems
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    • 제3권4호
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    • pp.375-383
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    • 1999
  • Gonadal development, gametogenesis, reproductive cycle, and first sexual maturity of Reishia clavigera were investigated monthly from July 1998 to June 1999 through cytological and histological observations. R. clavigera had separate sexes, and was an internal fertilizer. The ma1e penis was located near the two tentacles. The ovary and testis were composed of a great number of oogenic lobules and spermatogenic tubules, respectively. The size of ripe oocyte ranged from 130 to 140 ${\mu}$m in diameter. The peripheral cytoplasm of the germinal vesicle of the ripe oocyte in many cases were surrounded by smaller yolk granules, while the eccentric cytoplasm was occupied with larger ones. The reproductive cycle of R. clavigera could be classified into five successive stages: early active, late active, ripe, spawning, and recovery. Spawning of females occurred from early July to August when the seawater reached above 24.8$^{\circ}C$. Spawning of males occurred from early June to August in the water above 22.8$^{\circ}C$. Minimum size for sexual maturity of both sexes was above 10.0 mm in shell height. Each egg capsule was a cylinder or spindle in shape, 4-6 mm in length and 1-2 mm in width. Colors of newly spawned egg capsules showed yellowish white or pale yellow, while those with veliger larvae showed pale black, and released larvae or dead egg capsules showed black violet. The fecundity in an egg capsule ranged from 70 to 91 eggs (mean=80.28 eggs).

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한국 남해에 서식하는 눈볼대, blackthroat seaperch, Doderleinia berycoides (Hilgendorf)의 생식생태연구 (Reproductive ecology of the blackthroat seaperch, Doderleinia berycoides (Hilgendorf) in South Sea of Korean waters)

  • 차형기;강수경;오택윤;최정화
    • 수산해양기술연구
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    • 제46권4호
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    • pp.368-375
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    • 2010
  • Maturation and spawning of the Blackthroat seaperch, Doderleinia berycoides were investigated based on the samples captured in Korean waters from January 2008 to December 2009. Gonadosomatic index began to increase in June, and reached maximum between July to September. After spawning it began to decrease from October. Reproductive season was estimated to July-September, with peak in August. Fecundity was proportional to the size of the female, with the clutch size varying from 115,500 eggs in the smallest female (TL〓28.2cm) to 652,000 eggs in the largest (TL〓33.5cm). Size at 50% sexual maturity ($TL_{50}$), determined from mature females, was 29.6cm. Annual reproductive cycles of this species could be divided into six successive stages; immature stage (October-May), nucleolus stage (June-July), yolk vesicle stage (July-August), vitellogenic stage (June-September), ripe and spent stage (August-October).

Retinal Development and Opsin Gene Expression during the Juvenile Development in Red Spotted Grouper (Epinephelus akaara)

  • Kim, Eun-Su;Lee, Chi-Hoon;Lee, Young-Don
    • 한국발생생물학회지:발생과생식
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    • 제23권2호
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    • pp.171-181
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    • 2019
  • To produce healthy and stable seed production, we need to obtain information and understand vision that affects behavior of red spotted grouper. We examined their expression and retinal development during the juvenile development. Short-wavelength sensitive opsin (SWS2), a cone photoreceptor, began to be expressed from lens and ear vesicle formation stage and its expression increased until 10 days after hatching (dah). In case of middle-wavelength sensitive opsin (MWS), its expression was detected at 3 dah and reached the highest level at 21 dah. The expression of long-wavelength sensitive opsin (LWS) was first observed from 3 dah and their expression decreased thereafter. Rhodopsin, a rod photoreceptor, was found to be expressed from 2 dah and its expression reached the highest level at 50 dah. The outer nuclear layer (ONL), inner nuclear layer (INL) and ganglion cell layer began to differentiate at 2 dah, while choroid first appeared at 4 dah so that the eyes became black. These results indicate that the development of retina mostly completes around 4 dah. It seems that the development of the retina and the expression of the opsin genes are closely related to the behavior such as hunting prey, considering that the timing of the completion of the development of the retina, the timing of gene expression, and the timing of completion of yolk absorption are similar.

인공수정에 의한 Urechis unicinctus 난자의 난할형식 (Cleavage Pattern of Urechis unicinctus Eggs in Vitro Fertilization)

  • 신길상;이대희;고태영
    • Applied Microscopy
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    • 제34권1호
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    • pp.71-81
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    • 2004
  • 본 연구에서는 등황란인 U. unicinctus 수정란의 난할과정과 형식에 대하여 관찰된 바를 보고하였다. U unicinctus성숙란을 인공수정했을 때 난할은 핵 개방(germinal vesicle breakdown)과 제1, 2감수분열 후에 수행되었으며, 유생기 까지 난할은 등할(equal cleavage), 전할(holoblastic cleavage)이었고 난할형식은 나선형 난할(spiral cleavage)인 것으로 관찰되었다. 최초 3회의 난할이 경할$\rightarrow$경할$\rightarrow$수평할이었고, 이후 경할-수평할이 반복되는 것으로 보였다. 4세포기에 할구의 배열에서 일부 할구들이 동물극으로 융기한 것과 8세포기에서 식물극 할구 배열이 동물극 할구 배열에 대하여 사선 배열한 것 등은 나선형 난할에서만 볼 수 있는 특징이었으나 제 3차 난할인 수평할에서 등할, 전할인 것이 관찰되므로서 나선형 난할을 수행하는 Spiralian의 전형에 속하지는 않는 것으로 보였다. 4세포기 이후의 할구 배열이 사선배열, 즉 나선형인 근거를 항-$\alpha$-,-$\beta$-튜블린 처리에 의해 관찰된 유사분열 기구의 행위로서 볼 수 있었다. 4$\rightarrow$8세포기의 유사분열 기구는 동물극-식물극 축에 수직으로 발생하고 사선방향으로 선회한 후 난할하므로서 결과에서 수평할 및 할구의 사선배열이 가능한 것을 볼 수 있었다.