1. Introduction
Mesenchymal stem cells (MSCs) have been used in animal studies and clinical trials for decades. MSCs have the potential to differentiate into various mesenchymal cell types and exert immunomodulatory effects. Thus, significant achievements have been made in tissue regeneration and immune disorders using MSCs [
1]. MSCs can be isolated from various human tissues including skin, bone marrow, adipose tissue, placenta, and the umbilical cord [
2]. Among these, tonsil-MSCs (T-MSCs) can be acquired without unnecessary invasive procedures, because they are commonly harvested from waste tissue after tonsillectomy. Additionally, their relatively high proliferation rates and low immunogenic properties make them attractive sources of MSCs [
3,
4]. These unique characteristics of T-MSCs can be attributed to their typical isolation from young donors less than 10 years of age, unlike other sources of adult stem cells [
5].
Atopic dermatitis (AD) is the most common chronic inflammatory skin disease, and is characterized by intense itching and recurrent eczematous lesions. The incidence and prevalence of AD vary significantly depending on age, with children having a higher prevalence than adults [
6]. Clinical symptoms of AD also appear differently in adults and children; however, common features include recurrent dry and severe skin itching. The pathogenesis of AD is multifactorial and includes genetic predisposition, epidermal barrier disruption, and immune system involvement [
7]. Various studies have demonstrated that type 2 immune cytokines, including interleukin-4 (IL-4), IL-13, IL-17, IL-22, IL-31, and thymic stromal lymphopoietin, play important roles in the pathogenesis of AD [
8,
9,
10]. Th2 cells induce IgE class switching in B cells, resulting in increased IgE levels frequently observed in patients with AD [
11]. B cells also contribute to antigen-specific Th2 cell activation and expansion during allergic skin inflammation. Therefore, antigen-specific B cells are essential for Th2 cell development [
12]. The treatment of AD focuses on controlling disease progression and alleviating symptoms, because there is currently no cure for or prevention for AD. Thus, the treatment of AD targets underlying skin abnormalities such as xerosis, pruritus, and cutaneous inflammation [
13].
To date, several studies have demonstrated that MSCs derived from various tissues, such as bone marrow and adipose tissue, exert immunomodulatory effects in AD [
14,
15]. However, whether allergic progression in AD can be suppressed by T-MSCs has not yet been clearly defined. Therefore, this study aims to explore the potential immunomodulatory effects of T-MSCs on the pathogenesis of AD in vivo and in vitro.
2. Materials and Methods
2.1. Isolation and Characterization of T-MSCs
T-MSC isolation was approved by the Hallym University Hospital Institutional Review Board, and written informed consent was obtained from healthy donors. T-MSCs were isolated from tonsillar tissue as described previously [
16]. T-MSCs were characterized using the following antibodies: anti-CD31 (BioLegend, San Diego, CA, USA), anti-CD44 (BD Biosciences, San Diego, CA, USA), anti-CD45 (BioLegend), anti-CD105 (BioLegend), anti-CD73 (Biogems, Westlake Village, CA), anti-CD80 (BioLegend), anti-CD86 (BioLegend), anti-HLA class I (BioLegend), anti-HLA-DR (BioLegend), and anti-CD275 (BioLegend). Cell surface antigens were analyzed by flow cytometry (FACSCalibur or FACScanto II; BD Biosciences). Isotype-matched control antibodies were used as controls. The T-MSCs used in this study exhibited the typical phenotype.
2.2. Isolation and Stimulation of B Cells
To investigate whether primed T-MSCs directly regulated the activation of B cells, T-MSCs were treated with 10 ng/mL tumor necrosis factor-α (TNF-α) and 20 ng/mL interferon-γ (IFN-γ) for 24 h. We used tonsillar mononuclear cells (TMCs) containing B cell follicles obtained from pediatric tonsillectomy. Tonsillar tissues were dissected, cut into small tissue pieces, and treated with collagenase type I and DNase I (Sigma-Aldrich, St. Louis, MO, USA) for 30 min at 37 °C. This digested tissue was filtered through a 70 µm cell strainer and subjected to Ficoll-Paque (GE Healthcare, Little Chalfont, UK) density gradient centrifugation, following which TMCs were isolated. For B cell-activating conditions, the isolated TMCs (1 × 106 cells/mL) were co-cultured with T-MSCs or primed T-MSCs (1 × 105 cells/mL) in a 24-well plate and stimulated with 0.5 µg/mL of soluble CD40L (BioLegend), 1 µg/mL of CpG oligodeoxynucleotides (ODN 2006, Invivogen, San Diego, CA, USA), 20 ng/mL of recombinant human IL-2 (BioLegend), and 20 ng/mL of recombinant human IL-4 (BioLegend) for 5 days. For some experiments, B cells were isolated using the MojoSort Human Pan B Cell Isolation Kit (BioLegend), and CD4+ T cells were isolated from TMCs using a negative CD4+ T cell isolation kit (Miltenyi Biotec, Bergisch-Gladbach, Germany). Purified human CD4+ cells were polarized using a human Th2 cell differentiation kit (#CDK002, R&D Systems) at a density of 5.0 × 105 cells/mL. After 3 days, 5.0 × 105 cells/mL of B cells were co-cultured in a 24-well microplate (1 mL/well) at 5% CO2 at 37 °C for 3 d.
2.3. Cell Proliferation Assay
To examine the effect of primed T-MSCs on stimulated B cell proliferation, TMCs were labeled with carboxyfluorescein diacetate succinimidyl estercarboxyfluorescein diacetate succinimidyl ester (CFSE; Invitrogen, Waltham, MA, USA) according to the manufacturer’s instructions. The labeled cells were co-cultured with T-MSCs or primed T-MSCs for 5 d. After co-culture, flow cytometric analysis of cell division by CFSE dilution was conducted to assess B cell proliferation.
2.4. Real-Time PCR (RT-PCR)
To evaluate the mRNA expression of transcription factors related to B cell differentiation, we used CD19+ B cells isolated from TMCs co-cultured with T-MSCs or primed T-MSCs under B cell-activating conditions. CD19+ B cells were obtained using the Mojosort Human B Cell Isolation Kit (BioLegend) according to the manufacturer’s instructions. Also, to confirm the mRNA expression of IL-4 and IL-13 in skin lesions of the atopic dermatitis model, total RNAs were extracted from dorsal skin tissues. Total RNA was isolated using the easy-BLUE reagent (Intron Biotechnology, Seongnam, South Korea) according to the manufacturer’s recommendations. cDNA was synthesized from 2 μg of total RNA using an AccuPower cDNA Synthesis Kit (Bioneer, Daejeon, South Korea). The cDNA was then amplified and quantified using the SYBR Green master mix (Applied Biosystems, Foster City, CA, USA) with the following primers: human β-actin, forward 5′-GTG CTA TCC CTG TAC GCC TC-3′ and reverse 5′-GGC CAT CTC TTG CTCGAAGT-3′; human Blimp-1, forward 5′-TAC ATA CCA AAG GGC ACA CG-3′ and reverse 5′-TGA AGC TCC CCT CTG GAA TA-3′; human XBP-1, forward 5′-CCT GGT TGC TGA AGA GGA GG-3′ and reverse 5′-CCA TGG GGA GAT GTT CTG GAG -3′; human BCL-6, forward 5′- GAG AAG CCC TAT CCC TGT GA-3′ and reverse 5′-TGC ACC TTG GTG TTG GTG AT- 3′, mouse GAPDH, forward 5′-ACC ACA GTC CAT GCC ATC AC-3′ and reverse 5′-TGG ACC ACC CTG TTG CTG TA-3′; mouse IL-4, forward 5′- ACA GGA GAA GGG ACG CCA T′ and reverse 5′- GAA GCC CTA CAG ACG AGC TCA -3′; mouse IL-13, forward 5′- TCT TGC TTG CCT TGG TGG TCT CGC -3′ and reverse 5′- GAT GGC ATT GCA ATT GGA GAT GTT G -3′.
2.5. Western Blotting
To determine the signaling pathways affected by priming with TNF-α and IFN-γ, T-MSCs were pretreated with the signaling pathway inhibitor, AMGEN16 (non-canonical NF-κB pathway, 5 μmol/L; Sigma-Aldrich). After pretreatment with an inhibitor, the cells were incubated with TNF-α and IFN-γ for 24 h and then lysed in RIPA buffer. The lysates were separated using 10% sodium dodecyl sulfate-polyacrylamide gel electrophoresis and were transferred onto polyvinylidene fluoride membranes (Millipore, Billerica, MA, USA). The membranes were blocked with blocking solution and incubated with antibodies against phospho-p65 (#3033, Cell signaling Technology, Danvers, MA, USA), p65 (#8242, Cell signaling) of the canonical NF-κB pathway, and phospho-p100 (#4810, Cell signaling), p52 (#4882, Cell signaling), and RELB (#4922, Cell signaling) of the non-canonical NF-κB pathway (Cell signaling Technology, Danvers, MA, USA), an-ti-CD40 (# ab224639, abcam), and β-actin (#4970, Cell signaling Technology). The blots were visualized using horseradish peroxidase-conjugated secondary antibodies and an enhanced chemiluminescence (ECL) system (Pierce, Rockford, IL, USA).
2.6. Flow Cytometry
B cell activation was analyzed by detecting surface or intracellular markers using flow cytometry. Prior to staining for surface markers, dead cells were excluded by staining with LIVE/DEAD-fixable violet dye (Invitrogen). To examine the phenotype of antibody-secreting cells (ASCs) in B cell activation, the Fc receptors (FcR) were blocked using an FcR blocking reagent (Miltenyi Biotec, Bisley, Surrey, UK) and stained with allophycocyanin (APC) or phycoerythrin (PE) anti-human CD19 antibody (BioLegend), fluorescein isothiocyanate (FITC)-conjugated anti-human CD27 antibody (BioLegend), and APC/Cyanine7anti-human CD38 antibody (Biolegend). To detect IgE production by B cells, the cells were incubated with a fixation/permeabilization solution (eBioscience, San Diego, CA, USA) and stained with PE/Cy7 anti-IgE (BioLegend). After staining, the cells were analyzed using FACSCalibur or FACSCanto Ⅱ (Becton Dickinson, CA, USA), and the data were evaluated using BD FlowJo (BD Bioscience, La Jolla, CA).
2.7. SiRNA Transfection
T-MSCs were transfected with 40 pmol siRNA against human CD40 (sc-29250; Santa Cruz Biotechnology, Santa Cruz, CA, USA) or control siRNA (sc-37007; Santa Cruz Biotechnology) using siRNA transfection reagent (Santa Cruz Biotechnology). Twenty-four hours after transfection, the cells were primed with TNF-α and IFN-γ for 24 h, and the expression level of CD40 was analyzed. Primed T-MSCs with downregulated CD40 expression were co-cultured with TMCs under B cell-activating conditions.
2.8. Immunofluorescence
After the indicated treatments, T-MSCs were fixed with 4% paraformaldehyde (PFA) at room temperature for 10 min, permeabilized by incubation with a 0.05% Triton X-100 solution for 10 min, and blocked with 5% normal goat serum for 1 h. The cells were subsequently stained with specific primary antibodies against anti-CD40 (1:200; Abcam, Cambridge, MA, USA) and anti-RELB (1:100; Cell Signaling Technology, Danvers, MA, USA), followed by 2 h of incubation with Alexa 488 and Alexa 594-labeled secondary antibodies (1:1000; Molecular Probes, Eugene, OR, USA). For counterstaining, the nuclei were stained with DAPI. Images were captured using a confocal microscope (Carl Zeiss, Jena, Germany).
2.9. Mouse Model of AD
To evaluate whether primed T-MSCs affect the development of atopy in vivo, we used a 2,4-dinitrofluorobenzene (DNFB; Sigma-Aldrich, st. louis MO USA)-induced animal model of AD. Female C57BL/6J mice (6-weeks-old, n = 24) were divided into the following four groups (n = 6 per group): untreated mice (control), DNFB-sensitized and PBS-treated mice (DNFB-only group), DNFB-sensitized and T-MSC-treated mice (T-MSC group), and DNFB-sensitized and primed T-MSC-treated mice (primed T-MSC group). The mice received cutaneous administration of 25 μL of 0.15% DNFB in acetone/olive oil (AO) at a ratio of 3:1 into the right ears, and 100 μL 0.15% DNFB in AO was applied to the shaved dorsal skin on days 0 and 4. Sensitized mice were challenged by applying 0.2% DNFB in AO to the dorsal and ear skin on days 7, 9, and 11, and PBS, T-MSCs, or primed T-MSCs (1 × 106 cells) were injected subcutaneously on days 10 and 12. In this study, we used Matrigel® (MA, BD Biosciences, San Jose, CA, USA) as a scaffold for stem cells. Thus, T-MSCs in 20 μL of PBS were mixed with Matrigel® at a ratio of 1:10 to produce a final volume of 200 μL. We also used a PBS control group by combining 20 μL of PBS with 180 μL of Matrigel®. Next, the Matrigel®-embedded T-MSCs was subcutaneously administered to the dorsal skin using a 26-gauge sterile needle syringe. Thereafter, the mice were sacrificed, and the dorsal skin and serum were harvested for further examination. The severity of dermatitis was assessed based on the following symptoms: (1) edema, (2) erythema/hemorrhage, (3) dryness/scarring, (4) pruritus/itching, and (5) excoriation/erosion. Symptom scores were expressed as zero (none), one (mild), two (moderate), or three (severe), and each symptom score was assessed by two independent researchers and summed. To evaluate the histological events in AD mice, the dorsal skin was collected, fixed in 10% neutral formalin for 24 h, and embedded in white paraffin. The block was cut into 5 μm-thick sections, and the sectioned slides were stained with hematoxylin-eosin (H&E) or toluidine blue to analyze epidermis thickness and mast cell infiltration. To examine the localization of T and B cells in the skin, slides were stained with anti-mouse CD3 monoclonal antibody (BioLegend) and anti-mouse B220 monoclonal antibody (BioLegend). In this study, we detected the primary anti-mouse CD3 and B220 monoclonal antibodies with horseradish peroxidase-conjugated (HRP)-linked secondary antibody (goat anti-rabbit IgG, 1:1000, Santa Cruz). Then, HRP activity was detected with 3,3′-diaminobenzidine (DAB, Roche, Basel, Switzerland) substrate. Slides were imaged using microscopy (Carl Zeiss, Jena, Germany), and six different regions were analyzed using Image J software (Version 1.8.0). Moreover, IL-4 and IL-13 mRNA expression were assessed using RT-PCR in skin tissues.
2.10. IgE Detection
On day 24, whole blood samples were collected from the mice by removing the eyeballs after anesthesia. The blood was allowed to clot at 25 °C for 30 min, centrifuged at 1000× g for 10 min at 4 °C, and serum was collected and preserved at −80 °C until use. Serum IgE was detected using a mouse IgE enzyme-linked immunosorbent assay kit (#88-50460-22, Invitrogen) according to the manufacturer’s instructions.
2.11. Cell Viability Assay
To examine the cytotoxicity of NIKi, cell viability was evaluated using the CCK-8 assay. T-MSCs were seeded at a density of 1 × 104 cells per well in 96-well plates and cultured for 24 h. Then, cells were stimulated with various concentrations of NIKi with or without TNF-α and IFN-γ stimulation and incubated for 24 h. After incubation,10 μL of CCK-8 solution (Dojindo Laboratories, Kumamoto, Japan) was treated to each well for 2 h at 37 °C, and cell viability was measured using a microplate reader (Glomax; Promega, Seoul, Korea) at a wavelength of 450 nm.
2.12. Statistical Analysis
All data are presented as the mean ± standard error of the mean. Statistical differences were assessed by Student’s t-test or one-way ANOVA using GraphPad Prism (version 5; Graph Pad Software, San Diego, CA, USA). The statistical values are detailed in the figure legend.
4. Discussion
To our knowledge, this study is the first to investigate the immunomodulatory effects of primed T-MSCs on AD and B cell regulation. In the animal study, we found that primed T-MSCs exhibited greater therapeutic effects than naïve T-MSCs by inhibiting immune cell infiltration, IgE production, and cytokine expression in a mouse model of AD. In the in vitro study, the proportion of B cells producing IgE was significantly reduced when co-cultured with primed T-MSC with highly expressed CD40 than with T-MSCs. Additionally, we demonstrated that primed T-MSCs activated B cells by regulating BLIMP-1, XBP-1, and BCL6 expression in a contact-dependent manner. Moreover, to investigate the function of CD40 as a regulator of B cell activation by primed T-MSCs, we knocked down CD40 using CD40-specific siRNA. We found that the suppression of B cell activation by primed T-MSCs was dependent on CD40 expression and was mediated by the non-canonical NF-κB pathway.
T and B cells play important roles as immunologic factors in the pathogenesis of AD [
17]. Th2 cell activation and related cytokines lead to B cell activation, which elevates the production of allergen-specific IgE, increases skin inflammation, and aggravates skin barrier defects. One study demonstrated that bone marrow-derived MSCs suppressed the Th2 immune response in a mouse model of AD by inhibiting IL-4 and IgE production [
14]. Another study showed that adipose tissue-derived MSCs can alleviate AD in a mouse model of AD through regulating B cell-mediated IgE production [
15]. Umbilical cord blood-derived MSCs also decreased atopic inflammation in an animal model by regulating mast cell function [
18]. Another study showed that T-MSC injection in an AD mouse model reduced skin inflammation, mast cell infiltration, IgE production, and inflammatory cytokines such as IL6 and TNF-α [
19]. Although the sources of MSC isolation were different, our findings are consistent with those of previous studies on the immunomodulatory effects of MSC-based therapies in AD mouse models. In the present study, to explore and compare the therapeutic effects between primed T-MSCs and naïve T-MSCs, we subcutaneously injected primed T-MSCs or naïve T-MSCs in the DNFB-induced AD mouse model. Interestingly, primed T-MSCs suppress atopic inflammation more than naïve T-MSCs through the regulation of mast cell infiltration, Th2 cytokines, and IgE production in the mouse model of AD.
B cells play an essential role in the immune system, and their dysfunction can lead to various chronic inflammatory or autoimmune diseases [
20]. Although the immunosuppressive properties of MSC-based therapies are not fully understood, increasing evidence has revealed changes in B cell function after MSC transplantation. Previous studies have confirmed the inhibitory effects of MSCs on B cell proliferation, maturation, and IgE production, and the effects of MSCs on B cells have also been shown to be attenuated by the addition of a selective COX-2 inhibitor [
14,
21,
22]. Moreover, MSCs may induce regulatory B cells to secrete IL-10, which promotes the immunosuppressive function of B cells [
23,
24]. In our previous study, primed T-MSCs expressing CD40 showed immunomodulatory effects via Th1 and Th2 immune responses [
16]. Consistent with this, in the present study, we found that the proliferation of B cells and the proportion of IgE-producing B cells were significantly suppressed by primed T-MSCs expressing CD40. MSCs may regulate immune responses via cell-to-cell contact; thus, their downstream pathways could be directly involved in B cell production, activation, and differentiation [
25,
26,
27]. In line with this, in this study, we found that primed T-MSCs regulated B cell activation in a cell-to-cell contact-dependent manner.
One of the essential costimulatory molecules in the immune response is the receptor CD40, expressed on various cells such as B cells and antigen-presenting cells [
28]. CD40 binds its ligand CD40L, transiently expressed on T cells and other non-immune cells during inflammatory conditions. CD40/CD40L interactions exert profound effects on various cell types, including B cells, dendritic cells, and endothelial cells. In B cells, CD40 signaling promotes germinal center formation, immunoglobulin (Ig) isotype switching, and memory B cell survival [
29,
30]. A previous study revealed that CD40+ cells in bone marrow-derived MSCs may be a key immune regulatory element in the bone marrow [
31]. Our previous study demonstrated that CD40 may be a key molecule in the immunomodulatory capacity of primed T-MSCs [
16]. Thus, to assess the critical role of CD40 as a regulator of B cell activation in primed T-MSCs, we knocked down CD40 expression in primed T-MSCs using a CD40-specific siRNA. CD40-knockdown primed T-MSCs significantly increased the activation and differentiation of B cells, suggesting that CD40 is a key molecule in primed T-MSCs for B cell regulation. However, the downstream mechanisms of CD40/CD40L in MSCs remain poorly understood. Thus, to examine the downstream mechanisms of CD40/CD40L, we examined the noncanonical and canonical NF-κB pathways in primed T-MSCs. We found that under B cell activation, the non-canonical NF-κB pathway was activated more dramatically than the canonical NF-κB in primed T-MSCs, and that CD40 expression on primed T-MSCs was also regulated by the non-canonical NF-κB pathway. However, our study also has limitations. Our method for the CD40 knockout is impossible to achieve a complete knockout and it induces only knockdown. Thus, this is a partial knockout method. Moreover, to confirm the findings of in vitro experiments, in vivo investigation using CD40 knockout mice should be needed.
In conclusion, our results showed that primed T-MSCs significantly improve the inflammatory status in an AD mouse model, and that this effect was mediated by the modulation of B cell-mediated inflammatory responses. Additionally, our data suggest that the regulatory effect of T-MSCs is dependent on CD40 expressed on primed T-MSCs through the non-canonical NF-κB pathway. Nevertheless, MSC-based therapies still face important challenges, including the type of stem cells used, the number of transplanted cells, pretreatment of cell products, relevant treatment targets, routes, and frequency of administration. Thus, additional research regarding these issues is necessary for our findings to be applied in practical clinical treatment.