南方医科大学学报 ›› 2017, Vol. 37 ›› Issue (05): 594-.

• • 上一篇    下一篇

FABP7 在小鼠胎盘组织及人滋养层细胞HTR-8/Svneo中的表达

田鎏,廖晖淇,杨慧,马妮,张昌军,刁红录   

  • 出版日期:2017-05-20 发布日期:2017-05-20

Expression of FABP7 in mouse placenta tissue and human trophoblast HTR-8/Svneo cells

  • Online:2017-05-20 Published:2017-05-20

摘要: 目的探讨FABP7 在正常妊娠小鼠胎盘组织及HTR-8/Svneo 细胞中的表达。方法用Realtime-PCR 及原位杂交的方 法检测Fabp7 mRNA 在妊娠小鼠7.5~10.5 d 和14.5、18.5 d 子宫和胎盘组织中的表达,用冰冻切片免疫荧光的方法检测 FABP7 蛋白的表达。培养HTR-8/Svneo 细胞系,用细胞免疫荧光方法检测FABP7 蛋白表达。17β-雌二醇(E2)、孕酮(P4)和 E2+P4分别处理小鼠6 h 和24 h 后,用Realtime-PCR的方法检测小鼠子宫组织中Fabp7 mRNA的表达。结果Fabp7 mRNA在 妊娠小鼠7.5~10.5 d 子宫及胎盘组织中均有表达,FABP7 蛋白在妊娠小鼠子宫组织蜕膜化细胞及胎盘部位滋养层巨细胞核 中有表达;在HTR-8/Svneo 细胞中可以检测到mRNA和细胞核中蛋白的表达。P4和E2+P4联合处理6 h 及24 h 后,Fabp7 mRNA在小鼠子宫组织中的表达上调(P<0.05),而E2处理6 h 后Fabp7 mRNA表达变化不明显,但24 h 后其表达上调(P< 0.05)。结论FABP7 在妊娠小鼠子宫蜕膜化细胞、滋养层巨细胞及HTR-8/Svneo 细胞中有表达,说明其参与胎盘发育过程, 与妊娠的维持有关,且在子宫中的表达量受E2、P4激素的调节。

Abstract: Objective To detect the expression of FABP7 in the placenta of pregnant mice and in HTR-8/Svneo cells. Methods Real-time PCR and immunofluorescence were used to detect FABP7 mRNA and protein expressions in the uterine and placental tissue of pregnant mice at different days of gestation. FABP7 expression was also detected in cultured HTR-8/Svneo cells using immunofluorescence assay. The mice were treated with E2, P4 or their combination for 6 and 24 h and Fabp7 mRNA level in the uterus was detected with real-time PCR. Results At 7.5-10.5 days of gestation, the pregnant mice showed positive expressions of Fabp7 mRNA in the uterus and placenta, and FABP7 protein was detected in the decidualized cells and trophoblast giant cells. The expressions of FABP7 were detected at both the mRNA and protein levels in cultured HTR-8/Svneo cells. In mice treated with P4 alone or with E2+P4 for 6 and 24 h, the expression level of Fabp7 mRNA was upregulated in the uterus. Fabp7 upregulation was observed in mice at 24 h following E2 treatment but not at 6 h. Conclusion FABP7 is expressed in trophoblast giant cells and decidual cells in the placental tissue of mice and in cultured HTR-8/Svneo cells, suggesting the involvement of FABP7 in placental development and in maintenance of pregnancy. E2 and P4 can regulate the expression of FABP7 in mouse uterus.