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作 者:王毛毛[1,2] 毛伟[1,2] 曹金山[1,2] 董至恒[1,2] 刘博[1,2]
机构地区:[1]内蒙古农业大学兽医学院,呼和浩特010018 [2]农业部动物疾病临床诊疗技术重点实验室,呼和浩特010018
出 处:《中国畜牧兽医》2015年第6期1333-1339,共7页China Animal Husbandry & Veterinary Medicine
基 金:国家自然科学基金(31160490);新世纪优秀人才计划支持项目(NCET-11-109)
摘 要:本试验旨在观察前列腺素E2受体激动剂(布他前列腺素(butaprost))与雌激素对奶牛输卵管上皮细胞中转化生长因子β3(TGFβ3)表达的影响,阐明butaprost和雌激素对奶牛输卵管上皮细胞TGFβ3有无协同调控作用。采用胰酶消化法及机械法分离培养奶牛输卵管上皮细胞,分别将butaprost和雌激素作用于体外培养的奶牛输卵管上皮细胞,采用实时荧光定量PCR技术检测butaprost和雌激素对奶牛输卵管上皮细胞中TGFβ3mRNA表达的影响。结果显示,与0h作用组相比,雌激素作用16、24和48h时对奶牛输卵管上皮细胞TGFβ3的表达量均极显著升高(P<0.01),4h的表达量极显著降低(P<0.01);且受体激动剂butaprost和雌激素有协同调控TGFβ3的效应;加入吲哚美辛后能有效抑制内源性前列腺素对TGFβ3表达的作用。结果表明,butaprost和雌激素可调控奶牛输卵管上皮细胞TGFβ3mRNA的表达。This study was aimed to observe effect of the prostaglandin receptor agonists butaprost and estrogen on TGFβ3 mRNA expression and illustrate whether butaprost and estrogen had coor- dinated regulation on bovine oviduct epithelial cells (BOECs) transforming growth factor β3 (TGFβ3) or not. BOECs were isolated and cultured by mechanical and pancreatic enzyme digestion method;butaprost and estrogen acted on BOECs, respectively;mRNA expression of TGFβ3 was detected by Real-time PCR in BOECs. The results showed that after the action of estrogen, the expression of TGF133 at 16,24 and 48 h compared with 0 h were extremely significantly increased (P〈0.01), TGFβ3 mRNA expression reached minimal at 4 h (P〈0.01);The receptor agonist butaprost and estrogen had coordinated regulation on TGFβ3. Adding indomethacin could inhibit the expression of endogenous prostaglandin for TGFβ3. The results showed that butaprost and es- trogen could regulate the expression of TGFβ3 mRNA in BOECs.
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