• Journal of Marine Life Science
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• v.6 no.1
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• pp.23-30
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• 2021

The differentiation process of male germ cells and sperm morphology of the abalone Haliotis discus hannai were described in ultrastructure. The differentiation process of sperm was divided into four stages: spermatogonium, spermatocyte, spermatid and sperm. The process of differentiation from spermatogonium to spermatocyte did not show significant morphological changes. However, during the spermiogenesis there were distinct morphological changes such as chromatin condensation, morphological changes of the nucleus, and formation of acrosome, midpiece and flagellum. The sperm of the abalone consisted of head, midpiece and tail. The head of approximately 5.3 ㎛ in length was composed of a nucleus of high electron dense and bullet-shaped acrosome. The midpiece was composed of the basal body and mitochondria, and five mitochondria were arranged in single layer around the basal body. The cross section of the tail showed a "9+2" axonemal structure. These morphological and structural features are the result of showing that the sperm of H. discus hannai is a primitive type.

• Proceedings of the Malacological Society of Korea Conference
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• 2002.05a
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• pp.11-12
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• 2002

• Proceedings of the Korean Society of Developmental Biology Conference
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• 2003.02a
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• pp.15-15
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• 2003

• Proceedings of the Zoological Society Korea Conference
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• 1999.04a
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• pp.60.2-60
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• 1999

• Proceedings of the Malacological Society of Korea Conference
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• 2003.11a
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• pp.32-33
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• 2003

• The Korean Journal of Zoology
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• v.37 no.4
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• pp.514-523
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• 1994

꼬리명주나비(서ericinus montela) 조혈기관의 분포 및 미세구조를 광학현미경과 투과전자현미경을 이용하여 관찰하였다. 꼬리명주나비의 조혈기관은 흉부 제 2 · 3체절의 날개발생부위(imaginal wing disc)에 부착되었거나 인접해 있었다 각각의 조혈기관은 비세포성 기저 막으로 둘러싸인 여러 개의 조혈섬으로 구성되어 있었으며, 조혈 섬들은 compact islet(치밀하게 배열된 조혈섬)과 loose islet(느슨하게 배열된 조혈섬)으로 구분되었다. 혈구의 분화는 loose islet 내에서 진행되었으며, 시원세포로부터 원시혈구. 부정형혈구, 과립혈구, 소구혈구가 독자적 경로를 통해 분화되었다.

• Proceedings of the Korean Aquaculture Society Conference
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• 2006.05a
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• pp.629-630
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• 2006

• Proceedings of the Korean Society of Fisheries Technology Conference
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• 2002.05a
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• pp.625-626
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• 2002

• Proceedings of the Korean Aquaculture Society Conference
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• 2004.05a
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• pp.469-470
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• 2004

• Applied Microscopy
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• v.31 no.1
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• pp.49-57
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• 2001

In this study, the distribution of lectin receptors in culutured fibroblast was explored using colloidal gold label complexed with lectin WGA purified from wheat germ (Triticum vulgare). The lectin WGA gold complex, shown to recognize GlcNAc (N-acetylgalactosamine) and NeuNAc (N-acetylneuraminic acid) regions, was applied to detect binding sites in Lowicryl HM 20 sections viewed under electron microscope Labeled sections of the culutured fibroblast revealed gold particles specifically distributed on the cytoplasm and cell surface of the fibroblast. Labeling of 24 hours culutured fibroblast was then quantified and compared to that of 72 hours culutured fibroblast. 24 hours culutured fibroblast sections resulted in specific gold particle distribution on the cytoplasmic vesicle of the culutured fibroblast. These results indicate that lectin WGA receptors are located in the cytoplasmic vesicle and cell surface of the 24 hours culutured fibroblast, and on the cell surface of the 72 hours culutured fibroblast. Therefore, the GlcNAc and NeuNAc regions on the cell surface appear to be functionally associated with cell-recognition and protection from other cell of the tissue, and linked with secretion and exocytosis of the fibroblast cytoplasm.