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. 2017 Jan 6;7:39904. doi: 10.1038/srep39904

IFN type I and II induce BAFF secretion from human decidual stromal cells

Anna-Carin Lundell 1,a, Inger Nordström 1, Kerstin Andersson 1, Christina Lundqvist 1, Esbjörn Telemo 1, Silvia Nava 2, Helen Kaipe 2,3, Anna Rudin 1
PMCID: PMC5216379  PMID: 28057926

Abstract

B cell activating factor (BAFF) is a critical cytokine for maturation of immature B cells. In murine lymph nodes, BAFF is mainly produced by podoplanin-expressing stromal cells. We have previously shown that circulating BAFF levels are maximal at birth, and that farmers’ children exhibit higher BAFF levels in cord blood than non-farmers’ children. Here, we sought to investigate whether maternal-derived decidual stromal cells from placenta secrete BAFF and examine what factors could stimulate this production. We found that podoplanin is expressed in decidua basalis and in the underlying villous tissue as well as on isolated maternal-derived decidual stromal cells. Decidual stromal cells produced BAFF when stimulated with IFN-γ and IFN-α, and NK cells and NK-T-like cells competent of IFN-γ production were isolated from the decidua. Finally, B cells at different maturational stages are present in decidua and all expressed BAFF-R, while stromal cells did not. These findings suggest that decidual stromal cells are a cellular source of BAFF for B cells present in decidua during pregnancy.

B cell activating factor (BAFF) is critical for survival and differentiation of immature transitional B cells into mature naïve cells. BAFF-deficient mice present with normal B cell development up to the transitional stage but additional maturation in the spleen is hampered1,2. These mice also exhibit reduced antibody titers in response to both T-dependent and T-independent antigens1. Human BAFF-R-deficiency resembles the murine phenotype by arrested B cell maturity at the stage of transitional B cells and reduction in the numbers of all subsequent B cell maturational stages3. Although BAFF is required for B cell homeostasis and function, the cellular source(s) of BAFF remains to be explored further. Innate immune cells and epithelial cells produce BAFF in response to IFN type I (IFN-α) and type II (IFN-γ) in vitro4,5,6,7, but their ability to produce physiologically relevant BAFF levels in vivo has not been determined. Results from mouse models instead indicate that stromal cells are the main source of BAFF to support normal B cell homeostasis in vivo2.

Murine lymph nodes are comprised of a heterogeneous stromal network that can be distinguished by expression of podoplanin and CD31, e.g. fibroblastic reticular cells, follicular dendritic cells as well as lymphatic and blood endothelial cells8,9,10. In mice, podoplanin is crucial for the development of the lung and deep lymphatics, as podoplanin knock-out animals die soon after birth as a result of respiratory failure and generalized lymphedema11. An endogenous receptor of podoplanin is C-type lectin-like receptor-2 (CLEC-2), which is primarily expressed on platelets and dendritic cells12,13. On dendritic cells, CLEC-2 functions by facilitating efficient motility of activated dendritic cells along stromal podoplanin-expressing surfaces13. The murine stromal network also includes intertwined fibers that express the ER-TR7 antigen, which is detected by Erasmus University Rotterdam thymic reticulum antibody 710,14. Although ER-TR7 is localized in close proximity to podoplanin, and is used as a marker to identify fibroblastic reticular cells15, the antigen of ER-TR7 has yet to be determined. The fibroblastic reticular stromal cell network has been shown to function as a conduit system for immunocompetent cells to reach appropriate sites in order to cause immune reactions16. Over the past decade, discoveries relating to stromal cells have promoted these cells from bystanders to key players in immune responses8,13,17,18. Podoplanin-expressing follicular reticular cells were recently shown to be the primary cellular source for local BAFF in murine lymph nodes19. A similar podoplanin-positive reticular stromal cell network is also present in the T cell zone in human lymphoid tissue10, but if this network possesses the same functions as demonstrated in mice remains to be examined.

Longitudinal data regarding blood BAFF concentrations in early childhood have been lacking. We recently showed that BAFF levels in plasma were maximal at birth and that newborn children have higher levels than their mothers, the latter a finding also observed by others20,21,22. In the same study we also demonstrated that farmers’ children had elevated BAFF levels at birth compared to non-farmers’ children, and that higher neonatal BAFF levels were associated with an accelerated B cell maturation later in childhood20. Yet, both origin for BAFF in the fetal circulation and BAFF-inducing factors associated with a farming environment are unknown.

The placental basal plate (Fig. 1j) is an area of direct contact between maternal and fetal tissues, which includes maternal-derived decidua basalis and fetal-derived villi that are bathed in the circulating maternal blood. The outermost layer of the villi consists of syncytiotrophoblasts that form a continuous epithelium generated and maintained by the underlying cytotrophoblast cells. The latter layer of cells is supported by a basement membrane that separates it from the villous core, including stroma, capillaries and leukocytes (Fig. 1k). Decidual tissue is composed of stromal cells as well as different leukocyte subsets, including T cells, NK cells, NK-T cells and B cells23,24,25,26. B cells are found in the decidua during the whole pregnancy26,27, and it has been shown that fetal membranes have the ability to attract B cells in experimental settings28. Expression of podoplanin has been demonstrated in human placenta, mainly in the villous stroma, throughout gestation and BAFF is expressed intracellularly by decidual stromal cells25. Still, it is not known whether decidual stromal cells secrete BAFF and which stimuli that trigger its production. Although circulating B cell subsets, including transitional, mature/naïve, memory and regulatory B cells, have been characterized from late pregnancy to post-partum29, it remains to be elucidated if B cells at different maturational stages are present in decidua and if they express BAFF-R.

Figure 1. Podoplanin and ER-TR7 expression in placental tissue.

Figure 1

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Immunofluorescence staining of podoplanin (a), ER-TR7 (b) and merge of the two markers (c) in decidua basalis (DB) and in the underlying villous tissue (VT). Podoplanin is depicted in green, ER-TR7 in red and nuclei staining with Hoechst in blue (x10 magnification and scale bar 20 μm, one experiment out of two). Immunohistochemistry images of podoplanin (d), ER-TR7 (e), CD31 (f), CD45 (g), mouse and rat isotype control staining (h and i, respectively) in decidua basalis and underlying villous tissue (x10 magnification). Schematic illustrations, made by A–C Lundell, of a term placenta that show from which parts tissue and cells were isolated (j) and of the maternal-derived decidua and fetal-derived villous tissue (k).

In the present study we explored the role of decidual stromal cells as a possible source of BAFF. In placentas from full term normal pregnancies, we demonstrate that podoplanin is expressed in decidua basalis and in the underlying villous tissue as well as on isolated maternal-derived decidual stromal cells. We also found that decidual stromal cells produced BAFF when stimulated with IFN-γ and IFN-α, while cord blood mononuclear cells did not. NK cells as well as NK-T-like cells competent of providing IFN-γ to the stromal cells, and BAFF-R-expressing B cells at different maturational stages were present in the decidua. Thus, decidual stromal cells could be a cellular source of BAFF for decidual B cells as well as for BAFF in the fetal circulation, which could explain the environmental effects on BAFF levels in neonates.

Materials and Methods

Placenta and cord blood

Human term placentas and umbilical cord blood samples were obtained from unselected healthy vaginal deliveries at Mölndal delivery unit, the Sahlgrenska University Hospital (Göteborg, Sweden). All mothers were given oral information, and gave oral consent to participate in the study. According to the Swedish law (2003:460, §4 and §13) ethical approval was not needed as no personal information or identity was recorded and as placentas are normally discarded after delivery. For some of the experiments regarding isolation of decidual stromal cells, i.e. phenotypic characterization and measurement of BAFF secretion, term placentas were obtained from healthy mothers after cesarean section at Huddinge delivery unit, Karolinska University Hospital (Stockholm, Sweden) (Figs 2 and 3 and Supplementary Fig. S2 and S4, respectively). In that case personal information and identity was recorded and ethical approval was thus obtained from the Karolinska institutional ethical review board (2009/418-31/4 and 2010/2061-32). All experiments were carried out in accordance with the approved guidelines and regulations.

Figure 2. Isolated decidual stromal cells express podoplanin but not ER-TR7.

Figure 2

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(a) Flow cytometry contour plots depict podoplanin and CD31 expression on stromal cells isolated from decidua basalis at different passages. (b) The proportion of podoplanin-positive cells at different passages (n = 3). (c) Expression of characteristic stroma cell markers on cells isolated from decidua basalis. Specific markers are depicted in dark grey and FMO controls in light grey (one representative experiment out of three).

Figure 3. IFN-γ and IFN-α trigger BAFF production from decidual stromal cells.

Figure 3

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(a) BAFF production and relative BAFF mRNA levels to medium control by isolated decidual stromal cells in response to IFN-γ, IFN-α or LPS. (b) BAFF production and relative BAFF mRNA levels to medium control by cord blood mononuclear cells in response to IFN-γ, IFN-α or LPS. (c) BAFF-R expression on CD105-positive stromal cells isolated from decidua basalis or decidua parietalis after culture in the presence or absence of IFN-γ. (d) Histograms depict podoplanin expression on stromal cells isolated from decidua basalis or decidua parietalis and the scatter plot shows the percentage of podoplanin-positive cells after stimulation with IFN-γ or not. (e) Immunofluorescence staining of podoplanin on stromal cells isolated from decidua basalis stimulated with IFN-γ or not (podoplanin in green and nuclei staining with Hoechst in blue). Images from one donor in the upper panel are presented with x 10 magnification and images from a second donor in the lower panel are presented with x 25 magnification (scale bar 40 μm). Horizontal bars indicate median. *P ≤ 0.05, **P ≤ 0.01 and ****P ≤ 0.0001, Kruskal-Wallis test followed by Dunn’s multiple comparison test (Fig. 3a) and Wilcoxon signed-rank test (Fig. 3d).

Isolation and expansion of stromal cells from decidua basalis and parietalis

The placenta was moved to a sterile beaker containing PBS (HyCloneTM, Logan, USA). The maternal basal plate of the placenta was placed upward and small tissue pieces from the cotyledons, including decidua basalis and villous tissue, were cut out with a scalpel (about 10 mm2 and 2–3 mm deep). Tissue pieces were also dissected from decidua parietalis, including chorion and amnion, (about 10 mm2 and 1 mm deep) as previously described in detail30. A schematic drawing of a term placenta is shown in Fig. 1j to illustrate from which parts of the placenta tissue pieces were dissected. Tissue pieces were transferred to petri dishes for further extensive washing in PBS. Next, an equal volume of trypsin/EDTA (Thermo Fisher Scientific, Waltham, USA) was added for 10 minutes at 37° and was then discarded. Tissue pieces were then incubated twice in trypsin/EDTA for 40 min at 37°, and thereafter washed in Dulbecco’s modified Eagle’s low glucose medium (DMEM) (HyCloneTM) containing 10% fetal bovine serum (FBS, HyCloneTM) and gentamycin (Sigma-Aldrich, St. Louis, USA) (complete DMEM). The remains of tissues were cut into smaller pieces, and these were spread out and incubated in T182 flasks (VWR, Radnor, USA). Tissue pieces were removed from the flasks when colonies of fibroblast-like cells appeared after about 1 week of culture. When the cells from trypsin-digested tissue pieces were 90–95% confluent, cells were harvested with trypsin/EDTA, washed in complete DMEM, and seeded in new T182 flasks in complete DMEM. The cells were cultured to passage 1, 2 or 3 and frozen slowly in FBS containing 7.5% DMSO (Sigma-Aldrich). The stromal cells isolated from the decidua parietalis was confirmed to be of maternal origin31. To induce decidualization, stromal cells (2 × 105 cells/ml) were cultured in 24-well plates in complete DMEM in the presence of 300 nM progesterone (P4; Sigma-Aldrich) and 500 μM 8-bromo-cAMP (Sigma-Aldrich) for 7 days32. Half of the culture medium was changed on day 4, and P4 and cAMP were readded. Decidualization was assessed by prolactin secretion. The measurement of prolactin was performed in the laboratory of Clinical Chemistry at the Sahlgrenska University Hospital using the routine accredited method electrogenerated chemiluminescence33.

Immunofluorescence staining and immunohistochemistry

Immunofluorescence staining for detection of podoplanin and ER-TR7 was performed on 5–7-μm-thick frozen tissue sections from the maternal basal plate of the placenta, and on isolated decidual stromal cells attached to glass slides by cytospin centrifugation. Slides were counterstained with Hoechst 34580 (Thermo Fischer Scientific) and mounted with vectashield (Vector Laboratories, Berlingame, USA). Images were obtained by use of a confocal microscope equipped with 405-, 488-, 555- and 639-nm lasers (LSM 700, Zeiss, Oberkochen, Germany). Images were acquired with ZEN software (Zeiss). Discrimination of different cells, such as leukocytes, endothelial cells, epithelial cells and stromal cells, in decidua and villous tissue was examined with immunohistochemistry using ImmPRESSTM according to the manufacturer’s instructions (Vector Laboratories, Burlingame, USA; MP-7402 for mouse antibodies and MP-7444 for rat antibodies). Glucose oxidase was used for quenching of endogenous peroxidase activity. Primary antibodies used are indicated in Table 1. Sections were analyzed using a Leica DMR microscope.

Table 1. Antibodies used for flow cytometry, immunofluorescence and immunohistochemistry.

Flow cytometry Reactivity Conjugate Clone Reference Company
CD3 BV421 UCHT1 300434 Biolegend
CD3 FITC SK7 345763 BD Bioscience
CD4 FITC RPA-T4 561842 BD Bioscience
CD8 APC RPA-T8 555369 BD Bioscience
CD19 BV421 HIB19 562441 BD Bioscience
CD20 APC-H7 L27 641414 BD Bioscience
CD24 AF647 ML5 561644 BD Bioscience
CD31 PE WM59 555446 BD Bioscience
CD38 PE HB-7 345806 BD Bioscience
CD56 PE HCD56 318306 Biolegend
CD56 BV421 HCD56 318328 Biolegend
CD14/45 PE/FITC MφP9/2D1 342408 BD Bioscience
CD44 PE G44-26 555478 BD Bioscience
CD45 PerCP-Cy5.5 HI30 564105 BD Bioscience
CD73 FITC AD2 550257 BD Bioscience
CD90 FITC 5E10 329706 Biolegend
CD105 AF647 266 561439 BD Bioscience
CD105 PE 266 560839 BD Bioscience
CD303 (BDCA2) APC AC144 130-097-931 Miltenyi Biotec
BAFF-R FITC 8A7 11-9117-42 eBioscience
CXCR3 BV421 G025H7 353716 Biolegend
IFN-γ PE B27 562016 BD Bioscience
IFN-α PE LT27:295 130-099-098 Miltenyi Biotec
Flow cytometry, Immunofluorescence and Immunohistochemistry
Primary antibodies Reactivity Isotype Clone Reference Company
Podoplanin Mouse IgG1 D2-40 MCA2543 Serotec
ER-TR7 Rat IgG2a ER-TR7 Sc-73355 Santa Cruz
CD45 Mouse IgG1 HI30 564105 BD Bioscience
CD31 Mouse IgG1 WM59 555446 BD Bioscience
Flow cytometry Secondary antibodies Reactivity Host/Isotype Conjugate Reference Company
Mouse IgG Rabbit Ig Biotin E0464 DAKO
Streptavidin   BV421 405226 Biolegend
Rat IgG Goat IgG AF488 A11006 Thermo Fisher Scientific
Immunofluorescence Secondary antibodies Reactivity
Mouse IgG Rabbit IgG AF488 A11059 Thermo Fisher Scientific
Rat IgG Goat IgG AF555 A21434 Thermo Fisher Scientific
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Isolation of mononuclear cells from decidua and cord blood

Tissue pieces from the basal plate, as described above, and from decidua parietalis, with amnion removed, were placed in PBS with 2 mM EDTA (Media Department, Gothenburg University, Sweden) and cut into smaller pieces. Tissue pieces were then transferred into gentleMACS C tubes (Miltenyi Biotec, Bergisch Gladbach, Germany) containing RPMI-1640 and placed in a gentleMACS Dissociator (m_spleen 04.01 programme, Miltenyi Biotec). Next, 50 μg/ml Liberase TL (Roche Diagnostics, Basel, Switzerland) and 40 μg/ml DNase 1 (Sigma-Aldrich) was added to the dissociated tissue for 30 minutes at 37 °C on an orbital shaker. The digested suspension was then passed through 70-μm, followed by 40-μm cell strainers (Thermo Fisher Scientific and Corning Incorporated, New York, USA, respectively). LymphoprepTM (Axis-Shield PoC AS, Oslo, Norway) was then used to isolate mononuclear cells from the dissociated decidual tissue as well as from umbilical cord blood.

Stimulation of decidual stromal cells and mononuclear cells

Decidual stromal cells (2 × 105 cells/ml), cord blood and maternal-derived mononuclear cells (1 × 106 cells/ml) were cultured in flat 24- or 96-well plates. Stromal cell cultures were performed in complete DMEM and mononuclear cell cultures were performed in RPMI 1640 (PAA Laboratories GmbH, Pasching, Austria) supplemented with 10% FBS (HyCloneTM), gentamicin (50 μg/ml; Sigma-Aldrich) and L-glutamine (1 mM; Sigma-Aldrich) in the presence or absence of IFN-γ (10 ng/ml; R&D systems, Minneapolis, USA), IFN-α (10 ng/ml; PBL Biomedical Laboratories, Piscataway, USA), IL-2 (10 ng/ml; Peprotech, New Jersey, USA), TNF (10 ng/ml; R&D systems), polyinosinic-polycytidylic acid (polyI:C) (10 μg/ml; Sigma-Aldrich), E. coli LPS (100 ng/ml; Sigma-Aldrich), imiquimod acetate (10 μg/ml; Sequoia Research products, Pangbourne, UK) or CpG (10 ng/ml; InvivoGen, San Diego, USA) for 48 h in 5% CO2 at 37°.

BAFF ELISA

BAFF concentrations in culture supernatants from decidual stromal cells and cord blood mononuclear cells were determined by human BAFF DuoSet® ELISA (detection range 39.1–2,500 pg/mL) according to the manufacturer’s instructions (R&D Systems).

Flow cytometry

All antibodies used for characterization of decidual stromal cells, and for identification of decidual T cells, NK cells, NK-T cells, B cells and pDCs are listed in Table 1. To identify living leukocytes, cells were stained with Fixable Viability Dye (eFluor 506 or 780, eBioscience, San Diego, USA). For experiments analyzing intracellular IFN-γ and IFN-α production, isolated decidual mononuclear cells (106/ml) were cultured overnight with or without poly(I:C) together with IL-12 (10 μg/ml and 10 ng/ml (Nordic Biosite, Stockholm, Sweden), respectively). Brefeldin A (5 μg/ml, BD Biosciences, New Jersey, USA) was added for the last 3 hours. After surface staining cells were fixed and permeabilized using Cytofix/Cytoperm™ kit (BD Biosciences). Antibodies used for detection of IFN-γ and IFN-α are listed in Table 1. Samples were acquired in a FACSVerse or FACSCanto II (BD Biosciences) equipped with FACSSuite or FACSDiva software and analyzed with FlowJo software (TreeStar, Ashland, USA).

Quantitative Polymerase Chain Reaction (qPCR)

The relative levels of BAFF mRNA were measured in decidual stromal cells (2 × 105 cells/ml) cultured in complete DMEM with IFN-γ (10 ng/ml), IFN-α (10 ng/ml), E. coli LPS (100 ng/ml) or medium alone for 20 h. The cells were lysed with lysis buffer (Qiagen, Hilden, Germany). Total RNA was extracted using an RNeasy Micro kit (Qiagen) and treated with DNase (Qiagen) to remove genomic DNA. Complementary DNA was prepared in a random hexamer-primed SuperScript (Thermo Fisher Scientific) RT reaction. The mRNA levels were determined by qPCR on an ABI Prism 7500 Sequence Detection System using MicroAmp Optical 96-well reaction plates. Primer-probe pairs were as follows: GAPDH (Hs99999905_m1) and BAFF (Hs00198106_m1). Samples (10 ng of cDNA) were run in duplicate in a 20-μl reaction mix with TaqMan Universal PCR Master Mix using the comparative ΔΔCT method of relative quantification to calculate the differences in gene expression between stimulated and control cells. As an endogenous control, GAPDH was used to correct for variations in sample loading. Samples were normalized to medium control set to 1. All qPCR reagents were purchased from Thermo Fisher Scientific.

Statistics

The D’Agostino and Pearson omnibus normality test were used to assess if the data were normally distributed (GraphPad Prism, San Diego, USA). Data were analyzed by Kruskal-Wallis test followed by Dunn’s multiple comparison test or by Wilcoxon signed-rank test as described in figure legends (GraphPad Prism). A p value ≤ 0.05 was regarded as being statistically significant (*p ≤ 0.05, **p ≤ 0.01 and *** p ≤ 0.001).

Results

Podoplanin and ER-TR7 are expressed in decidua basalis and underlying villous core

In murine lymph nodes, podoplanin-expressing fibroblastic reticular stromal cells are the main local source of BAFF19. The lymph node stromal network also includes intertwined fibers that express the ER-TR7 antigen localized in close proximity to podoplanin14. Confocal imaging of tissue sections from the maternal basal plate of the placenta was performed to examine podoplanin and ER-TR7 expression in decidua basalis and villous tissue (Fig. 1j). As shown in Fig. 1a,b, podoplanin and ER-TR7 were expressed both in the decidua and in villous tissue. Merged images displayed co-localization of these two markers (Fig. 1c). Similar results were obtained when placental tissue from another donor was examined (Supplementary Fig. S1). Immunohistochemistry was also performed on the placental tissue sections to assess what cells among endothelial cells, leukocytes, stromal cells and epithelial cells that are podoplanin- and ER-TR-7-positive. A section including a blood vessel in the decidua was selected (Fig. 1d–i) and a schematic illustration of the maternal-derived decidua and fetal-derived villous tissue is shown in Fig. 1k. Podoplanin and ER-TR7 staining was observed close to the endothelium in the decidua and the two markers were also clearly expressed in the villous core (Fig. 1d,e, indicated by solid arrows). Endothelial cells were stained with CD31 both in the decidua and in the villous core (Fig. 1f, solid arrows). A scattered pattern of CD45-expressing leukocytes was observed in the decidua, while they were closely gathered within the villous core (Fig. 1g, solid arrows). The outermost layer of the villi composed of the trophoblastic epithelial cells was negative for all markers examined (Fig. 1d–g, dashed arrows). Negative isotype control stainings are shown in Fig. 1h,i. These results indicate that stromal cells express podoplanin and ER-TR7, while endothelial cells, leukocytes and epithelial cells do not. Hence, the placental basal plate, an area of direct contact between maternal and fetal tissues, might contain a stromal network that express podoplanin and ER-TR7 similar to what has been shown for lymph nodes.

Isolated decidual stromal cells express podoplanin but not ER-TR7

Next, we examined whether stromal cells isolated from decidua basalis expressed podoplanin and ER-TR7. By the use of flow cytometry we found that a majority of the cells expressed podoplanin, but not the endothelial marker CD31, in the first passage (Fig. 2a,b). However, the proportion of podoplanin-positive cells clearly decreased with time in culture (Fig. 2a,b and Supplementary Fig. S2). The isolated stromal cells displayed a homogenous phenotype with respect to expression of CD105, CD90, CD73 and CD44 that are all markers used to define human stromal cells (Fig. 2c)34. All cells were negative for the hematopoietic cell marker CD45 (Fig. 2c) and for CD14 (data not shown), which is in line with the characteristic stroma phenotype. The same phenotype was obtained for stromal cells isolated from the decidua after cesarean section (Supplementary Fig. S2). However, while podoplanin was expressed both in decidual tissue sections as well as on isolated stromal cells, ER-TR7 was not detected on the cultured decidual stromal cells (Fig. 2c and Supplementary Fig. S2). To confirm that the cells are authentic decidual stromal cells, decidualization of the cells was performed with progesterone and cAMP in vitro, which resulted in prolactin secretion (Supplementary Fig. S3).

IFN-γ and IFN-α trigger BAFF production from decidual stromal cells

Given the reported role for lymph node podoplanin-positive stromal cells in regulating B cell homeostasis by local production of BAFF19, we hypothesized that decidual stromal cells might produce BAFF. To answer this question and to examine if specific stimuli would elicit BAFF production, various cytokines and Toll-like receptor agonists were added to stromal cells isolated from both decidua basalis and parietalis. As shown in Fig. 3a, decidual stromal cells, both from basalis and parietalis, secreted BAFF in response to IFN-γ and IFN-α, but not after stimulation with LPS. No delivery mode-related differences in BAFF secretion were found between cells used from healthy vaginal deliveries and cesarean sections (Supplementary Fig. S4). Moreover, BAFF mRNA levels were clearly upregulated in response to IFN-γ and IFN-α but not to LPS, which supports increased BAFF secretion by these stimuli (Fig. 3a). Stimulation with TNF, IL-2 or Toll-like receptor agonists including Poly I:C (TLR-3), imiquimod (TLR-7) or CpG (TLR-9) did not induce BAFF secretion from stromal cells (data not shown). Contrary to decidual stromal cells, stimulation with IFN-γ and IFN-α or the other stimuli examined did neither trigger BAFF production nor BAFF mRNA expression by cord blood or decidual maternal-derived mononuclear cells (Fig. 3b and data not shown).

As decidual stromal cells produced BAFF, we examined if the main BAFF receptor, i.e. BAFF-R, was expressed on the cell surface. Flow cytometric analysis demonstrated that unstimulated CD105-positive stromal cells were negative for BAFF-R, and stimulation with IFN-γ did not induce BAFF-R or alter CD105 expression (Fig. 3c). These results thus suggest that decidual stromal cells do not secrete BAFF in an autocrine fashion.

Since IFN-γ was the most potent stimuli for BAFF secretion, we also investigated the effects of IFN-γ stimulation on podoplanin expression in decidual stromal cells. The cell cultures had a relatively low baseline expression of podoplanin as cells at later passages (3–4) were used (Fig. 3d). IFN-γ stimulation increased the proportion of podoplanin-positive stromal cells, both from decidua basalis and parietalis (Fig. 3d). These findings were corroborated by confocal imaging on decidual stromal cells from two additional donors. Immunofluorescence revealed that some, but not all, stromal cells from decidua basalis expressed podoplanin and that IFN-γ stimulation increased the number of positive cells (Fig. 3e). Similar results were obtained regarding stromal cells isolated from decidua parietalis (data not shown). Collectively, these data demonstrate that IFN-γ and IFN-α induce BAFF production from decidual stromal cells, which could be a potential cell source for BAFF in the placenta and possibly also for BAFF levels in the fetal circulation.

BAFF-R expressing B cells at different maturational stages are present in decidua

Although it is known that decidual tissue comprises different leukocyte subsets, including T cells, NK cells, NK-T cells and B cells23,24,25,26, it is unknown whether B cells at different maturational stages are present in decidua and if they express BAFF-R. From mother-infant pairs we isolated mononuclear cells from decidua basalis, decidua parietalis, and from cord blood and analyzed the presence of CD56+ NK cells, CD3+ T cells, CD56+ CD3+ NK-T-like cells and CD19+ CD20+ B cells. To distinguish different B cell maturation stages, a combination of CD24 and CD38 was used. First, live cells were gated using a viability dye that marks all dead cells. Next, the lymphocyte gate was set within CD45-expressing leukocytes (Fig. 4). We found clear populations of CD56+ NK cells and CD3+ T cells in decidua basalis and parietalis as well as in cord blood, while CD56+ CD3+ NK-T-like cells were only present in decidua (Fig. 4a–d). B cells were present in all three different cell sources, but a higher proportion of B cells within the lymphocyte gate was obtained from decidua basalis compared to parietalis (Fig. 4a–d). Additionally, the decidua comprised B cells at different maturation stages, i.e. immature/transitional, mature/naïve and memory cells, but the fraction of memory B cells was about threefold higher in decidua parietalis compared to basalis (Fig. 4a–c,e). As expected, the majority of B cells in cord blood were of an immature/naive phenotype (Fig. 4a–c,e). Finally, BAFF-R was expressed solely on B cells both in decidua, including all maturation stages, and in cord blood (Fig. 4a–c,f). Flow cytometry results from the other two mother-infant pairs are presented in Supplementary Fig. S5. Thus, since BAFF signaling via BAFF-R is pivotal for differentiation of immature B cells into mature naïve cells, BAFF production by decidual stromal cells could be of importance for local B cell homeostasis during pregnancy.

Figure 4. BAFF-R expressing B cells at different maturational stages are present in decidua.

Figure 4

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To identify lymphocytes, in the first panel to the far left, live cells were gated using a viability dye that marks all dead cells and the lymphocyte gate was then set within CD45-expressing singlet leukocytes. (a–c) Within lymphocytes, CD56+ NK cells, CD3+ CD56neg T cells, CD3+ CD56+ NK-T-like cells and CD19+ CD20+ B cells were identified (second and third panels). B cell maturational stages were distinguished based on CD24 and CD38 expression (fourth panel). The BAFF-R expression on the different lymphocyte populations is depicted to the far right. (d) The proportion of different cell subsets with in the lymphocyte gate and (e) the proportion of B cells at different maturational stages isolated from decidua basalis, decidua parietalis and cord blood. (f) The mean fluorescence intensity of BAFF on B cells at different maturational stages. Floating bars show minimum to maximum values, and horizontal bar indicates the median (n = 3). Approximately 40.000 cells were collected in the lymphocyte gate for d. basalis and CBMC and 20.000 for d. parietalis.

NK cells, NK-T-like cells and T cells able to produce IFN-γ are present in decidua basalis

As interferon stimulation triggered BAFF secretion from decidual stromal cells, we examined if immune cells present in decidua had the ability to produce IFN-α and IFN-γ. Mononuclear cells were isolated from decidua basalis and cultured overnight with or without poly(I:C) and IL-12, and the cells were thereafter examined for intracellular cytokine production. As shown in Fig. 5a, NK cells, NK-T-like cells and CD3+ T cells produced intracellular IFN-γ. The highest percentage of IFN-γ producing cells was found among NK-T-like cells followed by NK cells and lastly CD3+ T cells (Fig. 5a,c). Among CD3+ T cells, a small fraction of both CD8+ and CXCR3+ CD4+ T cells produced IFN-γ (Fig. 5b,c). Flow cytometry results from the other two experiments are presented in Supplementary Fig. S6. It is well known that plasmacytoid dendritic cells are a major source of IFN-α. Indeed, a small population of these cells was identified among the freshly isolated decidual mononuclear cells (Fig. 5d). However, they were not detected after overnight culture, and none of the other cell subsets analyzed produced intracellular IFN-α. These results demonstrate that various immune cells competent of producing IFN-γ are present in decidua basalis that may elicit BAFF production from stromal cells.

Figure 5. IFN-γ producing immune cells are present in decidua basalis.

Figure 5

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Mononuclear cells isolated from decidua basalis were left unstimulated or were stimulated with poly(I:C) in combination with IL-12 overnight (106/ml). To identify lymphocytes, live cells were gated using a viability dye that marks all dead cells and the lymphocyte gate was then set within CD45-expressing singlet leukocytes. (a) Flow cytometric analysis of NK cells, NK-T-like cells and CD3+ T cells producing intracellular IFN-γ. (b) Flow cytometric analysis of CD8+ T cells and CXCR3+ CD4+ T cells producing intracellular IFN-γ. (c) The proportion of IFN-γ-positive cells among NK-T-like cells, NK cells, CD3+ T cells, CD8+ T cells and CD4+ CXCR3+ T cells (n = 3). Approximately 20.000 cells were collected in the lymphocyte gate. (d) Identification of freshly isolated BDCA2+ plasmacytoid dendritic cells among decidual mononuclear cells.

Discussion

BAFF is a critical cytokine for peripheral B cell maturation and is mainly produced by stromal cells1,2,3,19. We recently demonstrated that the highest BAFF levels in blood during childhood were found already at birth, and that newborns had higher levels than their mothers. Additionally, cord blood BAFF levels did not correlate with those measured in maternal blood20. These findings together with the fact that the origin of circulating BAFF in newborns is unknown prompted us to explore the role of decidual stromal cells as a source of BAFF. For the first time, we here demonstrate that isolated stromal cells from the maternal-derived decidual membrane secreted BAFF when stimulated with IFN-γ and IFN-α. Moreover, podoplanin was expressed in placental tissue, and also by isolated decidual stromal cells. We also show that the decidua comprised BAFF-R-expressing B cells at different maturational stages as well as IFN-γ-producing NK-T-like cells and NK cells.

Podoplanin is expressed in human placenta, mainly as a network pattern in the fetal villous stromal core35. In addition to this finding, we here show that podoplanin is also expressed in decidua basalis. We also found that ER-TR7 was localized in close proximity to podoplanin in the decidua and in villous core, and that neither endothelial cells, leukocytes nor epithelial cells expressed these two markers. In both human and mice, the network of podoplanin-positive T cell-zone fibroblastic reticular cells is one of the hallmarks of secondary lymphoid organs10,19. Similar structures are also present in tertiary lymphoid tissues/follicles, which are often induced at sites of chronic inflammation, e.g. in salivary glands and in the lungs of patients with Sjögrens’s syndrome or chronic obstructive pulmonary disease (COPD), respectively10,15. Interestingly, BAFF levels are increased in lungs of COPD patients and found to be expressed in close surroundings of stromal cells within the lymphoid follicles15. In the present study, BAFF was not detected either in decidua or in fetal villous tissue, which could be due to that BAFF is not constitutively expressed in term placentas from healthy pregnancies or to that the immunofluorescence and immunohistochemistry methods were not sensitive enough. Still, the decidua may comprise a stromal network that control feto-maternal tolerance by regulating movement and function of leukocytes during pregnancy similar to what has been shown for secondary lymphoid tissue30,36,37 and reviewed in ref. 38.

While most studies have focused on cross-talk between decidual stromal cells and NK cells and T cells, results from the present study indicate that stromal cells in decidua may also influence B cells. We demonstrate that isolated stromal cells from decidua basalis and decidua parietalis secreted BAFF when stimulated with IFN-γ and IFN-α, a finding corroborated by interferon-specific upregulation of BAFF mRNA levels. Although interferon-induced BAFF release from decidual stromal cells was a novel finding, these cells have previously been shown to express BAFF intracellularly in early pregnancy25. Furthermore, decidual stromal cells did not express BAFF-R, which suggests that these cells do not secrete BAFF in an autocrine fashion. No functional experiments with trophoblast cells were performed in the present study. It has, however, been shown that fetal villous cytotrophoblast cells do not express BAFF mRNA while mesenchymal cells isolated from the villous stroma do39, which correspond with podoplanin expression demonstrated in our study and by others35. Combined, these results indicate that placental stromal cells could be a cellular source for local BAFF and possibly also for BAFF levels in the fetal circulation. In line with this hypothesis, animal models demonstrate that non-hematopoietic stromal cells are the primary source of BAFF in vivo2,19. By the use of radiation chimeras, it has been shown that radiation-resistant stromal cells are the most important source of BAFF for primary B cell homeostasis2. More recently, a specific stromal cell population, i.e. podoplanin-positive fibroblastic reticular cells, was shown to control B cell homeostasis in lymph nodes by being the main source of local BAFF19.

How maternal-derived BAFF could be transported to the fetal circulation is unknown, but placental transport of certain maternal-derived proteins is generally accepted. IgG is transported from maternal to fetal circulation, which requires movement across the cytotrophoblasts, the epithelial barrier that separates the two circulations40,41. Although the mechanisms for this transport is not fully clear, there is evidence for involvement of the neonatal Fc receptor42. Moreover, placental amino acid transfer is likely an active process as fetal amino acid concentrations are higher than maternal concentrations43.

It is well established that human decidua not only comprise stromal cells but also leukocytes that belong to both innate and adaptive immunity26,44,45 and reviewed in ref. 46. In the present study we confirmed presence of decidual CD56+ NK cells, CD3+ T cells, CD56+ CD3+ NK-T-like cells and B cells. A novel finding, however, was that B cells at different maturational stages, i.e. immature/transitional, mature/naïve and memory cells, were present in decidua. Although a lower proportion of B cells was found among lymphocytes from decidua parietalis compared to basalis, the B cell fraction from parietalis comprised a higher percentage of memory cells than that from basalis. All decidual B cells expressed BAFF-R, which is in accordance with studies showing that BAFF-R is expressed on all transitional, mature/naïve and memory B cells in blood47,48. Thus, decidual stromal cells could be an important source of BAFF that influence maturation of B cells present in decidua during pregnancy.

The functionality of the decidual B cells was not examined here, but it has been suggested that certain B cells by their ability to secrete IL-10 possess suppressive functions that may be of importance during pregnancy. The circulating number of these cells increase in normal pregnant compared to non-pregnant women, while they are not augmented in women suffering from miscarriage49. Recently, the proportions of different maturational stages of circulating B cells was characterized from late pregnancy to post-partum and compared to non-pregnant women29. In late pregnancy, the number of B cells as well as the proportion of transitional cells was decreased compared to non-pregnant women29. Even though it is likely that maternal B cells are recruited to the decidua, it still remains to be elucidated how they are attracted and if various B cell subsets differ in homing properties and functions.

The cell lineage of decidual stromal cells is not fully defined, but they appear to originate from a fibroblast-like stromal cell precursor already present in the endometrium24,50. In agreement with criteria for phenotypic definition of human mesenchymal stromal cells34, we found that isolated decidual stromal cells expressed CD105, CD90, CD73 and CD44, and were accordingly negative for CD45. Additionally, the majority of isolated decidual stromal cells expressed podoplanin in the first passage. However, the proportion of podoplanin-positive cells clearly decreased in later passages. The reason for this can only be speculated upon, but long time culture of these cells, when no longer present in the organized decidual stromal network, might affect the expression of stromal markers. In line with this reasoning, it has been shown that ER-TR7 is expressed by lymph node stromal cells only when in contact with other cells, i.e. lymphocytes51. Indeed, we found that ER-TR7 was highly expressed in the decidua but not detected on the isolated stromal cells.

We also found that IFN-γ stimulation increased the number of podoplanin-positive decidual stromal cells, while the expression of BAFF-R, CD105 and ER-TR7 was unaffected. Although the significance of this finding remains to be investigated further, it has been shown that podoplanin interacts with CLEC-2, a type II transmembrane protein, primarily expressed on dendritic cells and platelets. On dendritic cells, CLEC-2 functions by facilitating efficient motility of activated dendritic cells along stromal podoplanin-expressing surfaces13. Thus, podoplanin upregulation in response to inflammatory stimuli may be important for regulating immune responses in the placenta during inflammation.

Several studies have shown that human innate immune cells, including macrophages, dendritic cells and neutrophils, as well as epithelial cells from different tissue locations secrete BAFF4,5,6,7,52, but their ability to produce physiologically relevant BAFF levels in vivo has not been determined. Nevertheless, it has become clear from these studies that BAFF production is triggered by stimulation with type I and II interferons, which corresponds with our results showing interferon-induced BAFF secretion from decidual stromal cells. Indeed, BAFF expression is directly downstream of type I IFN signaling and members of the IFN regulatory factor family regulate BAFF53. However, since neither cord blood nor maternal-derived decidual mononuclear cells produced BAFF when stimulated with either IFN-γ or IFN-α in the present study, circulating immune cells in the fetus and mother are most likely not the main source for cord blood BAFF levels.

We have previously shown that children born by mothers living on a dairy farm during pregnancy have significantly higher levels of BAFF in cord blood compared to non-farmers’ children20. In view of the results in the present study, one could speculate that microbes or microbial products associated with a farming environment might reach the placenta where BAFF can be produced in response to these stimuli54. Although the TLR agonists examined in the present study had no direct effect on BAFF secretion from stromal cells there are both innate and adaptive immune cells present in decidua, as shown in the present study and by others26,44,45,46,56, which may produce IFN-α and IFN-γ in response to viruses and bacteria via TLR activation that could in turn elicit BAFF production by stromal cells. Indeed, we found decidual NK-T-like cells and NK cells to be potent producers of IFN-γ in response to the viral mimic poly(I:C) combined with IL-12. CD8+ and CD4+ T cells also produced IFN-γ, albeit to a lower extent than the two former cell subsets. In line with a previous study, IFN-γ production by CD4+ T cells was linked to CXCR3 expression57. Plasmacytoid DCs were also present in the decidua, but due to the very small population of cells, IFN-α may not be as important as IFN-γ in triggering BAFF production by the decidual stromal cells in healthy pregnancies.

In several autoimmune diseases, e.g. systemic lupus erythematosus (SLE), genomic studies have shown a marked overexpression of type I interferon inducible genes that include IFN-α, the so-called IFN signature58. Indeed, IFN-α serum levels are higher in SLE patients compared to healthy controls59 and serum levels of IFN-α correlate to the validated disease activity index SLEDAI60. However, higher IFN-γ protein concentrations in serum have also been reported in patients with SLE compared with healthy individuals59. Spontaneous germinal centre (GC) responses that are associated with autoantibody production are implicated in the pathogenesis of SLE. The pathways through which GC B cell tolerance break down are not clear, but in mouse models it was recently shown that IFN-γR signaling in B cells as well as B cell IFN-γ production were critical initial steps for spontaneous GC development leading to autoimmunity61,62. Interestingly, SLE patients also display increased BAFF serum levels that correlate with disease activity63. In accordance with this, BAFF blockade (belimumab) is the first U.S. Food and Drug Administration-approved treatment of SLE using a biologic. Since there are reports showing an increased rate of SLE flares during pregnancy64,65, the role of the placenta as an immunological organ may be of importance to investigate further in this context.

Additional Information

How to cite this article: Lundell, A-C. et al. IFN type I and II induce BAFF secretion from human decidual stromal cells. Sci. Rep. 7, 39904; doi: 10.1038/srep39904 (2017).

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Supplementary Material

Supplementary Information
srep39904-s1.pdf (889.3KB, pdf)

Acknowledgments

We are deeply grateful to the staff at Mölndal Delivery Unit, Sahlgrenska University Hospital in Gothenburg for collecting placentas and umbilical cord blood samples as well as midwives at the Department of Obstetrics and Gynecology, Karolinska University Hospital in Huddinge for collecting placentas. We thank Nina Dezfoolian for assistance with arrangement of decidual stromal cell cultures at our laboratory. This work was funded by: The Swedish Research Council (Grant K2012-57X-22047-01-6), by the Region Västra Götaland (agreement concerning research and education of doctors; ALF), by The Health and Medical Care Committee of the Regional Executive Board, Region Västra Götaland, by the Torsten and Ragnar Söderberg’s foundation, by the Hedberg foundation, by the Magnus Bergvall foundation and by the IngaBritt and Arne Lundberg’s foundation. H.K. was supported by grants from the Swedish Research Council (K2012-99X-22013-01-3), the Swedish Childhood Cancer Foundation (PR2013-0020), the Cancer Society in Stockholm (141193), the Swedish Cancer Foundation (CAN 2014/793), and Karolinska Institutet.

Footnotes

Author Contributions A-C.L. contributed to the design and performance of experiments, data analysis, designed all figures and wrote the paper. I.N. and K.A. contributed to the design and performance of experiments. C.L. contributed to the design and performance of immunofluorescence experiments. E.T. contributed to the design and performance of immunohistochemistry experiments. S.N. contributed with methods and arrangement of decidual stromal cell cultures at our laboratory. H.K. contributed to design and performance of experiments and with methods and arrangement of decidual stromal cell cultures at our laboratory. A.R. contributed to the design of the experiments and continuously supervised all aspects of the work.

References

  1. Schiemann B. et al. An essential role for BAFF in the normal development of B cells through a BCMA-independent pathway. Science 293, 2111–2114 (2001). [DOI] [PubMed] [Google Scholar]
  2. Gorelik L. et al. Normal B cell homeostasis requires B cell activation factor production by radiation-resistant cells. J Exp Med 198, 937–945 (2003). [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Warnatz K. et al. B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humans. Proc Natl Acad USA 106, 13945–13950 (2009). [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Nardelli B. et al. Synthesis and release of B-lymphocyte stimulator from myeloid cells. Blood 97, 198–204 (2001). [DOI] [PubMed] [Google Scholar]
  5. Scapini P. et al. G-CSF-stimulated neutrophils are a prominent source of functional BLyS. J Exp Med 197, 297–302 (2003). [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Ittah M. et al. B cell-activating factor of the tumor necrosis factor family (BAFF) is expressed under stimulation by interferon in salivary gland epithelial cells in primary Sjogren’s syndrome. Arthritis Res & Ther 8, R51 (2006). [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Woo S. J. et al. Induction of BAFF expression by IFN-gamma via JAK/STAT signaling pathways in human intestinal epithelial cells. J Leuk Biol 93, 363–368 (2013). [DOI] [PubMed] [Google Scholar]
  8. Link A. et al. Fibroblastic reticular cells in lymph nodes regulate the homeostasis of naive T cells. Nature Immunol 8, 1255–1265 (2007). [DOI] [PubMed] [Google Scholar]
  9. Broggi M. A., Schmaler M., Lagarde N. & Rossi S. W. Isolation of murine lymph node stromal cells. J Vis Exp, e51803 (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Link A. et al. Association of T-zone reticular networks and conduits with ectopic lymphoid tissues in mice and humans. Am J Pathol 178, 1662–1675 (2011). [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Schacht V. et al. T1alpha/podoplanin deficiency disrupts normal lymphatic vasculature formation and causes lymphedema. EMBO J 22, 3546–3556 (2003). [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Suzuki-Inoue K. et al. Involvement of the snake toxin receptor CLEC-2, in podoplanin-mediated platelet activation, by cancer cells. J Biol Chem 282, 25993–26001 (2007). [DOI] [PubMed] [Google Scholar]
  13. Acton S. E. et al. Podoplanin-rich stromal networks induce dendritic cell motility via activation of the C-type lectin receptor CLEC-2. Immunity 37, 276–289 (2012). [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Katakai T., Hara T., Sugai M., Gonda H. & Shimizu A. Lymph node fibroblastic reticular cells construct the stromal reticulum via contact with lymphocytes. J Exp Med 200, 783–795 (2004). [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Seys L. J. et al. Role of B Cell-Activating Factor in Chronic Obstructive Pulmonary Disease. Am J Resp Crit Med 192, 706–718 (2015). [DOI] [PubMed] [Google Scholar]
  16. Bajenoff M. et al. Stromal cell networks regulate lymphocyte entry, migration, and territoriality in lymph nodes. Immunity 25, 989–1001 (2006). [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Denton A. E., Roberts E. W., Linterman M. A. & Fearon D. T. Fibroblastic reticular cells of the lymph node are required for retention of resting but not activated CD8+ T cells. Proc Natl Acad Sci USA 111, 12139–12144 (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Astarita J. L. et al. The CLEC-2-podoplanin axis controls the contractility of fibroblastic reticular cells and lymph node microarchitecture. Nature Immunol 16, 75–84 (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Cremasco V. et al. B cell homeostasis and follicle confines are governed by fibroblastic reticular cells. Nature Immunol 15, 973–981 (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Lundell A. C. et al. Higher B-cell activating factor levels at birth are positively associated with maternal dairy farm exposure and negatively related to allergy development. J Allergy Clin Immunol 136, 1074–1082 e1073 (2015). [DOI] [PubMed] [Google Scholar]
  21. Kreuzaler M. et al. Soluble BAFF levels inversely correlate with peripheral B cell numbers and the expression of BAFF receptors. J Immunol 188, 497–503 (2012). [DOI] [PubMed] [Google Scholar]
  22. Bienertova-Vasku J. et al. The presence of B-cell activating factor (BAFF) in umbilical cord blood in both healthy and pre-eclamptic pregnancies and in human breast milk. J Reprod Immunol 109, 89–93 (2015). [DOI] [PubMed] [Google Scholar]
  23. Sindram-Trujillo A., Scherjon S., Kanhai H., Roelen D. & Claas F. Increased T-cell activation in decidua parietalis compared to decidua basalis in uncomplicated human term pregnancy. Am J Reprod Immunol 49, 261–268 (2003). [DOI] [PubMed] [Google Scholar]
  24. Richards R. G., Brar A. K., Frank G. R., Hartman S. M. & Jikihara H. Fibroblast cells from term human decidua closely resemble endometrial stromal cells: induction of prolactin and insulin-like growth factor binding protein-1 expression. Biol Reprod 52, 609–615 (1995). [DOI] [PubMed] [Google Scholar]
  25. Munoz-Fernandez R. et al. Human decidual stromal cells secrete C-X-C motif chemokine 13, express B cell-activating factor and rescue B lymphocytes from apoptosis: distinctive characteristics of follicular dendritic cells. Hum Reprod 27, 2775–2784 (2012). [DOI] [PubMed] [Google Scholar]
  26. Xu Y., Plazyo O., Romero R., Hassan S. S. & Gomez-Lopez N. Isolation of Leukocytes from the Human Maternal-fetal Interface. J Vis Exp, e52863 (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Haller H. et al. An immunohistochemical study of leucocytes in human endometrium, first and third trimester basal decidua. J Reprod Immunol 23, 41–49 (1993). [DOI] [PubMed] [Google Scholar]
  28. Gomez-Lopez N., Vadillo-Perez L., Nessim S., Olson D. M. & Vadillo-Ortega F. Choriodecidua and amnion exhibit selective leukocyte chemotaxis during term human labor. Am J Obstet Gynecol 204, 364 e369–316 (2011). [DOI] [PubMed] [Google Scholar]
  29. Lima J. et al. Characterization of B cells in healthy pregnant women from late pregnancy to post-partum: a prospective observational study. BMC Pregnancy Chilsbirth 16, 139 (2016). [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Karlsson H. et al. Stromal cells from term fetal membrane are highly suppressive in allogeneic settings in vitro. Clin Exp Immunol 167, 543–555 (2012). [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Ringden O. et al. Fetal membrane cells for treatment of steroid-refractory acute graft-versus-host disease. Stem Cells 31, 592–601 (2013). [DOI] [PubMed] [Google Scholar]
  32. Leno-Duran E. et al. Human decidual stromal cells secrete soluble pro-apoptotic factors during decidualization in a cAMP-dependent manner. Hum Reprod 29, 2269–2277 (2014). [DOI] [PubMed] [Google Scholar]
  33. Greaves R. F. et al. Hormone modeling in preterm neonates: establishment of pituitary and steroid hormone reference intervals. J Clin Endocrinol Metab 100, 1097–1103 (2015). [DOI] [PubMed] [Google Scholar]
  34. Dominici M. et al. Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement. Cytotherapy 8, 315–317 (2006). [DOI] [PubMed] [Google Scholar]
  35. Wang Y. et al. D2-40/podoplanin expression in the human placenta. Placenta 32, 27–32 (2011). [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Croxatto D. et al. Stromal cells from human decidua exert a strong inhibitory effect on NK cell function and dendritic cell differentiation. PloS one 9, e89006 (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Liu W. et al. Human placenta-derived adherent cells induce tolerogenic immune responses. Clin Transl Immunol 3, e14 (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Chang J. E. & Turley S. J. Stromal infrastructure of the lymph node and coordination of immunity. Trend Immunol 36, 30–39 (2015). [DOI] [PubMed] [Google Scholar]
  39. Langat D. L., Wheaton D. A., Platt J. S., Sifers T. & Hunt J. S. Signaling pathways for B cell-activating factor (BAFF) and a proliferation-inducing ligand (APRIL) in human placenta. Am J Pathol 172, 1303–1311 (2008). [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Fuchs R. & Ellinger I. Endocytic and transcytotic processes in villous syncytiotrophoblast: role in nutrient transport to the human fetus. Traffic 5, 725–738 (2004). [DOI] [PubMed] [Google Scholar]
  41. Cleal J. K. et al. Facilitated transporters mediate net efflux of amino acids to the fetus across the basal membrane of the placental syncytiotrophoblast. J Physiol 589, 987–997 (2011). [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Simister N. E. Placental transport of immunoglobulin G. Vaccine 21, 3365–3369 (2003). [DOI] [PubMed] [Google Scholar]
  43. Cetin I. et al. Maternal and fetal amino acid concentrations in normal pregnancies and in pregnancies with gestational diabetes mellitus. Am J Obstet Gynecol 192, 610–617 (2005). [DOI] [PubMed] [Google Scholar]
  44. Koopman L. A. et al. Human decidual natural killer cells are a unique NK cell subset with immunomodulatory potential. J Exp Med 198, 1201–1212 (2003). [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Heikkinen J., Mottonen M., Komi J., Alanen A. & Lassila O. Phenotypic characterization of human decidual macrophages. Clin Exp Immunol 131, 498–505 (2003). [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Erlebacher A. Immunology of the maternal-fetal interface. Ann Rev Immunol 31, 387–411 (2013). [DOI] [PubMed] [Google Scholar]
  47. Cuss A. K. et al. Expansion of functionally immature transitional B cells is associated with human-immunodeficient states characterized by impaired humoral immunity. J Immunol 176, 1506–1516 (2006). [DOI] [PubMed] [Google Scholar]
  48. Palanichamy A. et al. Novel human transitional B cell populations revealed by B cell depletion therapy. J Immunol 182, 5982–5993 (2009). [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Rolle L. et al. Cutting edge: IL-10-producing regulatory B cells in early human pregnancy. Am J Reprod Immunol 70, 448–453 (2013). [DOI] [PubMed] [Google Scholar]
  50. Oliver C., Montes M. J., Galindo J. A., Ruiz C. & Olivares E. G. Human decidual stromal cells express alpha-smooth muscle actin and show ultrastructural similarities with myofibroblasts. Hum Reprod 14, 1599–1605 (1999). [DOI] [PubMed] [Google Scholar]
  51. Katakai T. Marginal reticular cells: a stromal subset directly descended from the lymphoid tissue organizer. Front Immunol 3, 200 (2012). [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Kato A., Truong-Tran A. Q., Scott A. L., Matsumoto K. & Schleimer R. P. Airway epithelial cells produce B cell-activating factor of TNF family by an IFN-beta-dependent mechanism. J Immunol 177, 7164–7172 (2006). [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Sjostrand M. et al. The Expression of BAFF Is Controlled by IRF Transcription Factors. J Immunol (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Aagaard K. et al. The placenta harbors a unique microbiome. Sci Trans Med 6, 237ra265 (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Stout M. J. et al. Identification of intracellular bacteria in the basal plate of the human placenta in term and preterm gestations. Am J Obstet Gynecol 208, 226 e221–227 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Ban Y. L., Kong B. H., Qu X., Yang Q. F. & Ma Y. Y. BDCA-1+, BDCA-2+ and BDCA-3+ dendritic cells in early human pregnancy decidua. Clin Exp Immunol 151, 399–406 (2008). [DOI] [PMC free article] [PubMed] [Google Scholar]
  57. Pandya J. M. et al. Circulating T helper and T regulatory subsets in untreated early rheumatoid arthritis and healthy control subjects. J Leuk Biol 100, 823–833 (2016). [DOI] [PubMed] [Google Scholar]
  58. Higgs B. W. et al. Patients with systemic lupus erythematosus, myositis, rheumatoid arthritis and scleroderma share activation of a common type I interferon pathway. Ann Rheum Dis 70, 2029–2036 (2011). [DOI] [PubMed] [Google Scholar]
  59. Kim T. et al. Serum levels of interferons in patients with systemic lupus erythematosus. Clin Exp Immunol 70, 562–569 (1987). [PMC free article] [PubMed] [Google Scholar]
  60. Bengtsson A. A. et al. Activation of type I interferon system in systemic lupus erythematosus correlates with disease activity but not with antiretroviral antibodies. Lupus 9, 664–671 (2000). [DOI] [PubMed] [Google Scholar]
  61. Domeier P. P. et al. IFN-gamma receptor and STAT1 signaling in B cells are central to spontaneous germinal center formation and autoimmunity. J Exp Med 213, 715–732 (2016). [DOI] [PMC free article] [PubMed] [Google Scholar]
  62. Jackson S. W. et al. B cell IFN-gamma receptor signaling promotes autoimmune germinal centers via cell-intrinsic induction of BCL-6. J Exp Med 213, 733–750 (2016). [DOI] [PMC free article] [PubMed] [Google Scholar]
  63. Salazar-Camarena D. C. et al. Association of BAFF, APRIL serum levels, BAFF-R, TACI and BCMA expression on peripheral B-cell subsets with clinical manifestations in systemic lupus erythematosus. Lupus (2015). [DOI] [PubMed] [Google Scholar]
  64. Petri M., Howard D. & Repke J. Frequency of lupus flare in pregnancy. The Hopkins Lupus Pregnancy Center experience. Arthritis Rheum 34, 1538–1545 (1991). [DOI] [PubMed] [Google Scholar]
  65. Ruiz-Irastorza G. et al. Increased rate of lupus flare during pregnancy and the puerperium: a prospective study of 78 pregnancies. Br J Rheum 35, 133–138 (1996). [DOI] [PubMed] [Google Scholar]

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