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[FABP7在小鼠胎盘组织和人滋养层细胞HTR-8/Svneo中的表达]

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

作者信息

Tian Liu, Liao Hui-Qi, Yang Hui, Ma Ni, Zhang Chang-Jun, Diao Hong-Lu

机构信息

Reproductive Medicine Center, People's Hospital Affiliated to Hubei University of Medicine, Shiyan 442000, China.E-mail:

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2017 May 20;37(5):594-599. doi: 10.3969/j.issn.1673-4254.2017.05.05.

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 E, P 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 E+P 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 E 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. E and P can regulate the expression of FABP7 in mouse uterus.

摘要

目的

检测脂肪酸结合蛋白7(FABP7)在妊娠小鼠胎盘及HTR-8/Svneo细胞中的表达。

方法

采用实时荧光定量PCR和免疫荧光法检测不同妊娠天数的妊娠小鼠子宫和胎盘组织中FABP7 mRNA和蛋白的表达。采用免疫荧光法检测培养的HTR-8/Svneo细胞中FABP7的表达。对小鼠分别用雌激素(E)、孕激素(P)或其联合处理6小时和24小时,用实时荧光定量PCR检测子宫中Fabp7 mRNA水平。

结果

在妊娠7.5 - 10.5天时,妊娠小鼠子宫和胎盘中Fabp7 mRNA呈阳性表达,在蜕膜化细胞和滋养层巨细胞中检测到FABP7蛋白。在培养的HTR-8/Svneo细胞中检测到FABP7在mRNA和蛋白水平均有表达。单独用P4或E + P处理小鼠6小时和24小时后,子宫中Fabp7 mRNA表达水平上调。E处理24小时后的小鼠中观察到Fabp7上调,但6小时时未观察到。

结论

FABP7在小鼠胎盘组织的滋养层巨细胞和蜕膜细胞以及培养的HTR-8/Svneo细胞中表达,提示FABP7参与胎盘发育和维持妊娠。E和P可调节小鼠子宫中FABP7的表达。

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