Preimplantation factor is an anti-apoptotic effector in human trophoblasts involving p53 signaling pathway

被引:23
|
作者
Moindjie, Hadia [1 ]
Dos Santos, Esther [1 ,2 ]
Gouesse, Rita-Josiane [1 ]
Swierkowski-Blanchard, Nelly [3 ]
Serazin, Valerie [1 ,2 ]
Barnea, Eytan R. [4 ,5 ]
Vialard, Francois [1 ,3 ]
Dieudonne, Marie-Noelle [1 ]
机构
[1] Univ Versailles St Quentin En Yvelines Paris Sacl, GIG EA7404, Unite Format & Rech Sci Sante Simone Veil, Montigny Le Bretonneux, France
[2] Ctr Hosp Poissy St Germain, Serv Biol Med, Poissy, France
[3] Ctr Hosp Poissy St Germain, Dept Biol Reprod Cytogenet Gynecol & Obstet, Poissy, France
[4] Soc Invest Early Pregnancy, Cherry Hill, NJ USA
[5] BioIncept LLC, Cherry Hill, NJ USA
来源
CELL DEATH & DISEASE | 2016年 / 7卷
关键词
FACTOR PIF-ASTERISK; INTRAUTERINE GROWTH RESTRICTION; VILLOUS TROPHOBLAST; EMBRYO DEVELOPMENT; OXIDATIVE STRESS; CELL-DEATH; IN-VITRO; EXPRESSION; INVASION; PROLIFERATION;
D O I
10.1038/cddis.2016.382
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
From the earliest stages of gestation, embryonic-maternal interaction has a key role in a successful pregnancy. Various factors present during gestation may significantly influence this type of juxta/paracrine interaction. PreImplantation Factor (PIF) is a recently identified factor with activity at the fetomaternal interface. PIF is secreted by viable embryos and directly controls placental development by increasing the invasive capacity of human extravillous trophoblasts (EVTs). To further specify PIF's role in the human placenta, we analyzed the genome-wide expression profile of the EVT in the presence of a synthetic PIF analog (sPIF). We found that sPIF exposure altered several pathways related to p53 signaling, survival and the immune response. Functional assays revealed that sPIF acts through the p53 pathway to reduce both early and late trophoblast apoptosis. More precisely, sPIF (i) decreases the phosphorylation of p53 at Ser-15, (ii) enhances the B-cell lymphoma-2 (BCL2) expression and (iii) reduces the BCL2-associated X protein (BAX) and BCL2 homologous antagonist killer (BAK) mRNA expression levels. Furthermore, invalidation experiments of TP53 allowed us to demonstrate that PIF's effects on placental apoptosis seemed to be essentially mediated by this gene. We have clearly shown that p53 and sPIF pathways could interact in human trophoblast and thus promotes cell survival. Furthermore, sPIF was found to regulate a gene network related to immune tolerance in the EVT, which emphasizes the beneficial effect of this peptide on the human placenta. Finally, the PIF protein levels in placentas from pregnancies affected by preeclampsia or intra-uterine growth restriction were significantly lower than in gestational age-matched control placentas. Taken as a whole, our results suggest that sPIF protects the EVT's functional status through a variety of mechanisms. Clinical application of sPIF in the treatment of disorders of early pregnancy can be envisioned.
引用
收藏
页码:e2504 / e2504
页数:12
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