The orphan nuclear receptor NUR77 promotes trophoblast invasion at early pregnancy through paracrine placental growth factor

被引:9
|
作者
Li, Xiao-Cui [1 ]
Yin, Xiang-Jie [1 ]
Hong, Wei [1 ]
Liu, Jie [2 ]
Jin, Feng [3 ]
Wang, Bei-Ying [1 ]
Wang, Yu-Mei [1 ]
Tian, Fu-Ju [4 ,5 ]
机构
[1] Tongji Univ, Dept Gynecol & Obstet, Shanghai Matern & Infant Hosp 1, Sch Med, Shanghai 201204, Peoples R China
[2] Qingdao Municipal Hosp, Reprod Med, Qingdao 266071, Shandong, Peoples R China
[3] Shanghai Jiao Tong Univ, Dept Obstet & Gynecol, Affiliated Peoples Hosp 6, Shanghai 200233, Peoples R China
[4] Shanghai Jiao Tong Univ, Int Peace Matern & Child Hlth Hosp, Sch Med, Shanghai 200030, Peoples R China
[5] Shanghai Key Lab Embryo Original Dis, Shanghai 200030, Peoples R China
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 2019年 / 97卷 / 09期
基金
中国国家自然科学基金;
关键词
NUR77; PGF; Trophoblast invasion; Syncytiotrophoblast; Early pregnancy; IN-VITRO DIFFERENTIATION; RECURRENT MISCARRIAGE; FACTOR PIGF; NGFI-B; CELLS; EXPRESSION; KINASE; VEGF; PLGF; IDENTIFICATION;
D O I
10.1007/s00109-019-01819-4
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
NR4A1 (NUR77) is an orphan nuclear receptor that has been implicated in both cell survival and apoptosis. However, the role of NUR77 in trophoblast function during early placenta development has not been fully elucidated. In this study, we showed that NUR77 expression was significantly lower in the villi of the recurrent miscarriage (RM) group compared to that in the healthy controls (HCs) group. We used immunohistochemistry and found that NUR77 was highly expressed in human placental villi during early pregnancy, especially in syncytiotrophoblast (STB), and was expressed at a much lower level in STB from the RM group than in those from HC group. Western blotting data further confirmed that NUR77 was highly expressed in primary human term placental STB and the FSK-induced BeWo cell line. Moreover, antibody array screening and ELISA revealed that NUR77 promoted significant placental growth factor (PGF) expression during trophoblast fusion. Ectopic overexpression and knockdown experiments demonstrated that PGF was a novel downstream target of NUR77, and serum PGF expression correlated positively with trophoblast NUR77 mRNA levels in HCs and RM patients. Importantly, bioinformatics analysis identified two NUR77 binding sites in the PGF promoter region, and chromatin immunoprecipitation (ChIP) coupled with Western blotting analysis further verified that NUR77 bound directly to the PGF promoter region and promoted PGF expression. Furthermore, in a BeWo/HTR-8 co-culture system, FSK-induced BeWo-secreted PGF promoted HTR-8 cell migration and invasion, and an anti-PGF antibody reversed this effect. Collectively, these results indicated that NUR77 may play a key role in regulating trophoblast invasion at early pregnancy. Key messages NUR77 expression was significantly decreased in the syncytiotrophoblast of the recurrent miscarriage group compared to that in the healthy control group. NUR77 promoted PGF expression during trophoblast fusion. ChIP and western blotting experiments verified that NUR77 bound directly to the PGF promoter region and activated PGF expression in trophoblast. Trophoblast-derived PGF promoted HTR-8 cell migration and invasion in a cell co-culture system.
引用
收藏
页码:1359 / 1373
页数:15
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