Biomedical Research

Research Article - Biomedical Research (2017) Volume 28, Issue 10

Upregulation of SOCS1 and SOCS3 in pediatric patients with Henoch-Schoenlein purpura

Fengying Wang1, Xiaozhong Li1*, Lusheng Huang2 and Kang Xu2

1Department of Nephrology and Rheumatology, Children's Hospital of Soochow University, Suzhou, Jiangsu, PR China

2Department of Pediatrics, Affiliated Taixing Hospital of Yangzhou University, Taixing, Jiangsu, PR China

*Corresponding Author:
Xiaozhong Li
Department of Nephrology and Rheumatology
Children's Hospital of Soochow University
PR China

Accepted date: February 28, 2017

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Abstract

Suppressors of Cytokine Signaling (SOCS) family members are inhibitors of cytokine signaling pathways. Emerging evidence suggests the involvement of SOCS1 and SOCS3 in a variety of diseases, including allergy, autoimmune diseases, and inflammation. This study aimed to investigate the expression of SOCS1 and SOCS3 in the development of Henoch-Schoenlein Purpura (HSP) in children. Peripheral Blood Mononuclear Cells (PBMC) were isolated from children with HSP (HSP group, n=20) and healthy children (control group, n=15). The mRNA and protein levels of SOCS1 and SOCS3 in PMBC were detected by real time Reverse Transcription-Polymerase Chain Reaction (RT-PCR) and Western bot analysis. The results showed that the mRNA and protein levels of SOCS1/3 were upregulated in HSP group compared to control group (P<0.01). These data demonstrate that SOCS1 and SOCS3 are upregulated in children with HSP, and suggest that SOCS1 and SOCS3 are involved in the pathogenesis of HSP.

Keywords

Suppressors of cytokine signaling 1/3, Mononuclear cell, Henoch-Schoenlein purpura, Children

Introduction

Henoch-Schoenlein Purpura (HSP) is a major disease in the capillaries of allergic diseases, and is a common disease in children. In recent years, the incidence of HSP keeps increasing. The pathogenesis of HSP has not yet been completely understood [1]. Numerous studies have shown significant immune dysfunction during acute phase of HSP, including the disturbance of humoral immunity and T-lymphocyte subsets function, as well as cytokine secretion.

Suppressors of Cytokine Signaling (SOCS) families include at least 8 members of cytokine-induced proteins, namely SOCS1 to SOCS7 and CIS (Cytokine-inducible SH2 protein). These molecules negatively regulate Janus Kinase/Signal Transducers and Activators of Transcription (JAK-STAT) signaling pathway to modulate the activation, development, differentiation and function of monocyte-macrophages, dendritic cells and T-lymphocytes, and play important roles in autoimmune and inflammatory diseases [2-5]. Among all members of SOCS family, SOCS1 and SOCS3 have attracted more attention because they are crucially involved in immune diseases [4,5]. However, the roles of SOCS1 and SOCS3 in HSP remain unclear. In this study, we performed Reverse Transcriptase-Polymerase Chain Reaction (RT-PCR) and Western blot analysis to investigate SOCS1/SOCS3 mRNA and protein levels in Peripheral Blood Mononuclear Cells (PBMC) in children with HSP.

Subjects and Methods

Subjects

HSP patients and healthy control children were selected as the objects. Children with HSP were included if they met the following inclusion criteria: age 3-12 years old; exhibited diagnostic criteria for HSP; for children with initial onset, the course was 3 days; 4 weeks without using any corticosteroid or cytotoxic drugs; had no other associated medical problems. Healthy children were included if they met the following inclusion criteria: matched for age and gender of the children with HSP; had no history of allergic disease; 4 weeks without using any corticosteroid or cytotoxic drugs. This study was approved by Hospital Ethics Committee, and all the parents gave informed consent.

Blood collection

2 ml peripheral blood were collected from the children with HSP and healthy controls and put into anticoagulant sodium heparin tube, PBMC was isolated by density gradient centrifugation. The number of PMBC was counted by using a hemacytometer.

RT-PCR

Total RNA was extracted from 1.5 × 106 PBMC using Trizol reagent (Invitrogen, USA) following the manufacturer’s protocol. The integrity of total RNA was examined by 1% agarose gel electrophoresis. In addition, the absorbance of RNA samples at 230, 260 and 280 nm and ratios of D260:D280 and D260:D230 were calculated to estimate the purity of total RNA. cDNA was produced by reverse transcription at 42°C for 60 min using RT kit (Promega, Madsion, WI, USA) following the manufacturer’s protocol, followed by incubation at 70°C for 10 min to inactive reverse transcriptase. Quantitative PCR was performed using SYBR Green I Kit on ABI Prism7500. The total reaction volume of 25 μL included 12.5 μL SYBR Green qPCR Master Mix (2X), 0.25 μL Forward Primer, 0.25 μL Reverse primer, 0.25 μL cDNA, and 11.75 μL Diethylpyrocarbonate (DEPC) treated water. The primers used were as follows: SOCS1 CTTCCCCTTCCAGATTTG (forward) and TCCAGGCAAGTAATAACAA (reverse); SOCS3 TCTCCTTCAATTCCTCAG (forward) and GTTGGAAAGTTTGAAGATTC (reverse); β-actin ACCCTGAAGTACCCCATCGAG (forward) and ACATGATCTGGGTCATCTTCTCG (reverse). PCR reaction conditions were as follows: 1 min at 95°C for degeneration (one cycle) and then 10 s at 95°C, 20 s at 58°C, 20 s at 72°C for 40 cycles. The relative mRNA levels of SOCS1 and SOCS3 were compared to that of β-actin and calculated by the 2-ΔΔCt method. Each Ct value used for these calculations was the mean of the triplicate for each reaction.

Western blot analysis

Total protein was extracted from PBMC using protein extraction kit (Beyotime, Wuhan, China) according to the manufacturer’s protocols. Equal amounts of proteins (30 μg) were separated by SDS-PAGE and transferred onto nitrocellulose membranes. The membranes were blocked and then incubated with primary antibodies for SOCS-1, SOCS-3 and β-actin (Santa Cruz Biotechnology, Santa Cruz, CA, USA) at 4°C overnight. The membranes were washed and then incubated with horseradish peroxidase conjugated secondary antibody (Santa Cruz Biotechnology, Santa Cruz, CA, USA) at 37°C for 1 h. Protein bands were detected by using ECL kit (Amersham, Uppsala, Sweden).

Statistical analysis

SPSS17.0 statistical software was used for statistical analysis. Measurement data were expressed as mean ± standard deviation. Comparison between groups was analysed by t-test. P<0.05 was considered significant difference.

Results

General information of the subjects

We selected 20 HSP patients, including 11 males and 9 females (mean age 7.36 ± 2.22 years old, range 3-12 years old); and 15 healthy control children, including 8 males and 7 females (mean age 7.24 ± 1.64 years old, range 4-11 years old). The age and gender of the children in two groups showed no significant difference (t=0.175, χ2=0.115, P >0.05).

High SOCS1 and SOCS3 mRNA levels in HSP patients

The mRNA expression levels of SOCS1 and SOCS3 were detected by RT-PCR. Representative melting curves of PCR for SOCS1 was shown in Figure 1. SOCS1 and SOCS3 mRNA levels were significantly higher in HSP group than in control group (Table 1). These data suggest that abnormal high expression of SOCS1 and SOCS3 is involved in HSP.

biomedres-Quantitative-PCR

Figure 1: Quantitative PCR analysis of SOCS1 mRNA level. Shown were representative melting curves.

Group HSP (n=20)    Control (n=15)       t  p
SOSC1 mRNA level 1.37 ± 0.38     0.85 ± 0.12       5.03 <0.001
SOCS3 mRNA level   1.87 ± 0.53     0.77 ± 0.12        7.89 <0.001

Table 1: Relative SOSC1 and SOCS3 mRNA levels in HSP patients and controls.

High SOCS1 and SOCS3 protein levels in HSP patients

The protein expression levels of SOCS1 and SOCS3 were detected by Western blot analysis. SOCS1 and SOCS3 protein levels were significantly higher in HSP group than in control group (Figure 2). These data confirm that abnormal high expression of SOCS1 and SOCS3 is involved in HSP.

biomedres-Western-blot

Figure 2: Western blot analysis of SOCS1 and SOCS3 protein levels. Shown were representative blots from three independent experiments with similar results. β-actin was loading control.

Discussion

The etiology of HSP is complex, involving immune abnormalities, environmental factors and genetic factors. Th cells play an important role in the regulation of immune response. Immune disorders caused by the imbalance of Th cells, in collaboration with other factors, lead to autoimmune diseases. The newly discovered CD4+CD25+ regulatory T cells (Treg) and Th17 cells are important causes of immune imbalance in HSP [6,7]. In addition, a variety of cytokines such as TNF-α, IL-2, IL-4, IL-6, IL-10, IL-26, and IL-28 are implicated in the pathogenesis of HSP.

SOCS is not only a target gene of JAK/STAT signaling pathway, but also an important negative feedback regulator of this pathway. SOCS mRNA level is normally low in unstimulated cells but SOCS is induced rapidly at high levels after cytokine stimulation. In addition, microenvironmental factors affect the expression of SOCS mRNA [8]. Recent studies suggest that SOCS1 and SOCS3 regulate Treg cell differentiation and function, especially the balance of Th1/Th2 [9-11]. SOCS1 expression level in Thl cells is 5 times of Th2 cells, while SOCS3 expression in Th2 cells is 23 times of Thl cells [12,13]. SOCS1 can inhibit IL-4/STAT6 signaling, thus inhibiting Th2 cell differentiation and promoting Th1 cell differentiation, leading to enhanced Thl response. In contrast, SOCS3 can inhibit IL-4/STAT6 signaling, thus inhibiting Th1 cell differentiation and promoting Th2 cell differentiation, leading to enhanced Th2 response [14,15]. Therefore, SOCS1 and SOCS3 are involved in many inflammatory diseases, especially in autoimmune diseases associated with Th1/Th2 imbalance. SOCS1 and SOCS3 participate in ocular uveitis, Crohn's disease, systemic lupus erythematosus, rheumatoid arthritis, multiple sclerosis, allergic reactions, asthma, psoriasis, and type I diabetes [16].

In this study, we compared SOCS1 and SOCS3 mRNA levels in 20 children at acute stage of HSP to 15 healthy control children matched at the age and gender. The results showed that both SOCS1 and SOCS3 mRNA levels were significantly higher in HSP patients than in controls. Moreover, the increase of SOCS3 mRNA level was bigger than the increase of SOCS1 mRNA level in HSP patients. Therefore, after the antagonistic effects of SOCS1 and SOCS3, surplus SOCS3 seems to favor enhanced Th2 response and contribute to the development of HSP. In addition, Western blot analysis confirmed that SOCS1 and SOCS3 protein levels were significantly higher in HSP group than in control group. Previous studies have suggested that SOCS signaling could be therapeutically targeted for the treatment of various immune diseases [15-17]. Considering our results, we speculate that the dysregulation of SOCS1 and SOCS3 is implicated in the pathogenesis of HSP. The modulation of SOCS1 and SOCS3 expression levels may provide novel therapeutic approach for the prevention and treatment of HSP.

Conflict of Interest

None

References