MicroRNA-21-5p protects melanocytes via targeting STAT3 and modulating Treg/Teff balance to alleviate vitiligo

Abstract

Vitiligo (VIT) is caused by loss and degradation of functional epidermal melanocytes. Studies have indicated that melanocyte destruction may be associated with an imbalance between regulatory T cells (Treg cells) and effector T cells (Teff cells). The current study aimed to investigate the molecular mechanism through which Treg/Teff balance affects VIT pathogenesis. To explore this, peripheral blood mononuclear cells were isolated from patients with VIT and healthy individuals. The present study revealed that the proportions of CD4⁺ T cells, Treg cells and T helper 1 (Th1) cells were decreased in patients with VIT, but those of Teff cells (Th17 and Th22 cells) were increased; additionally, Foxp3 expression was decreased, but the expression levels of interferon-γ, interleukin (IL)-17A and IL-22 were increased. Furthermore, in patients with VIT, microRNA (miR)-21-5p expression was decreased, while that of STAT3 was increased. Further in vitro experiments in CD4⁺ T cells revealed that STAT3 was targeted by miR-21-5p. Functional analysis further indicated that miR-21-5p overexpression in Th17-polarized CD4⁺ T cells decreased the proportion of Teff cells and associated cytokines, such as IL-17A and IL-22, but increased the proportion of Treg cells and Foxp3. However, the effects of miR-21-5p overexpression were partly reversed by STAT3 overexpression. Increased apoptosis of melanocytes was detected after co-culture with Th17-polarized CD4⁺ T cells in the presence of a miR-21-5p mimic. However, this indirect effect of the miR-21-5p mimic on melanocytes was decreased via STAT3 overexpression. Therefore, miR-21-5p may protect melanocytes via targeting STAT3 and regulating Treg/Teff balance. The current findings may provide a possible treatment method for managing VIT.

Introduction

Vitiligo (leukoderma, VIT) is characterized by pigment loss in skin patches and is defined as a long-term skin condition in which patches of affected skin turn white with obvious color margins (1). The disease incidence was 0.5–2% worldwide in 2017, independently of sex or ethnicity factors (2). There is increasing evidence that loss and degradation of functional epidermal melanocytes may cause the onset of VIT (2,3). It has been speculated that autoimmunity, cytotoxic metabolites and oxidative stress induction may be the factors causing VIT development and progression (4), and therefore, may explain the molecular mechanisms underlying the degradation of melanocytes. However, the pathogenesis of VIT requires further investigation.

Melanocytes are melanin-producing neural crest-derived cells (5). Recent studies have demonstrated that VIT is an autoimmune disease that targets melanocytes and that melanin loss is the main cause of morbidity, regardless of ethnicity (6). Therefore, protecting melanocytes from being targeted may have potential for slowing down the development and progression of VIT (7).

Melanocytes may be targeted or destroyed by T-cell-mediated immune responses initiated by autoimmune diseases (8). Effector T cells (Teff cells), mainly T helper 1 (Th1) and Th17 cells, are pro-inflammatory T cells that may induce the development and progression of autoimmune processes, while regulatory T cells (Treg cells) serve protective and anti-inflammatory roles (9) and are downregulated in autoimmune diseases (10). In multiple diseases, including skin diseases, an imbalance between Treg and Teff cells is detected, as Treg cells are decreased and Teff cells are increased (11). Additionally, a study has demonstrated that microRNAs (miRNAs/miRs) serve key roles in regulating the balance between Treg and Teff cells (12). However, the detailed molecular mechanisms remain unclear.

At present, miRNAs have been reported to have critical functions in the development and progression of VIT (13,14). Overexpression of pre-miR-21 has been demonstrated to regulate Treg/Teff balance following gastric cancer resection (15). Another study revealed that low miR-21-5p expression was associated with an imbalance of Treg/Teff cells in patients with rheumatoid arthritis (16). Therefore, the present study hypothesized that miR-21-5p (also known as miR-21) may be a crucial regulator during the differentiation of Treg/Teff cells, which is rarely reported in VIT. Additionally, the mechanism through which miR-21-5p participates in VIT affecting the differentiation of Treg/Teff cells remains unclear. A study on the analysis of the miRNA signature in Treg cells indicated that miR-21 is highly expressed in Treg cells and positively regulates FOXP3 expression (17), which is considered to be a main regulator of Treg development. It is well known that the transcription of miR-21 can be activated by STAT3 signaling (18). However, in the present study, TargetScan 7.2 (targetscan.org) predicted that STAT3 may be a potential target of miR-21-5p.

Therefore, the present study aimed to investigate the role of miR-21-5p and its underlying mechanism associated with STAT3 in Treg/Teff balance, and its potentially indirect effect on melanocytes, hoping to find a potential therapeutic treatment for VIT.

Materials and methods

Ethics statement

The present study was approved by the Ethics Committee of Dezhou People's Hospital (approval no. PFK20181006; Dezhou, China). All participants provided written informed consent.

Isolation of peripheral blood mononuclear cells (PBMCs)

PBMCs were isolated using Ficoll-Hypaque-based density gradient centrifugation (19). Peripheral blood samples were obtained from 15 patients with VIT and 15 healthy individuals and stored at 4°C to minimize cell activation. Whole blood samples were mixed with PBS (Biologos, LLC) and manually layered over a lymphocyte separation medium (Thomas Scientific), and centrifuged at 2,000 × g for 30 min at room temperature. The layer containing PBMCs was carefully harvested and then washed twice with PBS. The cells were resuspended in PBS and were counted manually using a Neubauer chamber (Ningbo Finer Medical Instruments Co., Ltd.) and light microscope (magnification, ×100).

Flow cytometry

For analysis of lymphocyte subsets, PBMCs (1×10⁶ cells/well) obtained from patients with VIT or healthy individuals were suspended in RPMI-1640 medium supplemented with 10% FBS (Invitrogen; Thermo Fisher Scientific, Inc.), 25 ng/ml phorbol myristate acetate, 1 µg/ml ionomycin and 1 µg/ml brefeldin A at 37°C with 5% CO₂ for 5 h. All data were analyzed by FlowJo software (version 7.6.1; FlowJo LLC).

Subsequently, cells were incubated and stained with the following PE-Cyanine5-conjugated monoclonal antibodies (mAbs): Anti-CD4 (RPA-T4; 1:40; cat. no. 15-0049-42), anti-CD8 (3B5; 1:500; cat. no. MHCD0818), anti-CD25 (PC61.5; 1:100; cat. no. 61-0251-82), anti-CD127 (A7R34; 1:700; cat. no. 15-1271-82), anti-interferon (IFN)-γ (R4-6A2; Biotin; 1:400; cat. no. 36-7312-85), anti-interleukin (IL)-17 (50104; 1:100; cat. no. MA5-23748) and anti-IL-22 (22URTI; 1:500; cat. no. 12-7229-41) at 4°C for 10 min; all antibodies were purchased from Thermo Fisher Scientific, Inc., and the experiments were performed according to the manufacturer's protocol. The lymphocyte subsets were then analyzed by flow cytometry. Differences in the proportions of Teff cells (Th1, ^CD4+CD8−IFN-γ⁺/CD4⁺; Th17, CD4⁺CD8⁻IL-17⁺/CD4⁺; Th22, CD4⁺CD8⁻IL-22⁺/CD4⁺) and Treg cells (CD4⁺CD25⁺CD127⁻/CD4⁺) in patients with VIT and in healthy controls were detected and measured using a CytoFLEX Flow Cytometry assay (B96622; Beckman Coulter, Inc.).

Cell apoptosis was detected using an Annexin V-fluorescein isothiocyanate/propidium iodide (PI) apoptosis kit (cat. no. K101; BioVision, Inc.) according to the manufacturer's protocol. Briefly, the cells were harvested 48 h after transfection, washed twice with cold PBS and treated with Annexin V and PI together for 15 min at room temperature in the dark. Cell apoptosis was detected using a flow cytometry assay (APO006; FLISP Serine Protease Detection kit; Bio-Rad Laboratories, Inc.). The Annexin V⁺ PI⁺ cells were considered to be the apoptotic cells. The apoptosis rate was assessed according to the proportion of Annexin V⁺ PI⁺ cells.

Enzyme-linked immunosorbent assay (ELISA)

ELISA was performed to measure the protein expression levels of cellular cytokines (IFN-γ, IL-17A and IL-22) in the peripheral blood of patients with VIT and of healthy individuals, or from CD4⁺T cells or melanocyte supernatant. The PBMCs and supernatant were separated by centrifugation at 2,000 × g for 15 min at 4°C and stored in aliquots at 80°C. The expression levels of inflammatory factors (IFN-γ, IL-17A and IL-22) in CD4⁺T cells or melanocyte supernatant were determined using their corresponding ELISA kits (cat. nos. KHC4021 for IFN-γ, BMS2017 for IL-17A and BMS2047 for IL-22; Invitrogen; Thermo Fisher Scientific, Inc.). OD values were detected and measured using a Crocodile 4-in-one assay miniWorkstation (Titertek-Berthold).

RNA isolation and reverse transcription-quantitative (RT-q)PCR

Total RNA was extracted from PBMCs from patients with VIT or healthy controls using TRIzol^® reagent (Invitrogen; Thermo Fisher Scientific, Inc.) and preserved at 4 or −80°C. The RNA preserved at 4°C was used for cDNA, while the RNA kept at −80°C was for long-term storage. The concentration of total RNA was detected using a biological spectrometer (NanoDrop 2000; Thermo Fisher Scientific, Inc.). A total of 1 µg of total RNA was reverse transcribed into cDNA at 37°C for 60 min and 4°C for 5 min using a First-strand cDNA Synthesis kit (cat. no. E6300L; New England BioLabs, Inc.) according to the manufacturer's protocol. RT-qPCR was conducted using the SYBR PremixEx Taq II kit (cat. no. RR820L; Takara Bio, Inc.) in an AriaMx real-time PCR system (cat. no. G8830A; Agilent Technologies, Inc.). Samples were run using the following thermocycling parameters: Initial denaturation at 95°C for 15 min, 94°C for 15 sec, followed by 40 cycles of 60°C for 30 sec and final extension at 72°C for 30 sec. Primer sequences are shown in Table I. GAPDH (for STAT3) and U6 (for miR-21-5p) were used as internal references. The relative expression levels of genes were quantified using the 2^−ΔΔCq method (20).

Table I.

Primers used for reverse transcription-quantitative PCR.

Gene	Primers (5′→3′)
Foxp3
Forward	GAGAAGCTGAGTGCCATGC
Reverse	AGCCCTTGTCGGATGATG
MicroRNA-21-5p
Forward	TGTTGAGTCGTATCCAGTGCAA
Reverse	GTATCCAGTGCGTGTCGTGG
STAT3
Forward	GAGGACTGAGCATCGAGCA
Reverse	CATGTGATCTGACACCCTGAA
U6
Forward	GAGAAAGTTAGCACGGCTTCTG
Reverse	CAAAATATGGAATGCTTCAAAGAG
GAPDH
Forward	GATCAACACGTACCAGTGCAA
Reverse	CGCCTGTACACTCCACCAC

Western blot analysis

Western blot analysis was performed to measure the protein levels of relative mRNAs in PBMCs from patients with VIT or healthy controls as previously described (21). Proteins were lysed and extracted using RIPA buffer (P0013C; Beyotime Institute of Biotechnology) shortly after cell collection, and protein concentration was measured using a BCA protein kit (Sigma-Aldrich; Merck KGaA). A total of 30 µg protein/lane was separated via 12% SDS-PAGE (cat. no. P0012A; Beyotime Institute of Biotechnology) and transferred onto polyvinylidene fluoride membranes (cat. no. FFP28; Beyotime Institute of Biotechnology), which were then blocked using 5% skimmed milk for 2 h at room temperature. The membranes were incubated at 4°C overnight with the following primary antibodies: Anti-STAT3 antibody (mouse; 1:5,000; cat. no. ab119352; Abcam) and anti-GAPDH antibody (rabbit; 1:10,000; cat. no. ab181602; Abcam). GAPDH was used as the internal reference. The membranes were subsequently incubated at room temperature for 1 h with secondary horseradish peroxidase-conjugated antibodies: goat anti-mouse IgG H&L (1:2,000; cat. no. ab205719; Abcam) and goat anti-rabbit IgG H&L (1:2,000; cat. no. ab205718; Abcam). The membranes were washed three times with TBST (0.1% Tween-20) and developed using an enhanced chemiluminescence kit (EMD Millipore). The grey values of the strips were quantified by ImageJ (version 5.0; National Institutes of Health).

Th17 cell polarization

PBMCs were isolated from patients with VIT using Ficoll-Hypaque-based density gradient centrifugation. CD4⁺ T cells used in the experiments were purified using CD4 microbeads (cat. no. 130-045-101; Miltenyi Biotec, Inc.) for PBMCs in peripheral blood with 95% purity. To induce Th17 cell polarization, CD4⁺ T cells were cultured with 5 µg/ml anti-CD3 mAb (cat. no. 17-0038-42; Thermo Fisher Scientific, Inc.) in 24-well culture plates, and anti-CD28 mAb (cat. no. CD2804; Thermo Fisher Scientific, Inc.) at a final concentration of 2 µg/µl and incubated in RPMI-1640 medium (Thermo Fisher Scientific, Inc.) at 4°C for 30 min 5% CO₂. Cell were treated with 5 ng/ml tumor growth factor (TGF)-β, 20 ng/ml IL-6 and 25 ng/ml IL-23 to induce the polarization of Th17 cells at 4°C for 30 min.

Target prediction and Dual-Luciferase reporter assay

Target gene and potential binding sites of miR-21-5p and STAT3 were predicted using TargetScan 7.2 (targetscan.org), and subsequently confirmed via Dual-Luciferase reporter assay.

A PMIR-REPORT Luciferase vector (cat. no. AM5795; Thermo Fisher Scientific, Inc.) containing wild-type (WT) or mutated (MUT) STAT3 sequences was cloned into the pMirGLO reporter vector (Promega Corporation) to generate STAT3-WT and STAT3-MUT, respectively. CD4⁺ T cells (5×10³ cells/well) from 1 normal control were cultured in 96-well plates and co-transfected with STAT3-WT (sequence, 5′-ACUCUUCAGUACAUAAUAAGCUU-3′) or STAT3-MUT (sequence, 5′-ACUCUUCAGUACAUAGGCCAUGU-3′), and a miR-21-5p mimic or a mimic control using Lipofectamine^® 3000 (Thermo Fisher Scientific, Inc.) according to the manufacturer's protocol at 37°C. The Renilla luciferase gene of the pMirGLO reporter vector served as an internal control. Cells were harvested 48 h after transfection for the detection of luciferase activity using a dual-luciferase reporter assay (cat. no. E1910; Promega Corporation) according to the manufacturer's protocol. Firefly luciferase activity was normalized to Renilla luciferase activity.

Cell co-culture and transfection

For cell co-culture, Th17-polarized CD4⁺ T cells obtained from patient with VIT were cultured in the upper chamber, whereas primary melanocytes were cultured in the lower chamber. Cells were cultured in 0.4 µM Transwell inserts for 24-well plates (Greiner Bio-One International GmbH) at 37°C in a 5% CO₂ atmosphere. The culture medium for both chambers was Ham's F12 nutrient mixture (Thermo Fisher Scientific, Inc.).

For cell transfection, Th17-polarized CD4⁺ T cells were cultured at a density of 5×10⁵ cells/well in a 96-well plate for 24 h at room temperature in 5% CO₂ atmosphere. miR-21-5p mimic (sequence, 5′-UAGCUUAUCAGACUGAUGUUGA-3′) and the miR-21-5p inhibitor (sequence, 5′-UCAACAUCAGUCUGAUAAGCUA-3′) were purchased from Sigma-Aldrich (Merck KGaA). STAT3 was overexpressed using a pcDNA3.1 plasmid (Thermo Fisher Scientific, Inc.). The medium in the 96-well plates was replaced after 24 h, and the cells were transfected with 100 ng miR-21-5p mimic or miR-21-5p inhibitor, and STAT3 using Lipofectamine^® 3000 (Thermo Fisher Scientific, Inc.), according to the manufacturer's protocol. The cells were harvested 48 h after transfection and used for subsequent experiments.

Primary melanocytes were isolated from the skin of the 15 patients with VIT by suction blistering (4) and subsequently cultured in the lower chamber containing Hu 16 medium, which was supplemented with 50 µg/ml gentamicin, 20 ng/ml fibroblast growth factor (Sigma-Aldrich; Merck KGaA), 20 µg/ml isobutylmethylxanthine (Sigma-Aldrich; Merck KGaA) and 10 ng/ml cholera toxin (Sigma-Aldrich; Merck KGaA), at 37°C with 5% CO₂ for 4 h. The cell density in the culture flasks was 5×10⁵ cells/ml.

Subsequently, Th17-polarized CD4⁺ T cells (in the upper chamber) and primary melanocytes (in the lower chamber) were co-cultured in a 6-well plate at a density of 1×10⁵ cells/well for 72 h at 37°C. The cells were harvested for subsequent experiments to detect the survival of primary melanocytes after various treatments.

Tyrosinase activity detection

Levodopa (L-DOPA) solution (cat. no. 333786; Sigma-Aldrich; Merck KGaA) was used for the detection of tyrosinase activity. Briefly, after co-culturing Th17-polarized CD4⁺ T cells obtained from patients with VIT for 72 h, melanocytes were washed once with PBS. Subsequently, cells were pretreated with 90 µl 1% Triton X-100 solution at −80°C for 30 min and allowed to thaw at room temperature. A total of 0.1% L-DOPA solution (100 µl/well) was then added into cells at 37°C for 2 h. OD values at 490 nm were measured and recorded using a microplate reader (model 680; Bio-Rad Laboratories, Inc.). The tyrosinase activity in each group relative to the control group was calculated as follows: Relative tyrosinase activity=(OD values_sample-OD values_{control group})/OD values_{control group} ×100.

Detection of melanin

For melanin detection of melanocytes obtained from the skin of patients with VIT, the supernatant was discarded and the cells were washed once with PBS, and treated with 500 µl 1 mol/l NaOH diluted into DMSO in a water bath at 70°C for 2 h to dissolve melanin. Subsequently, lysates in the 6-well plate were transferred to a 96-well plate (100 µl for each plate). OD values at 405 nm were measured and recorded using a microplate reader (model 680; Bio-Rad Laboratories, Inc.).

Statistical analysis

The data are expressed as the mean ± SD (n≥3). Statistical analysis was performed using SPSS 20.0 software (IBM Corp.). Statistical significance was analyzed using unpaired Student's t-test to compare control and VIT groups or one-way ANOVA followed by Dunnett's post hoc test for other experiments. P<0.05 was considered to indicate a statistically significant difference.

Results

Proportion of Treg cells is decreased, but that of Teff cells is increased in CD4⁺ T cells of patients with VIT

Treg/Teff cell imbalance has been identified in multiple diseases, including skin diseases (11). Therefore, Treg and Teff subset populations in CD4⁺ T cells from patients with VIT and from normal healthy controls were measured. The proportions of Th17 cells (CD4⁺CD8⁻IL-17⁺) and Th22 cells (CD4⁺CD8⁻IL-22⁺) in CD4⁺ T cells from patients with VIT were significantly increased compared with those from normal individuals (P<0.001; Fig. 1B and C). a significant difference is shown in Fig. 1A and 1D, indicating that Th1 (CD4⁺CD8⁻IFN-γ⁺) and Treg cells (CD4⁺CD25⁺CD127⁻) in patients with VIT were significantly decreased compared with controls (P<0.01; Fig. 1A, P<0.001; Fig. 1D). Therefore, the proportion of Treg cells was decreased, while that of Teff cells was increased in CD4⁺ T cells of patients with VIT.

Figure 1.

Imbalance of T effector/Treg cells and dysregulation of miR-21-5p in patients with VIT. Percentages of (A) Th1, (B) Th17, (C) Th22 and (D) Treg cells in CD4⁺ T cells of peripheral blood mononuclear cells in patients with VIT and healthy controls (n=15 for each group) were measured via flow cytometry. Protein levels of (E) IFN-γ, (F) IL-17A and (G) IL-22 in the peripheral blood of patients with VIT and healthy controls were measured via enzyme-linked immunosorbent assay. Relative expression levels of (H) Foxp3 and (I) miR-21-5p in the peripheral blood of patients with VIT and healthy controls were measured via reverse transcription-quantitative PCR. GAPDH and U6 were used as the internal controls, respectively. **P<0.01; ***P<0.001. VIT, vitiligo; Th, T helper; IFN, interferon; IL, interleukin; miR, microRNA; Treg cells, regulatory T cells.

Expression levels of the Teff cell cytokines IFN-γ, IL-17A and IL-22 are increased, while those of the Treg cell cellular marker Foxp3 is decreased in patients with VIT

To further explore why Treg cells were decreased but Teff cells were increased in CD4⁺ T cells of patients with VIT, the expression levels of the Teff cell cytokines IFN-γ, IL-17A and IL-22, and those of the Treg cell marker Foxp3 were determined using ELISA and RT-qPCR, respectively. The present results indicated that the expression levels of the Teff cytokines IFN-γ, IL-17A and IL-22 were increased, while Foxp3 expression was decreased in PBMCs of patients with VIT compared with in those of normal healthy controls (P<0.001; Fig. 1E-H).

STAT3 is a target of miR-21-5p, and miR-21-5p expression is downregulated while STAT3 expression is increased in patients with VIT

In order to investigate the role of miR-21-5p in patients with VIT, miR-21-5p expression in PBMCs of patients with VIT and normal healthy controls was detected by RT-qPCR. The results revealed that miR-21-5p expression was significantly decreased in patients with VIT compared with in normal healthy controls (P<0.001; Fig. 1I).

TargetScan successfully predicted that the target gene of miR-21-5p was STAT3, and its conserved binding sites are shown in Fig. 2A. To further confirm that miR-21-5p could bind to STAT3, a Dual-Luciferase reporter vector containing the STAT3 3′-UTR was built. The Dual-Luciferase reporter assay demonstrated that the relative luciferase activity of the STAT3-WT-mimic (STAT3-WT-M) group was significantly decreased compared with that of the STAT3-WT-mimic control (STAT3-WT-MC) group (P<0.001), while that of the STAT3-MUT-M group was not affected compared with that of the STAT3-MUT-MC group (Fig. 2B), indicating that STAT3 was the target gene of miR-21-5p.

Figure 2.

STAT3 is a target of miR-21-5p. (A) Binding sites of the WT and MUT STAT3 sequences to miR-21-5p were predicted using TargetScan. (B) Dual-Luciferase reporter assay confirmed that STAT3 was a target gene of miR-21-5p. ***P<0.001 vs. MC. (C) Relative STAT3 protein expression in the control and VIT groups was detected via western blot analysis. GAPDH was used as the internal control. (D) Relative STAT3 mRNA expression in the control and VIT groups was detected via reverse transcription-quantitative PCR. GAPDH was used as the internal control. ***P<0.001 vs. control. miR, microRNA; M, miR-21-5p mimic; MC, mimic control; WT, wild-type; MUT, mutant; VIT, vitiligo.

To determine the role of STAT3 in VIT, the protein and mRNA levels of STAT3 were detected by western blot analysis and RT-qPCR, respectively. As shown in Fig. 2C and D, the relative protein and mRNA levels of STAT3 in patients with VIT were significantly increased compared with in the control group (P<0.001).

miR-21-5p mimic increases miR-21-5p expression but inhibits STAT3 expression

The association between miR-21-5p and STAT3 in patients with VIT was studied via transfections using a miR-21-5p mimic and STAT3 overexpression plasmids into CD4⁺ T cells. The present results revealed that after miR-21-5p mimic transfection (M+NC), miR-21-5p expression was significantly increased compared with the MC+negative control (MC+NC) group (P<0.001; Fig. 3A), while mRNA and protein levels of STAT3 were significantly decreased (P<0.001; Fig. 3B and C). STAT3 overexpression did not affect miR-21-5p expression levels, whereas miR-21-5p mimic significantly decreased STAT3 expression levels (Fig. 3A-C). In addition, mRNA and protein levels of STAT3 in CD4⁺ T cells of patients with VIT were significantly increased after STAT3 overexpression (MC+STAT3; P<0.05 vs. MC+NC; Fig. 3B and C); however, these were reversed by concomitant miR-21-5p overexpression (M+STAT3; P<0.01 vs. MC+STAT3; P<0.001 vs. M+NC; Fig. 3B and C).

Figure 3.

miR-21-5p mimic inhibits STAT3 expression in T helper 17-polarized CD4⁺ T cells of patients with vitiligo. (A) Relative expression levels of (A) miR-21-5p and (B) STAT3 of the control, MC+NC, M+NC, MC+STAT3 and M+STAT3 groups were measured via reverse transcription-quantitative PCR. U6 and GAPDH were used as internal controls, respectively. *P<0.05 and ***P<0.001 vs. MC+NC; ^{^^}P<0.01 and ^{^^^}P<0.001 vs. MC+STAT3; ^###P<0.001 vs. M+NC. (C) Relative STAT3 protein expression of the control, MC+NC, M+NC, MC+STAT3 and M+STAT3 groups were measured via western blot analysis. GAPDH was used as the internal control. *P<0.05 vs. MC+NC; ***P<0.001 vs. MC+NC; ^###P<0.001 vs. M+NC; ^{^^}P<0.01 vs. MC+STAT3. miR, microRNA; M, miR-21-5p mimic; MC, mimic control; NC, negative control.

miR-21-5p overexpression increases the proportion of Treg cells but decreases that of Teff cells by reversing the effects of STAT3

To explore the effects of miR-21-5p and STAT3 on the proportion of Treg/Teff cells in patients with VIT, miR-21-5p was overexpressed in the Th17-polarized CD4⁺ T cells, and the proportion of Treg and Teff (Th17 and Th22 cells) cell subsets in CD4⁺ T cells was measured. Flow cytometry assays demonstrated that after miR-21-5p overexpression, the proportion of Teff cells (Th17 and Th22 cells) in CD4⁺ T cells was decreased, but that of Treg cells was increased compared with the MC+NC group (P<0.01; Fig. 4A-C). STAT3 overexpression resulted in the opposite results, with increased Teff cells and decreased Treg cells (P<0.01); however, this was partially reversed by miR-21-5p overexpression (P<0.01 vs. MC+STAT3 and vs. M+NC; Fig. 4A-C).

Figure 4.

miR-21-5p overexpression regulates T effector/Treg cell balance via STAT3. Percentages of (A) Th17, (B) Th22 and (C) Treg cells in CD4⁺ T cells of the control, MC+NC, M+NC, MC+STAT3 and M+STAT3 groups were measured via flow cytometry. Protein levels of (D) IL-17A and (E) IL-22 of T cells in the control, MC+NC, M+NC, MC+STAT3 and M+STAT3 groups were measured via enzyme-linked immunosorbent assay. (F) Relative Foxp3 expression in the control, MC+NC, M+NC, MC+STAT3 and M+STAT3 groups were measured via reverse transcription-quantitative PCR. GAPDH was used as the internal control. *P<0.05, **P<0.01 and ***P<0.001 vs. MC+NC; ^{^}P<0.05 and ^{^^}P<0.01 vs. MC+STAT3; ^##P<0.01 and ^###P<0.001 vs. M+NC. Th, T helper; IL, interleukin; miR, microRNA; Treg cells, regulatory T cells; M, miR-21-5p mimic; MC, mimic control; NC, negative control.

miR-21-5p overexpression decreases the expression levels of IL-17A and IL-22 cytokines in Teff cells but increases Foxp3 expression in Treg cells by reversing the effects of STAT3

Subsequently, expression levels of the Teff cell cytokines IL-17A and IL-22, and those of the Treg cell marker Foxp3 in CD4⁺ T cells of patients with VIT and normal healthy controls were detected via ELISA and RT-qPCR, respectively. The present results revealed that IL-17A and IL-22 expression levels were decreased, while Foxp3 expression was significantly increased after miR-21-5p overexpression compared with the MC+NC group (P<0.01 and P<0.001; Fig. 4D-F). However, after STAT3 overexpression, IL-17A and IL-22 expression levels were increased compared with the MC+NC group (P<0.05; Fig. 4D-E). Furthermore, miR-21-5p overexpression reversed the effects of STAT3 overexpression on the expression levels of Teff cell cytokines and the Treg cell marker (P<0.01 vs. MC+STAT3; P<0.01 and P<0.001 vs. M+NC; Fig. 4D-F).

miR-21-5p/STAT3 axis in Th17-polarized CD4⁺ T cells regulates the apoptosis of melanocytes

In order to further determine the effects of the miR-21-5p/STAT3 axis on Th17-polarized CD4⁺ T cells in melanocytes protection, the apoptosis of melanocytes after co-culture with pretreated CD4⁺ T cells was examined via flow cytometry. It was observed that the apoptosis of melanocytes was decreased by miR-21-5p overexpression in Th17-polarized CD4⁺ T cells (P<0.001 vs. MC+NC), but increased after STAT3 overexpression (P<0.05 vs. MC+NC), suggesting that STAT3 overexpression in CD4⁺ T cells could induce apoptosis of melanocytes (Fig. 5A). In addition, miR-21-5p overexpression in Th17-polarized CD4⁺ T cells reversed the effects of STAT3 overexpression on the apoptosis of melanocytes (P<0.01 vs. MC+STAT3; P<0.001 vs. M+NC; Fig. 5A).

Figure 5.

miR-21-5p overexpression may protect melanocytes via regulating T effector/regulatory T cell balance through STAT3. (A) Apoptosis rates of melanocytes in the control, MC+NC, M+NC, MC+STAT3 and M+STAT3 groups were measured via flow cytometry. Protein levels of (B) IL-17A and (C) IL-22 in the lower chamber of Transwell inserts after co-culture of melanocytes and Th17-polarized CD4⁺ T cells in the control, MC+NC, M+NC, MC+STAT3 and M+STAT3 groups was measured via enzyme-linked immunosorbent assay. (D) Tyrosinase activity and (E) relative melanin content in melanocytes in the control, MC+NC, M+NC, MC+STAT3 and M+STAT3 groups were measured using a microplate reader. *P<0.05, **P<0.01 and ***P<0.001 vs. MC+NC; ^{^}P<0.05 and ^{^^}P<0.01 vs. MC+STAT3; ^##P<0.01 and ^###P<0.001 vs. M+NC. Th, T helper; IL, interleukin; miR, microRNA; M, miR-21-5p mimic; MC, mimic control; NC, negative control.

miR-21-5p/STAT3 axis in Th17-polarized CD4⁺ T cells regulates the release of IL-17A and IL-22 cytokines

After co-culture of CD4⁺ T cells and melanocytes, the levels of released cytokines (IL-17A and IL-22) were measured via ELISA, and it was observed that after miR-21-5p overexpression in Th17-polarized CD4⁺ T cells, the expression levels of IL-17A and IL-22 in the lower chamber were decreased compared with the MC+NC group (P<0.001 and P<0.01; Fig. 5B and C, respectively); however, these were reversed by STAT3 overexpression (P<0.05 and P<0.01; Fig. 5B and C, respectively). miR-21-5p overexpression in Th17-polarized CD4⁺ T reversed the effects of STAT3 overexpression on the release of IL-17A and IL-22 (P<0.01 vs. MC+STAT3; P<0.001 and P<0.01 vs. M+NC; Fig. 5B and C, respectively).

miR-21-5p/STAT3 axis in CD4⁺ T cells regulates tyrosinase activity and melanin synthesis

The effects of the miR-21-5p/STAT3 axis in CD4⁺ T cells on tyrosinase activity and melanin synthesis of melanocytes were explored. Tyrosinase activity and melanin content in melanocytes were detected using a microplate reader. As shown in Fig. 5D and E, tyrosinase activity and melanin content of melanocytes were increased after miR-21-5p overexpression in Th17-polarized CD4⁺ T (P<0.01 vs. MC+NC), but STAT3 overexpression in Th17-polarized CD4⁺ T resulted in opposite results, with both tyrosinase activity and melanin synthesis being decreased compared with the MC+NC group (P<0.01) (Fig. 5D and E). Furthermore, miR-21-5p overexpression in Th17-polarized CD4⁺ T cells reversed the effects of STAT3 overexpression on tyrosinase activity and melanin content of melanocytes (P<0.05 vs. MC+STAT3; P<0.01 vs. M+NC; Fig. 5D and E). Finally, a potential mechanism has been constructed (Fig. 6), which indicated that miR-21-5p protected melanocytes via targeting STAT3 and modulating the Treg/Teff balance to alleviate VIT.

Figure 6.

Potential mechanism of the interaction between miR-21-5p and STAT3 in vitiligo. Low miR-21-5p expression may induce the differentiation of CD4⁺ T cells towards Teff cells, causing a pro-inflammatory response and thereby increasing apoptosis in melanocytes. However, miR-21-5p mimic treatment promoted the balance of Treg/Teff cells and thereby had a benefit on the survival of melanocytes. Th, T helper; IFN, interferon; IL, interleukin; miR, microRNA; Treg/Teff cells, regulatory T/effector T cells.

Discussion

The balance between Treg and Teff cells has been the focus of the pathological examination of numerous autoimmune disorders, such as uveitis, scleroderma and rheumatoid arthritis (9,10,22). Treg cells, which are a subset of T cells, serve a vital role in peripheral immune tolerance maintenance (23), and Teff cells have the function of regulating immunity and inflammation (9). Decreased activity of Treg cells enhances the activity of Teff cells, particularly the activity of Th17 cells (24). The present study observed an imbalance between Treg and Teff cells in CD4⁺ T cells in patients with VIT; specifically, the proportion of Teff cells was increased but that of Treg cells was decreased in CD4⁺ T cells of patients with VIT compared with those of healthy controls, with the expression levels of the Treg cellular marker Foxp3 being decreased and the secretion of Teff cell cytokines (IFN-γ, IL-17A and IL-22) being increased. It was noted that the proportion of Th22 cells in patients with VIT had a higher SD compared with other T-cell subtypes; this high SD may be due to individual differences among patients with VIT, although there is currently no evidence to support this hypothesis.

miRNAs regulate the balance of Treg/Teff cells (25), consistent with the findings of the present study, in which miR-21-5p expression in patients with VIT was decreased compared with in healthy individuals. Therefore, a miR-21-5p mimic was transfected into Th17-polarized CD4⁺ T cells to overexpress miR-21-5p and study its potential effects. The present data revealed that miR-21-5p overexpression regulated the Treg/Teff balance in CD4⁺ T cells, which was consistent with a previous study suggesting that miR-21-5p may regulate Treg/Teff balance in CD4⁺ T cells (15). Therefore, miR-21-5p may be a potential regulator of Treg/Teff balance.

miRNAs target mRNAs to regulate their expression and functions (26). A previous study has demonstrated that STAT3 can bind to the promoter of the miR-21 gene and thereby enhances the expression levels of pre-miR-21 and mature miR-21 in CD4⁺ T cells induced upon IL-21 stimulation in Sezary syndrome (27). Similar results have been observed in cellular transformation in which STAT3 directly activates the transcription of miR-21 (28). By contrast, the present study indicated that miR-21-5p could regulate STAT3 expression in CD4⁺ T cells. Therefore, it is inferred that a feedback loop may exist between STAT3 and miR-21 in CD4⁺ T cells, which should be further explored in future studies.

STAT3 may be modulated by arsenic trioxide in treatment-naïve patients with rheumatoid arthritis and may improve the Treg/Teff balance (29). STAT3 has been detected in VIT pathogenesis (30), but the association between STAT3 modulation and Treg/Teff balance in VIT is less explored. The present study demonstrated that STAT3 was the target of miR-21-5p and that its expression in patients with VIT was increased compared with in normal controls, causing an imbalance between Treg and Teff cells; however, this effect was reversed by miR-21-5p overexpression. Nevertheless, the mechanism through which miR-21-5p/STAT3 regulates the Treg/Teff balance in CD4⁺ T cells requires further elucidation.

Melanocytes serve an important role in VIT pathogenesis, and interaction between intrinsic and extrinsic melanocyte defects may be a key factor causing the onset of VIT (31). Therefore, protection of melanocytes may be a possible clinical method for VIT treatment. Zhou et al (32) revealed that IL-10 may contribute to the survival of primary melanocytes via the activation of the STAT3 and PI3K/Akt/NF-кB signaling pathways. The present study demonstrated that miR-21-5p overexpression indirectly ensured the survival of melanocytes with increasing tyrosinase activity and melanin synthesis via regulating the Treg/Teff balance, and that the effect of miR-21-5p overexpression was reversed by overexpression of its target gene, STAT3.

Additionally, it should be noted that there are some limitations in the present study, such as that only cellular assays were performed and that the analysis of CD4⁺ T cells from patients with VIT were preliminary. Therefore, more comprehensive experiments are required to confirm the effects of miR-21-5p in the development and progression of VIT using an animal model.

In conclusion, the present study identified a potential novel role for miR-21-5p in patients with VIT involving the protection of melanocytes via regulating the Treg/Teff balance. During this process, STAT3 may be a crucial target gene. Therefore, miR-21-5p may be used as a potential therapeutic target for treating VIT.

Funding

No funding was received.

Availability of data and materials

The datasets generated and/or analyzed during the current study are available from the corresponding author on reasonable request.

Authors' contributions

JH substantially contributed to the conception and design of the present study. TL, FL, XS and XH were involved in the data acquisition, analysis and interpretation, and in drafting and critically revising the manuscript for important intellectual content. All authors have read and approved the final manuscript.

Ethics approval and consent to participate

All experiments performed in the present study involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Declaration of Helsinki and its later amendments or comparable ethical standards. The present study was approved by the Ethics Committee of Dezhou People's Hospital (approval no. PFK20181006; Dezhou, China). All participants provided written informed consent.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.