The present study recruited 58 patients diagnosed with primary IgA nephropathy by renal biopsy between February 2016 and December 2017 from The Affiliated Hospital of Nantong University (Nantong, China). The recruited patients included 23 women and 35 men, with an average age of 39.21±9.3 years. In addition, 20 patients with renal necrosis caused by renal tumors were recruited as the control group from the Department of Urology, The Affiliated Hospital of Nantong University between February 2016 and December 2017. The patients in the control group comprised 12 women and 8 men, with an average age of 49.32±11.27 years. The study protocol was approved by the medical ethics committee of The Affiliated Hospital of Nantong University, and all subjects provided written informed consent.

This study excluded patients with secondary kidney disease, such as systemic lupus erythematosus, Henoch-Schonlein purpura, ankylosing spondylitis, liver disease and tumors. Patients were not systematically treated and did not use immunosuppressive agents prior to the start of the study.

A total of 8 ml anticoagulated blood was collected from the upper arms of patients that were fasted for 1 night. Each collected sample was centrifuged at 1,200 × g for 10 min at room temperature, and the plasma was collected and maintained in an Eppendorf tube at −80°C for storage. For examination, the frozen plasma was rapidly thawed at 37°C. Urine was collected at 8:00 AM and urine samples were subsequently taken for 24 h; toluene (4–5 ml) was added to prevent corrosion. The kidney tissue specimens of patients with IgA nephropathy were obtained by ultrasound-guided percutaneous nephrolithotomy. The kidney tissue specimens of patients with renal tumors were collected from normal kidney tissues away from the tumor site following removal of the kidney. The obtained kidney tissues were partially fixed for 2 h at room temperature in 10% formalin solution post-surgery, and partial kidney tissues were placed in liquid nitrogen and stored at −80°C.

The protein in urine was added to 1.5% sodium tungstate and centrifuged at 3,000 × g for 5 min at room temperature, and was then quantitatively determined by the biuret method (24). The concentration of creatinine in urine and plasma was measured using the Modular P800 Automatic Biochemistry Analyzer (Roche Diagnostics), and urine volume was measured for 24 h. The Cockcroft formula (25) was used to calculate the clearance rate of endogenous creatinine for 24 h.

An ELISA kit (cat. no. ab188391; Abcam) was used to detect BAFF levels in plasma samples, according to the manufacturer's protocol. The absorbance was measured at 450 nm, according to the manufacturer's protocol. A standard curve was generated according to the dilution concentration, in order to calculate the concentration of BAFF in each specimen.

The obtained kidney tissues were fixed for 2 h at room temperature with 4% formalin, dehydrated in an ascending series of ethanol, and permeabilized by xylene. Sections were then immersed in wax, embedded in paraffin, sliced into 2-µm sections, dried, dewaxed and subjected to antigen retrieval with 0.01 M citrate buffer for 40 min at 92°C. The slides were then incubated with 3% H₂O₂ for 10 min at room temperature to quench endogenous peroxidase activity, placed in 0.01 mmol/l citrate buffer (pH 6.0) and rinsed three times with 0.01 mol/l PBS for 3 min. Anti-human BAFF antibody (1:50; cat. no. AF124; R&D Systems, Inc.), anti-p-NF-κBP65 (1:1,000; cat. no. ab86299; Abcam) or rabbit anti-TRAF6 antibody (1:100; cat. no. sc-8409; Santa Cruz Biotechnology, Inc.) were used to incubate slides overnight at 4°C. PBS was used to rinse slides following primary antibody incubation. Horseradish peroxidase (HRP)-labeled secondary antibody (1:500; cat. nos. A0181 and A0208; Beyotime Institute of Biotechnology) was then added for 30 min at room temperature, followed by washing with PBS. PBS was used instead of primary antibodies as a negative control. 3,3′-Diaminobenzidine was used to stain the slides for 20 min, and hematoxylin was used for counterstaining for 1 min at room temperature. The slides were then dehydrated and mounted. Light microscopy was employed for observations and image capturing. Brown-yellow particles were regarded as positive cells and six fields were randomly selected from each slice. The integrated optical density values were determined using Image-ProPlus 6.0 image analysis processing software (Media Cybernetics, Inc.), and the average value was used to determine the expression level.

According to the Katafuchi score (26) of IgA nephropathy, the score of glomerular lesions was classified as 0–12 points, including: i) The degree of glomerular mesangial cell and mesangial matrix hyperplasia (0–4 points); ii) segmental glomerular lesions, such as crescent formation, glomerular adhesion, segmental sclerosis and segmental capillary fibrinous necrosis (0–4 points); and iii) glomerular sclerosis (0–4 points). The integral evaluation criteria were: 1, none, 0 points; 2, <25%, 1 point; 3, 25–50%, 2 points; 4, 51–75%, 3 points; and 5, >75%, 4 points. A total of 58 patients with IgA nephropathy were divided into four groups according to the scores: 0–3 points (group I), 4–6 points (group II), 7–9 points (group III), and 10–12 points (group IV).

The animal protocol in the present study was approved by the Medical Ethics Committee of The Nantong University Affiliated Hospital. Two male Sprague-Dawley rats (age, 8 weeks; weight, 220–260 g), supplied by the laboratory animal center of Nantong University, were housed under the following conditions: Temperature, 18–26°C; relative humidity, 40–70%; noise, <85 dB; ammonia concentration, <20 ppm; air exchange, 8–12 times/h; 15 g food added every 24 h; drinking water, pH 2.5–2.8 acidified water, changed 2–3 times/week. Animal health and behavior were monitored every 12 h. The rats were intraperitoneally anesthetized with 50 mg/kg sodium pentobarbital after weighing. After disinfection, the abdominal cavity was opened, saline was fully perfused into the apex cordis of the heart; once the kidneys turned pale, they were quickly moved onto ice. Rats were euthanized with an intraperitoneal injection of 150 mg/kg sodium pentobarbital following surgery. Subsequently, the renal capsule was discarded from the kidneys and the renal cortex along the boundary of the medulla was obtained to generate a homogenate. The tissue was then consecutively filtered through 60-, 100- and 200-mesh screens, after which, the tissue was collected and the separated glomeruli were obtained. Subsequently, 0.1% collagenase IV (cat. no. 17104019; Thermo Fisher Scientific, Inc.) was added for 10 min at 37°C. The glomeruli (2×10⁴) were transferred to a culture flask with DMEM (cat. no. 31600-091; Thermo Fisher Scientific, Inc.) containing 20% fetal bovine serum (FBS; cat. no. M6546; Macklin, Inc.). After the glomeruli were adherent to the culture flask wall, the cells were cultured for 4 weeks, and the cells were digested with trypsin, subcultured and purified. The third generation of cells was used in experiments.

Cells were cultured at 37°C in an atmosphere containing 5% CO₂, in saturated humidity. The cells were cultured to the 8th-10th generation. When the proliferating cells reached 80–90% confluence, 0.25% trypsin was used to digest cells. A single cell suspension was prepared from DMEM containing 20% FBS). After supplementing cells with serum-free low glucose DMEM for 24 h, the glomerular mesangial cells were randomly divided into five groups: Control (con)-short hairpin RNA (shRNA) group; con-shRNA + BAFF (20 ng/ml; cat. no. PHC1674; Thermo Fisher Scientific, Inc.) group, in which BAFF was added to transfected cells for 48 h at 37°C; con-shRNA + BAFF + BAFF-receptor (R)-Fc chimera protein (500 µg/ml; cat. no. 1162-BR-050; R&D Systems, Inc.) group, in which BAFF-R-Fc was added to transfected cells and after 30 min BAFF was added for 48 h at 37°C; TRAF6-shRNA group; and TRAF6-shRNA + BAFF (20 ng/ml) group, in which BAFF was added to transfected cells for 48 h at 37°C.

Glomerular mesangial cells (10⁶/ml) were seeded into 24-well plates at 500 µl per well. Cells were transfected after reaching 40% confluence. A total of 100 µl 6 pmol TRAF6-shRNA (cat. no. sc-156004-SH; Santa Cruz Biotechnology, Inc.), 2 µl Rfect (cat. no. 11011; Changzhou Baidai Biotechnology Co., Ltd.) and serum-free medium were added to each well and mixed; the cells and transfection agents were cultured at 37°C for 48 h. After transfection, the cells were further cultured in RPMI-1640 medium (containing 200 U/ml penicillin G, 10 mg/l gentamicin and 10% FBS) overnight at 37°C. Cells in the control group were transfected with the Con-shRNA (5′-AAGAAACCATGCAAAGTAAGGTT-3′; Santa Cruz Biotechnology, Inc.).

A total of 60 Sprague-Dawley male rats (age, 8 weeks; weight, 220–260 g), supplied by the laboratory animal center of Nantong University, were randomly divided into four groups: Con-small interfering RNA (siRNA; 0.2 µM), con-siRNA (0.2 µM) + IgA, BAFF-RFc chimera protein (2 µg/ml) + IgA, and TRAF6-siRNA (0.2 µM) + IgA. Rats were housed under the following conditions: Temperature, 18–26°C; relative humidity, 40–70%; noise, <85 dB; ammonia concentration, <20 ppm; air exchange, 8–12 times every hour; 15 g food was added every 24 h; drinking water, pH 2.5–2.8 acidified water, changed 2–3 times every week. Animal health and behavior were monitored every 12 h.

TRAF6-siRNA (cat. no. sc-156004; Santa Cruz Biotechnology, Inc.) was mixed with Entranster™ in vivo (cat. no. 4000-3; Engreen Biosystem) at a ratio of 1:2. A total of 1 ml solution was injected through the tail vein in rats, and the relevant experiments were performed after 24 h. Rats in the control group were injected with Con-siRNA (cat. no. A06001; Shanghai GenePharma Co., Ltd.). Rats were injected with siRNAs 24 h prior to IgA nephropathy model generation (27).

To establish the IgA nephropathy model, Sprague-Dawley rats were acclimated for 1 week. Subsequently, the rats were anesthetized by intraperitoneal injection of 1% sodium pentobarbital (40 mg/kg) and the left kidney was removed. After 1 week, 3 mg BSA (cat. no. Abs9157; Shanghai Absin Biotechnology) mixed with complete Freund's adjuvant medium was injected into both hind footpads of the mice, followed by repeated subcutaneous multi-site injections of the same solution every 2 weeks. A total of 2 weeks after the injection of BSA into the footpads, 6 mmol/l hydrochloric acid-acidified water containing 0.1% BSA was administered every other day. Blood was drawn after three immunization injections of BSA, and the serum anti-BSA antibody titer was measured using the double immunodiffusion method (28). When the antibody titer reached 1:16, 3 mg BSA was intraperitoneally injected daily. After 3 weeks, 100 µg lipopolysaccharide (cat. no. L2880; Sigma-Aldrich; Merck KGaA) was intraperitoneally injected. The model was established after 4 weeks (28). After fasting for 12 h, the rats were placed in a metabolic cage, urine was collected over 24 h, urine volume was recorded and the 24-h urine protein quantity was measured, as aforementioned. All rats were euthanized via an intraperitoneal injection of 150 mg/kg sodium pentobarbital. Once the heartbeat stopped and pupils dilated, serum was obtained, and Scr and BAFF were detected. The methods of measurement were the same as those aforementioned for analysis of human specimens. In addition, the left kidney was removed and fixed in 10% neutralized formaldehyde solution for 2 h at room temperature. The samples were stored at −80°C for further testing.

Cells were treated according to the aforementioned grouping and dosing methods. Subsequently, the cells were harvested, and the nuclei were extracted using the BestBio Nucleus/Cytoplasmic Isolation kit (Bestbio). Subsequently, 5–10×10⁶ cells were centrifuged at 500 × g for 3 min at 4°C to collect cells. Cells were washed twice with PBS, and a mixture consisting of cold Buffer A and protease inhibitor was added. After shaking twice, the solution containing cells was centrifuged at 16,000 × g for 5 min at 4°C. The mixture of cold Buffer B and protease inhibitor was then added to the pellet. After shaking, the cell suspension was centrifuged at 16,000 × g for 10 min at 4°C, and the supernatant was quickly transferred into a precooled, clean centrifuge tube to obtain nuclear proteins.

Rat kidney samples were cut into small pieces. After adding PBS, the tissues were homogenized using a tissue homogenizer, until bulky solids were not visible after settling on ice for 5 min. The supernatant was carefully transferred into a precooled clean centrifuge tube, followed by centrifugation at 500 × g for 2–3 min at 4°C. The supernatant was then discarded and the same procedure as aforementioned was performed to extract nuclear proteins.

The cells were collected and lyzed on ice for 30 min with RIPA lysis buffer (cat. no. P0013B; Beyotime Institute of Biotechnology). Centrifugation was then conducted at 8,000 × g for 5 min at 4°C. Total proteins were extracted from cells and the protein concentration was determined using the bicinchoninic acid (BCA) assay. After the proteins were mixed with loading buffer for 5 min, 30 µg protein was separated by SDS-PAGE on 8% gels. Proteins were then transferred to a nitrocellulose membrane and blocked with 50 g/l skim milk powder in TBS-0.05% Tween (TBST). Membranes were then incubated with anti-BAFF-R antibody (1:1,000; cat. no. ab5965; Abcam) overnight at 4°C. The corresponding HRP-labeled goat anti-rabbit secondary antibody (1:4,000; cat. no. ab205718; Abcam) was added to the membrane at 4°C for 2 h. Proteins were detected using an enhanced chemiluminescence (ECL) system (cat. no. PE0010; Beijing Solarbio Science & Technology Co., Ltd.). An Odyssey^® CLx Imaging system (LI-COR Biosciences) was used to capture images and densitometric analysis was conducted using Image Lab 3.0 software (Bio-Rad Laboratories, Inc.). β-actin (1:5,000; cat. no. ab95437; Abcam) was used to incubate membranes at 4°C overnight and was employed as a loading control.

For flow cytometric detection of BAFF-R, glomerular mesangial cells (10⁷/ml) were seeded into 24-well plates at 500 µl/well. Cells were incubated with primary mouse anti-BAFF-R antibody (1:1,000; cat. no. ab233775; Abcam) for 30 min in PBS supplemented with 3% FBS at 4°C. Subsequently, cells were incubated with FITC-conjugated anti-mouse secondary antibody (1:5,000; cat. no. ab6785; Abcam) for 30 min at 4°C. Rat Ig (cat. no. AS10-923; Agrisera) at the same concentration was used as a negative control. BAFF-R expression on the mesangial cell membrane was detected using an Attune NxT Flow Cytometer (Thermo Fisher Scientific, Inc.). Attune™ NxT software version 2.1 (Thermo Fisher Scientific, Inc.) was used to analyze the results.

After cells were treated with the aforementioned reagents, they were harvested. RNA extraction was performed using TRIzol^® reagent (Invitrogen; Thermo Fisher Scientific, Inc.). A total of 1 ml TRIzol^® was added to every 1×10⁶ cells. The integrity of the extracted product was evaluated by 1% TBE-agarose electrophoresis, and the concentration was measured using a spectrophotometer. cDNA was synthesized using a RT kit (RevertAid First Strand cDNA synthesis kit; cat. no. K1621; Thermo Fisher Scientific, Inc.). The reactions were carried in a 12-µl volume: 3 µg RNA template, 11 µl primer and RNase-free ddH2O. The reaction was maintained at 70°C for 5 min and was placed in an ice bath for 30 sec. After centrifugation (8,000 × g for 3 min at room temperature), the following reagents were added: 4 µl 5X Reaction Buffer, 1 µl RNase Inhibitor (20 U/µl), 2 µl dNTP Mix (10 mmol/l), and the sample was incubated at 37°C for 5 min. Subsequently, 1 µl M-MLV RT (20 U/µl) was added, and the sample was incubated at 37°C for 60 min and 70°C for 10 min. SYBR Green II qPCR reagent (SYBR premix Ex Taq II; cat. no. DRR820A; Takara Bio, Inc.) was used for qPCR with an ABI 7300 cycler (Applied Biosystems; Thermo Fisher Scientific, Inc.). For consistent amplification efficiency, each specimen was tested for TRAF6, CTGF, FN, NF-κBP65 and GAPDH gene expression. The total reaction system comprised 20 µl, which included 10 µl 2X Real Master Mix, 0.4 µl ROX, 0.8 µl each of the upstream and downstream primers, and 2 µg cDNA as a reaction template. The thermocycling conditions were as follows: Initial denaturation at 95°C for 3 min, followed by 40 cycles of denaturation at 95°C for 15 sec, primer annealing at 62°C for 30 sec and elongation at 72°C for 30 sec, and a final elongation step at 72°C for 7 min. The fluorescence signal was recorded after reading the plate to obtain a melting curve; the melting curve was then analyzed. Samples were randomly selected for 2% agarose gel electrophoresis to determine whether the amplified products were the desired fragments. Quantum CX5 (Vilber Lourmat) was used to capture images and densitometric analysis was conducted using AlphaImager 2000 image analyzer (Alpha Innotech). With GAPDH as the housekeeping gene, 2^−∆∆Cq ×100% indicated the relative expression of each gene: ∆Cq(test)=Cq(target,test)-Cq(ref,test); ∆Cq(calibrator)=Cq(target,calibrator)-Cq(ref,calibrator); ∆∆Cq=∆Cq(test)-ΔCq (calibrator). Calibrator refers to the control group; test refers to the experimental group(s); ref refers to the housekeeping gene; target refers to the gene of interest. Three replicate wells were set for each reaction to calculate the mean value for each ΔCq (29). Primers were designed by Shanghai Bioengineering, as follows: TRAF6, forward (F) 5′-TGATAGTGTGGGTGGAACTGC-3′, reverse (R) 5′-CAGATGGGGCATTCATACTTG-3′; FN, F 5′-CCGGTGGCTGTCAGTCAAAG-3′, R 5′-AAACCTCGGCTTCCTCCATAA-3′; CTGF, F 5′-CCCTGACCCAACTATGATGC-3′, R 5′-CCTTACTCCCTGGCTTTACG-3′; NF-κBP65, F 5′-TTCCTGGCGAGAGAAGCAC-3′, R 5′-AAGCTATGGATACTGCCCTCT-3′; and GAPDH, F 5′-ACGGATTTGCTCGTATTG-3′ and R 5′-GGAAGATGGTGATGGGATT-3′

Glomerular mesangial cells were treated according to cell groups for 48 h, after which, total protein was extracted by lysing cells on ice with 150 µl RIPA lysis solution in each well of a 6-well plate. The protein concentration was determined using a BCA protein quantitative kit (Beyotime Institute of Biotechnology). Total and nuclear proteins (60 µg/well) were separated by SDS-PAGE on 8% gels and were transferred to a nitrocellulose membrane. The membranes were blocked with TBST containing 5% skim milk powder at room temperature for 1 h, and were then incubated with anti-TRAF6 (1:1,000; cat. no. ab33915; Abcam), anti-FN (1:1,000; cat. no. MA517075; Thermo Fisher Scientific, Inc.), anti-CTGF (1:1,000; cat. no. ab6992; Abcam), anti-p-NF-κBP65 (1:1,000; cat. no. ab86299; Abcam), anti-NF-κBP65 (1:1,000; cat. no. ab16502; Abcam), anti-β-actin (1:5,000; cat. no. ab95437; Abcam) and anti-Histone H3 (1:5,000; cat. no. ab176842; Abcam) overnight at 4°C. After sufficient washing with TBST (5 min/three times), HRP-conjugated secondary antibodies (1:5,000; cat. no. ab205718; Abcam; and cat. no. 31430; Thermo Fisher Scientific, Inc.) was added at room temperature for 1 h. Proteins were detected using an ECL system. An Odyssey^® CLx Imaging system (LI-COR Biosciences) was used to capture images and densitometric analysis was conducted using Image Lab 3.0 software (Bio-Rad Laboratories, Inc.). β-actin was used as a cytoplasmic loading control; Histone H3 was used as nuclear-specific loading control.

A total of 200 µl RIPA lysis solution (Beyotime Institute of Biotechnology) was added per 20 mg kidney tissue samples to extract proteins. The extracted total and nuclear protein samples (60 µg/well) were subjected to SDS-PAGE on 8% gels. After electrophoresis, the samples were transferred to polyvinylidene difluoride membranes, which were blocked with TBST containing 5% skim milk powder at 4°C overnight. Membranes were then washed twice with TBST, and incubated with anti-BAFF (1:1,000; cat. no. ab8396; Abcam), anti-FN (1:1,000), anti-TRAF6 (1:1,000), anti-CTGF (1:1,000) anti-β-actin (1:5,000), anti-Histone H3 (1:5,000), anti-NF-κBP65 (1:1,000) and anti-p-NF-κBP65 (1:1,000) at 37°C for 2 h, and were washed twice with TBST for 10 min. The membranes were then incubated with the aforementioned secondary antibodies (1:2,000) at 37°C for 2 h, and washed with TBST four times (10 min/wash). The chemiluminescence method (GE Healthcare) was used for visualization. The Odyssey imaging system was used to develop images. ImageJ software (National Institutes of Health) was used for densitometric analysis; grayscale values of target proteins were normalized to the loading proteins. β-actin was used as a cytoplasmic loading control; Histone H3 was used as nuclear-specific loading control.

Statistical analysis was performed using SPSS statistical software for Windows, version 17.0 (SPSS, Inc.). The experiments were conducted three times. Data are expressed as the mean ± standard deviation. Data were analyzed by one-way ANOVA followed by a Tukey post hoc test for multiple groups, and by Student's t-test for two groups. The correlation between two variables was analyzed using Pearson's correlation. P<0.05 was considered to indicate a statistically significant difference.

With the aggravation of pathological damage, the proteinuria level of patients with IgA nephropathy increased. In addition, plasma BAFF levels were significantly increased and the endogenous creatinine clearance rate was decreased. Pairwise comparisons were made between the groups, and these differences were statistically significant (P<0.05; Fig. 1). Proteinuria (r=0.45; P<0.05) and BAFF levels (r=0.62; P<0.05) were positively correlated with the Katafuchi score of renal damage (data not shown). The endogenous creatinine clearance rate was negatively correlated with the Katafuchi score of renal damage (r=−0.72; P<0.05) (data not shown). The expression levels of BAFF, TRAF6, FN, p-NF-κBp65 and CTGF were markedly higher in the kidneys of patients with IgA nephropathy than those in the control group. The overexpression of proteins was mainly concentrated in the glomerular mesangial area (Fig. 2).

Western blotting was used to detect the expression of BAFF-R protein. The results revealed that there was a small amount of BAFF-R protein expression in mesangial cells. Following the addition of 20 ng/ml BAFF for 48 h, the protein expression levels of BAFF-R were significantly increased in mesangial cells (P<0.05). The presence of BAFF-R on the surface of the mesangial cell membrane was confirmed by flow cytometry (Fig. 3).

Following the addition of 20 ng/ml BAFF to glomerular mesangial cells for 48 h, the mRNA expression levels of FN, TRAF6, CTGF and NF-κBP65 were significantly increased in the glomerular mesangial cells (P<0.05 vs. the control group). Glomerular mesangial cells transfected with the shRNA-TRAF6 plasmid exhibited reduced expression of TRAF6 mRNA (P<0.05 vs. the control group), and following treatment with 20 ng/ml BAFF for 48 h, the mRNA expression levels of NF-κBP65 were significantly lower than those observed in the con-shRNA + BAFF group, and the mRNA expression levevls of FN and CTGF were also decreased (P<0.05 vs. the con-shRNA + BAFF group; Fig. 4).

Following the addition of 20 ng/ml BAFF to the glomerular mesangial cells for 48 h, the protein expression levels of TRAF6 in mesangial cells and p-NF-κBP65 in the nuclei of mesangial cells were significantly increased. Notably, total NF-κB protein expression in the cells did not change, and the proportion of p-F-κBP65/NF-κBP65 was significantly higher (P<0.05 vs. the control group). In addition, the expression levels of the downstream proteins, FN and CTGF, were enhanced by BAFF treatment (P<0.05 vs. the control group). Mesangial cells transfected with the shRNA-TRAF6 plasmid exhibited reduced expression of TRAF6 protein (P<0.05 vs. the control group), and after 48 h of treatment with 20 ng/ml BAFF, the protein expression levels of p-NF-κBP65 in the nucleus were significantly lower than those observed in the con-shRNA + BAFF group, and FN and CTGF protein expression was also decreased (P<0.05 vs. con-shRNA + BAFF group; Fig. 5).

When TRAF6-siRNA was administered into the tail vein of rats, the protein expression levels of TRAF6 in the kidneys of rats with IgA nephropathy were significantly decreased (P<0.05). These findings suggested that TRAF6 expression in the kidneys of rats with IgA nephropathy was successfully inhibited by TRAF6-siRNA (Fig. 6).

Proteinuria, serum creatinine concentration and plasma BAFF concentration of rats in the IgA nephropathy group were significantly higher than those in the control group (P<0.05). In the Fc + IgA and TRAF6-siRNA groups, plasma BAFF concentration was not significantly different compared with the IgA nephropathy group (P>0.05); however, the other two markers were significantly lower than those in the IgA nephropathy group (P<0.05; Fig. 7).

The expression levels of BAFF, TRAF6, p-NF-κBp65, FN and CTGF in the kidneys of rats with IgA nephropathy were markedly increased compared with in the control group (P<0.05), and these proteins were mainly distributed in the glomerular mesangial area. The expression levels of BAFF in the TRAF6-siRNA + IgA and Fc groups were not significantly different from those in the IgA nephropathy group (P>0.05); however, the expression levels of TRAF6, p-NF-ΚBP65, FN and CTGF were significantly lower than those observed in the IgA nephropathy group (P<0.05; Fig. 8).

The expression levels of BAFF, TRAF6, FN, CTGF and nuclear p-NF-κBP65 proteins in rats with IgA nephropathy were significantly higher than those in the control group (P<0.05). Notably, total NF-κB protein expression in the cells did not change, whereas the proportion of p-NF-κBP65/NF-κBP65 was significantly higher (P<0.05 vs. the control group). In the TRAF6-siRNA + IgA and Fc groups, the protein expression levels of BAFF were not significantly different from those in the IgA nephropathy group (P>0.05); however, the expression levels of TRAF6, FN, CTGF and nuclear p-NF-κBP65 proteins were significantly lower than those in the IgA nephropathy group (P<0.05; Fig. 9).