CTGF siRNA ameliorates tubular cell apoptosis and tubulointerstitial fibrosis in obstructed mouse kidneys in a Sirt1-independent manner
Authors Ren Y, Du C, Yan L, Wei J, Wu H, Shi Y, Duan H
Received 16 April 2015
Accepted for publication 19 May 2015
Published 31 July 2015 Volume 2015:9 Pages 4155—4171
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 6
Editor who approved publication: Prof. Dr. Wei Duan
Yunzhuo Ren,* Chunyang Du,* Li Yan, Jingying Wei, Haijiang Wu, Yonghong Shi, Huijun Duan
Department of Pathology, Hebei Medical University, Shijiazhuang, Hebei, People’s Republic of China
*These authors contributed equally to this work
Abstract: Transforming growth factor-β1 (TGF-β1) plays an important role in the pathogenesis and progression of chronic kidney disease. Connective tissue growth factor (CTGF) is a critical fibrogenic mediator of TGF-β1. Mammalian sirtuin 1 (Sirt1) is reported to attenuate renal fibrosis by inhibiting the TGF-β1 pathway. This study was designed to detect whether the delivery of CTGF siRNA in vivo directly ameliorates renal fibrosis. Furthermore, the relationship with Sirt1 underlying the protective effect of CTGF siRNA on interstitial fibrosis and apoptosis was explored. Here, we report that the expressions of CTGF and TGF-β1 were increased while Sirt1 expression and activity were both dramatically decreased in mouse kidneys with unilateral ureteral obstruction. Recombinant human TGF-β1 treatment in HK-2 cells increased CTGF levels and remarkably decreased Sirt1 levels and was accompanied by apoptosis and release of fibrosis-related factors. Recombinant human CTGF stimulation also directly induced apoptosis and fibrosis. The CTGF siRNA plasmid ameliorated tubular cell apoptosis and tubulointerstitial fibrosis, but did not affect Sirt1 expression and activity both in vivo and in vitro. Furthermore, overexpression of Sirt1 abolished TGF-β1-induced cell apoptosis and fibrosis, while Sirt1 overexpression suppressed CTGF expression via stimulation by TGF-β1. This study provides evidence that treatment strategies involving the delivery of siRNA targeting potentially therapeutic transgenes may be efficacious. Our results suggest that the decrease in Sirt1 is associated with the upregulated expression of CTGF in renal fibrosis, and may aid in the design of new therapies for the prevention of renal fibrosis.
Keywords: ureteral obstruction, Sirt1, CTGF, fibrosis, apoptosis
Interstitial fibrosis is correlated with the progression of chronic renal diseases and has been proposed as a final common pathway to end-stage renal diseases.1 Unilateral ureteral obstruction (UUO) results in a number of pathophysiological and morphological changes in the renal parenchyma, including interstitial fibrosis and inflammation and apoptotic changes in tubular and interstitial cells.2 Apoptosis is a process of normal cell death that maintains tissue homeostasis, but excessive apoptosis or its dysregulation can lead to various pathological fibrosis processes, such as those seen in patients with idiopathic pulmonary fibrosis3 and several liver fibrosis diseases.4 Renal tubular cells comprise the bulk of the renal cortex, and apoptosis of the tubular cells combined with epithelial–mesenchymal transition (EMT) is the major cause of tubular atrophy.5 Moreover, apoptosis has been found in renal tubular cells from patients with diabetic nephropathy.6 A variety of cytokines are known to affect the processes of interstitial fibrosis (ie, PAI-1 and TIMP-1). α-SMA is a molecular hallmark of fibroblast activation during the fibroblast-to-myofibroblast transition. Therefore, we examined the levels of PAI-1, TIMP-1, and α-SMA. An increase in Bax and a concomitant decrease in Bcl-2 are common markers of apoptosis. Following the original study by Gobe and Axelsen,7 there have been numerous reports concerning the role of tubular apoptosis in mediating eventual tubular atrophy as a consequence of chronic UUO.8 Clinical and experimental studies have identified a key role for connective tissue growth factor (CTGF/CCN2) in the development of interstitial fibrosis. CTGF, a member of the CCN (Cyr61, CTGF, Nov) family of secretory proteins, is involved in various cellular functions (ie, adhesion, migration, proliferation, and extracellular matrix production), and plays a critical role in many fibrotic conditions, including kidney fibrosis.9,10 CCN proteins regulate many aspects of cellular functions including apoptosis. It has also been demonstrated that CTGF induces apoptosis in human mesangial cells11 and that CTGF siRNA ameliorates retinal cell apoptosis in streptozotocin-induced diabetic rats.12
Mammalian sirtuin 1 (Sirt1), a nicotinamide adenine dinucleotide (NAD+)-dependent protein class III deacetylase, is widely expressed in almost all mammalian organs. Sirt1 is a key modulator of cell proliferation, hormone responses, stress responses, apoptosis, and cell metabolism13,14 through the deacetylation of the lysine residues of not only histone proteins but also those of some nuclear proteins, such as p53, the forkhead family proteins, and c-Myc. A recent study demonstrated that Sirt1 activation ameliorated renal fibrosis by inhibiting the TGF-β1 (transforming growth factor-β1)/Smad3 pathway.15 Sirt1 was shown to be capable of interacting with TGF-β1 signaling and reducing apoptosis in TGF-β1-treated mesangial cells.16 Moreover, the Sirt1 activator SRT1720 significantly reduced TdT-dUTP nick end labeling (TUNEL)-positive apoptosis and collagen I expression in the medulla of the obstructed kidney after UUO.17
In this study, we explored the role of CTGF siRNA in matrix accumulation, EMT, apoptosis, and Sirt1 expression using an in vivo model of progressive kidney fibrosis induced by UUO. We also performed studies in vitro to determine whether Sirt1 was involved in the TGF-β1-induced CTGF increase and its profibrotic action.
Materials and methods
Animal model and experimental design
Twelve-week-old male CD-1 mice (Charles River Laboratories, Vitalriver, Beijing, People’s Republic of China) were housed in the animal facilities of the Hebei Medical University with free access to food and water. The animals were randomly divided into three groups: a sham operation group (Sham), a UUO group (UUO), and a UUO group administered a pBAsi mU6 Neo CTGF siRNA plasmid (Takara Bio Inc., Shiga, Japan) (siRNA) (N=8 per group). UUO surgery was performed under general anesthesia. Complete ureteral obstruction was performed by double-ligating the left ureter using 4.0 silk after a midline abdominal incision. Sham-operated mice had their ureters exposed and manipulated, but not ligated. Plasmids were administered into mice by electroporation. The kidney received 100 μL containing 50 μg of DNA. The injection was done with one 50 μL delivery to the lower portion of the kidney, and the other 50 μL to the upper portion. Both injections were given in the medulla. The control vector contained sequences necessary for transcription, but no exogenous DNA was added to the vector. Tweezer electrodes (BTXT weezertrodes Model #522, Harvard Apparatus, Holliston, MA, USA) connected to an electro-stimulator (Electro Cell Manipulator™, ECM® 830, BTX, a division of Genentronics, Harvard Apparatus) were placed on opposite sides of the kidney, and 20 pulses were administered at 200 V, each lasting 20 milliseconds, at 1,000 Hz.18 The animals were sacrificed by exsanguination under general anesthesia, and the kidneys were harvested at 7 days after the UUO or sham operation. All procedures were performed in compliance with the guidelines established by the Ethics Review Committee for Animal Experimentation of Hebei Medical University.
Generation of the pBAsi mU6 Neo CTGF siRNA plasmid
Three CTGF siRNA plasmids were constructed on the basis of the U6 siRNA expression vector pBAsi mU6 Neo (Takara, Mie, Japan), which includes a mouse U6 promoter and an amp-resistance gene. The following sets of sense and antisense oligonucleotides were annealed and ligated into the vector: sense oligo 1: 5′-GATCCGATACCAATGCACTTGCCTGTAGTGCTCCTGGTTGCAGGCAAGTGCATTGGTATCTTTTTTA-3′; antisense oligo 1: 5′-AGCTTAAAAAAGATACCAATGCACTTGCCTGCAACCAGGAGCACTACAGGCAAGTGCATTGGTATCG-3′; sense oligo 2: 5′-GATCCGGACATACAGGGCTAAGTTCTAGTGCTCCTGGTTGGAACTTAGCCCTGTATGTCCTTTTTTA-3′; antisense oligo 2: 5′-AGCTTAAAAAAGGACATACAGGGCTAAGTTCCAACCAGGAGCACTAGAACTTAGCCCTGTATGTCCG-3′; sense oligo 3: 5′-GATCCGCTATGATGCGAGCCAACTGTAGTGCTCCTGGTTGCAGTTGGCTCGCATCATAGCTTTTTTA-3′; and antisense oligo 3: 5′-AGCTTAAAAAAGCTATGATGCGAGCCAACTGCAACCAGGAGCACTACAGTTGGCTCGCATCATAGCG-3′.
To test the efficiency of the three pBAsi mU6 Neo CTGF siRNA plasmids, mouse mesangial cells cultured under high-glucose conditions were transfected with the plasmids, and the plasmids were delivered by electroporation into UUO mice in vivo. CTGF expression was evaluated by Western blotting and immunohistochemistry. The most effective plasmid (oligo 1) was used for the study. One group of UUO mice received an injection of CTGF siRNA plasmid DNA at 1 mg/kg body wt at day 1 before the operation, and every 5 days thereafter, while another group received an injection of pBAsi mU6 Neo control plasmid in an identical manner.
Kidneys were fixed in 4% paraformaldehyde overnight and embedded in paraffin. Sections (2 μm) were stained with Masson’s trichrome for light microscopic observation. The fibrotic area was measured quantitatively using HPIAS-2000 image analysis software (Champion Image Company, Wuhan, People’s Republic of China). Thirty randomly selected fields were examined by two investigators without knowledge of the treatment protocol. The results were expressed as the percent area of interstitial fibrosis.19
Kidney sections (4 μm) were deparaffinized with xylene and rehydrated in graded ethanol. Endogenous horseradish peroxidase (HRP) activity was blocked with 3% H2O2 in methanol for 30 minutes. Antigen retrieval was performed by microwave treatment in 10 mM citrate buffer for 15 minutes. The sections were incubated with α-SMA, TIMP-1, and PAI-1 (Santa Cruz Biotechnology, Santa Cruz, CA, USA) antibodies overnight at 4°C. Then, the sections were washed and incubated with biotinylated secondary antibody and HRP-conjugated streptavidin. Labeling was visualized with 3,3-diaminobenzidine (DAB; Sigma, St Louis, MO, USA) to produce a brown color, and the sections were counterstained with hematoxylin.
In vivo detection of apoptotic cells
Apoptotic cells in kidneys were identified using the Dead End TM Colorimetric TUNEL System (Promega, Madison, WI, USA). Briefly, 4 μm paraffin sections were treated with freshly diluted 20 μg/mL proteinase K for 15 minutes at room temperature. After treatment with equilibration buffer for 10 minutes, the recombinant terminal deoxynucleotidyl transferase reaction mix was added for 60 minutes at 37°C. Endogenous peroxidase activity was blocked by incubating the sections in 0.3% H2O2 in phosphate-buffered saline (PBS) for 5 minutes. Streptavidin HRP solution was added to each slide and incubated for 30 minutes at room temperature. Then, the sections were washed, developed in DAB, and counterstained with a light hematoxylin. The numbers of the tubular and interstitial TUNEL-positive apoptotic cells in the entire cortex were scored on the slides.
Cell culture and transient transfection
HK-2 cells (ATCC, American Type Culture Collection, Manassas, VA, USA) were cultured in Dulbecco’s Modified Eagle Medium: Nutrient Mixture F-12 (DMEM-F12) medium supplemented with 5% fetal bovine serum, 2 mM L-glutamine, 100 U/mL penicillin, and 100 μg/mL streptomycin in a 95% air, 5% CO2 atmosphere. HK-2 cells were divided into the normal group (NG), TGF-β1 (5 ng/mL) (Abgent, San Diego, CA, USA) stimulation group, and TGF-β1 (5 ng/mL) plus CTGF siRNA group. Meantime, to examine the direct effect of CTGF on interstitial fibrosis, HK-2 cells were randomly divided into two groups: the NG group and the CTGF (10 ng/mL) stimulation group. Furthermore, we transfected cells with Sirt1 overexpression plasmid20 (addgene.com, plasmid 1791) to observe the effect of Sirt1 overexpression on interstitial fibrosis and CTGF in the presence of rhTGF-β1. HK-2 cells were randomly divided into three groups: NG, the TGF-β1 (5 ng/mL) stimulation group, and the TGF-β1 (5 ng/mL) plus Sirt1 overexpression group. Transfections of HK-2 cells with CTGF siRNA plasmid or Sirt1 overexpression plasmid were performed with Lipofectamine 2000 according to the manufacturer’s instructions. A negative control plasmid was transfected at the same time.
HK-2 cells were grown on chamber slides and fixed with 96% alcohol after 24 hours under experimental conditions. After washing with PBS (0.14 M NaCl, 0.004 M KCl, and 0.01 M Na2HPO4·12H2O), the cells were incubated with primary mouse monoclonal antibodies against Sirt1 (Abcam, ab110304) overnight at room temperature. Then, the cells were incubated with biotin-conjugated goat antimouse secondary antibody (Dako) and exposed to streptavidin-peroxidase and DAB. Negative controls were obtained by incubating with nonimmune serum instead of the Sirt1 antibody.
In vitro detection of apoptosis
Apoptosis was assessed by TUNEL, and then the apoptotic cells were counted. Apoptotic cells were defined by chromatin condensation or nuclear fragmentation. Apoptotic cells in different groups were determined using an Annexin V/PI (propidium iodide) apoptosis detection kit according to manufacturer’s protocol (Multi Sciences Biotech, Hangzhou, People’s Republic of China). Briefly, the cell pellet was resuspended in 1× binding buffer, followed by incubation with 5 mL of Annexin V (conjugated with fluorescein isothiocyanate) and 10 mL of PI in the dark for 5 minutes. Then, cell fluorescence was analyzed using a flow cytometer (FCM) (Epics-XLII, Beckman Coulter, Inc, Pasadena, CA, USA). This test discriminates intact cells (Annexin V−/PI−), early apoptotic cells (Annexin V+/PI−), and late apoptotic cells (Annexin V+/PI+). Finally, Hoechst 33258 staining was also used to detect apoptotic cells. Briefly, the cells were washed with PBS, fixed in 10% formaldehyde solution for 5 minutes at room temperature, and resuspended in 50 mL of PBS before deposition onto coverslips. The adhered cells were incubated with Hoechst 33258 dye (Invitrogen, Carlsbad, CA, USA) for 20 minutes at room temperature. The coverslips were rinsed with PBS and imaged by fluorescence microscopy (BX3-CBH Olympus, Tokyo, Japan). The apoptotic cell counts were expressed as a percentage of the total number of cells emitting fluorescence.
Western blot analysis
Whole kidneys were homogenized in ice-cold radioimmunoprecipitation assay lysis buffer, then centrifuged at 14,000× g for 25 minutes at 4°C prior to collection of the supernatants. The protein concentration was measured by Bradford’s method, and the supernatants were stored at −80°C. The cell lysates (50 μg of protein/lane) or whole HK-2 cell extracts (40 μg of protein/lane) were loaded, separated by sodium dodecyl sulfate–polyacrylamide gel electrophoresis, and transferred to polyvinylidenedifluoride membranes (Millipore, Billerica, MA, USA). The membranes were incubated overnight at 4°C with primary antibodies for CTGF (Abcam, Cambridge, UK), TGF-β1, collagen type I (Col1), α-SMA, TIMP-1, PAI-1, E-cad, or β-actin (Santa Cruz Biotechnology). Subsequently, the membranes were incubated with goat antirabbit IgG or goat antimouse IgG HRP conjugate, and then immersed in ECL Plus Western Blotting Detection Reagent (Amersham, Piscataway, NJ, USA) and exposed to Hyperfilm ECL (Amersham). The intensity of the bands was measured using Lab Works 4.5 software (UVP, Upland, CA, USA).
Real-time quantitative PCR analysis
Total RNA and cDNA were prepared from whole kidney samples using the SV Total RNA Isolation System (Promega, Madison, WI, USA) or cultured cells using TRIzol reagent (Invitrogen, Carlsbad, CA, USA) and RT-PCR kits (Promega, Madison, WI, USA). Real-time polymerase chain reaction (PCR) was performed in a 96-well optical reaction plate using SYBR Premix Ex TaqTMII. Reverse transcriptase polymerase chain reactions (RT-PCRs) were performed on Agilent Mx3000P QPCR Systems (Agilent, CA, USA). The levels of mRNA were normalized to the eukaryotic 18s rRNA expression level and calculated using the 2(-ΔΔCT) method.21 The cycling conditions were as follows: initial denaturation at 95°C for 30 seconds, followed by 40 cycles at 95°C for 5 seconds, 60°C for 30 seconds, and 72°C for 30 seconds. Primer sequences are available upon request.
Sirt1 deacetylase activity assay
Sirt1 deacetylase activity was colorimetrically measured in vivo and in vitro using the Sirt1 Deacetylase Activity Assay Kit (Genmed Scientifics Inc., Arlington, MA, USA) following the manufacturer’s instructions. The kit provided a Sirt1 substrate with an acetylated peptide fragment derived from p53 (which is known to be deacetylated by Sirt1) that was prelabeled with p-nitroaniline. After deacetylation by Sirt1, the aminopeptidase cleaved the deacetylated substrate and generated a highly chemiluminescent molecule group of p-nitroaniline. The optical densities at a wavelength of 405 nm were recorded with a spectrophotometer (Diareader ELX800G, Dialab GmbH, Vienna, Austria). Sirt1 deacetylation activity was expressed as a percentage of the control.
Data were presented as the mean ± SD. Statistical analysis was performed by one-way ANOVA. Statistical significance was defined as P<0.05.
Treatment with CTGF siRNA reduced UUO-induced increases in CTGF, the percentage areas of interstitial fibrosis, and Col1, α-SMA, PAI-1, and TIMP-1 expression, but not TGF-β1 expression
As shown in Figure 1A, Masson’s trichrome staining revealed increased collagen deposition in the kidneys from UUO mice compared with sham mice. We determined the percentage area of interstitial fibrosis in UUO kidneys. The kidneys in the sham treatment group showed very little, if any, fibrosis in the tubules or interstitium. In contrast, the percentage of fibrotic areas in the UUO kidneys was increased compared with the sham group (Figure 1B). We also analyzed total kidney tissue lysates by Western blotting for Col1. As shown in Figure 1C and D, an increase in Col1 protein expression was observed in the obstructed kidneys compared with the sham kidneys. Consistent with the result of Col1 protein expression, the Col1 mRNA level was increased in UUO mice (Figure 1E). Moreover, treatment with the CTGF siRNA plasmid resulted in a notably reduced percentage of renal fibrotic areas (Figure 1A and B) and Col1 mRNA and protein expression (Figure 1C–E). The delivery of CTGF siRNA to UUO obstructed kidneys did not affect the mRNA and protein levels of TGF-β1 (Figure 1C–E). Compared with the UUO group, the mRNA and protein expression did not change in cells treated with control siRNAs (data not shown).
A variety of cytokines are known to affect the processes of interstitial fibrosis (ie, PAI-1 and TIMP-1). α-SMA is a molecular hallmark of fibroblast activation during the fibroblast-to-myofibroblast transition. Therefore, we examined the levels of PAI-1, TIMP-1, and α-SMA in vivo. The mRNA and protein levels of PAI-1, TIMP-1, and α-SMA detected by Western blotting and real-time RT-PCR were all significantly increased in the obstructed kidneys of the UUO group compared with the CTGF siRNA plasmid transfection group and the sham group (Figure 1C–E). Moreover, immunohistochemistry (Figure 2) indicated that areas staining positive for PAI-1, TIMP-1, and α-SMA were located mainly in tubular epithelial cells from the UUO kidneys, and that the delivery of CTGF siRNA greatly downregulated the expression of PAI-1, TIMP-1, and α-SMA. Compared with the UUO group, the mRNA and protein expression did not change in cells treated with control siRNAs (data not shown).
Treatment with CTGF siRNA attenuated the UUO-induced increase in Bax expression, apoptosis rate, and decrease in Bcl-2 expression
The number of tubular epithelial cells containing TUNEL-positive nuclei was increased in UUO mice compared with sham mice; this increase was markedly decreased by the delivery of CTGF siRNA (Figure 3A–D). Furthermore, in the obstructive kidney UUO group, 7 days of UUO resulted in a significant decrease in Bcl-2 protein and mRNA expression compared with the sham operation kidney group. In contrast, Bax mRNA and protein levels were significantly increased in the obstructive kidney UUO group. Administration of CTGF siRNA attenuated the changes in Bcl-2 and Bax expression (Figure 3E–G). Compared with the UUO group, the mRNA and protein expression did not change in cells treated with control siRNAs (data not shown).
rhCTGF increased α-SMA, TIMP-1, PAI-1, and Col1 expression, and decreased E-cad expression in HK-2 cells
In the following in vitro experiments, we determined whether CTGF was the direct inducer of EMT, interstitial matrix accumulation, and interstitial fibrosis in HK-2 cells. The EMT was identified by the observation of dramatical downregulation of E-cad that is expressed in epithelial cells only, and upregulation of α-SMA and CTGF as mensenchymal-specific features. When HK-2 cells were treated with recombinant human CTGF (rhCTGF), the mRNA levels of α-SMA, TIMP-1, PAI-1, and Col1 were significantly increased, and E-cad was decreased compared with the NG (Figure 4E). Western blotting showed that the protein levels of α-SMA, TIMP-1, PAI-1, and Col1 were all greatly elevated after stimulation with rhCTGF, while the E-cad protein level was significantly downregulated (Figure 4C and D).
rhCTGF increased the apoptosis rate and Bax expression, and decreased Bcl-2 expression in HK-2 cells
To detect the direct effect of rhCTGF on apoptosis, the cells were cultured in DMEM-F12 medium containing rhCTGF for 24 hours. rhCTGF treatment significantly promoted the cell apoptosis rate examined by TUNEL, Hoechst 33258 staining, and FCM compared with the control group (Figure 4A and B). Next, we examined whether the rhCTGF-induced cell apoptosis was linked to the expression of Bax and Bcl-2. As shown in Figure 4C–E, rhCTGF upregulated the expression of the Bax mRNA and protein compared with the NG, whereas it inhibited the expression of Bcl-2 (Figure 2).
Transfection of CTGF siRNA altered the increased expression of CTGF, α-SMA, TIMP-1, PAI-1, and Col1, and decreased the expression of E-cad via stimulation of TGF-β1 in HK-2 cells
We found that the expression of the CTGF protein was increased in HK-2 cells in the rhTGF-β1-stimulated group (Figure 5A and B). rhTGF-β1 also increased CTGF mRNA levels (Figure 5C). Western blot analysis revealed that CTGF expression was significantly decreased after treatment with CTGF siRNA (Figure 5A and B). Furthermore, we analyzed the role of CTGF in the rhTGF-β1-induced increases of fibrogenesis-associated factors. Administration of CTGF siRNA markedly attenuated the increase in the mRNA and protein levels of α-SMA, TIMP-1, PAI-1, and Col1, and decreased the level of E-cad stimulated by rhTGF-β1 (Figure 5). Compared with the TGF-β1 group, the mRNA and protein expression did not change in cells treated with control siRNAs (data not shown).
Transfection of CTGF siRNA inhibited the increase in the apoptosis rate and Bax expression, and the decrease in Bcl-2 expression via stimulation of TGF-β1 in HK-2 cells
As shown in Figure 6A and B, exposure to rhTGF-β1 significantly increased cell apoptosis compared with NG. This increase was efficiently inhibited by transfection with CTGF siRNA as detected by FCM. As shown in Figure 6C–E, rhTGF-β1 stimulation of HK-2 cells for 24 hours decreased Bcl-2 levels and increased Bax levels compared with their expression levels in normal medium. Compared with the cells treated with rhTGF-β1, delivery of CTGF siRNA significantly ameliorated the decrease in Bcl-2 and the increase in Bax. Compared with the TGF-β1 group, the mRNA and protein expression did not change in cells treated with control siRNAs (data not shown).
Delivery of CTGF siRNA did not affect the decrease in Sirt1 induced by UUO in vivo or TGF-β1 in vitro
Figure 7A–C shows the decrease in the Sirt1 protein and mRNA levels in UUO kidneys. Likewise, Sirt1 activity was significantly decreased in UUO kidneys compared with the sham kidneys (Figure 7C). Sirt1 mRNA and protein levels were not altered by the delivery of CTGF siRNA compared with the UUO kidney (Figure 7A–C). There was also no difference in Sirt1 deacetylase activity between the UUO group and the CTGF siRNA plasmid group (Figure 7D). Next, we examined Sirt1 expression in TGF-β1-stimulated HK-2 cells. Sirt1 expression was confirmed to be decreased in the TGF-β1 group compared with the NG by immunocytochemistry (Figure 8A and B). Delivery of CTGF siRNA did not ameliorate the decrease of Sirt1 positive staining in vitro (Figure 8C). Concordantly, Sirt1 mRNA and protein levels measured by real-time RT-PCR and Western blotting were both decreased after TGF-β1 stimulation (Figure 8D–F); as expected, Sirt1 activity was also markedly decreased (Figure 8G). Furthermore, Sirt1 mRNA, protein levels, and deacetylase activity were not altered by the delivery of CTGF siRNA compared with rhTGF-β1-stimulated HK-2 cells (Figure 8D–G). Compared with the TGF-β1 group, the Sirt1 expression did not change in cells treated with control siRNAs (data not shown).
Overexpression of Sirt1 ameliorates TGF-β1-induced increases in CTGF, α-SMA, TIMP-1, PAI-1, and Col1, and decrease in E-cad expression in HK-2 cells
The overexpression of Sirt1 in HK-2 cells was confirmed by Western blotting (Figure 9A and B). The Sirt1 activity assay demonstrated that the overexpression of Sirt1 significantly increased Sirt1 deacetylase activity (Figure 9C). Western blotting and real-time RT-PCR both showed that HK-2 cells overexpressing Sirt1 significantly attenuated rhTGF-β1-induced increases in α-SMA, TIMP-1, PAI-1, and Col1, and the decrease in E-cad expression at 24 hours compared with the rhTGF-β1-stimulated group (Figure 9D–F), supporting the protective effect of Sirt1 on renal fibrosis. Sirt1 overexpression attenuated the increase in CTGF expression at the protein level by Western blotting analysis (Figure 9D and E) and the mRNA level based on real-time RT-PCR analysis (Figure 9F) in rhTGF-β1-induced HK-2 cells. Compared with the TGF-β1 group, the mRNA and protein expression did not change in cells treated with control siRNAs (data not shown).
Overexpression of Sirt1 reduces the rhTGF-β1-induced increase in the apoptosis rate and Bax expression and decreased Bcl-2 expression in HK-2 cells
As shown in Figure 10A and B, the percentage of apoptotic cells in the rhTGF-β1 HK-2 cell group at 24 hours was increased significantly compared with the NG. The administration of Sirt1 overexpression significantly reduced the percentages of apoptotic cells induced by rhTGF-β1. As shown in Figure 10C–E, Sirt1 overexpression increased Bcl-2 protein and mRNA levels, and decreased Bax protein and mRNA levels. Compared with the TGF-β1 group, the mRNA and protein expression did not change in cells treated with control siRNAs (data not shown).
Renal fibrosis inevitably progresses to end-stage renal disease with a progressive, irreversible decline in renal function, regardless of whether the origin is inflammatory or immunological, obstructive, metabolic, or systemic.22 To the best of our knowledge, in this study, we have provided the first evidence that the in vivo delivery of CTGF siRNA ameliorated tubular cell apoptosis and tubulointerstitial fibrosis in obstructed mouse kidneys. Our in vitro data also suggest the possible involvement of Sirt1 in the profibrotic action of CTGF in the presence of rhTGF-β1.
The pathogenesis of renal fibrosis has been depicted as a continuum of four overlapping phases: priming (localized inflammatory response), activation (activation and recruitment of matrix producing cells), execution (accumulation of matrix protein), and progression (loss of cells and renal function).23 CTGF and TGF-β, key mediators of kidney fibrosis, were identified on the basis of their contribution to these phases. CTGF is a cysteine-rich matricellular protein belonging to the CCN family of proteins, which have many diverse functions in processes such as angiogenesis, fibrosis, and apoptosis. TGF-β, a ubiquitously expressed cytokine, has also been demonstrated to promote tissue repair, but its excessive expression can mediate diverse profibrotic events in the liver,24 lung,25 kidney,26 and breast.27 CTGF enhances TGF-β signaling and facilitates TGF-β binding to TGF-β receptors.28 Moreover, correlative studies in humans and animals with tissue fibrosis support a link between CTGF and TGF-β. Most models postulate that CTGF acts either downstream or cooperatively with TGF-β.29,30 In this study, we found that the expression of CTGF and TGF-β1 were both increased in UUO obstructed kidneys and that rhTGF-β1 (5 ng/mL) treatment of HK-2 cells for 24 hours remarkably increased CTGF levels. In turn, this increase was accompanied by a significant upregulation of matrix accumulation, EMT, and apoptosis. This result is consistent with the observation that the expression of TGF-β and CTGF is increased in human and experimental models of chronic kidney disease and correlates with the severity of renal fibrosis.22,31–33
We used siRNA targeting to silence the CTGF gene, which is a valuable tool for investigating the function of gene products in tissues. To the best of our knowledge, this is the first report to show the effect of delivery of CTGF siRNA to a UUO mouse kidney. In this study, delivery of CTGF siRNA effectively downregulated the expression of CTGF in UUO kidneys in a sequence-specific manner, causing significant inhibition of tubular cell apoptosis and tubulointerstitial fibrosis. TGF-β1 is a potent inducer of CTGF, and CTGF acts downstream of TGF-β1 to promote fibrosis. Not surprisingly, TGF-β1 expression was not altered following CTGF siRNA plasmid treatment in obstructive kidneys after 7 days.
The elucidation of the molecular mechanisms of the profibrotic action of CTGF may provide clues to understand the pathogenesis of renal fibrosis associated with TGF-β1. Growing evidence has revealed that sirtuins (NAD-dependent protein deacetylases) play a regulatory role in the process of different renal diseases. The antifibrotic function of Sirt1 has been reported in patients with heart failure,34 cardiac fibrosis,35 hepatic steatosis,36 diabetic nephropathy,37 and UUO.17 In this study, we found that Sirt1 expression and activity were both dramatically decreased in UUO obstructed mouse kidneys. Recently, growing evidence has shown that Sirt1 is associated with TGF-β in endothelial cells,38 vascular smooth muscle cells,39 bronchial epithelial cells,40 and mesangial cells.15 Moreover, Sirt1 overexpression attenuated TGF-β1-induced extracellular matrix expression in cultured mesangial cells.15 Studies have suggested that the TGF-β1–Smad–SIRT6 pathway may play a critical role in the regulation of vascular smooth muscle cells differentiation in response to the cyclic strain.39 Indeed, the overexpression of Sirt6 efficiently inhibited TGF-β1-induced senescence in idiopathic pulmonary fibrosis.40 Therefore, we treated cultured HK-2 cells with rhTGF-β1 (5 ng/mL) to determine the role of Sirt1 in TGF-β1 profibrogenic activity. Our data showed that TGF-β1 treatment for 24 hours remarkably decreased the Sirt1 level, which was accompanied by a significant upregulation in matrix accumulation and EMT. Furthermore, we showed that overexpression of Sirt1 also abolished TGF-β1-induced upregulation of Col1, TIMP-1, and PAI-1 expression. These findings indicate that Sirt1 may functionally participate in the fibrogenesis induced by TGF-β1 in HK-2 cells, and suggest a beneficial role for Sirt1 in protecting the kidney from fibrosis; this result supports previous studies that showed an antifibrotic effect for resveratrol.41–43
We also demonstrated that Sirt1 overexpression effectively attenuated apoptosis in TGF-β1-treated HK-2 cells. TUNEL analysis, Hoechst 33258 staining, and FCM Annexin V/PI staining assay all exhibited the inhibition in the rhTGF-β1-induced apoptosis rate in HK-2 cells overexpressing Sirt1 at 24 hours. Western blotting and real-time RT-PCR revealed that Sirt1 overexpression increased Bcl-2 protein and mRNA levels, and decreased Bax protein and mRNA levels. Several studies have reported a protective effect for Sirt1 on apoptosis in multiple organs and tissues, such as the liver,44 lung,45 thyroid,46 pancreas,47 stomach,48 neurons,49 retina,50 and kidney, against injury due to diverse causes. H2O2-induced apoptosis was significantly attenuated in Sirt1-overexpressing murine mesangial cells (MMCs), but enhanced in Sirt1-knockdown MMCs.51 Moreover, the downregulation of Sirt1 expression in diabetes promoted podocyte apoptosis.52 The UUO model of kidney injury induced markedly increased renal apoptosis and fibrosis in Sirt1+/− mice compared with wild-type controls, while pharmacologic Sirt1 activation substantially attenuated apoptosis and fibrosis in wild-type mice.17 These findings further support the proposal that Sirt1 may be a promising therapeutic target of a common pathway of renal apoptosis and fibrosis.
In this study, we observed a close association between increased CTGF expression or decreased Sirt1 expression and renal fibrogenesis. These data suggest the possibility of a relationship between Sirt1 and CTGF. We found that Sirt1 expression and activity were significantly decreased in the UUO obstructed mouse kidney. In contrast, Sirt1 expression and activity were not altered following CTGF siRNA plasmid treatment in obstructive kidneys for 7 days. rhTGF-β1 (5 ng/mL) treatment for 24 hours remarkably increased CTGF levels and decreased Sirt1 levels in HK-2 cells. Nevertheless, the decrease in Sirt1 induced by rhTGF-β1 was not attenuated by CTGF siRNA. To further evaluate the relationship between Sirt1 and CTGF, we transfected HK-2 cells with a Sirt1 overexpression plasmid, and then investigated the effect of overexpressed Sirt1 on CTGF. Our results showed that overexpression of Sirt1 dramatically suppressed CTGF expression at the protein level in the presence of rhTGF-β1. These in vitro findings support the notion that it is likely that Sirt1 attenuates renal fibrogenesis and apoptosis by altering CTGF expression.
Only a few studies have discussed the relationship between Sirt1 and CTGF. Mao et al53 reported that the expression of Sirt1 was significantly upregulated in tumor samples from hepatocarcinoma patients, and Sirt1 mRNA levels positively correlated with CTGF mRNA levels. The results of our study and Mao’s study seem to lead to diametrically opposite conclusions. It has been demonstrated that Sirt1 is overexpressed in prostate, colon, breast, gastric, liver, and pancreatic tumors,54 while Sirt1 deficiency under various stress conditions, such as metabolic or oxidative stress or hypoxia, has been implicated in the pathophysiologies of age-related diseases including diabetes, cardiovascular diseases, neurodegenerative disorders, and renal diseases.55 Taken together, it is reasonable to speculate that the discrepancy between the two conclusions is due to the presence of tumors or other disease. This hypothesis requires further study.
In summary, we detected increased TGF and CTGF, and decreased Sirt1 expression levels in obstructed mouse kidneys. CTGF plays a direct and substantial role in the development of interstitial fibrosis in the kidney. This study also provides evidence that treatment strategies involving the delivery of siRNA targeting potentially therapeutic transgenes may be efficacious. Our results suggest that a decrease in Sirt1 is associated with the upregulated expression of CTGF in renal fibrosis. Additional insight into the relationship between Sirt1 with TGF-β1/CTGF in vivo will require with appropriate genetic, pharmacological, and physiological tools. Once this is achieved, it is expected that Sirt1 could become potential interesting targets for future therapies against fibrosis-related diseases (Figure 11).
The authors would like to acknowledge and thank Dr Michael E Greenberg for valuable contributions on providing free Sirt1 overexpressing plasmid. This work was supported by the National Natural Science Foundation of China (number 81200532) and the Natural Science Foundation of Hebei Province (number H2012206132).
The authors report no conflicts of interest in this work.
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