Regulation of Proinflammatory Molecules and Tissue Factor by SARS-CoV-2 Spike Protein in Human Placental Cells: Implications for SARS-CoV-2 Pathogenesis in Pregnant Women

SARS-CoV-2 infects cells via binding to ACE2 and TMPRSS2, which allows the virus to fuse with host cells. The viral RNA is detected in the placenta of SARS-CoV-2-infected pregnant women and infection is associated with adverse pregnancy complications. Therefore, we hypothesize that SARS-CoV-2 infection of placental cells induces pro-inflammatory cytokine release to contribute to placental dysfunction and impaired pregnancy outcomes. First, expression of ACE2 and TMPRSS2 was measured by qPCR in human primary cultured term cytotrophoblasts (CTBs), syncytiotrophoblast (STBs), term and first trimester decidual cells (TDCs and FTDCs, respectively), endometrial stromal cells (HESCs) as well as trophoblast cell lines HTR8, JEG3, placental microvascular endothelial cells (PMVECs) and endometrial endothelial cells (HEECs). Later, cultured HTR8, JEG3, PMVECs and HEECs were treated with 10, 100, 1000 ng/ml of recombinant (rh-) SARS-CoV-2 S-protein ± 10 ng/ml rh-IFNγ. Pro-inflammatory cytokines IL-1β, 6 and 8, chemokines CCL2, CCL5, CXCL9 and CXCL10 as well as tissue factor (F3), the primary initiator of the extrinsic coagulation cascade, were measured by qPCR as well as secreted IL-6 and IL-8 levels were measured by ELISA. Immunohistochemical staining for SARS-CoV-2 spike protein was performed in placental specimens from SARS-CoV-2–positive and normal pregnancies. ACE2 levels were significantly higher in CTBs and STBs vs. TDCs, FTDCs and HESCs, while TMPRSS2 levels were not detected in TDCs, FTDCs and HESCs. HTR8 and JEG3 express ACE2 and TMPRSS2, while PMVECs and HEECs express only ACE2, but not TMPRSS2. rh-S-protein increased proinflammatory cytokines and chemokines levels in both trophoblast and endothelial cells, whereas rh-S-protein only elevated F3 levels in endothelial cells. rh-IFNγ ± rh-S-protein augments expression of cytokines and chemokines in trophoblast and endothelial cells. Elevated F3 expression by rh-IFNγ ± S-protein was observed only in PMVECs. In placental specimens from SARS-CoV-2-infected mothers, endothelial cells displayed higher immunoreactivity against spike protein. These findings indicated that SARS-CoV-2 infection in placental cells: 1) induces pro-inflammatory cytokine and chemokine release, which may contribute to the cytokine storm observed in severely infected pregnant women and related placental dysfunction; and 2) elevates F3 expression that may trigger systemic or placental thrombosis.

Introduction

Coronaviruses (CoV) family members are large, enveloped, single-stranded, and positive sense RNA viruses that present in many avian and mammalian species. In humans, CoV usually causes mild to moderate upper-respiratory tract illnesses. However, Severe Acute Respiratory Syndrome (SARS)-CoV and Middle East Respiratory Syndrome (MERS)-CoV can have fatal outcomes (1, 2). A novel SARS-like CoV, SARS-CoV-2, was identified in Wuhan, China, in December 2019, and rapidly spread and mutated (3–5), producing the current prolonged pandemic of coronavirus disease 2019 (COVID-19) (6). The SARS-CoV-2 virus primarily infects the respiratory tract (7), and infected patients exhibit a wide range of symptoms from mild to severe respiratory distress (1, 8). However, SARS-CoV-2 infection can result in additional disease-associated symptoms in different organ systems such as poor appetite, nausea, vomiting, and diarrhea in the digestive system, headache and confusion in the nervous system, and chest distress and cardiac injury in the cardiovascular system (1, 8).

SARS-CoV-2 infects host cells that express angiotensin-converting enzyme 2 (ACE2) mainly located in lung, heart, ileum, and kidney (9). The initial step of viral entry is mediated by spike (S) protein on the viral surface. The S-protein binds to its ACE2 receptor via its receptor-binding domain (9), and is proteolytically activated by type II transmembrane serine protease (TMPRSS2), present on the surface of the host cell (10). S-proteins activation leads to conformational changes that allow viral entry, release the viral RNA into cytoplasm to generate new viral particles (11). SARS-CoV-2 entry into host cells is a crucial factor for viral permissiveness and pathogenesis.

Pregnant women represent a vulnerable population for COVID-19 infection. Moreover, SARS-CoV-2 infection in pregnant women results in more severe symptoms compared with non-pregnant women, although pregnancy does not increase susceptibility to infection (12, 13). Recent studies reported that SARS-CoV-2 infected pregnant women are more likely to be hospitalized with increased risk for intensive care unit admission and higher mortality rates versus infected non-pregnant women (12, 14, 15). Furthermore, SARS-CoV-2 infection increases rates of cesarean delivery and preterm birth (PTB) and/or other pregnancy outcomes including low birth weight, stillbirth, abruption, and preeclampsia (13, 16, 17), especially when women are infected in the third trimester (18, 19). These complications may be related to the unique adaptation of the maternal immune system at different stages of pregnancy: a pro-inflammatory state that enhances implantation and the initiation of labor in the 1^st and 3^rd trimesters, respectively and an anti-inflammatory state facilitating fetal growth in the 2^nd trimester (20). Although, vertical transmission of SARS-CoV-2 remains highly debated, viral RNA is detected in placental villi, predominantly in syncytiotrophoblasts, cytotrophoblasts, villous fibroblasts, Hoffbauer cells, and endothelial cells (21, 22).

Therefore, we hypothesized that SARS-CoV-2 induces utero-placental pro-inflammatory cytokine and chemokine release, as well as activation of the coagulation cascade, consistent with the cytokine storm and prothrombotic state associated with severe infections. This, in turn, places pregnant women and their fetuses at higher risk for severe complications. Thus, we initially compared expression levels of potential viral entry receptors in maternal (decidual), fetal (trophoblastic), and endothelial cell cultures, and then explored the expression levels of pro-inflammatory cytokines, chemokines, and coagulation factor III (F3; aka tissue factor) in recombinant (rh-) spike (S)-protein of SARS-CoV-2-treated trophoblast and endothelial cell cultures.

Materials and Methods

Cell Culture and Recombinant Proteins

This study was approved by the University of South Florida Institutional Review Boards (Pro00019480). Human first trimester immortalized extravillous trophoblast cells (HTR8/SV^neo) and choriocarcinoma trophoblast cells (JEG3) (ATCC, Manassas, VA) were cultured in phenol-free basal medium (DMEM/F12, Thermo Fisher Scientific, Waltham, MA) with 10% fetal bovine serum (Thermo Fisher Scientific) and 1% antibiotic-antimycotic complex (Gibco, Thermo Fisher Scientific). We chose human placental microvascular endothelial cell (PMVEC), which is an excellent in vitro model to study vascularization in the placenta (23), to evaluate fetal microvascular endothelial responses against SARS-CoV-2 S-protein, whereas human endometrial endothelial cells (HEECs) were chosen to evaluate maternal microvascular endothelial responses against SARS-CoV-2 S-protein. Frozen PMVECs is a kindly gift from Dr. Hana Totary-Jain (USF), purchased from ScienCell Research Laboratories (Carlsbad, CA). According to the manufacturer’s instruction, PMVECs are obtained from healthy pregnant women and characterized by immunofluorescence with antibodies specific to vWF/Factor VIII. As characterized previously (24), frozen HEECs were isolated from endometrial biopsies obtained from healthy women, who were not under hormonal treatment. Frozen PMVECs and HEECs were thawed and cultured in EGM-2 medium supplemented with low serum growth supplement (Gibco, Thermo Fisher Scientific) with 1% antibiotic-antimycotic complex. SARS-CoV-2 rh-S-protein was provided by BEI Resources (Manassas, VA). Human recombinant interferon gamma (rh-IFNγ) was purchased from R&D systems (Minneapolis, MN).

Experimental Design

Confluent HTR8, JEG3, HEECs and PMVECs cultures were trypsinized and seeded in 6-well culture plates (1×10⁵ cells/well). The next day, the cells were exposed to either mock (control) or rh-S-protein at concentrations of 10, 100 and 1000 ng/ml, or 10ng/ml rh-IFNγ ± 10 ng/ml rh-S-protein in 500 µl serum free media and then shaken every 15 min to enhance rh-S-protein binding to cells at 37°C for 1 hour. Thereafter, 1500 µl fresh media with serum was added into cells. After 24 hours, plates were washed 3 times with ice-cold PBS and stored at −80°C for further RNA extraction.

RNA Isolation, Reverse Transcription, and qPCR

Total RNAs from HTR8, JEG3, PMVECs and HEECs cultures were isolated using RNeasy Mini Kit (Qiagen, Germantown, MD) followed by DNase I treatment (Qiagen) to eliminate genomic DNA contamination. To compare endogenous expression of SARS-CoV-2 entry molecules, ACE2 and TMPRSS2 in fetal and maternal cells, previously isolated RNAs from primary cultured term cytotrophoblasts, syncytiotrophoblasts, term decidual cells, first trimester decidual cells and human endometrial stromal cells were employed (25). Reverse transcription using RETROscript kit (Ambion, Austin, TX) was performed as described (26) and qPCR performed using TaqMan gene expression assays to detect gene expression levels of: 1) pro-inflammatory cytokines interleukin (IL)-1β, IL-6, and IL-8; 2) chemokines C-C motif chemokine ligand (CCL)2 -5 as well as C-X-C motif chemokine ligand (CXCL) 9 and 10; and 3) tissue factor (F3) (Applied Biosystems, Grand Island, NY, TaqMan assay ID given in Supplementary Table 1). All reactions were performed in duplicate. Expression of the target genes was normalized to β-actin levels, and the 2^−ΔΔCT method was used to calculate relative expression levels (27).

Enzyme-Linked Immunosorbent Assay

Media from HTR8 and PMVEC cultures treated with vehicle 10 or 1000 ng/ml rh-S-protein or 10 ng/ml IFNΥ ± 10 ng/ml rh-S-protein for 24 hours were collected, centrifuged and the resultant supernatants were stored at -80⁰C. Secreted IL-6 and IL-8 levels were measured using specific enzyme-linked immunosorbent assay (ELISA) kits (R&D Systems; Minneapolis, MN). Briefly, 96-well ELISA microplates were coated with a capture antibody; after blocking with 5% BSA, 1:4 diluted samples were added to the coated plates for 2 h, followed by a biotin-conjugated detection antibody. Antibody binding was measured with horseradish peroxidase-conjugated avidin along with a soluble colorimetric substrate. The absorbance was read at 450 nm using a microplate reader (Bio-Rad). Each sample was measured in duplicate

Immunohistochemical Staining

After receiving IRB approval, placental specimens from SARS-Cov-2 infected mothers (n=3) who tested positive for COVID-19 in the third trimester and gestational age-matched normal pregnancies (n=3) were obtained from Clinical Pathology Laboratories at Tampa General Hospital. 5 μm formalin-fixed paraffin embedded placental sections were processed for immunohistochemistry as described previously (28). Briefly, after deparaffinization and rehydration, paraffin-embedded sections were boiled in 10 mM citric acid solution (pH: 6.0) for antigen retrieval for 20 min and incubated in 3% H₂O₂ for endogenous peroxidase quenching for 10 min. The slides were incubated with 10% goat serum (Vector Labs, Burlingame, CA) for 30 min at room temperature, then overnight with mouse monoclonal anti-SARS-Cov-2 Spike RBD (monoclonal mouse IgG2A, clone no. 1035423, 10µg/ml dilution; R&D Systems, Minneapolis, MN). For negative control, placental sections were incubated with non-immune mouse IgG_2a in place of primary antibody at the same concentration. All sections were washed in PBS containing 0.1% Tween-20 (PBS-T) and incubated with biotinylated anti-mouse IgG antibody (1/400 dilution; Vector Labs) for 30 min. Following several rinses in PBS-T, the sections were incubated in streptavidin–peroxidase complex (Elite ABC Kit, Vector Labs) for 30 min. After washing, slides were exposed to diaminobenzidine tetrahydrochloride dehydrate (Vector Labs) as a chromogen for 3 min and counterstained with hematoxylin before permanent mounting.

Statistical Analysis

Results were analyzed by One-Way ANOVA followed with a post-hoc Tukey test if normally distributed or using the Kruskal-Wallis test followed by the post-hoc Student-Newman-Keuls’ test if non-parametrically distributed using SigmaStat version 3.0 software (Systat Software, San Jose, CA), P<0.05 was considered statistically significant.

Results

Expression of ACE2 and TMPRSS2 Viral Entry Molecules in Fetal and Maternal Cells

To elucidate SARS-CoV-2 cell tropism in the placenta, we first investigated the expression levels of the cell entry receptor, ACE2, and priming protease, TMPRSS2 at the maternal-fetal interface including primary cultured term cytotrophoblasts, syncytiotrophoblasts, term decidual cells, and first trimester decidual cells as well as human endometrial stromal cells obtained from non-pregnant women. qPCR analysis revealed that ACE2 mRNA levels are significantly higher in both cytotrophoblasts and syncytiotrophoblasts (Ct < 30) vs. term or first trimester decidual cells as well as endometrial stromal cells (Ct > 33) (Figure 1A). While both trophoblastic cells displayed weak TMPRSS2 expression (Ct > 33), maternal stromal decidual cells did not express TMPRSS2 (Figure 1B). Subsequently, we compared ACE2 and TMPRSS2 levels in trophoblastic cell lines HTR8, and JEG3, and detected significantly higher ACE2 (~ 4.9-fold) and TMPRSS2 (~9-fold) levels in JEG3 than HTR8 cells (Figure 1C). In addition to trophoblast cells, we also compared ACE2 and TMPRSS2 levels in fetal and maternal endothelial cell types PMVECs from placental specimens and HEECs, respectively to explain COVID-19 severity in pregnancy. qPCR results revealed weak ACE2 mRNA levels in both cell types and a slightly higher in HEECs (Mean ± SEM; 1.02 ± 0.13) compared to PMVECs (0.52 ± 0.08) (Figure 1D). In contrast, TMPRSS2 levels were undetectable in both endothelial cell types.

FIGURE 1

Figure 1 Comparison of SARS-CoV-2 entry receptor ACE2 and TMPRSS2 mRNA levels among various decidual (maternal) and placental (fetal) cell types at the maternal-fetal interface. Expression levels of ACE2 (A) and TMPRSS2 (B) in human term cytotrophoblast (CTBs), syncytiotrophoblast (STBs), term decidual cell (TDCs), first trimester decidual cell (FTDCs), and human endometrial stromal cell (HESCs) cultures; Expression levels of ACE2 and TMPRSS2 in trophoblastic cell lines HTR8 and JEG3 (C); as well as expression levels of ACE2 in placental microvascular endothelial (PMVECs) and human endometrial endothelial cell (HEECs) cultures (D) by qPCR. Bars represent mean ± SEM, n=4; * P<0.05 vs. CTB or STB (A); * P<0.05 vs. HTR8 (C); * P<0.05 vs. HEECs (D).

Increased Inflammatory Cytokine Expression Induced by rh-S-protein in Trophoblast and Endothelial Cells

To mimic inflammatory changes induced by SARS-CoV-2 in the placenta, and to explore virus-induced pregnancy outcomes, HTR8 and JEG3 cell lines as well as PMVECs and HEECs were treated with 10, 100, 1000 ng/ml rh-S-protein for 24 hours and the expression of pro-inflammatory cytokine genes IL-1β, IL-6, and IL-8 measured by qPCR. In HTR8 cells, rh-S-protein treatment significantly increased levels of IL-1β and IL-6 vs. controls, displaying a clear dose-response effect to increasing concentrations of rh-S-protein, whereas only 1000 ng/ml rh-S-protein significantly induced mRNA expression of IL-8 (Figure 2A). In contrast, in JEG3 cells, IL-1β and IL-8 mRNA levels were undetectable in all groups (not shown); additionally, no rh-S-protein concentration altered basal IL-6 levels (Figure 2B). In PMVECs, IL-1β and IL-6 levels were significantly elevated by rh-S-protein again with a clear dose response evident, while only highest concentration of rh-S-protein significantly induced IL-8 levels (Figure 2C), similar to the pattern seen with HTR8. However, in HEECs, IL-1β levels increases did not attain statistical significance; while IL-6 levels were significantly induced by 100 and 1000ng/ml of rh-S-protein, and IL-8 levels were only elevated by the highest concentration of rh-S-protein (Figure 2D). Similarly, ELISA analysis revealed significantly higher levels of IL-6 and IL-8 secretion in culture supernatants of HTR8 (Figure 2E) and PMVECs (Figure 2F) treated with 1000 ng/ml rh-S-protein vs. control, validating S-protein mediated increase in IL-6 and IL-8 transcription in HTR8 and PMVECs. However, 10 ng/ml rh-S-protein treatment did not induce secretion levels of either cytokine in these cell types. These findings indicate: 1) low concentrations of S-protein appear sufficient to induce of IL-1β and IL-6 levels, but a higher concentration is required to induce IL-8 levels in HTR8, PMVECs and HEECs; 2) only higher concentration of rh-S-protein induces secretion of IL-6 and IL-8 levels in HTR8 and PMVECs; and 3) there is a clear inflammatory response to COVID-19 in vascular endothelial cells, potentially contributing to viral pathogenesis in pregnant women.

FIGURE 2

Figure 2 Induction of pro-inflammatory cytokine in trophoblast and endothelial cell cultures by rh-S-protein. SARS-CoV-2 induced expression of pro-inflammatory cytokines IL-1β, IL-6 and IL-8 mRNA levels in trophoblastic cells HTR8/SV^Neo (A) and JEG3 (B) as well as PMVEC (C) and HEEC cultures (D) treated with 10, 100, or 1000 ng/ml rh-S-protein vs. mock-treated control treatment. Bars represent mean ± SEM, n=4; * P<0.05 vs. control; and IL-8 mRNA * P<0.05 vs. control or 10 or 1000 ng/ml rh-S protein (A, C, D). Secreted IL-6 and IL-8 protein levels in culture supernatants of HTR8 (E) and PMVECs (F) treated with control or 10 or 1000 ng/ml rh-S-protein. Bars represent mean ± SEM, n=3; * P<0.05 vs. control (E, F).

Enhanced Chemokine Expression by rh-S-Protein in Trophoblast and Endothelial Cells

Following confirmation that rh-S-protein treatment resulted in an alteration of pro-inflammatory gene expression, we compared mRNA expression levels of chemokines CXCL9, CXCL10, CCL2, and CCL5 in HTR8, JEG3, PMVECs, and HEECs cultures. The qPCR analysis revealed that compared to mock-treated cells, levels of CCL2 and CCL5 in both HTR8 (Figure 3A) and JEG3 cells (Figure 3B) were not altered by any rh-S-protein exposure. Moreover, levels of CXCL9 and CXCL10 were undetectable and not induced by any rh-S-protein concentration in both HTR8 and JEG3 cells. In contrast, in PMVECs cultures, CCL2 levels were significantly induced by all rh-S-protein concentrations in a dose-response fashion, while CCL5 levels were only significantly increased at concentrations of rh-S-protein of 100 or 1000 ng/ml and whereas basal CXCL9 and CXCL10 levels were unchanged (Figure 3C). Again, in contrast to PMVECs, rh-S-protein did not affect expression of these cytokines in HEECs (Figure 3D).

FIGURE 3

Figure 3 Expression chemokines mRNA in trophoblastic and endothelial cells cultures treated by rh-S-protein. qPCR analysis revealed to measure of expression levels of CCL2, CCL5, CXCL9 and CXCL10 in HTR8/SV^Neo (A), JEG3 (B), PMVEC (C) and HEEC (D) cultures treated with 10, 100, or 1000 ng/ml rh-S-protein vs. control. Bars represent mean ± SEM, n=4; * P<0.05 vs. control.

Elevated Tissue Factor (F3) Expression by rh-S-protein in Endothelial Cells, but Not Trophoblasts

Thrombotic complications are frequent in COVID-19 patients and are associated with disease severity and mortality (29). F3 that is the primary initiator of coagulation is not normally expressed by endothelial cells or trophoblast, though its expression can be induced by proinflammatory cytokines. Thus, we evaluated expression levels of F3 in cells treated with 10, 100, and 1000 ng/ml rh-S-protein to explore potential etiologies of placental thrombosis in SARS-CoV-2 infected pregnant women. After 24 hours treatment, qPCR results displayed no significant difference in mRNA expression levels of F3 in either HTR8 (Figure 4A) or JEG3 (Figure 4B). However, 1000 ng/ml of rh-S-protein significantly increased F3 levels in PMVECs (Figure 4C), whereas all concentrations induced F3 levels in HEECs compared to control groups (Figure 4D).

FIGURE 4

Figure 4 Increased tissue factor mRNA levels by rh-S-protein in endothelial cell, but not in trophoblast cell cultures. qPCR analysis measured tissue factor (F3) mRNA expression in trophoblast cell lines HTR8/SV^Neo (A) and JEG3 (B) as well as endothelial PMVEC (C) and HEEC (D) cultures treated with mock-treated control or 10, 100, or 1000 ng/ml rh-S-protein. Bars represent mean ± SEM, n=3; * P<0.05 vs. control, 10 or 100 ng/ml rh-S-protein in PMVECs; and * P<0.05 vs. control in HEECs.

IFNγ Treatment in Combination With rh-S-Protein Augments Expression of Pro-Inflammatory Cytokines and Chemokines

To explore whether the immunological state of pregnancy can promote adverse pregnancy outcomes in SARS-CoV-2 infected pregnant women, HTR8, JEG3, PMVECs and HEECs cultures were treated with 10 ng/ml rh-IFNγ ± 10 ng/ml rh-S-protein since a significant positive correlation was reported between IFNγ levels and disease severity in pregnant women (30). The expression of pro-inflammatory cytokines and chemokines levels were then measured. The qPCR analysis revealed that compared to mock-treated controls: 1) in HTR8 cells, rh-IFNγ alone significantly increased mRNA levels of the pro-inflammatory cytokines IL-1β, IL-6, IL-8. However, the combination of rh-IFNγ with rh-S-protein further elevated IL-8 levels, but not IL-1β or IL-6 levels (Figure 5A); 2) in JEG3 cells, rh-IFNγ alone or in combination with rh-S-protein did not alter IL-6 levels, whereas IL-1β and IL-8 levels were undetectable (Figure 5B); 3) in PMEVCs, rh-IFNγ alone significantly increased IL-1β, IL-6 and IL-8 levels, which are further induced by the combination of rh-IFNγ and rh-S-protein (Figure 5C); and 4) rh-IFNγ alone enhanced IL-6 levels, and addition of rh-S-protein did not further induce cytokine mRNA levels in HEECs (Figure 5D). Further analysis by ELISA revealed that HTR8 (Figure 5E) and PMVEC cultures (Figure 5F) treated with 10 ng/ml IFNΥ displayed significantly higher IL-6 and IL-8 secretion levels, which are the further increased by the addition of rh-S-protein (Figures 5E, F).

FIGURE 5

Figure 5 IFNγ with or without S-protein significantly increases expression of pro-inflammatory cytokines in trophoblastic and endothelial cell cultures. Expression of pro-inflammatory cytokines genes IL-1β, IL-6, IL-8 was measured in HTR8/SV^neo (A), JEG3 (B), PMVECs (C), and HEECs (D) treated with either control or 10 ng/ml rh-IFNγ ± 10 ng/ml rh-S-protein by qPCR. Bars represent mean ± SEM, n=3; * P<0.05 vs. control and + P<0.05 vs. rh-IFNγ alone. ELISA results revealed to measure secreted IL-6 and IL-8 protein levels in HTR8 (E) and PMVECs (F) by treatment with 10 ng/ml rh-IFNγ or rh-IFNγ + 10 ng/ml rh-S-protein. Bars represent mean ± SEM, n=3; *P<0.05 vs. control. + P<0.05 vs. IFNγ alone. C, Control; I, rh-IFNγ; and I+S, rh-IFNγ + rh-S-protein.

Following the same protocol with Figure 5, we evaluated the impact of rh-IFNγ on chemokine expression in these cells by qPCR and noted that mRNA levels of CXCL9, CXCL10 (Figure 6A), and CCL2 and CCL5 (Figure 6B) were significantly enhanced by rh-IFNγ, but not further altered by addition of rh-S-protein in HTR8. In JEG3 cells, only CCL5 levels were induced by rh-IFNγ, but again not further increased by adding rh-S-protein, whereas CCL2 levels did not attain significance in any incubation condition (Figure 6C). Interestingly, in JEG3 cells, CXCL9 and CXCL10 levels were undetectable in both the control and rh-IFNγ treatment groups. Finally, rh-IFNγ significantly induced expression of CXCL9, CXCL10 (Figures 6D, F), and CCL2 and CCL5 (Figures 6E, G) in both PMVECs and HEECs, and rh-S-protein further elevated their expression in PMVECs, but not HEECs (Figures 6D–G).

FIGURE 6

Figure 6 Recombinant IFNγ with or without S-protein significantly increases mRNA levels of chemokines in trophoblastic and endothelial cell cultures. Expression of chemokines CXCL9, CXCL10 (A); CCL2 and CCL5 (B) in HTR8/SV^neo, expression of chemokines CCL2 and CCL5 (C) in JEG3; expression of chemokines CXCL9, CXCL10 (D), CCL2 and CCL5 (E) in PMVECs; expression of chemokines CXCL9, CXCL10 (F), CCL2 and CCL5 (G) in HEECs treated with either control or 10 ng/ml rh-IFNγ ± 10 ng/ml rh-S-protein treated cells. Bars represent mean ± SEM, n=3; *P<0.05 vs. control. + P<0.05 vs. IFNγ alone. C, Control; I, rh-IFNγ; and I+S, rh-IFNγ + rh-S-protein.

Elevated F3 Expression by rh-IFNγ in Combination With rh-S-Protein in Only PMVEC Cultures

We next investigated whether enhanced rh-IFNγ contributes to the risk of thrombosis by measuring F3 expression in trophoblastic HTR8 and JEG3 as well as endothelial PMVECs and HEECs cultures. Figure 7 shows that F3 mRNA levels are not induced by either rh-IFNγ alone or in combination with rh-S-protein in both HTR8 (Figure 7A) and JEG3 cells (Figure 7B). However, compared to control, F3 mRNA levels were significantly higher in PMVECs treated with 10ng/ml rh-IFNγ and the combination of rh-IFNγ +10 ng/ml rh-S-protein further increased F3 expression in PMVECs (Figure 7C). Interestingly, F3 expression was not induced by either rh-IFNγ alone or in combination with rh-S-protein in HEECs, suggesting that interferon blocked spike protein induction of tissue factor (Figure 7D).

FIGURE 7

Figure 7 IFNγ with or without S-protein significantly increases tissue factor (F3) levels in only PMVECs. Expression of F3 was measured in HTR8/SV^neo (A), JEG3 (B), PMVECs (C), and HEECs (D) treated with either control or 10 ng/ml rh-IFNγ alone or in combination with 10 ng/ml rh-S-protein. Bars represent mean ± SEM, n=4 * P<0.05 vs. control. + P<0.05 vs. rh-IFNγ alone. C, Control; I, rh-IFNγ; and I+S, rh-IFNγ + rh-S-protein.

Detection of SARS-CoV-2 Spike Protein Expression in Placenta

Analysis of placental sections immunostained with anti-SARS-CoV-2 spike RBD revealed that endothelial cells as well as trophoblast layer displayed immunoreactivity in placental villi obtained from mothers who tested COVID-19 positive in the third trimester (Figure 8), whereas no reaction was detected in either endothelial cells or other cells in the placental villi obtained from gestational age-matched normal pregnancies (Figure 8).

FIGURE 8

Figure 8 SARS-CoV-2 spike protein immunostaining in placental villi from women tested positive for Covid-19. Endothelial cells and trophoblastic layers display strong to weak SARS-CoV-2 spike protein immunoreactivity in placental sections from COVID-19 infected mothers (n=3), but not in cells in placental sections from non-infected mothers (n=3). Inset picture represents negative control incubated with non-immune IgG_2a at the same monoclonal IgG_2a primary antibody concentration. PS, Placental specimen; Original magnification: 40X.

Discussion

Viral infections are a major cause of global morbidity and mortality. During pregnancy, viral infections that breach the placental barrier are frequently responsible for devastating effects on fetal development and maternal health (31). Pregnant women are more susceptible to several viral infections related to pregnancy-specific immune adaptation, which promotes maternal tolerance of the semi-allogenic fetus and enables viral infections (20, 32). Therefore, pregnant women represent a vulnerable population that has been carefully monitored during the COVID-19 pandemic. Several studies have reported that compared to non-pregnant reproductive age women, COVID-19 infected pregnant women are at higher risk for: 1) severe illness; and 2) preterm birth and cesarean delivery as well as other adverse pregnancy outcomes (12, 13, 18). Therefore, this study evaluated the underlying mechanism(s) associated with the placental pathology observed in these women (33) to help explain both disease severity and adverse human pregnancy outcomes.

The presence of COVID-19 infection in pregnant patients raises the question concerning vertical transmission of SARS-CoV-2 to the fetus (21). Although rare, vertical transmission of SARS-CoV-2 has been reported with detectable SARS-CoV-2 in the placenta, predominantly in syncytiotrophoblasts (22, 34, 35). These findings indicate the importance of identifying cellular tropisms for SARS-CoV-2 at the maternal-fetal interface. Therefore, we first examined the cell specific expression of the documented viral entry receptors, ACE2 and TMPRSS2, in primary cultured cells from the maternal-fetal interface. Our results reveal high expression of ACE2 and TMPRSS2 in syncytiotrophoblasts, and cytotrophoblasts compared to maternal first and third trimester decidual cells, consistent with the pathological detection of SARS-CoV-2 viral RNA in the placenta. Surprisingly, these expression profile for SARS-CoV-2 viral entry receptors are the opposite of those found with Zika virus infection since Zika virus viral entry molecules are highly expressed in maternal decidual cells compared to trophoblast (25), indicating the importance of confirming individual virus-specific mechanisms in the placenta. Previous studies demonstrated ACE2 expression in syncytiotrophoblasts, cytotrophoblasts, endothelial and vascular smooth muscle cells in placenta villi (36, 37). These data were further supported by recent studies using single cell RNA-sequence analysis (15, 38). However, co-expression of both entry molecules was observed only in the chrorioamnionic membranes, whereas TMPRSS2 levels were not detected in several placental cells (38). Similarly, we detected ACE2, but not TMPRSS2 expression in decidua cells, PMVECs and HESCs, suggesting the likelihood that SARS-CoV-2 could infect placental cells by using alternative host entry molecule(s) recently identified by Gordon et al. (39). Thus, further studies are required to identify other molecules that play a role in host infection, for example, cathepsin L and furin are other candidate proteases that prime the S-protein of SARS-CoV-2 (40).

An excessive inflammatory response to SARS-CoV-2 is a major cause of disease severity as well as mortality in COVID-19 patients and is associated with high levels of circulating cytokines i.e., IL-1β, IL-6, IL-7, IFNγ and TNFα and chemokines i.e., CCL2, CLL3 and CXCL10 (1, 41, 42). Maternal infection and inflammation associated with COVID-19 could prompt potential pregnancy complications through this “cytokine storm”. Several studies reported increased expression of inflammatory biomarkers in pregnant women with COVID-19 (21, 30, 43). Thus, we assessed the impact of SARS-CoV-2 infection during pregnancy on placental inflammation as a potential cause of adverse pregnancy outcomes. We found that rh-S-protein treatment triggers increase of pro-inflammatory cytokines IL-1β, IL-6, IL-8 and chemokines CXCL9, CXCL10, CCL2, CCL5 in a cell-type specific manner. The increase levels of these inflammatory markers could exaggerate the fetal and maternal immune system that is associated with stillbirth, fetal growth restriction, preeclampsia and/or PTB. COVID-19 has been linked to an increase occurrence of preeclampsia (44) as well as a preeclamptic-like illness (45). Preeclampsia is also associated with increased IL-6 levels (46). Interestingly, we found elevated IL-6 levels in HTR8 and endothelial cells, suggesting a potential similar pathogenesis.

Also, we previously reported that IL-1β and IL-6 are responsible for chorioamnionitis-associated PTB and weakened fetal membrane through intense generation of extracellular matrix degrading metalloproteases (26, 47, 48). In addition, IL-1β is a potent inhibitor of decidual cell progesterone receptor expression, which accompanies chorioamnionitis (48). Therefore, the higher pro-inflammatory cytokine and chemokine responses observed in SARS-CoV-2 infected pregnant women may help explain the association between SARS-CoV-2 infection and inflammation-associated PTB. COVID-19 infected pregnant women are potentially at increased risk of developing coagulopathy and/or thromboembolic complications since pregnancy represents a physiological pro-thrombotic stage (49). A recent study found that the placentas from women infected with COVID-19 displayed a type of injury associated with uteroplacental vascular insufficiency which has been associated with stillbirth, fetal growth restriction, preeclampsia, abruption and preterm birth (50). Therefore, we investigated F3 levels in rh-S-protein treated endothelial and trophoblast cell cultures and found rh-S-protein induced F3 levels in only endothelial PMVEC and HEEC cells.

F3 initiates the coagulation process by binding to activated factor VII to activate factor IX and X, and subsequently generate thrombin, which activates endothelial cells, platelets, leukocytes and propagates microvascular thrombosis (51). Our previous studies reported decidual cells generate tissue factor during decidualization contributing uterine and placental hemostasis (52, 53). Decidual hemorrhage induces significant thrombin from decidual cell tissue factor accounting for the associated consumptive coagulopathy as well as the link between abruption and development of preterm premature rupture of membranes and spontaneous preterm birth. Thrombin promotes the production of decidual cell-derived pro-inflammatory cytokines, and matrix-degrading metalloproteinases (54, 55) and inhibits decidual cell progesterone receptor expression by activation of the ERK1/2 pathway (56). Thus, these findings provide clear evidence of potential molecular mechanisms to account for the observed histopathological changes in the placenta from women infected with COVID-19.

IFNγ, a pleiotropic lymphokine, exerts important regulatory effects on many cell types, and is essential for the initiation of uterine vascular modifications, directly and through the recruitment of Natural Killer (NK) cells and maintenance of decidual integrity (57). Conversely, excess decidual IFNγ expression may inhibit uterine NK cell migration (58). Recently, Tanacan et al., reported significantly higher levels of IFNγ in COVID-19 infected pregnant women, most prominently in the third trimester samples (30). Therefore, we investigated the impact of rh-IFNγ on SARS-CoV-2 placental pathogenesis and observed that rh-IFNγ treatment significantly increased mRNA levels of pro-inflammatory cytokines IL-1β, IL-6, IL-8, chemokines CXCL9, CXCL10, CCL2, CCL5 and F3 in both trophoblast and endothelial cell lines. Moreover, rh-IFNγ in combination with rh-S-protein further induces the expression of pro-inflammatory cytokines, chemokines and F3 in placental endothelial cells PMVECs, but not in HEECs isolated from the endometrium of non-pregnant women. Combination of results showing in vitro and in situ detection of SARS-Co-V-2 spike protein expression in endothelial cells in placental villi suggest that IFNγ and S-protein synergistically induce inflammation and vascular thrombosis specifically in placenta endothelial cells, which likely play an important role in linking COVID-19 infections with adverse pregnancy outcomes.

In conclusion, our results revealed that in placental cells, SARS-CoV-2 S-protein induces release of pro-inflammatory cytokines and chemokines, which likely contributes to the “cytokine storm” in pregnant women and potential cause of placental dysfunction as well as elevated F3 levels that may trigger the vascular thrombosis seen in the placentas of women infected with COVID-19. These findings also support the concept that SARS-CoV-2 infection in the presence of enhanced IFNγ levels amplifies pro-inflammatory cytokine release from placenta to cause utero-placental and/or feto-placental endothelial dysfunction, contributing to SARS-CoV-2-associated adverse pregnancy outcomes such as PTB, abruption, still birth, fetal growth restriction, and/or preeclampsia.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics Statement

The studies involving human participants were reviewed and approved by University of South Florida. The patients/participants provided their written informed consent to participate in this study.

Author Contributions

OG-K, UK, FS, and CL designed research studies. OG-K, UK, and XG discussed results and wrote the manuscript. OG-K and UK supervised experiments, contributed to data analyses. XG, NS, and VA performed experiments and contributed to data analyses. TS supplied placental specimen paraffin blocks. All authors performed critical evaluation of final version of results and agreed to submit manuscript for publication.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Acknowledgments

Authors thank Dr. Hana Totary-Jain (Department of Molecular Pharmacology and Physiology, USH Health, Morsani College of Medicine, Tampa, FL) for her kindness to provide us the human placental microvascular endothelial cells.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fimmu.2022.876555/full#supplementary-material

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