ヒラメ白血球の長期培養
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- Ozaki Tomoki
- Laboratory of Fish Diseases, Department of Veterinary Science, Nippon Veterinary and Life Science University
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- Hatakeyama Hitoshi
- Laboratory of Fish Diseases, Department of Veterinary Science, Nippon Veterinary and Life Science University
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- Wada Shinpei
- Laboratory of Fish Diseases, Department of Veterinary Science, Nippon Veterinary and Life Science University
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- Kurata Osamu
- Laboratory of Fish Diseases, Department of Veterinary Science, Nippon Veterinary and Life Science University
書誌事項
- タイトル別名
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- Long-term Culture of Japanese Flounder Paralichthys olivaceus Leukocytes
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抄録
We developed a long-term culture system for Japanese flounder Paralichthys olivaceus leukocytes supported by JFF07-1 feeder cells established from Japanese flounder fin tissue. Kidney leukocytes were seeded onto a monolayer of the feeder cells in enriched RDF medium supplemented with 20% fetal bovine serum and 2.5% flounder serum. Several colonies adhered to the feeder cells after 7 days of cultivation, demonstrating leukocyte proliferation. Increasing numbers of floating cells, which signified colony growth, were observed as the length of the culture period increased. The optimum culture conditions consisted of an incubation temperature of 25°C, the addition of 2.5% flounder serum to the medium and the inoculation of kidney leukocytes at a density of 2 × 106 cells/mL. The proliferated cells were grouped into three types based on May-Grünwald Giemsa staining: basophilic cytoplasmic cells (65%), neutrophilic cytoplasmic cells (30%) and large cells containing many vacuoles (5%). The cells showed acid-phosphatase activity (90%), peroxidase activity (31%) and non-specific esterase activity (57%). Electron microscopy revealed that many of the cells contained endoplasmic reticula and mitochondria, but not specific granules with the fibrillar structure that characterizes flounder granulocytes. A monocyte lineage thus appeared to be the dominant population among the proliferated cells in the culture system. The composition of growing cells was also kept after 20 passages.
収録刊行物
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- 魚病研究
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魚病研究 46 (1), 11-18, 2011
日本魚病学会
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詳細情報 詳細情報について
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- CRID
- 1390001206461926272
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- NII論文ID
- 10027836476
- 130000674859
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- NII書誌ID
- AN00063165
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- ISSN
- 18817335
- 0388788X
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- NDL書誌ID
- 11051482
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- IRDB
- NDL
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