ウシ子宮内膜の上皮細胞および間質細胞の単離・継代・凍結保存法の開発
スポンサーリンク
概要
- 論文の詳細を見る
To establish a storage system for isolated endometrial cells, we investigated the basal, oxytocin (OT)- and tumor necrosis factor (TNF) α-stimulated production of prostaglandin (PG) F2α in bovine-passaged and frozen-thawed endometrial cells. Stromal and epithelial cells obtained from cows in the early stage of the estrous cycle (Days 2-5) were frozen at -80 C or further cultured and/or passaged until passage 4 in DMEM/Hams F-12 supplemented with 10% calf serum. A fresh-unfrozen primary culture and one-time passaged fresh-unfrozen cells were used as the control. When both unfrozen and frozen cells reached confluence, the culture medium was replaced with fresh medium with 0.1% BSA and the cells were stimulated with OT (100 ng/ml) or TNFα (1 ng/ml) for 4 h. The passage and freezing of the endometrial cells did not affect their morphology. In primary culture of frozen and unfrozen endometrial cells, OT strongly stimulated PGF2α production in epithelial cells, and TNFα strongly stimulated PGF2α production in stromal cells (P<0.05). The basal output of PGF2α in frozen stromal cells was similar to that in unfrozen stromal cells. However, the basal output of PGF2α in frozen epithelial cells was significantly lower than that unfrozen cells (P<0.05). On the other hand, in passaged cells, the basal level of PGF2α production was retained until passage 1 in epithelial cells, whereas it was retained until passage 4 in stromal cells. Although epithelial cells responded to OT in PGF2α production until passage 2 (P<0.05), the stromal cells showed a significant response to TNFα until passage 4 (P<0.05). These results suggest that stored cells could be used for studying the physiology of bovine endometrium in vitro until passage 1 in endometrial epithelial cells, and until passage 4 in stromal cells.
- 日本繁殖生物学会の論文
著者
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OKUDA Kiyoshi
Laboratory of Reproductive Endocrinology, Okayama University
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SHIBAYA Masami
Laboratory of Reproductive Endocrinology, Graduate School of Natural Science and Technology, Okayama
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Okuda Kiyoshi
Laboratory Of Reproductive Endocrinology Graduate School Of Natural Science And Technology Okayama U
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村上 周子
岡山大学大学院自然科学研究科バイオサイエンス専攻生殖内分泌学
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村上 周子
岡山大学・農学部
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Shibaya Masami
Laboratory Of Reproductive Endocrinology Graduate School Of Natural Science And Technology Okayama U
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Murakami Shuko
Laboratory of Reproductive Endocrinology, Okayama University, Okayama 700-8530, Japan
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SKARZYNSKI Dariusz
Division of Reproductive Endocrinology and Pathophysiology, Institute of Animal Reproduction and Foo
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竹内 宏佑
岡山大学・農学部
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TAKEUCHI Kosuke
Laboratory of Reproductive Endocrinology, Faculty of Agriculture, Okayama University
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- ウシ子宮内膜の上皮細胞および間質細胞の単離・継代・凍結保存法の開発
- ウシ子宮内膜の上皮細胞および間質細胞の単離・継代・凍結保存法の開発
- Effects of Tumor Necrosis Factor α and Interferon γ on the Viability and mRNA Expression of TNF Receptor Type I in Endothelial Cells from the Bovine Corpus Luteum
- Progesterone Stimulation by Prostaglandin F_ Involves the Protein Kinase C Pathway in Cultured Bovine Luteal Cells
- Secretion of Prostaglandins E_2 and F_ by the Bovine Endometrium in Response to Oxytocin during the Estrous Cycle
- Gene Expression of 11β-HSD and Glucocorticoid Receptor in the Bovine (Bos taurus) Follicle During Follicular Maturation and Atresia : The Role of Follicular Stimulating Hormone
- Effects of Storage and Passage of Luteal Endothelial Cells on Endothelin-1 and Prostaglandin F2α Production
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