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首页> 外文期刊>The Journal of Reproduction and Development >Effects of storage and passage of bovine luteal endothelial cells on endothelin-1 and prostaglandin F2 alpha production.
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Effects of storage and passage of bovine luteal endothelial cells on endothelin-1 and prostaglandin F2 alpha production.

机译:牛黄体内皮细胞的储存和传代对内皮素-1和前列腺素F2α产生的影响。

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摘要

To establish a storage system for isolated bovine luteal endothelial cells (LECs), we investigated the basal and tumour necrosis factor (TNF) alpha -stimulated production of endothelin-1 (ET-1) and prostaglandin (PG) F2 alpha in unfrozen and frozen-thawed LECs until passage 10. LECs were obtained from developing corpora lutea (CL; days 5-7 of the oestrous cycle) using enzymatic digestion and magnetic beads coated with lectin BS-1. The LECs were frozen at -80 C or further cultured and/or passaged until passage 10 in DMEM/Ham's F-12 supplemented with 10% calf serum. The hormonal productions of unfrozen and frozen/thawed LECs were compared through passages 2-10. When both the unfrozen and frozen/thawed cells reached confluence, the culture medium was replaced with fresh medium containing 0.1% bovine serum albumin (BSA), and the cells were incubated with TNF alpha (50 ng/ml) for 12 h. The basal productions of ET-1 and PGF2 alpha by the unfrozen and frozen/thawed LECs were similar at passage 2. The basal production of PGF2 alpha by LECs was not altered by passage and storage at -80 C, whereas the basal production of ET-1 decreased from passage 2 and 3 to passage 4 in the unfrozen LECs and from passage 2 to passage 3 in the frozen/thawed LECs. However, production of ET-1 by the unfrozen and frozen/thawed LECs was similar between passages 4-10 and passages 3-10, respectively. Exposure of LECs to TNF alpha increased (P<0.05) ET-1 and PGF2 alpha production by the unfrozen and frozen-thawed LECs in all passages examined. Thus, LECs obtained from developing CLs and stored until passage 10 can be used for study of the physiology of LECs in vitro..
机译:为了建立分离的牛黄体内皮细胞(LECs)的存储系统,我们研究了基础和肿瘤坏死因子(TNF)α刺激的未冻结和冷冻状态下内皮素1(ET-1)和前列腺素(PG)F2α的产生。融化的LEC,直到第10代。使用酶消化和涂有凝集素BS-1的磁珠从发育的黄体(CL;发情周期的第5-7天)获得LEC。将LEC在-80℃下冷冻或进一步培养和/或传代直至在补充有10%小牛血清的DMEM / Ham's F-12中传代第10代。通过第2-10段比较未冷冻和冷冻/解冻的LEC的激素产生。当未冷冻的细胞和冷冻/融化的细胞都达到汇合时,将培养基替换为含有0.1%牛血清白蛋白(BSA)的新鲜培养基,并将细胞与TNFα(50 ng / ml)孵育12小时。在第2代,未冻结和冷冻/解冻的LEC产生的ET-1和PGF2α的基础产量相似。在-80 C下通过和储存,LEC产生的PGF2α的基础产量没有改变,而ET的基础产生-1在未冻结的LEC中从通道2和3下降到通道4,在冻结/解冻的LEC中从通道2下降到通道3。但是,在第4-10代和第3-10代之间,未冻结的和冷冻/解冻的LEC产生的ET-1相似。在所有检查的传代中,未冷冻和冻融的LEC对LEC的TNFα暴露量增加(P <0.05)ET-1和PGF2α的产生。因此,从发育中的CL获得并保存到第10代的LEC可用于体外研究LEC的生理学。

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