- Open Access
Spatiotemporal expression of SERPINE2 in the human placenta and its role in extravillous trophoblast migration and invasion
© Chern et al; licensee BioMed Central Ltd. 2011
- Received: 8 June 2011
- Accepted: 2 August 2011
- Published: 2 August 2011
SERPINE2, one of the potent serpins belonging to the plasminogen activator (PA) system, is involved in the tissue remodeling. We previously demonstrated the expression patterns of Serpine2 in the mouse placenta and uterus, indicating that Serpine2 is a major PA inhibitor in the placenta and uterus during the estrous cycle, pregnancy, and lactation. In this study, we further investigated the expression pattern of SERPINE2 in the human placenta and explored possible functional roles of SERPINE2 in regulating trophoblast activity.
Placental tissues from various trimesters were collected for real-time reverse-transcription polymerase chain reaction quantification. Immunohistochemical staining was performed in placental tissues to assure localization of SERPINE2. SERPINE2 small interfering (si) RNA was applied to suppress its expression in villous explants and extravillous trophoblast-like 3A cells. Subsequent experiments to evaluate SERPINE2 levels, villous outgrowth, trophoblast invasion, and tube formation were performed.
SERPINE2 messenger RNA was detected in the human placenta during pregnancy with the highest levels in the third trimester. The SERPINE2 protein was present in villous syncytiotrophoblasts and trophoblasts of chorionic villi for anti-SERPINE2 immunostaining. Extravillous trophoblasts in the chorionic plate and basal plate confronting the invasive face of anchoring villi were also positive. In most decidual cells, SERPINE2 was observed in the cytoplasm. In addition, fibrinoid deposit was weakly immunoreactive. Introduction of SERPINE2 siRNA into villous explants and trophoblast cells led to significantly reduced villous outgrowth, and trophoblastic migration and invasion. Moreover, capillary-like network formation of 3A cells in Matrigel was greatly attenuated by SERPINE2 siRNA and SERPINE2 antiserum.
These data identify the temporal and spatial SERPINE2 distribution in the human placenta and suggest its possible role in modulating tissue remodeling of extravillous trophoblasts in the placenta during pregnancy.
- Human Placenta
- Trophoblast Cell
- Placental Tissue
- Vasculogenic Mimicry
- Decidual Cell
SERPINE2, also called protease nexin-1 and glial-derived neurite promoting factor, is a 44-kDa member of the serine protease inhibitor (SERPIN) superfamily. It was shown to be a potent inhibitor of the urokinase-plasminogen activator (uPA), tissue-type PA (tPA), thrombin, trypsin, factor XIa, and prostasin [1–5].
SERPINE2 is widely expressed in various tissues, including endothelial cells, fibroblasts, smooth muscle cells, tumor cells, glial cells, neurons, and placental cells [6–9]. Expression patterns of SERPINE2 in the placenta are quite dissimilar in different species. Expression levels of SERPINE2 in the monkey endometrium and placenta during early pregnancy were below the level of detection . In rats, Serpine2 messenger RNA (mRNA) expression was only detected in endometrial stromal cells of the uterus, particularly at the time of implantation . It was reported that SERPINE2 is highly expressed in the human placenta throughout pregnancy .
We demonstrated that Serpine2 is extensively expressed in various cell types in the mouse placenta and uterus, and in the human uterine endometrium [13, 14]. In the murine uterus and placenta, it was prominently expressed in decidual stromal cells, metrial glands, endometrial epithelium, trophoblasts of the labyrinth, and spongiotrophoblasts during gestation. In humans, the SERPINE2 protein is highly expressed in the endometrium during the secretory phase . These findings suggest a role for SERPINE2 in modulating tissue remodeling during implantation. Although SERPINE2 was found to be expressed by trophoblasts in various animals, the temporal expression of SERPINE2 in the human placenta during gestation still remains unclear .
Recent reports on human cancers indicated that SERPINE2 levels were elevated in pancreatic tumors , breast tumors , colorectal tumors , oral squamous carcinomas , and liposarcomas . In contrast, the physiological function of SERPINE2 in placental extravillous trophoblasts that possess "pseudomalignant" features is less well documented .
In addition to previous findings of the relatively abundant levels of SERPINE2 in female reproductive tissues, existing microarray gene expression profiles of normal human tissues deposited in the NCBI GEO database (http://www.ncbi.nlm.nih.gov/geo/; GDS596, GDS1096, and GDS3113) show that the placenta expresses the highest levels of SERPINE2 among all probed tissues except seminal vesicles. In the present study, we investigated the spatiotemporal expression of SERPINE2 in the human placenta. Further, knock-down experiments with SERPINE2 were performed to examine if the suppression of SERPINE2 in villous explants and trophoblast cells could modulate trophoblast invasion in vitro.
Placental tissue collection
Human placental tissues from the first (7~12 wk of gestation; n = 5), second (13~24 wk of gestation; n = 4), and third trimesters (31~38 wk of gestation; n = 10) were obtained from the Department of Obstetrics and Gynecology, Mackay Memorial Hospital. Signed, written consent was obtained from each patient before sample collection. The use of placental tissue specimens and the consent forms were approved by the Institutional Review Board of Mackay Memorial Hospital. Tissues were collected and washed three times in sterile saline, then they were (a) fixed in 10% neutral formalin (Merck, Darmstadt, Germany), embedded in paraffin, (b) stored in either RNAlater (Ambion, Austin, TX, USA) at -80°C for subsequent RNA extraction, and/or (c) finely minced with a surgical knife and resuspended in culture medium (Medium 199 containing 10% fetal calf serum (FCS), penicillin/streptomycin, and amphoteracin B).
Cell/explant culture and treatment
3A cells, derived from first-trimester human trophoblast by SV40 ts30 transformation , were purchased from ATCC (CRL-1584; Rockville, MD, USA). Cells were cultured in medium 199 (M199, Invitrogen, Carlsbad, CA, USA) supplemented with 10% FCS (Invitrogen) and 100 IU/ml penicillin/streptomycin (Invitrogen), and maintained at 37°C in 5% CO2. Preparation of placental explants was performed as described elsewhere . Villous tips were dissected under a microscope to approximately 2~3 mm3 and incubated for 16 h in culture medium at 37°C and 5% CO2. An extracellular matrix (ECM) gel solution was prepared using 1 ml neutralized collagen I (4 mg/ml, Sigma-Aldrich, St Louis, MO, USA) mixed with 1 ml Matrigel (10 mg/ml, BD Biosciences, San Jose, CA, USA). The ECM gel for explants was formed by adding 85 μl of the ECM solution onto the surface of 6-well culture dishes (Nunc, Roskilde, Denmark). After hardening of the gels, the villous tips (explants) were put on top of the gel and immersed in medium for 2~4 h to allow adherence to the ECM. Explants were then flooded with 1 ml M199 medium in the absence or presence of small interfering RNA (siRNA). Three ECM gels in each well containing 9~12 and 30~36 explants of each placenta were utilized. Four placentas (with respective gestational ages of 9, 12, 16, and 20 wk) were subjected to explant culture. Villous outgrowth and migration of trophoblasts were evaluated following a previously published protocol . Briefly, the explant morphology was carefully analyzed by two observers to judge explant outgrowth. The numbers of outgrowth sites of villous explants were recorded at 72 h. Migration of trophoblast cells in the ECM was scored at 120 h on a scale of 0-5 (0, no migration; 1, one or two sites of localized migration; 2, several sites of localized migration; 3, moderate migration; 4, moderate to extensive migration; and 5, extensive migration from several sites around the explant).
SERPINE2-targeted siRNAs and corresponding scrambled siRNAs were obtained from Sigma-Aldrich (for sequences see Additional file 1, Table S1). 3A cells (3 × 106) were transiently transfected with 0.05 μM of siRNAs using the Lipofectamine 2000 (Invitrogen) reagent, whereas villous cultures directly gained 1 μM siRNAs by an active transport mode . After 24 h of transfection, 3A cells were trypsinized for subsequent experiments, including RNA extraction following a reverse-transcription polymerase chain reaction (RT-PCR), wound-healing assay, invasion assay, and tube formation as described below. During the culture of explants, the medium was collected at 16 and 24 h for the Western blot analysis. At the end of the experiment, explants were harvested and processed for Western blotting, RNA extraction, and RT-PCR.
A batch of explants (at a gestational age of 14 wk) was cultured for 10 days in Matrigel to allow the ECM gel shank. The gel containing villi was fixed in 10% neutral buffered formalin for 24 h and processed for the immunohistochemical analysis.
Immunocytochemical staining was performed as previously described . Briefly, placental tissues were collected, fixed in neutralized formalin, embedded in paraffin, and cut into 5-μm sections. After the sections were deparaffinized and hydrated, they were treated with 3% hydrogen peroxide in phosphate-buffered saline (PBS, Invitrogen) for 15 min to quench any endogenous peroxidase activity, then blocked with 10% normal goat serum in PBS for 1 h. Immunocytochemistry for the SERPINE2 and trophoblast-specific CK7 marker was performed on tissues using anti-SERPINE2 antiserum (1:700)  and anti-human CK7 (1:100) (Dako, Copenhagen, Denmark) in blocking solution at 4°C for 16 h. Negative controls were performed by replacing primary antibodies with serum pretreated with SERPINE2-conjugated beads at the same concentration. After washing, slides were treated with biotin-conjugated goat anti-rabbit immunoglobulin G (IgG; ~3 μg/ml) (Zymed, San Francisco, CA, USA). Slides were then incubated with horseradish peroxidase (HRP)-conjugated streptavidin (~1 μg/ml) (Zymed) in the blocking solution for 40 min at room temperature. Protein signals were detected by 3-amino-9-ethylcarbazole (Zymed) staining. Slides were then counterstained with hematoxylin (Vector Laboratories, Burlingame, CA, USA) and photographed using a Zeiss AxioImager Z1 microscope system (Wetzlar, Germany) equipped with a digital camera and an automated acquisition system (TissueGnostics, Vienna, Austria).
RNA isolation and real-time RT-PCR
Total RNA of placental tissues and 3A cells was extracted using a QuickPrep RNA extraction kit (GE Healthcare Life Sciences, Uppsala, Sweden). To examine SERPINE2 gene expression, an RT-PCR was conducted. PCR primers (for sequences see Additional file 1, Table S1) were designed to cross the junction between the exon and intron. Four micrograms of total RNA was reverse-transcribed using an iScript complementary DNA synthesis kit (Bio-Rad, Hercules, CA, USA) according to the manufacturer's instructions. The PCR was performed in a total volume of 20 μl, and 25 ng of cDNA was added to the PCR mix made with 2-fold pre-mix containing fluorescein (Kapa SYBR Fast qPCR Kit, KAPA Biosystems, Woburn, MA, USA). Amplification conditions were as follows: 95°C for 10 min, and then 40 cycles at 95°C for 15 s and at 60°C for 1 min using the CFX96 real-time PCR system (BioRad) in triplicate. The PCR amplification efficiency for each gene was tested to be sure it was equivalent to that of RPLPO mRNA examined in a cDNA dilution series. Product purity was checked through a melting curve analysis at the end of the real-time PCR. The accuracy of the PCR products was confirmed by DNA sequencing. Relative gene expression levels were determined using the threshold cycle (CT) method (2-ΔΔCt method) with reference to the endogenous RPLPO control . Gene expression was normalized to RNA loading using primers for RPLPO as an internal standard.
Western blot analysis
Tissue extract proteins were separated by sodium dodecylsulfate-polyacrylamide gel electrophoresis (SDS-PAGE) on a 4%~15% gradient gel (Invitrogen) and were transferred to nitrocellulose membranes for immunostaining. Membranes were blocked with 10% (w/v) skim milk in PBS (blocking solution) for 2 h, and then incubated with anti-SERPINE2 antiserum (1:3000) or monoclonal anti-β-actin (1:5000, Sigma-Aldrich) in blocking solution for 1 h at room temperature. After gentle agitation in four changes of PBS for 15 min each, the membranes were immunoreacted with HRP-conjugated goat anti-rabbit IgG (1:10000, GE Healthcare Life Sciences) or HRP-conjugated anti-mouse IgG (1:15000; GE Healthcare Life Sciences) in blocking solution for 1 h. Immunoreactive bands were revealed using an enhanced chemiluminescence (ECL) substrate according to the manufacturer's instructions (Pierce, Rockford, IL, USA).
Collected medium (25 μl) from explants and 3A cell cultures were subjected to Blue Sepharose (GE Healthcare Life Sciences) chromatography to remove albumin and analyzed by Western blotting. Residual albumin was taken as the loading control and immunodetected by a rabbit anti-BSA polyclonal antibody (1:2500, GeneTex, San Antonio, TX, USA).
Invasion assays were carried out using Matrigel Invasion Chambers (BD Biosciences). Briefly, cells transfected with siRNAs (scrambled or SERPINE2) were trypsinized and seeded on Matrigel inserts in triplicate at a density of 5 × 104 cells/well in 200 μl of culture medium. Following an incubation period of 48 h, the filter inserts were removed and washed three times with PBS. Cells were fixed with 4% paraformaldehyde (Merck) and stained with hematoxylin for 3 min. Cells on the upper side of the transwell membrane were removed with a cotton tip swab. Cell numbers on the filters were counted under a microscope (IX71, Olympus, Tokyo, Japan).
Migration scratch assay
3A cells with or without siRNA treatment were harvested after 24 h of transfection, seeded into 10-cm dishes, and grown to about 95% confluence. A wound about 1 mm wide was created on cell monolayers by scraping them with a pipette tip. The dishes were washed with PBS to remove detached cells and incubated for 16 h at 37°C in the culture medium. After incubation, images were taken on an inverted light microscope (Olympus IX71) equipped with a digital camera. For quantification, these images were analyzed with the TScratch software tool . This free software is able to automatically measure the area occupied by cells in the image. The cell-free area correlated with the ability of 3A cells to migrate into the scratch, and closure of the controls was used for normalization.
In vitro angiogenesis assay (tube-formation assay)
Matrigel was thawed on ice overnight, and 10 μl was pipetted with ice-cold pipette tips into the lower chambers of an angiogenesis slide (IBIDI, München, Germany) and allowed to harden for 30 min at 37°C. Then, 7500 cells with or without siRNA treatment were seeded on the chamber and incubated overnight in the absence or presence SERPINE2 anti-serum (1:100) in the medium. Images were taken using an Olympus DP71 microscope with a camera system and analyzed using Image-Pro Plus software vers. 6.0 (Media Cybernetics, Houston, TX, USA). Network formation was quantified by measuring the branch point, and total cord lengths were compared between silenced and non-silenced cells.
Data are expressed as the mean ± standard error of the mean (SEM). Results were subjected to a statistical analysis by Student's t-tests as appropriate using Prism 5.0c (GraphPad Prism, San Diego, CA, USA), and significance was accepted when p < 0.05. * p < 0.05; ** p < 0.01; *** p < 0.001. All experiments were repeated three or more times with similar results.
Spatiotemporal expression of SERPINE2 in the human placenta
Immunohistochemistry was used to localize SERPINE2 in placental tissues obtained from the second trimester (n = 3). SERPINE2 protein expression was visible in extravillous trophoblast cells and decidual cells of the chorionic plate (Figure 1B). However, it was strongly expressed in villous syncytiotrophoblasts, cytotrophoblasts, decidual cells, extravillous trophoblasts anchoring the villous cell column (av-cc) adjunction zone, spiral arteries, and decidual stroma cells (Figure 1C, D). The immunoreaction was evident in extravillous trophoblasts invading the basal plate, where cytoplasm of most decidual cells were positively stained (Figure 1D). No detectable signal was found in septal endometrial stromal cells or mesenchymal cores of chorionic villi. Lower immunoreactivity was observed in fibrinoid deposits (Figure 1D). CK-7-positive extravillous trophoblasts were observed in the cell column (Figure 1E). Syncytiotrophoblasts and cytotrophoblasts in floating villi were strongly positive for SERPINE2 (Figure 1F, upper-left panel). Furthermore, most endothelia of spiral artery were both SERPINE2 and CK-7 positive (Figure 1F, lower panels). However, when slides were immunostained with control antiserum, no signal was detected (Figure 1G).
The trophoblast-derived cell line, 3A-sub E (3A) [21, 27], was applied for the in vitro studies of SERPINE2 in extravillous trophoblasts. Of note, 3A cells express HLA-G, CD9, and CK-7 mRNAs, which are characteristics of invasive extravillous trophoblasts [27, 28], as shown by an RT-PCR study (Additional file 2, Figure S1). Furthermore, SERPINE2 mRNA levels in 3A cells resembled those of the first trimester placenta tissue (data not shown).
Knockdown of SERPINE2
In this study, we demonstrated that SERPINE2 was extensively expressed in several cell types that exist in the human placenta. It was highly expressed in syncytiotrophoblasts, cytotrophoblasts, and extravillous trophoblasts in the placenta, while it was relatively weakly expressed in decidual cells (Figure 1D). These results were similar to a previous report on the term human placentas  which showed strong SERPINE2 immunofluorescence in amnion, chorion, and trophoblastic epithelia; lower intense and interspersed signals in decidual cells and stroma. We further specified the co-localization of SERPINE2 and invaded extravillous trophoblasts at the basal plate and the endothelium of the spiral artery. Recently, we demonstrated that Serpine2 was extensively expressed in labyrinthine trophoblasts, spongiotrophoblasts, and decidual cells, but was less expressed in giant cells in the mouse placenta. The expression pattern of the placental SERPINE2 protein greatly differs in various species. In rhesus monkeys, SERPINE2 protein expression in the compartments of the endometrium and placenta was lower or undetectable . However, the SERPINE2 protein is extensively expressed in human and murine placentas.
Interestingly, the pattern of SERPINE2 expression in the human placenta presented here during gestation parallels circulating uPA and tPA levels during pregnancy [31, 32]. However, SERPINE2 has broad-spectrum activity specific to serine proteases, including trypsin, thrombin, factor XIa , and prostasin . The question of what the cognate protease is in the human placenta needs to be further investigated.
Serine proteases and their cognate inhibitors were documented to play key roles in matrix remodeling and degradation in the uterus. Accordingly, a well-regulated balance between levels of protease and its inhibitor during endometrial matrix remodeling and restricted trophoblast invasion are essential for a successful pregnancy . We herein showed that downregulation of SERPINE2 mediated by siRNA effectively suppressed the outgrowth of villous explants and tended to inhibit extravillous trophoblast invasion (Figure 4). In trophoblast-derived 3A cells, SERPINE2 siRNA significantly impaired both migration and invasion (Figure 5). It seems that the depletion of SERPINE2 disturbs the balance between proteases and protease inhibitors, causes a shift in the ECM profile, and further affects the activity of trophoblasts.
During the first trimester of pregnancy, spiral arteries transform into wide-caliber, low-resistance vessels, extravillous trophoblasts invade through the maternal decidua to the spiral arteries, and then differentiate into tube structures, lining the artery walls with endothelial cells. Blockage of SERPINE2 inhibited 3A cell formation of capillary-like networks in Matrigel (Figure 6B), suggesting that SEPINE2 is essential for invading trophoblasts to develop vasculogenic mimicry. We therefore propose the following scenario for the regulation of extravillous trophoblasts in tissue remodeling by SERPINE2. SERPINE2 in the ECM establishes a micro-environment that facilitates trophoblast cell migration, and further promotes trophoblast cells aligning with themselves or with the maternal endothelium to establish vasculature structures via an unknown signaling pathway. Additionally, SERPINE2 in the ECM may originate from trophoblasts themselves or from maternal decidual cells in a coordinated manner.
Plasminogen activator inhibitor-1 (PAI-1 or SERPINE1), the phylogenetically closest relative of SERPINE2, is more deeply studied, as exemplified by a body of published work . Actually, SERPINE1 mRNA seems to be the major PA inhibitor in the human placenta (our unpublished data). The uPA-uPAR system and PAI-1 are undoubtedly associated with malignances through regulating tumor cell proliferation, migration, invasion, metastasis, and apoptosis [35–38], although contrary to what would be expected for the function of a cellular protease inhibitor. Likewise, SERPINE2 is reported to be upregulated in various tumors [15–19]. Further studies of serine proteases and cognate inhibitors' effects on placental tissue development will greatly enhance our understanding of the physiological and pathophysiological mechanisms of tissue remodeling.
SERPINE2 is highly expressed in the human placenta during pregnancy. Blockage of SERPINE2 results in inhibition of extravillous trophoblast activity in vitro, including migration, invasion, and tube formation. Taken together, these data suggest that SERPINE2 plays important roles in modulating placental tissue remodeling during pregnancy. Our studies may provide helpful insights into the roles of SERPINE2 in placental remodeling.
This work was supported by grants (NSC99-2628-B-195-001-MY3 and NSC97-2314-B-195-006-MY3) from the National Science Council and Mackay Memorial Hospital (MMH-E-100-04), Taipei, Taiwan. We wish to thank Dr. CL Chang for his helpful discussions.
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