• Title/Summary/Keyword: 생식세포

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Ultrastructure of Germ Cells, Cyst Epithelial Cells and Interstitial Cells during Spermatogenesis of the Stone Flounder, Kareius bicoloratus (돌가자미 Kareius bicoloratus의 정자형성과정 중 생식세포, Cyst 상피세포 및 간질세포의 미세구조)

  • Jun, Je-Cheon;Chung, Ee-Yung;Yang, Young Chul
    • Korean Journal of Ichthyology
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    • v.18 no.4
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    • pp.311-318
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    • 2006
  • Ultrastructure of germ cells, the cyst epithelial cells and interstitial cells during spermatogenesis of the stone flounder, Kareius bicoloratus (Pleuronectidae) sampled on the west coast of Korea were investigated by electron microscopic observations. In the primary spermatocyte, the synaptonemal complexes appear in the zygotene stage of the prophase during maturation division. In the growing testis, especially, the interstitial cells (Leydig cells) appear near the primary, secondary spermatocytes and spermatids. Well-developed interstitial cells (steroid hormone secreting cells) which are located in the interlobular space in growing testis have three morphological characteristics of a vesicular nucleus, mitochondria with tubular cristae and smooth endoplasmic reticulum. During spermatogenesis, the primary and secondary spermatocytes attach to the cyst epithelial cell (Sertoli cell) having an elongated ovoid or triangular nucleus and several mitochondria in the cytoplasm. In the growing testis, lipid droplets, the mitochondrial rosettes and glycogen particles appear in the cytoplasm of the cyst epithelial cells near the secondary spermatocytes and spermatids. Particularly, the mitochondria, endoplasmic reticulum, little lipid droplets and the large amount of glycogen particles are present in the cytoplasm of the cyst epithelial cell in the late growing testis. In the late stage of spermiogenesis, the proximal centriole is joined to the nuclear envelope, the distal centriole forms the basal body of the flagellum and gives rise to the axial filament of the flagellum. No acrosome of the sperm is formed as seen in other teleost fish. The head of the spermatozoon is approximately $3{\mu}m$ in length and its tail is about $30{\mu}m$ in length. The axoneme of the tail flagellum of the spermatozoon consists of nine outer doublet microtubules at the periphery and two centrial singlet microtubules at the center. The spermatozoon of this species has two axonemal lateral fins. Especially, the cyst epithelial cells which located near groups of gametes in the various stages, show three functions: nutrition, phagocytosis and steroidogenesis. Especially, the nuclei of cyst epithelial cells in the recovery stage of the testicular developmental stages appear to be irregular in shape after spermiation. Of three functions of the cyst epithelial cell, several characteristics of phagocytosis are showed in the cytoplasm of the cyst epithelial cells in the recovery stage of the testicular developmental stages. At this stage, therefore, it is assumed that the cyst epithelial cells are involved in degeneration and resorption of undischarged germ cells after spermiation.

A Morphological Study on the Male Genital Organs of a Land Snail, Nesiohelix samarangae (동양달팽이의 웅성 생식기관에 대한 형태학적 연구)

  • 이훈섭;정계헌;박종안
    • The Korean Journal of Malacology
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    • v.8 no.1
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    • pp.61-71
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    • 1992
  • 동양달팽이 (Nesiohelix samarangae)는 동양달팽이속(Nesiohelix)에 속하는 종으로 한국에서 동양?팽이속으로는 유일하게 발견되는 종이다. 본 실험에서는 동양달팽이의 웅성생식기관의 각 부분 즉, 난정소(ovotestis), 양성관(hermaphrodite duct), 수정실(fertilization chamber), 전립선(prostate), 수정관(vas deferens), 상음경(epiphallus), 음경(penis)등의 배열 상태를 관찰하고 이들에 대한 광학현미경적 관찰을 위해 Hematoxylin- Eosin염색과 Mallory 염색을 실시하였다. 난정소(ovotestis)는 많은 수의 선포(acini)로 이루어져 있으며 각 선포는 배상피세포층(germinal epithelial cell layer)과 영양세포(nurse cell), 생식세포(gamete cell)들로 이루어져 있었다. 선포(acini)는 원주상피로 덮여있었다. 양성관(hermaphrodite duct)은 가늘고 긴 관으로 내벽은 섬모입방상피세포와 얇은 결합조직층으로 이루어져 있었으며 내강은 농축된 정자로 가득 차 있었다 . 수정관(fertilization chamber)은 3개의 도관이 결합조직에 의해 둘러싸인 형태로 이루어져 있었다. 도관의 상피세포는 뚜렷한 위중층섬모원주세포로 되어 있었다. 전립선(prostaoe)은 분비기능을 가진 것으로 사료되는 세포들과 실제 분비가 일어나는 실(chamber)로 이루어져 있었으나 다른 염색법 또는 전자현미경적 관찰에 의해 다른 구조들의 존재유무를 확인 해야할 것으로 사료된다. 실(chamber)은 분비포로 보이는 세포들과 접해 있었다. 수정관(vas deferens)은 결합조직으로 이루어진 근육질의 두꺼운 벽을 가지고 있었으며 내강은 돌출부위에 의해 4부분으로 갈라져 있었다. 내강에 연한 상피는 원주세포로 되어 있었다. 상음경(epiphallus)의 벽은 근섬유 다발은 벽의 외곽으로 갈수록 밀도가 높아졌다. 상부에 내강과 연결되는 함입구조(groove)를 가지며, 내강에 연한 상피는 섬모가 없는 원주세포로 이루어져 있었다. 음경(penis)은 근섬유가 산재된 두꺼운 벽을 가졌으며 상음경보다 굵은 원통형이었다. 내강은 많은 돌출부에 의해 복잡하게 나뉘어 있으며 상피세포는 원주 세포로 이루어져 있었고 섬모는 관찰되지 않았다. 내강 내의 분비물과 세포의 형태로 보아 내강상피세포는 분비기능을 가진 것으로 사료된다.

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Effects of the Heavy Metal Pollution on the Primordial Germ Cells of Developing Amphibia (중금속 오염이 양서류 시원생식세포 발생에 미치는 영향)

  • Hah, Jae-Chung
    • The Korean Journal of Zoology
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    • v.21 no.2
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    • pp.43-58
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    • 1978
  • Heavy metal treatment on the fertilized frog eggs before the first cleavage results in a quantitative alteration in the number of PGCs. The formation of PGCs is inhibited by a limited range of heavy metal during the early embryonic development. Total doses of lead above 70ppm and doses of cadmium above 4ppm result in a partial reduction of germ cells at the mitotically dormant stage. After this stage the germ cell number increases almost at the same rate as the untreated control tadpoles. In contrast, on mercury treated eggs, total doses above 0.8ppm cause more damage to germ cell formation. Their proliferation rate thereafter seems to be lower compared with the others. These facts seem to suggest that the heavy metal treatment on frog eggs prior to the first cleavage division is not highly effective in the complete elimination of PGCs in constrast with UV irradiation, even though cytolysis of the tissue occurs in the tadpoles.

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Expression of Apoptosis-Related Proteins on Germ Cells in Neonatal Mouse Ovary (생쥐 신생자 난소내 생식 세표에서 세포 사멸 관련 단백질의 발현)

  • Cho Dong-Jae;Park Cheol-Hong;Yang Hyunwon;Park Joo-Hyun;Yun Jeong-Mi;Kim Sei-Kwang;Yoon Yong-Dal
    • Development and Reproduction
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    • v.8 no.1
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    • pp.27-33
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    • 2004
  • To investigate the mechanism of germ cell death in postnatal stage of mouse, the involvement of apoptotic executioners, caspase-3 and caspase-activated DNase(CAD), and apoptotic initiators, Bax Fas and Fas ligand, in the germ cell death has been studied. Immune-labels of active caspase-3 and CAD were located in TUNEL-positive, apoptotic, oocytes as well as normal oocytes of primary or secondary follicles. CAD immune-labels were also detected in the nucleus of TUNEL-positive oocytes. Most of oocytes showing positive immune-labeling of active caspase-3 or CAD had vacuoles in their cytoplasm, which is the morphological characteristic of oocyte during folliclar atresia. Bax immune-stains were detected in the atretic oocytes which showed the vacuole in their cytoplasm. Positive immune-labels for Fas ligand was localized in TUNEL-positive or atretic oocytes. Presence of immunoreactivity of active caspase-3 and CAD in TUNEL-positive germ cells implicate that active raspase-3 and CAD might play a role in germ cell apoptosis during early development of mouse ovarian follicle. Immunohistochemical localization of Bax and Fas ligand in TUNEL-positive oocytes suggests that these might be the most plausible modulator of oocyte apoptosis.

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Probing Cell-Type Specific Gene Expression in the Ovarian Cells of Drosophila by P-Element Mediated Enhancer Detection (P-요소를 이용한 노랑초파리 난소에서의 세포특이적 유전자발현의 검출)

  • 계명찬;조경상;김경진;이정주
    • The Korean Journal of Zoology
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    • v.38 no.4
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    • pp.505-513
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    • 1995
  • P-lement mediated enhancer detector lines (EDla) were screened for reporter gene (1acZ expression In the ovary of Drosophila mejanogaster Cell-type spedfic 1acZ expression can be grouped Into three parts such as in the geimline, soma, and both. LacZ expression In germline cells was devided into 2 types; expression in nurse cells or in both of the nurse cells and oocote. In the stage-9 to stage-lO follicles, lacZ expression was observed either In the whole follicle cells around oocote or in the subpopulation of follicle cells in egg chamber. lacZ expression in the subset of follicle cells are showed in the centripetal follicle cells or the columnar follicle cells except centripetal follicle cells. Several lines showed anterior to postedor gradient pattern of lacZ expression in the follicle cells. Interestingly there were 3 lines in which lacZ was expressed In the polar cells and/or the horder cells of egg chamber. These lacZ expression patterns in the different ovarian cells of independent EDla reflect the cell type-spedflc expression of maternal genes nesr the P-element insertion, and might provide a basis for cloning of genes involved in oogenesis of Drosophila.

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