INTRODUCTION
Rheumatoid arthritis (RA) is a chronic autoimmune inflammatory disease that causes progressive articular damage, functional loss, and comorbidity. RA affects approximately 1% of the population, can develop at any age, and is more prevalent in women than in men [
1]. An improved understanding of RA pathogenesis has led to several therapeutic options; however, additional studies are needed to avoid side effects and improve the quality of life of RA patients [
2]. Current treatment strategies involve traditional disease-modifying anti-rheumatic drugs and novel biologic agents targeting T cells, B cells, pro-inflammatory cytokines including tumor necrosis factor (TNF) or interleukin (IL)-1, and tyrosine kinase activity both markedly improve the clinical outcomes of RA patients [
2,
3]. However, at least 30% of RA patients show poor responses to the available therapies, suggesting that novel mediators are needed for targeting of other disease-specific pathways or cell lineages.
Fibroblast-like synoviocytes (FLSs), also known as synovial fibroblasts, are a quite unique cell type that distinguishes RA from other inflammatory conditions of the joints and are key effector cells in the pathogenesis of RA [
4]. FLSs from RA patients exhibit a unique progressive phenotype that increases invasiveness into the extracellular matrix and further exacerbates joint damage. This invasiveness of FLSs is considered equivalent to that of tumor cells [
5]. Numerous studies showed that FLSs participate in cell inflammation by secreting cytokines and chemokines, particularly TNF-α, IL-1β, and IL-6, and result in joint tissue damage in RA [
6]. Furthermore, inflammatory cytokines secreted by FLSs increase the total number of FLSs and promote the development of systemic inflammation, such as chronic anemia and cardiovascular disease [
7]. Therefore, understanding the molecular mechanism of dysregulation of cytokines expression in RA patients, particularly in FLSs, may provide novel treatment strategies.
MicroRNAs (miRNAs) are endogenous small noncoding RNA molecules that modulate the expression of multiple protein-encoding genes at the post-transcriptional level [
8]. Accumulating evidence has shown that these small RNA molecules play important roles in various pathological conditions, including rheumatic and other autoimmune diseases [
9,
10]. Several studies suggested that miRNAs are involved in controlling the inflammatory response of immune and non-immune cells. For instance, miR-124 mediates the anti-inflammatory action by suppressing production of the pro-inflammatory cytokines IL-6 and TNF-α [
11]. Lucas Philippe et al. observed dysregulated expression of miR-20a decreased IL-6 and CXCL10 released by RA FLSs and IL-1β and TNF-α by activated THP-1 cells [
12]. Recent studies suggested that miR-410-3p is involved in inflammation, angiogenesis, and tumorigenesis [
13‐
15]. Furthermore, as a key regulatory factor in the pathogenesis of systemic lupus erythematosus (SLE), miR-410-3p was found to be decreased in T cells of SLE patients and regulated the expression of IL-10 [
16]. However, no studies have examined miR-410-3p expression and its roles in RA.
In this study, we explored the expression of miR-410-3p in FLSs and synovial tissues of RA patients, its role in inflammatory cytokine secretion in RA-FLSs, and the underlying mechanisms.
METHODS
Cell Lines and Tissues
Human RA fibroblast-like synoviocytes (HFLS-RA) and human normal fibroblast-like synoviocytes (HFLS) were purchased from Jennio Biotech Co., Ltd. (Guangzhou, China). HFLS-RA were cultured in DMEM (Gibco, Life Sciences, MD), and HFLS were cultured in MEM (Gibco), supplemented with 10% heat-inactivated fetal bovine serum (FBS) (Gibco), penicillin (final concentration, 100 U/ml), and streptomycin (final concentration, 0.1 mg/ml) (all from Hyclone, Logan, UT), in a humidified atmosphere of 5% CO2 and 95% air at 37 °C. Cells were passaged every 4–5 days. Cells from the 3rd–8th passages were used for the following experimental procedures.
Synovial tissues were obtained from RA patients at the time of arthroscopic biopsy or total joint replacement from the Department of Orthopaedics in the Shengjing Hospital of China Medical University. All five RA patients met the 1987 American College of Rheumatology (ACR) criteria for the classification of RA [
17]. Four control synovial tissue samples were obtained from patients with joint trauma during routine arthroscopy or open joint surgery for diagnostic and therapeutic procedures. All patients were informed of the purpose of the study and gave written consent. The study was approved by the Ethics Committee of the Shengjing Hospital of China Medical University.
Transfection Experiments
The experimental setup consisted of five groups: the blank group, miR-410-3p mimics group (transfected with miR-410-3p mimics), mimics-negative control (transfected with miR-410-3p mimics-negative control sequence), miR-410-3p inhibitor group (transfected with miR-410-3p inhibitor), and inhibitor-negative control (transfected with miR-410-3p inhibitor-negative control sequence). miR-410-3p-related sequences were synthesized by GenePharma (Shanghai, China). HFLS-RA cells were seeded into six-well plate, transfected using Lipofectamine™ 3000 Reagent (Invitrogen, USA). The respective miR-410-3p sequences and Lipofectamine 3000 were mixed separately with Opti-MEM (Invitrogen) and then incubated together at room temperature for 10 min under serum-free conditions to form transfection complexes. The HFLS-RA was washed twice with PBS and the corresponding transfection complexes were added to each well. Complete DMEM media was replaced 6 h later. The transfection efficiency was verified by fluorescence microscopy at 24 h, and cells at 48 h and 72 h post-transfection were used for further analysis.
miR-410-3p Quantification
HFLS-RA cells were first transfected with miR-410-3p mimics, inhibitor, or NC for 48 h. Quantification of miR-410-3p was performed with real-time RT-PCR as previously described with modifications [
18]. In brief, total RNA containing small-size RNA was isolated or extracted from synovial tissues and cells with RNAiso Plus reagent (Takara, Japan). Total RNA (3 μg) was reversely transcribed to cDNA using a Mir-XTM miRNA First-Strand Synthesis kit (Takara). Next, the cDNA was amplified with a SYBR® Premix Ex Taq™ II (Tli RNaseH Plus) kit (Takara). U6 was used as an internal control and the relative expression of miR-410-3p was calculated using the 2-ΔΔ
CT method. The PCR primers were commercially obtained from Sangon Biotech (Shanghai, China).
Western Blot
HFLS-RA cells were first transfected with miR-410-3p mimics, inhibitor, or NC for 72 h, and then were harvested and lysed using RIPA buffer (Beyotime Biotechnology, Shanghai, China). The protein concentration was determined with a BCA kit (Beyotime Biotechnology) according to the protocol. Equal amounts of protein corresponding to approximately 30 μg were subjected to SDS-PAGE. Then, proteins were transferred to polyvinylidene difluoride (PVDF) membranes and incubated with 5% BSA for 2 h. Diluted primary antibodies (IκB-α, p-IκBα, p65, and p-p65; Cell Signaling Technology, USA; GAPDH and β-actin; ZSGB-BIO, China) were added into the membranes, and the mixture was incubated at 4 °C overnight. The membranes were washed with Tris-buffered saline Tween-20 (TBST). Horseradish peroxidase-labeled secondary antibodies (ZSGB-BIO) were added and the mixture was incubated at room temperature for 2 h. The membrane was then washed with TBST three times for 10 min once. The bands were visualized by enhanced chemiluminescence (ECL) according to the instructions (Millipore). The protein bands were quantitatively analyzed by using Image J software, normalized to GAPDH or β-actin.
Assessment of NF-κB Nuclear Translocation
NF-κB activation and nuclear translocation assay was performed according to the reagent manufacturer’s instructions (Beyotime Biotechnology). Briefly, 24 h after being plated in six-well plate, HFLS-RA cells were transfected with miR-410-3p mimics, inhibitor, or NC for 72 h, then fixed and blocked at room temperature. After incubation with rabbit anti-p65 NF-κB antibody overnight at 4 °C, cells were added with fluorescent secondary antibody. Eventually, the nuclear was dyed with DAPI (Beyotime Biotechnology). The fluorescence microscope was used to take pictures.
Enzyme-Linked Immunosorbent Assay
HFLS-RA cells were seeded into 24 well plates and transfected with miR-410-3p mimics, inhibitor, or NC for 48 h, with or without BAY 11-7082 treatment (Beyotime Biotechnology). The concentrations of TNF-α, IL-1β, IL-6, and MMP-9 in the cell culture supernatants were determined by a sandwich enzyme-linked immunosorbent assay (ELISA) (R&D Systems, Minneapolis, MN) according to the manufacturer’s instructions. A standard curve was performed for each plate and used to calculate the absolute concentrations of the indicated cytokines.
Statistical Analysis
All data were expressed as the mean ± standard deviation from at least three independent experiments and normally distributed. The differences between two groups were analyzed using the two-tailed Student t test. For the differences among three groups, one-way ANOVA followed by Tukey’s multiple comparisons test was used. P values below 0.05 was considered as statistically significant (ns, non-significant, *p < 0.05). All calculations were performed using the GraphPad Prism version 7.00 (GraphPad Software, Inc., San Diego, CA, USA).
DISCUSSION
RA is a systemic chronic inflammatory disease mainly characterized by hyperplastic synovial pannus tissue, which mediates the destruction of cartilage and bone [
19]. FLSs are key components of this invasive synovium and play a major role in the initiation and perpetuation of destructive joint inflammation. As primary promoters of inflammation, FLSs from RA patients also display unique aggressive features. These FLS cells contribute to the inflammatory microenvironment and recruit and activate immune cells to the damaged synovium by secreting multiple pro-inflammatory cytokines and chemokines, particularly TNF-α, IL-1β, IL-6, and MMPs [
20]. Elevated levels of cytokines and chemokines in the synovium modulate the expression of growth factors and result in further activation of FLSs, which undergo hyperplasia, a hallmark event in RA. Activated FLSs can undergo migration and enhance the production of pro-inflammatory cytokines and chemokines, particularly MMPs, which in turn mediate tissue destruction [
21].
An increasing number of studies have focused on the abnormal expression of microRNAs in RA. Thus, understanding the disease-associated mechanisms of these small non-coding RNAs may provide a novel approach for the diagnosis and treatment of RA. Here, we showed that the expression of miR-410-3p was significantly lower in synovial tissues and FLSs of RA patients compared to that in healthy controls. Considering the downregulation of miR-410-3p in RA patients, this miRNA may have a critical role in RA development. Furthermore, we observed that miR-410-3p suppressed the inflammatory cytokine release of RA-FLS. Since abnormally activated NF-κB signaling pathway was responsible for the inflammation and excess proliferation of FLSs in RA [
22], we further investigated whether miR-410-3p suppresses the cytokine release of RA-FLS by regulating the NF-κB signaling pathway.
miR-410-3p is abnormally expressed in a variety of diseases, including cancer, inflammation, and autoimmune diseases and is involved in multiple biological processes, such as proliferation, apoptosis, differentiation of stem cells, and drug resistance [
13,
16,
23‐
25]. Previous studies showed that miR-410-3p was highly expressed in the lung and colorectal cancer, and promoted the proliferation, invasion, and migration of cancer cells [
23,
26‐
28]. In contrast, miR-410-3p was reported to suppress the proliferation, migration, and invasion of breast cancer and pancreatic cancer [
25,
29,
30]. These data indicate that dysregulation of miR-410-3p occurs in a tissue-specific manner in different types of diseases. A recent study showed that miR-410-3p attenuated renal fibrosis in lupus nephritis mice
via directly targeting IL-6 [
13]. Additionally, miR-410-3p was found to be involved in the development of osteoarthritis through modulating the differentiation of mesenchymal stem cells (MSCs) into chondrocytes [
31]. However, the roles of miR-410-3p in RA are unknown. Nuclear translocation and subsequent DNA binding of NF-κB in inflamed synovium transactivate the expression of its target genes, including TNF-α, IL-1β and IL-6, and MMP-9 [
32]. Therefore, NF-κB signaling has been extensively studied to identify its role in the pathogenesis of RA, and NF-κB inhibition has been examined as a therapeutic approach for the disease. Our results demonstrated that miR-410-3p suppressed NF-κB activation in cultured HFLS-RA by suppressing the phosphorylation of IκB-α, thus resulting in low phosphorylation of p65. As transcription targets, elevations of TNF-α, IL-1β, IL-6, and MMP-9 induced by miR-410-3p inhibition were restored by NF-κB inhibitor. Together, these findings suggest that miR-410-3p is involved in cytokine release by suppressing the NF-κB signaling pathway. These results suggest that miR-410-3p is an inflammatory suppressor in RA progression. However, there are still some limitations. First, the number of synovial tissue samples is relatively small. Additionally, certain animals’ experiments are needed to evaluate the effect of miR-410-3p on cytokine release
in vivo.
Although miR-410-3p regulates multiple biological processes in a variety of diseases, its upstream regulating mechanism is unknown. It was reported that internalized miR-410-5p, derived from pre-miR-410, degraded miR-410-3p by base pairing and thus inhibited its function; blockade of the miR-410-5p upregulated the expression of miR-410-3p [
14]. In contrast, CpG islands in the upstream regions of miR-410-3p were methylated; however, the expression level of miR-410-3p was not regulated by a DNA methylation inhibitor [
33]. Additionally, some transcription factors were found to regulate the expression of miR-410-3p, such as myocyte enhancer factor 2 (MEF2) [
34] and E2F [
35]. However, little is known about the underlying mechanism of aberrant expression of miR-410-3p in RA, which requires further investigation.
In conclusion, we demonstrated that miR-410-3p acts as an inflammatory suppressor in RA by suppressing the NF-κB signaling pathway. These data suggest the potential diagnostic and therapeutic applications of miR-410-3p in RA.
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