Human endogenous retrovirus-FRD envelope protein (syncytin 2) expression in normal and trisomy 21-affected placenta
© Malassiné et al; licensee BioMed Central Ltd. 2008
Received: 03 October 2007
Accepted: 23 January 2008
Published: 23 January 2008
Human trophoblast expresses two fusogenic retroviral envelope proteins, the widely studied syncytin 1, encoded by HERV-W and the recently characterized syncytin 2 encoded by HERV-FRD. Here we studied syncytin 2 in normal and Trisomy 21-affected placenta associated with abnormal trophoblast differentiation. Syncytin 2 immunolocalization was restricted throughout normal pregnancy to some villous cytotrophoblastic cells (CT). During the second trimester of pregnancy, syncytin 2 was immunolocalized in some cuboidal CT in T21 placentas, whereas in normal placentas it was observed in flat CT, extending into their cytoplasmic processes. In vitro, CT isolated from normal placenta fuse and differentiate into syncytiotrophoblast. At the same time, syncytin 2 transcript levels decreased significantly with syncytiotrophoblast formation. In contrast, CT isolated from T21-affected placentas fused and differentiated poorly and no variation in syncytin 2 transcript levels was observed. Syncytin 2 expression illustrates the abnormal trophoblast differentiation observed in placenta of fetal T21-affected pregnancies.
Human endogenous retroviruses (HERV) comprise approximately 8% of the human genome [1, 2]. Most of the identified elements are defective due to mutations and/or deletions within their genes, but some elements have conserved intact open reading frames. A systematic search for non-defective endogenous retrovirus envelope protein genes has led to the identification of 16 genes . Among them, two can induce cell-cell fusion when expressed in different cells and are highly and specifically expressed in the human placenta [4–6]. The products of these two genes are glycoproteins named HERV-W Env glycoprotein (syncytin 1) and HERV-FRD Env glycoprotein (syncytin 2).
In vitro isolated mononuclear cytotrophoblasts aggregate and fuse together to form a non proliferative, multinucleated syncytiotrophoblast which secretes human chorionic gonadotropin (hCG) and human placental lactogen (hPL), specific to pregnancy [8, 9].
Trisomy of chromosome 21 (T21), which causes the phenotype known as Down syndrome, is the major known genetic cause of mental retardation and is found in around 1:800 live births. Little is known about placental development in this aneuploid condition. However, a defect in syncytiotrophoblast formation in T21-affected placentas is observed. Cultured cytotrophoblasts, isolated from T21-affected placentas, aggregate but fuse poorly or belatedly [10–13].
Trophoblast fusion and differentiation directly involves different molecular actors . Among them, the HERV-W envelope glycoprotein named syncytin 1 is expressed in all trophoblastic cells [15, 16] and directly involved in human trophoblast fusion and differentiation . HERV-FRD Env glycoprotein (or syncytin 2) has been more recently shown to be expressed in the human placenta [1, 4, 18]. The aim of this work was therefore to study in situ and in vitro the expression and localization of syncytin 2 in human placenta at different stages of gestation, in normal and T21-affected pregnancies.
Syncytin 2 is immunolocalized in cytotrophoblastic cells throughout normal pregnancy
Syncytin 2 immunostaining of cytotrophoblastic cells differs between T21 and gestational age-matched control placentas
With time in culture Syncytin 2 transcript levels decrease in normal but not in T21 cells
The role of endogenous retroviruses in placental morphogenesis and trophoblast differentiation was hypothesized 10 years ago . More recent studies point to the presence of HERV-R (ERV 3), HERV-FRD, HERV-W, HERV-F, HERV-K and HERV-T in human placenta, coding for intact retroviral Env proteins . However the role of theses retroviral envelope proteins is still poorly understood.
A role for the ERV-3 envelope protein (produced by the single-copy human endogenous retrovirus ERV-3) have been suggested in trophoblast proliferation and differentiation [20, 21]. However, the physiological knockout of the ERV-3 envelope (lacking both the fusion peptide and the immunosuppressive domain) in 1% of the Caucasian population  suggests that no essential function in placentation is associated with the expression of the ERV-3 envelope protein.
HERV-W envelope protein, syncytin 1, is directly involved in villous trophoblast fusion and differentiation . The syncytin 1 is expressed in all trophoblastic cells, villous and extravillous trophoblast, independently of their differentiation stage [15, 16].
In this study, we show that throughout pregnancy, HERV-FRD envelope protein, syncytin 2 is detected in some villous cytotrophoblastic cell and therefore this localization differs from syncytin 1 localization. All along pregnancy, the syncytiotrophoblast regenerates from the fusion of the underlying cytotrophoblasts. This process includes the continuous trophoblast turnover including proliferation of cytotrophoblast progenitors, the withdrawal of cytotrophoblasts from the cell cycle to G0, the recruitment of these post-mitotic cells to syncytiotrophoblast after membrane fusion and progression of syncytiotrophoblast towards apoptosis. Therefore the expression of syncytin 2 in some cytotrophoblastic cells suggest that it is expressed when the cytotrophoblastic cell is engaged in the fusion stage. As illustrated in second trimester placenta cytotrophoblastic cells are immunostained for syncytin 2 more frequently at the level of the cell membrane and this staining occurs at the sites of contact with the syncytiotrophoblast. Localization at this interface is precisely that expected for a protein directly involved in the fusion of the mononuclear cytotrophoblastic cells into the syncytiotrophoblast.
In addition, the syncytin 2 immunolabeling reflects the structural changes of the cytotrophoblastic layer during pregnancy. Indeed, as recently demonstrated, the cytotrophoblastic cell layer becomes thinner: the cuboidal cells are transformed to flat cells with many cellular processes that together with those of the adjacent syncytiotrophoblast eventually cover the basal lamina in a complex network of interdigitations .
In T21-affected placentas, localization of the labeled syncytin 2 differs notably from that in gestational age-matched control placentas. Syncytin 2 is mainly located in the cytoplasm of cuboidal cytotrophoblastic cells. This observation highlights in situ the delay in the fusion process of T21 trophoblastic cells and the delay in the maturation of the chorionic villi from T21-affected placentas [24, 25] (Fig. 3).
In addition the transcript levels of syncytin 2 decreased significantly during in vitro differentiation of normal cytotrophoblastic cells into syncytiotrophoblast. In contrast in isolated T21 cytotrophoblastic cells, which did not fuse transcript levels of syncytin 2 did not vary with time in culture. Interestingly, we recently demonstrated that the in vitro defect of syncytiotrophoblast formation in T21 is reversible when cytotrophoblastic cells are treated with biosynthetic human chorionic gonadotropin. These results point to a major role of abnormal hCG and its receptor in T21 placental defect .
Envelope glycoprotein of HERV-W (syncytin 1)  interacts with its identified receptor RDR, also known as the neutral aminoacid transporter SLC1A5/ASCT2 [5, 27]. Syncytin 2 entered the primate genome earlier than syncytin 1, namely before the split between New World and Old World Monkeys (i.e >40 Myrs ago). It also differs in its receptor, as demonstrated by ex vivo cell-cell fusion assays using different cell types . The identification of this receptor and the direct role of syncytin 2 of in human syncytiotrophoblast formation need to be investigated.
Recently, other retroviral envelope proteins have been identified in placenta from other species. In mouse placenta two related env genes (syncytin A and syncytin B) were characterized  and it was demonstrated that the endogenous Jaagsiekte sheep retrovirus envelope regulates trophectoderm growth and differentiation in perimplantation ovine conceptus . The role of these retroviral envelope proteins in fetoplacental development is still poorly known but their pleiotropic functions, including immunosuppressive activity argue for a critical role [1, 30, 31].
In summary data presented here show that the highly fusogenic retroviral FRD envelop protein, syncytin 2, is expressed in human placenta throughout pregnancy in some cytotrophoblastic cells, which might be in the fusion stage. Syncytin 2 expression highlights the abnormal trophoblast differentiation observed in placenta of fetal T21-affected pregnancies.
First trimester placentas were obtained from legal induced abortions (8–12 weeks of gestation). Term placentas were obtained after elective cesarean section from healthy mothers near term with uncomplicated pregnancies. Samples of second trimester placental tissues were collected at the time of termination of pregnancy at 12–25 weeks of gestation (in weeks of amenorrhea) in T21-affected pregnancies (n = 5) and gestational age-matched control cases (n = 5) as previously described . Fetal Down syndrome was diagnosed by karyotyping of amniotic fluid cells, chorionic villi or fetal blood cells. Termination of pregnancy was performed in control cases affected by severe bilateral or low obstructive uropathy or major cardiac abnormalities. The karyotype of placental cells was checked in all cases (free trisomy 21 or normal). The use of these biological samples was approved by our local ethical committee.
Placental samples were fixed in 4% formalin for 4–12 h at room temperature and then embedded in paraffin. Briefly, paraffin sections were dewaxed in xylene and rehydrated in ethanol/water. Some sections were classically stained with H&E. Immunostaining was performed with an universal streptavidin-peroxidase immunostaining kit (Dako LSAB, Glostrup, Danemark) using a syncytin 2 monoclonal antibody . All controls, performed with a mouse isotypic IgG1 at the same concentration as the primary antibody were negative.
For in vitro culture villous cytotrophoblastic cells were isolated from second trimester placentas (gestational age-matched controls and T21-affected placentas). 90%–95% of the cells isolated from the normal or T21 placentas were cytokeratin 7-positive. Cells plated in triplicate were cultured for 3 days. Trophoblastic fusion was monitored by desmoplakin immunostaining and nuclei counting as previously described .
Quantification of specific transcripts by real-time RT-PCR
Total RNA was extracted from villous trophoblastic cells cultured for 24 h and 72 h using QIAGEN RNeasy mini kit. cDNA synthesis and PCR amplification were performed as described previously . All PCR reactions were performed using an ABI Prism 7700 Sequence Detection System and the SYBER Green PCR Core Reagents kit (Perkin-Elmer). We used the following primers: FRD (+) 5'-GCCTGC A AATAGTCTTCTTT-3' and FRD (-) 5'-ATAGGGGCTATTCCCATTAG-3'. RNA from the RPLP0 gene encoding the human acidic ribosomal phosphoprotein-P0 was used as an internal control and each sample was normalized to RPLP0 transcript content. The RPLP0 primers used for amplification were: (+) 5'-GGCGACCTGGAA GTCCAAT-3' and (-) 5'-CCATCAGCACCA CAGCCTTC-3'.
The hCG concentration was determined in culture medium at 24 h and 72 h of culture, using an enzyme.
The authors wish to thank Prof. Foidart (Université de Lièges, Belgium) and the staff of the Obstetrics Department of the Cochin, Saint Vincent de Paul, Broussais, Beaujon and Robert Debré Hospitals (Paris, France), for assistance with specimen collections, as well as Patrick Saunier and the Translational Research Laboratory (Institut Gustave-Roussy, 94805 Villejuif) for expertise in RT-PCR analysis, Jean Guibourdenche for expertise in hCG assay and Christian Lavialle for critical reading of the manuscript.
This work was supported by la Caisse d'Assurance Maladie des Professions Libérales Province and la CANAM.
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