• Title/Summary/Keyword: 난자형성과정

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Changes of Morphology and Morphometric Characteristics of the Oocyte during Oogenesis of the Abalone Haliotis discus hannai (북방전복 Haliotis discus hannai 난자형성과정 동안 난모세포의 형태 및 계측형질 변화)

  • Ju, Sun Mi;Lee, Jung Sick
    • The Korean Journal of Malacology
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    • v.32 no.1
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    • pp.1-7
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    • 2016
  • The developmental stage of germ cells during oogenesis can be categorized into six stages with histological features: (1) oogonium, (2) previtellogenic oocyte, (3) initial vitellogenic oocyte, (4) early active vitellogenic oocyte, (5) late active vitellogenic oocyte and (6) ripe oocyte. The size of oocyte, nucleus and nucleolus illustrated the increase tendency but size ratio of nucleolus to nucleus was decreased during oogenesis. During oogenesis the stainability in the cytoplasm of oocyte changes from basophilic to eosinophilic in H-E stain. And egg stalk and outer jelly membrane was developed in the oocyte. These histological changes are seemed to be yolk accumulation in the oocyte and preparation process for spawning.

Autoradiographic Studies on the Protein Synthesis in the egg chamber during Oogenesis of Drosophila melanogaster (노랑초파리의 난자형성에 따른 난실 내의 단백질 합성에 대한 자기방사적 연구)

  • 박성순;이양림
    • The Korean Journal of Zoology
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    • v.38 no.2
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    • pp.145-152
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    • 1995
  • 노랑초파리의 난실에서의 단백질 합성을 난자형성과정의 단계별로 자기방사법을 이용하여 관찰하였다 단백질은 영양세포에서 난자형성 초기에 미약한 정도로 함성되는 것으로 나타나지만, 가장 활발하게 합성되는 세포는 여포세포이다. 난모세포와 영양세포에서는 단백질이 거의 합성되지 않고 있다. 여포세포에서 합성된 단백질은 Stage 10 이후의 단계에서만 난모세포로 이동하는 것으로 관찰되었다 난모세포에 괸만하게 분포된 은입자는 난자 형성을 위한 다양한 목적을 위해 여포세포로 부터 이입된 단백질로 짐작된다. 특히 난황립의 형성에 여포세포의 단백질이 최소한도 부분적으로 관여한다는 사실을 알 수 있었다.

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Changes of Protein Synthesis during Oogenesis of Drosophila melanogaster (노랑초파리의 난자형성과정에서의 단백질 합성의 변화)

  • 박성순;이양림
    • The Korean Journal of Zoology
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    • v.30 no.1
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    • pp.10-28
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    • 1987
  • Changes of protein synthesis in the isolated egg chambers were studied during oogenesis of Drosophila melanogaster. Protein synthesis did not change much in quantity except that the activity was slightly enhanced at the stages 11 and 12, when new structures such as vitelline membranes and yolk granules were made, but considerably changed in quality during oogenesis. Protein synthesis was believed to occur mainly in the follicle cells, and a number of stage-specific proteins were found to differ at various stages. The observations suggest that proteins synthesized in the cells within chambers as well as those from the outside of the chambers might be directly required for the growth and maturation of oocytes in Drosophila.

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Fertilization Process in Porcine Oocytes Following Intracytoplasmic Injection of Porcine, Human, Bovine or Mouse Spermatozoon (돼지, 사람, 소 및 생쥐 정자 미세주입에 의한 돼지난자의 수정과정)

  • 전수현;도정태;이장원;김남형;이훈택;정길생
    • Korean Journal of Animal Reproduction
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    • v.22 no.2
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    • pp.195-202
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    • 1998
  • We demonstrated, for the first time, pronuclear formation and apposition in porcine ooc-ytes following intracytoplasmic injection of porcine, human, bovine and mouse spermatozoon. Microtubule organization and chromatin configuration were investigated in these oocytes during pronuclear apposition. Following intracytoplasmic injection of porcine spermatozoon, the microtubular aster was organized from the neck of spermatozoon, and filled the whole cytoplasm. This male derived microtubules appear to move both pronuclei to the center of oocytes. In contrast, following injection of spermatozoa from different species such as human, bovine and mouse, microtubules were organized from the cortex of the oocytes and concentrated to the pronuclei, which seems to move both male and female pronuclei to the center of oocyte. This organization is similar to what has been shown in the parthenogenetically activated por-cine oocytes. These results suggested that the porcine, human, bovine and mouse sperm chromatin can be formed pronucleus and apposited in the center of oocytes in the absence of male derived microtubule when they were injected into porcine oocytes.

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Ultrastructural Description on Oogenesis of the Melania Snail, Semisulcospira libertina libertina (Gastropoda: Pleuroceridae) (다슬기, Semisulcospira libertina libertina의 난자형성과정에 관한 미세구조적 기재)

  • Kim, Eun-Kyoung;Lee, Jung-Sick
    • The Korean Journal of Malacology
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    • v.25 no.2
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    • pp.145-151
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    • 2009
  • The ultrastructural changes in germ cells during oogenesis of the melania snail, Semisulcospira libertina libertina have been investigated by light and electron microscopy. The ovary is located on the surface of the hepatopancreas in the spiral posterior region. The ovary exhibited greenish color in the gonadal mature season. The ovary was composed of a number of oogenic follicles. Oogenesis was divided into five stages with histological features: (1) oogonia, (2) previtellogenic, (3) initial vitellogenic, (4) active vitellogenic, and (5) mature stages. Oogonia were oval in shape, $4-6\;{\mu}m$ in diameter, and had a large nucleus. Previtellogenic oocytes were about $20\;{\mu}m$ in diameter and the cytoplasm reacted with hematoxylin in H-E satin. Initial vitellogenic stage, oocytes were $60-80\;{\mu}m$ in diameter, and small yolk granules of low electron density are scattered in the cytoplasm. Oocytes in the initial vitellogenic stage were connected with ovarian follicle by egg stalk. Active vitellogenic oocyte were $100-120\;{\mu}m$ in diameter. Electron density, size and quantity of yolk granules that are distributed in the cytoplasm have increased from the previous stage. Result of TEM observations, the oocyte contains well-developed Golgi complex, endoplasmic reticula and tubular mitochondria in the cytoplasm. Cytoplasm of mature oocyte was filled with proteinaceous yolk globules of high electron density. In this stage, the length of microvilli in the egg envelope was approximately $1.1\;{\mu}m$.

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The Oogenesis of Glow-light Tetra, Characidae, Teleost (경골어류 카라신과 glow-light tetra의 난자형성과정)

  • Lee, Kyu-Jae;Chang, Byung-Soo;Teng, Yung-Chien;Kim, Dong-Heui
    • Applied Microscopy
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    • v.38 no.4
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    • pp.315-319
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    • 2008
  • Glow-light tetra, Hemigrammus erythrozonus is a teleost belonging to Characidae. The natural habitate of this fish is the wild in the Essequibo river, Guyana and South America. The oogenesis of glow-light tetra was investigated by light microscopy to compare with those of other families. A pair of ovary was located between swim bladder and intestines. The ovary was of white color and ellipsoidal shape with the major axis 11 mm and the minor axis 4 mm. Cytoplasm of oogonia was basophilic and many nucleoli were located at inside of nuclear membrane. In primary oocytes, yolk vesicles were distributed only in the marginal area and egg envelope was not formed on the outside of an egg. In secondary oocytes, the egg envelope was formed and yolk vesicles in the cytoplasm were increased than the earlier stage. The amount of basophilic substance was decreased. In case of matured egg, thickness of egg envelope and size of egg were increased, basophilic substance was distributed in only around the egg envelope. The yolk vesicles were changed to yolk mass in accordance with development. In conclusion, the oogenesis of glow-light tetra, Hemigrammus erythrozonus was characterized by the increase in cell size, the formation and accumulation of yolk, and the decrease of basophilia a in the cytoplasm. The oogenesis of glow-light tetra seems to share common patterns in Characidae, teleost and have a similar pattern with other teleost.

Ultrastructural Changes at the Surfaces of Oocytes during Oogenesis of the starfish, Asterina pectinifera (Muller and Troschel) (별불가사리(Asterinapectinifera)의 난자형성 과정 중 난모세포 표면의 미세구조적 변화)

  • 이양림;한지원
    • The Korean Journal of Zoology
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    • v.37 no.2
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    • pp.203-212
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    • 1994
  • 별불가사리 난자형성 중 난모세포(직경 7-l7O Um) 표면의 구조적 변화를 투과 전자현미경으로 관찰하였다. 직경 25-855 Um의 난모세포에서 'endocvtosis'와 관련된 구조인 coated pit, coated vesicle과 내포소낭이 존재하였으며. 내포소낭은 난황립과 융합하였다. 특히, 이러한 융합은 직경 130-155 Um의 난모세포에서 많이 관찰되었다 난자형성 초기에 난모세포의 미세융모는 세포막을 따라 무질서하게 분포하고. 인접한 세포와 맞닿아 있었다. 직경 15 Um에서 65 Um에 이르는 난모세포는 세포막 부위에 따라서 미세융모의 굵기와 길이, 그리고 형태가 다르게 나타났고, 직경 100 Um 이상의 난모세포에서는 잘 발달된 미세음모가 난뢍층에 존재하였다 여포세포로부터 나온 돌기는 직경 7 Um의 난모세포와 난자형성 후기의 난모세포에서 난황층을 윤고 세포막과 닿아 'junctional complex'를 형성하였다. 이와같은 난모세포 표면의 다양한 구조적 변화는 난모세포의 세포막을 통한 물질투과 기능의 분화와 관련이 있을 것으로 생각된다.

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Histological Description of Oogenesis in Largehead Hairtail Trichiurus lepturus (Teleostei: Trichiuridae) (갈치 Trichiurus lepturus 난자형성과정의 조직학적 기재)

  • Shin, So Ryung;Kim, Hyeon Jin;Oh, Han Young;Kim, Jae Won;Lee, Jung Sick
    • Journal of Marine Life Science
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    • v.7 no.1
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    • pp.55-59
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    • 2022
  • This study was conducted to provide basic information on the sexual mature and reproductive biology of Trichiurus lepturus. During the oogenesis, size of oocyte and nucleus showed the increase tendency but size ratio of nucleolus to nucleus was decreased. In the result of H-E stain, the stainability of the cytoplasm was changed from basophilic to eosinophilic. The egg diameter of initial vitellogenic oocyte was about 63.2 (±12.7) ㎛. In the cytoplasmic cortex, eosinophilic yolk nucleus was observed. The size of mature oocyte was 216.6 (±24.7) ㎛ and GVBD (germinal vesicle breakdown) was observed. The size of ripe oocyte was 317.9 (±80.9) ㎛ and the thickness of zona radiata was 4.2 (±1.7) ㎛. The oocyte developmental type is considered to belong to the group synchronous type. The accumulation of yolk in the oocyte, like most teleost, is thought to be of two types: exogenous and endogenous accumulation.

The Oogenesis of Three Spot Gourami, Belontiidae, Teleostei (경골어류 등목어과 Three spot gourami의 난자형성과정)

  • Chang, Byung-Soo;Jung, Han-Suk;Joo, Kyung-Bok;Kim, Dong-Heui
    • Applied Microscopy
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    • v.41 no.3
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    • pp.155-161
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    • 2011
  • Three spot gourami (Trichogaster trichopterus Pallas, 1770) is a teleost belonging to Belontiidae. The oogenesis of three spot gourami was investigated by light microscope. The ovary was of light peach color and ellipsoidal shape with the major axis 2 cm and the minor axis 1 cm. Cytoplasm of oogonia was basophilic and many nucleoli were located at inside of nuclear membrane. In primary oocyte, lipid droplets were distributed only in the marginal area first, than at nuclear envelope near. In secondary oocyte, the egg envelope was formed and yolk vesicles was formed in the marginal area. The basophilic substance of cytoplasm was changed to acidic. In case of matured egg, thickness of egg envelope and size of egg were increased. The yolk vesicles were changed to yolk mass in accordance with development. The fertilized eggs were the colorless, transparent, spherical, adhesive and pelagic type. A large oil droplet was located in vitelline membrane of the fertilized egg. In conclusion, the oogenesis of three spot gourami was characterized by the increase in cell size, the formations of lipid droplets and yolk, the decrease of basophilic substance in the cytoplasm, and formation of one large oil droplets.

Ultrastructural Changes of Oocytes Related to the Yolk Formadon dudng Oogenesis of Pseudopotamilla occelata Moore (안점의꽃갯지렁이(Pseudopotamilla occelata Moore)의 난모세포의 난황립형성에 따른 미세구조의 변화)

  • 강화선;이양림
    • The Korean Journal of Zoology
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    • v.34 no.2
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    • pp.217-227
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    • 1991
  • Ultrastmctura changes of multivesicular bodies and mitochondria of oocytes of PseudopotamU- Ia occelata Moore were examined with transmission electron microscope in order to follow the process of yolk formation. Yolk granules begin to form at the previtellogenic stages of 50 $\mu$m diameter from multivesicular bodies. Small vesicles and membranous structures within the multivesicular bodies are fused to form the precursors of core bodies of yolk granules. Some vesicles from cytoplasm are also coalesced into the multivesicular bodies. Mature yolk granules are composed of electron-dense core bodies which are seperated from each other by electronopaque small vesicle-like structures. Structural changes of cristae into vesicular shapes and increase in electron density of matrix in mitochondria strongly suggested that mitochondria are in the process of transformation. The transformed mitochondria appear to be basic structures which later become multivesicular bodies.

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