RBP4 regulates trophoblastic cell proliferation and invasion via the PI3K/AKT signaling pathway.

Insufficient trophoblast invasion is associated with preeclampsia (PE) development. Retinol-binding protein 4 (RBP4) is important for regulating cell differentiation, migration and invasion. The aim of the present study was to determine RBP4 expression and function in the human placenta and to examine the underlying mechanisms. In the present study, RBP4 expression was determined in serum samples from 35 pregnant women with PE and 30 healthy pregnant women using enzyme-linked immunosorbent assays. Cell proliferation was assessed by Cell Counting Kit-8 assays, and cell invasion was examined with transwell assays. RBP4 concentrations were significantly lower in the PE group when compared with the control group. RBP4 overexpression enhanced HTR8/SVneo cell proliferation and invasion, and the levels of phosphorylated (p-) phosphoinositide 3-kinase (PI3K) and p-protein kinase B (AKT) in HTR8/SVneo cells. RBP4 knockdown significantly inhibited HTR8/SVneo cell proliferation and invasion, and repressed the expression of matrix metalloproteinases. In addition, RBP4 knockdown significantly reduced the levels of p-PI3K and p-AKT in HTR8/SVneo cells. Taken together, the results of the present study demonstrated that RBP4 overexpression increased HTR8/SVneo cell proliferation and invasion by suppressing PI3K/AKT signaling and RBP4 knockdown induced the opposite effects.

Introduction

Preeclampsia (PE) is a pregnancy-specific clinical disorder that affects approximately 3–8% of all pregnant women (1). PE is defined by new-onset hypertension and proteinuria after 20 weeks of gestation and is a leading cause of maternal and perinatal mortality (2). A successful pregnancy depends on well-regulated trophoblast invasion into the uterine decidua and moderate uterine spiral artery remodeling. To date, the pathophysiology of PE has not been fully elucidated.

Serum retinol-binding protein 4 (RBP4) is a binding partner of retinol, which is delivered into the circulation by the carrier protein transthyretin (TTR) (3); the formation of this complex increases the molecular weight of RBP4, thus preventing its glomerular filtration and subsequent catabolism in the kidneys. Under physiological conditions, the liver is the major source of RBP4, producing approximately 80% of this protein. However, RBP4 can also be produced in adipose tissues (4). Chen et al (5) showed that RBP4 is not only a carrier of retinol but also acts as a circulating cytokine. Our previous study using surface-enhanced laser desorption ionization time-of-flight mass spectrometry (SELDI-TOF-MS) revealed that RBP4 is downregulated in PE (6). Serum samples were analyzed using a peptide ligand library conjugated to beads and liquid chromatography-mass spectrometry/mass spectrometry; RBP4 concentrations were found to be significantly lower in women with severe PE than in women with a healthy pregnancy. Immunohistochemistry (IHC) demonstrated significantly lower RBP4 expression (brown) in preeclamptic placental tissues than in normal placental tissues (7).

During placental development, trophoblasts with reduced invasive ability fail to deeply invade the myometrium and to appropriately remodel the uterine spiral arteries, resulting in a shallow placental bed and ultimately leading to PE. In our study, we hypothesized that RBP4 participates in the regulation of trophoblastic cell invasion and migration. The aim of the present study was to investigate the effect of RBP4 on the biological behavior of trophoblasts and to explore the potential signaling pathways involved in this process.

Materials and methods

Patients and clinical samples

The study protocol was approved by the Ethics Committee of Beijing Chao-Yang Hospital (Beijing, China). All women enrolled in the present study were Chinese patients at the Department of Obstetrics and Gynecology in Chao-Yang Hospital, Capital Medical University in Beijing, China, and all patients provided written informed consent before inclusion. Thirty-five patients with PE and thirty healthy pregnant women were recruited for enzyme-linked immunosorbent assay (ELISA) analysis. PE was defined as the onset of hypertension (systolic blood pressure ≥140 mmHg and/or diastolic blood pressure ≥90 mmHg on at least two occasions, 4 h to 1 week apart) after 20 weeks of gestation with proteinuria (≥300 mg in 24-h urine collection or at least one dipstick measurement ≥2+). The control patients were pregnant women who underwent cesarean section because of malposition and premature rupture of membranes. None of the participants had any history of hypertension, diabetes, cardiovascular disease, kidney disease, hyperthyroidism, smoking, alcoholism, chemical dependency, intrauterine fetal death, fetal congenital or chromosomal abnormalities or pregnancies conceived by in vitro fertilization. Blood was drawn via venipuncture and collected in a serum-separator tube. Serum was separated by centrifugation at 1,300 × g and 4°C for 10 min within 2 h of collection and was stored at −80°C until analysis.

ELISA

ELISAs were conducted according to the manufacturer's instructions (Cloud-Clone Corp., Katy, TX, USA). In brief, 100 µl of diluted standards was added to each well containing the quality control and the samples, and the plate was incubated on an orbital microplate shaker at room temperature for 1 h. After the wells were washed three times, 100 µl of conjugate solution was added, and the plate was then incubated for 1 h at room temperature while shaking at 300 rpm. The plate was washed three times with wash buffer, 100 µl of the substrate solution was added to each well, and the plate was incubated for approximately 10 min to enable the reaction to develop. Absorbance at 450 nm was measured using an ELISA plate reader.

IHC

RBP4 expression in placenta tissue was assessed using PV-9000 (standard polymer detection system) for immunohistological staining. IHC was performed to detect RBP4 expression and localization in the placenta. Tissue samples were fixed with sodium phosphate buffer containing 10% formalin, embedded in paraffin and sliced into 5-µm continuous sections. The sections were deparaffinized, rehydrated, and incubated with 3% H2O2 in methanol for 30 min to quench endogenous peroxidase activity. After a short rinse, the sections were heated in a 37°C water bath for 15–20 min in citrate buffer. Following cooling and rinsing, the sections were incubated with a rabbit polyclonal anti-RBP4 antibody (1:50) for 30 min at room temperature, overnight at 4°C, and for 30 min at room temperature while shaking. Antibody binding was amplified for 10 min using biotin and horseradish peroxidase-conjugated streptavidin. The slides were counterstained with hematoxylin, dehydrated in gradient ethanol, cleared in dimethylbenzene, and observed under a microscope. Normal controls for IHC were prepared under the same conditions, 5 placental specimens for each group. The immunostained sections were examined using a Leica DMLA light microscope (Leica Microsystems, Wetzlar, Germany) to assess the prevalence of DAB-positive staining and immunostaining localization within the tissues. All sections were assessed on a microscope for positive DAB staining. Trophoblast cells with unequivocal staining of granular cytoplasm were considered positive. RBP4 expression was evaluated via a computer assessment and scored based on the cytoplasmic staining intensity throughout the entire section. Immunohistochemical staining pictures were taken with the same exposure time by microscope (MOTIC BA400) coupled with camera device (MOTICCAM 2306) in the same microscope environment and conditions. The expressions of target proteins were quantified and the average optical density (AOD) was analyzed by Motic Image Advanced v.3.2 software (MOTIC, Xiamen, China).

Cell culture

The human immortalized trophoblast cell line HTR8/SVneo was obtained from ATCC. The cells were transiently transfected to overexpress or knockout RBP4, and unaltered HTR8/SVneo cells served as the control. The cells were cultured in RPMI 1640 medium (HyClone; GE Healthcare Life Sciences, Logan, UT, USA) supplemented with 10% fetal bovine serum (FBS; Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA), 100 U/ml penicillin, and 100 mg/ml streptomycin in a 37°C humidified incubator (5% CO2). The cells were subcultured at a 1:3 ratio when they reached 80–90% confluence (8).

Lentivirus infection

cDNA containing the human RBP4 sequence was cloned into a pLVX-mCMV-ZsGreen-PGK-Puro vector using EcoRI and BamHI digestion. A sequencing analysis was conducted to confirm correct insertion of the DNA fragment. 293T cells (Xi Bei Hong Cheng Biological Technology, Co., Beijing, China) were used to generate packaging lentiviruses for transduction. HTR cells were infected with the pLVX-RBP4-mCMV-ZsGreen-PGK-Puro construct. Finally, stable cell lines were screened.

We used pLVX-shRNA2-Puro lentiviral vectors carrying short hairpin RNAs (shRNAs). The shRNA vectors were obtained from Health and Biological Company, and the lentiviruses were obtained via overnight triple co-transfection of 293T cells. Knockdown efficiency was determined by reverse transcription-polymerase chain reaction (RT-PCR). We found that the best interference effect was achieved using shRNA2-RBP4-2. HTR cells were infected with the pLVX-shRNA2-RBP4-Puro construct, followed by puromycin selection to establish stable cell lines.

Western blotting

Total cell protein was extracted from cells in each group. After centrifugation at 12,000 rpm and 4°C for 15 min, the protein concentration in the supernatant was determined with a BCA protein assay. Equal amounts of total protein (30 µg) were loaded and separated on 10% sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) gels and transferred to nitrocellulose (NC) membranes using standard procedures.

The primary antibodies rabbit polyclonal anti-MMP2 (1:1,000; Abcam, Cambridge, UK), rabbit polyclonal anti-MMP9 (1:1,000; Abcam), rabbit polyclonal anti-AKT (1:1,000; Abcam), rabbit polyclonal anti-p-AKT (Thr308, Ser473) (1:1,000; Abcam), mouse polyclonal anti-PI3K (1:1,000; Abcam), rabbit polyclonal anti-p-PI3K (1:1,000; Abcam), rabbit polyclonal anti-Bcl-2 (1:2,000; Abcam), rabbit polyclonal anti-GAPDH (1:2,000; Abcam), and rabbit polyclonal anti-RBP4 were used. GAPDH served as the internal loading control.

The membranes were probed with primary antibodies diluted in 5% SBS/PBS-Tween 20 (PBST-20) overnight at 4°C, rinsed three times with PBST-20 and then incubated with secondary antibodies (1:3,000) for 2 h at room temperature. Excess secondary antibody was removed by four washes in PBST-20. The targeted protein bands were visualized and imaged using an ECL western blotting kit (CWBiotech, Beijing, China), and densitometry was performed using ImageJ (v.1.49e; National Institutes of Health, Bethesda, MD, USA).

In vitro invasion assay with Matrigel

Cell invasion was assessed using transwell chambers (24-well inserts; 8-µm pore size) precoated with Matrigel (200 µg/ml; BD Biosciences, Franklin Lakes, NJ, USA). Briefly, 24 h after transfection, HTR8-SVneo cells (RBP4 knockdown, RBP4 overexpression, and control) were trypsinized and seeded into the upper chambers (5×105 cells/chamber) in serum-free medium, and the lower chambers were filled with 600 µl of RPMI 1640 medium containing 10% FBS as a chemoattractant. After incubation of the plates for 48 h, the cells on the upper surface of the membrane were gently removed, and the invasive cells on the lower surface of the membrane were fixed in methanol and stained with crystal violet. The invasive cells in four randomly selected fields of view were imaged using a light microscope and counted.

Cell treatment

RBP4 knockdown, RBP4 overexpression and control HTR8/SVneo cells (5,000/well) were seeded into 96-well plates. A CCK8 Assay Kit was used to assess cell survival at different time points (0, 24, 48, 72, 96 and 144 h). Optical density (OD) was measured at 450 nm. These experiments were performed three times.

Statistical analysis

Statistical analysis was performed using SPSS v.20.0 software (IBM Corp., Armonk, IL, USA). The data were tested for normality using unpaired t-tests, one-way analysis of variance with a least significant difference post hoc test and nonparametric tests (median test). Normally distributed data are presented as the mean ± standard deviation, and non-normally distributed data, as the median (interquartile range). P<0.05 was considered to indicate a statistically significant difference.

Results

Subject characteristics

Blood samples from thirty-five patients with PE and thirty healthy pregnant women were analyzed via ELISA. The patient characteristics are listed in Table I.

Table I.

Subject characteristics for ELISA.

Characteristics	Controls (n=30)	PE (n=35)	P-value
Age (years)	33.3±2.4	33±3.6	0.328
Gestational age (weeks)	37±6.5	34.7±7.4	0.066
Blood pressure (mmHg)
SBP	119.2±15.3	166.4±13.2	<0.0001
DBP	75.5±9.3	96.8±12.6	<0.0001

SBP, systolic blood pressure; DBP, diastolic blood pressure; PE, preeclampsia.

IHC to assess RBP4 expression in the placenta

IHC analysis showed that RBP4 localized to syncytiotrophoblasts (STBs). RBP4 expression in PE placenta tissue (n=5) was significantly decreased compared with that in normal controls (n=5; Fig. 1). Normal placenta tissue stained for RPB4 at 0.79±0.05; PE placenta tissue stained for RPB4 at 0.39±0.02.

Figure 1.

IHC analysis of RBP4 expression in the placenta. Example of immunostaining: Positive antibody staining is brown. (A) RBP4 immunostaining of the CTRL group; and (B) RBP4 immunostaining of the PE group (magnification, ×10 and ×40, as indicated). *P<0.05, as indicated. IHC, immunohistochemistry; RBP4, Retinol-binding protein 4; CTRL, control; PE, preeclampsia.

Serum RBP4 expression was compared between patients with PE and healthy pregnant women using ELISA (PE median, 129.3 ng/ml vs. control median, 166.7 ng/ml; P=0.046; standard curve line y=0.0176× + 0.1724 (R2=0.9527); Fig. 2).

Figure 2.

Serum RBP4 expression based on ELISA. Serum RBP4 concentrations were significantly lower in the PE group when compared with the control group. *P<0.05, as indicated. RBP4, Retinol-binding protein 4; CTRL, control; PE, preeclampsia.

RBP4 regulates HTR8/SVneo cell proliferation in vitro

We investigated whether RBP4 affects the proliferation of trophoblasts. We found that overexpression of RBP4 increased cell proliferation after 120 and 144 h, whereas siRNA-mediated knockdown of RBP4 significantly decreased HTR8/SVneo cell proliferation at 24, 48 and 72 h (Fig. 3). Two bands for RBP4 should be present in the western blot of the RBP4 overexpression group. However, RBP4 was cloned into the vector without including vsgreen in the frame, resulting in overexpression of RBP4 without any tags. Therefore, only one band was observed when blotting with the anti-RBP4 antibody. Western blot analysis of RBP4 to confirm overexpression and knock down was successful.

Figure 3.

RBP4 regulates HTR8/SVneo cell proliferation in vitro. (A) RBP4 overexpression increased cell proliferation, and RBP4 knockdown inhibited HTR8/SVneo cell proliferation. The proliferation of control cells, RBP4-overexpressing cells and RBP4 knockdown cells at 0, 24, 48, 72, 120 and 144 h was determined by Cell Counting Kit-8 assays. The absorbance of viable cells was determined at 450 nm (optical density 450). Proliferation of RBP4-overexpressing cells was significantly higher than that of the control cells at 96 and 144 h. Proliferation of RBP4-knockdown cells was significantly lower than that of the control cells at 48, 72, 96 and 144 h. *P<0.05 vs. NC. (B) Western blot analysis of RBP4 protein expression to confirm that overexpression and knockdown were successful. *P<0.05, as indicated. All quantitative data are presented as the mean ± standard deviation of three independent experiments. RBP4, Retinol-binding protein 4; NC, normal control; RBP4OV, RBP4 overexpression group; RBP4KD, RBP4 knockdown group.

In vitro invasion assay

Cell invasion assays were employed to investigate the effect of RBP4 expression on HTR8/SVneo cell invasion (Fig. 4). RBP4 overexpression promoted the invasion of HTR8/SVneo cells (A group), and RBP4 knockdown decreased the invasion of HTR8/SVneo cells (B group).

Figure 4.

In vitro invasion assay: RBP4 reduces cell invasion. Cell invasion across Matrigel was determined by transwell assays. Images of representative invasive cells are shown on the left (magnification, ×10), and quantification analysis is presented on the right. (A) There was significantly increased trophoblast cell invasion in the RBP4 overexpression group. (B) Compared with the control group, cells with RBP4 knockdown displayed significantly reduced invasion ability. All quantitative data are presented as the mean ± standard deviation of three independent experiments. *P<0.05 and **P<0.01, as indicated. RBP4, Retinol-binding protein 4; CTRL, control; RBP4OV, RBP4 overexpression group; RBP4KD, RBP4 knockdown group.

Effect of RBP4 on MMP2, MMP9 and Bcl-2 expression

MMP2, MMP9, and Bcl-2 are associated with invasion and apoptosis. Therefore, we measured the protein levels of MMP2, MMP9 and Bcl-2 via western blotting. Overexpression of RBP4 significantly increased MMP2, MMP9 and Bcl-2 expression in HTR8/SVneo cells (B group), and knockdown of RBP4 decreased MMP2, MMP9 and Bcl-2 expression in HTR8/SVneo cells (A group). Each experiment was repeated three times (Fig. 5).

Figure 5.

Effect of RBP4 on MMP2, MMP9 and Bcl-2 expression. Effects of RBP4 knockdown and overexpression on the expression of proteins associated with invasion. (A) MMP2, MMP9 and Bcl-2 protein expression was downregulated in the RBP4KD group when compared with the NC group. (B) MMP2, MMP9 and Bcl-2 expression was upregulated in the RBP4OV group when compared with the NC group. *P<0.05, **P<0.01 and ***P<0.001, as indicated. RBP4, Retinol-binding protein 4; NC, normal control; RBP4OV, RBP4 overexpression group; RBP4KD, RBP4 knockdown group; MMP, matrix metalloproteinase; Bcl-2, B-cell lymphoma 2.

Effect of RBP4 on the PI3K/AKT signaling pathway in HTR8/SVneo cells

To elucidate the mechanisms by which RBP4 promotes trophoblast invasion, we evaluated PI3K/AKT signaling in trophoblast cells. We examined PI3K, AKT, p-PI3K and p-AKT expression via western blotting. Each experiment was repeated three times (Fig. 6). p-AKT (Ser473) and p-PI3K were significantly upregulated in the RBP4 overexpression group compared with the normal control group, and there were no differences in AKT and PI3K levels between the groups (B group). p-AKT (Ser473), p-AKT (Thr308) and p-PI3K were significantly downregulated in the RBP4 knockdown group compared with the normal control group (A group).

Figure 6.

Effect of RBP4KD and RBP4OV on the PI3K/AKT signaling pathway. (A) p-AKT (Ser473), p-AKT (Thr308) and p-PI3K were significantly downregulated in the RBP4KD group when compared with the NC group. (B) p-AKT (Ser473) and p-PI3K were significantly upregulated in the RBP4OV group when compared with the NC group. There were no differences in AKT and PI3K levels between the groups. *P<0.05 and **P<0.01, as indicated. RBP4, Retinol-binding protein 4; NC, normal control; RBP4OV, RBP4 overexpression group; RBP4KD, RBP4 knockdown group; p-, phosphorylated; AKT, protein kinase B; PI3K, phosphoinositide 3-kinase.

Discussion

PE is generally defined as new-onset hypertension accompanied by proteinuria or complications in multiple organs at or after the 20th week of gestation (9,10). Although extensive studies have demonstrated that immunologic, antigenic, genetic, metabolic, and environmental factors are associated with PE (11), the pathophysiology of PE has not yet been fully elucidated. Moreover, there are no reliable biomarkers for predicting PE during early pregnancy.

Maintenance of a normal pregnancy depends on placental development and function. Moderate invasion of human extravillous trophoblast cells into the maternal decidual stroma and spiral arteries is essential for establishing a successful pregnancy. Similar to tumor cells, trophoblasts have invasive ability; however, unlike tumor invasion, trophoblast invasion is a strictly controlled physiological event. Abnormal trophoblast differentiation is associated with a variety of pregnancy-associated diseases. Insufficient trophoblast invasion and proliferation are correlated with PE development (12,13).

Recent studies have suggested that RBP4, an integral member of a trimer with retinol and TTR that is transported to specific tissues and organs in the body, may be linked to insulin resistance, type 2 diabetes mellitus, renal dysfunction, atherosclerosis and hypertension in women (14). RBP4 is a 21-kDa protein and a specific carrier of retinol (vitamin A) from the liver to peripheral tissues (15). In the present study, IHC analysis showed that RBP4 is localized in STBs, and RBP4 expression in PE placenta tissue was significantly decreased compared with that in normal controls. In the present study, serum RBP4 concentration as determined by ELISA was found to be significantly lower in patients with PE than in healthy pregnant women, consistent with the results of our previous study (7).

The trophoblast invasion process requires degradation and remodeling of the decidual extracellular matrix. Because the MMP family is involved in breakdown of the extracellular matrix, to gain a greater understanding of the mechanisms underlying RBP4-regulated cell invasion, we examined the expression of MMP2 and MMP9, which were previously found to increase the invasiveness of trophoblasts (16–18). We found that RBP4 knockdown decreased cell invasion, and RBP4 overexpression increased the invasion of HTR8/SVneo cells. Moreover, the production of MMP2 and MMP9 was decreased in RBP4-knockdown HTR8/SVneo cells and dramatically increased in RBP4-overexpressing cells. These results indicated that MMP2 and MMP9 likely contribute to RBP4-induced trophoblast invasion. Thus, it is worthwhile to ascertain whether RBP4 acts directly on MMP2 and MMP9 promoters or functions indirectly through some other factor.

The PI3K/AKT signaling pathway plays important roles in cell growth, proliferation, migration and invasion (19). We found that RBP4 overexpression did not increase HTR8/SVneo cell proliferation at 24, 48 or 72 h, and thus, we cultivated the cells for longer periods of time. After 96 and 144 h (20,21), we found that the overexpression of RBP4 increased cell proliferation, whereas siRNA-mediated RBP4 knockdown significantly decreased HTR8/SVneo cell proliferation at 24, 48, 72, 96 and 144 h. Activation of PI3K/AKT signaling inhibits apoptosis (22) through Bcl-2 (23), an anti-apoptotic protein that is downstream of the PI3K/AKT pathway. Bcl-2 is associated with or may be necessary for cell growth and survival. In our study, Bcl-2 was increased in RBP4-overexpressing cells and decreased in RBP4-knockdown cells. RBP4 is known to activate PI3K/AKT signaling in HTR8/SVneo cells. We found that RBP4 knockdown decreased AKT (Ser473 and Thr308) and PI3K phosphorylation, although the total protein expression of AKT and PI3K remained constant. Therefore, blockade of the PI3K/AKT pathway may be one reason for the cell growth inhibition after RBP4 knockdown.

In summary, our data show that RBP4 is involved in the proliferation and invasion of trophoblastic cells. Additionally, RBP4 can activate the PI3K/AKT signaling pathway and upregulate MMP2 and MMP9 expression. Based on the results of the current study, we hypothesize that RBP4 regulates trophoblastic cell proliferation and invasion by activating the PI3K/AKT pathway. Decreased RBP4 expression in the placenta may contribute to PE development by decreasing the invasive ability of trophoblasts.

Therefore, placental trophoblast cell differentiation indeed involves an EMT-like process, which will be the focus for our follow-up research. The present study is the first to detect the effect of RBP4 on the invasion ability of trophoblast cells and changes in MMP-related molecules, including Snail, Slug, Vimentin, and E-Cadherin, which are directly related to cell invasion ability. We plan to conduct additional studies in the future to further elucidate these mechanisms.