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作 者:刘红改[1] 王璐[1] 代盈盈[1] 于得水[1] 赵慧英[1]
机构地区:[1]西北农林科技大学动物医学院,陕西杨凌712100
出 处:《解剖学报》2015年第2期265-269,共5页Acta Anatomica Sinica
基 金:抗病转基因牛新品种培育重点专项基金资助项目(2009ZX08007);西北农林科技大学2013年大学生创新训练资助项目
摘 要:目的探讨雌激素膜性受体G蛋白耦联受体30(GPR30)在子宫免疫中的作用。方法将80只小鼠分为假手术(sham)组、卵巢摘除(OVX)组、OVX注射0.1nmol、0.5nmol和2.5nmol GPR30激动剂G1组及OVX小鼠注射0.1nmol、0.5nmol和2.5nmol GPR30拮抗剂G15组,分别采用免疫组织化学SP法及实时定量PCR技术,对子宫中toll样受体4(TLR4)的分布及TLR4 mRNA的表达量进行研究。结果 TLR4免疫反应阳性产物主要分布在小鼠子宫的内膜上皮、腺上皮及间质细胞;G1高浓度组中TLR4的免疫组织化学阳性着色强度显著低于其他组(P<0.01),去卵巢小鼠给予GPR30拮抗剂G15后,TLR4的相对表达量随G15浓度的升高而升高,各浓度组间TLR4的相对表达量显著性变化差异同OVX+G1组。各组小鼠子宫中TLR4 mRNA的表达量变化与TLR4相对表达量变化一致。结论 GPR30可下调子宫中TLR4的表达,并可能介导雌激素参与子宫的局部免疫功能的调节。Objective To investigate the role of G protein-coupled receptor 30( GPR30) on the uterine immunity.Methods A total of 80 mice were used in this study. Immunochemistry SP method and fluorescent real-time quantitative PCR technology were used to study the distribution of toll-like receptor( TLR4) and the expression of TLR mRNA in sham group,ovariectomized( OVX) group,OVX + 0. 1nmol G1 group,OVX + 0. 5nmol G1 group,OVX + 2. 5nmol G1 group,OVX + 0. 1nmol G15 group,OVX + 0. 5nmol G15 group,OVX + 2. 5nmol G15 group. Results TLR4 was mostly localized to the cell membrane and cytoplasm of the luminal,glandular epitheliumcells and mesenchymal cells. The intensities of the immunohistochemical positive staining for TLR4 were significantly lower in G1 high concentration group than those in other groups( P〈0. 01). After administrating the antogonist G15 to the OVX mice,the relative expression of TLR4 was increased with G15 concentration increasing. The significant difference on the relative expression of TLR4 in OVX + G15 group was coincidence with OVX + G1 group. The result of fluorescent real-time quantitative PCR showed that the expression level change of TLR4 mRNA in uterus of mice between groups was consistent with the relative expression of TLR4. Conclusion These results indicate that GPR30 can inhibit the expression of TLR4 in the uterus,and that GPR30 may participate in regulating the uterus local immune function.
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