Figures
Abstract
Altered nucleoside levels may be linked to pathogenic signaling through adenosine receptors. We hypothesized that adenosine dysregulation contributes to fibrosis in diabetic kidney disease. Our findings indicate that high glucose levels and experimental diabetes decreased uptake activity through the equilibrative nucleoside transporter 1 (ENT1) in proximal tubule cells. In addition, a correlation between increased plasma content of adenosine and a marker of renal fibrosis in diabetic rats was evidenced. At the cellular level, exposure of HK2 cells to high glucose, TGF-β and the general adenosine receptor agonist NECA, induced the expression of profibrotic cell activation markers α-SMA and fibronectin. These effects can be avoided by using a selective antagonist of the adenosine A3 receptor subtype in vitro. Furthermore, induction of fibrosis marker α-SMA was prevented by the A3 receptor antagonist in diabetic rat kidneys. In conclusion, we evidenced the contribution of purinergic signaling to renal fibrosis in experimental diabetic nephropathy.
Citation: Kretschmar C, Oyarzún C, Villablanca C, Jaramillo C, Alarcón S, Perez G, et al. (2016) Reduced Adenosine Uptake and Its Contribution to Signaling that Mediates Profibrotic Activation in Renal Tubular Epithelial Cells: Implication in Diabetic Nephropathy. PLoS ONE 11(1): e0147430. https://doi.org/10.1371/journal.pone.0147430
Editor: Jean-Claude Dussaule, INSERM, FRANCE
Received: April 23, 2015; Accepted: January 3, 2016; Published: January 25, 2016
Copyright: © 2016 Kretschmar et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: Funded by grants FONDECYT 1130414 to RSM, 3150548 to WG and 1121121 to CQ from Comisión Nacional de Ciencia y Tecnología-Chile (CONICYT-Chile), www.conicyt.cl. Funded by grant S-2013-15 to CO from Universidad Austral de Chile, www.uach.cl. Funded by grant SAF2011-23660 to MPA from Ministerio de Economía de España, www.mineco.gob.es. SA hold doctoral fellowship from Comisión Nacional de Ciencia y Tecnología-Chile (CONICYT-Chile), www.conicyt.cl. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Diabetes mellitus is produced by a chronic metabolic unbalance and its incidence rate has dramatically increased worldwide [1]. Diabetic nephropathy (DN) is a long-term complication affecting up to 30–40% of diabetic patients and is the major cause of end-stage renal disease worldwide [2]. DN is also a major risk factor for cardiovascular disease and can be a life threatening condition. The economic and social impact of the illness is high, due to the fact that DN predisposes patients to undergo organ replacement therapies at advanced stages [3,4]. To date, strict controls of glycaemia and arterial blood pressure as well as the use of blockers of the renin-angiotensin system have only been modestly effective in slowing the evolution of DN [5]. Thus, DN remains incurable and there is an urgent demand for new therapies.
Incipient DN is characterized by the occurrence of podocytopathy and alterations in the filtration barrier which are clinically evidenced by hyperfiltration and microalbuminuria. As the disease advances an extensive renal fibrosis arises, characterized as a progressive and irreversible process [6]. A key event in this process is the transition of epithelial cells to a mesenchymal phenotype (EMT) acquiring the properties to mediate renal fibrosis and probably migrate to the interstitium. Typically, the expression of alpha smooth muscle actin (α-SMA) and fibronectin have been used as markers of profibrotic cells activation. Emerging evidence has shown that cytokines such as transforming growth factor-beta 1 (TGF-β), high glucose levels and advanced glycation end products influence profibrotic activation in kidney cells phenotype [7,8]. The discovery of mediators of this pathogenic process is a major current focus due to their valuable therapeutic potential.
Recently, it was demonstrated that a systemic rise of plasma adenosine and derived metabolites occurring in DN patients correlate with the progression of the disease, while the nucleoside levels were basal in diabetic patients without renal complication similar to those observed in healthy people [9,10]. Extracellular adenosine arises from the adenine nucleotide metabolism, thus becoming a crucial step the hydrolysis of AMP [11]. In addition, the equilibrative nucleoside transporters (ENTs), recognized by their sodium-independent facilitative transport activity, mediates the adenosine uptake to be metabolized intracellularly whereas nucleoside can be accumulated outside when the transport activity is reduced. Consequently, it has been described that ENTs could play a major contribution to adenosine availability for autocrine or paracrine signaling through adenosine receptors [12–22]. Notably, the transition from the epithelial to the mesenchymal phenotype was shown in the renal epithelial tubular cells line HK2 knocked down for the equilibrative nucleoside transporter member 1 (ENT1) [23]. These observations suggest a link between altered adenosine handling and profibrotic activation of cells. Adenosine modifies cell function by signaling via the P1 purinoceptor family [24]. While A1 and A2A subtypes have high affinity for their ligand, the A2B and A3 receptors require increased levels of adenosine to mediate a cellular response. Functionally, a protective role for adenosine A2A receptor subtype in diabetic nephropathy by attenuating inflammatory responses has been described [25]. Absence of A1 adenosine receptor results in an increase of both the diabetic hyperfiltration and the glomerular damage, thus suggesting that it also plays a protective task [26,27]. In contrast, the A2B receptor subtype mediates pathogenic events that trigger diabetic glomerulopathy [22]. While a role for the A3 receptor subtype has been recently associated with the progression of renal fibrosis in a model of chronic kidney disease [28], its contribution to the pathogenesis of diabetic renal disease remains to be analyzed.
The goal of this study was determine the mechanism that mediates altered adenosine handling in the diabetic kidney and its relation with purinergic signaling and renal fibrosis. We provide evidence of a decreased adenosine uptake occurring in the epithelial tubule cells of the diabetic kidney concomitant with the progression of renal disease. We also demonstrate the contribution of adenosine receptor signaling to the phenotypic transition of cells.
Material and Methods
Materials
Pharmacological modulators of adenosine receptors and inhibitors of nucleoside transporters were purchased from Tocris Biosciences. Culture mediums, serum, antibiotics and supplements were purchased from Invitrogen. Chemicals and streptozotocin were purchased from Merck KGaA. Tritiated adenosine was obtained from American Radiolabeled Chemicals.
Cell culture
Human proximal epithelial tubule cell line (HK2) was obtained from ATCC. The cells were propagated in Keratinocyte Serum Free Medium (K-SFM) supplemented with 0.05 mg/ml of bovine pituitary extract (BPE) and 5 ng/ml human recombinant epidermal growth factor (EGF) and antibiotics, at standard condition of 5% CO2 at 37°C in a humidified atmosphere.
Animal models
Diabetes was induced in male rats (Sprague-Dawley) weighing 250 g by single intravenous administration of streptozotocin (STZ) at 55 mg/kg dissolved in citrate buffer, pH 4.5. Controls rats were injected with an equivalent volume of vehicle. The diabetic groups included animals presenting blood glucose levels ≥ 25 mmol/L. Animals were monitored up to four months. Also diabetic rats were treated with the adenosine A3 receptor antagonist MRS1220 at doses 0.1 mg/kg via intraperitoneal administration from days 31 to 60 post diabetes induction, and animals were then sacrificed. Ent1 knockout mice were originally generated by Choi et al. [16]. Renal samples were obtained from the University of Barcelona´s own colony.
Ethics statement
All animal procedures were approved by the Institutional Committee on the Use of Live Animals in Research at the University Austral de Chile (Ref. 2012/59). Animal welfare was monitored daily and all efforts were made to minimize suffering. Any animal showing signs of limited movement or significant weight loss were euthanized by intra-peritoneal injection of sodium thiopental (200 mg/kg body weight).
Human biopsies
Human renal samples were obtained from patients controlled in the nephrology department of Fundació Puigvert, Barcelona, Spain. Use of samples was approved by the Comité Ético de Investigación Clínica (CEIC) from Fundació Puigvert (Ref. 2010/19). Percutaneous kidney biopsies from 9 diabetic patients with nephropathy and normal kidney tissue from 3 patients affected by renal carcinoma were used for the study. The biopsies were obtained for diagnosis in all patients before 2005, without further follow up in Fundació Puigvert, the study was submitted to ethic committee considering that following the current legislation, were not required informed consent for participate in this study.
Proximal convoluted tubule (PCT) isolation
Renal PCT were extracted from healthy and diabetic rats as described previously [29]. The kidneys were perfused through the renal artery, first with Hank's Balanced Salt Solution (HBSS) and then with HBSS containing 1mg/ml collagenase type II. Renal cortical slices were incubated for 10 minutes with HBSS/collagenase and maintained at 37°C, 50 mg/ml BSA was then added, maintaining the agitation for another 5 minutes. The homogenate was poured through gauze to eliminate non digested tissue. The extracts were centrifuged at 300 x g for 3 minutes and then the pellets were washed with HBSS without CaCl2 and centrifuged. The remaining material was resuspended in 45% percoll (GE Health Care) in solution HBSS without CaCl2 and centrifuged at 7900 x g for 15 minutes at 4°C, obtaining 3 phases. The middle phase, containing the PCT was extracted and washed. The pellet was diluted between 8 to 14 times depending of the amount. The PCT extracts were used immediately for transport activity assays. Purity of extracts was assessed by detecting the enrichment of the PCT marker aquaporin 1 and loss of glomerular nephrin and podocin.
Nucleoside transport activity
HK2 cells were cultured in 24 well plates in presence of 5mM or 25mM glucose for 24 h. Nucleoside transport activity was assayed in choline buffer (in mM: 5.4 KCl, 1.8 CaCl2, 1.2 MgSO4, 10 Hepes, 137 choline chloride, pH 7.4) supplemented with [3H]-adenosine (2mCi/nmol) and 10μM of adenosine at 22°C. Incubation was stopped after 20 seconds by washing the monolayers twice in 2 ml of cold buffer composed of 137 mM choline chloride and 10 mM Tris-Hepes, pH 7.4. Cells were then lysed in 0.250 ml of 1M NaOH. Aliquots were taken for protein determination and for radioactivity counting. Particular uptake rates for equilibrative nucleoside transporters 1 or 2 (ENT1, ENT2) were assigned to transport activities which were inhibited by 1 μM S-(4-nitrobenzyl)-6-thio-inosine (NBTI) or 2 mM hypoxanthine, respectively [30]. Total nucleoside uptakes in cells mediated by concentrative and equilibrative systems were also measured using transport buffer containing sodium chloride. Sodium-dependent uptake rates were obtained by subtracting adenosine uptakes in choline buffer to the total adenosine uptakes in buffer containing sodium chloride.
Nucleoside transport activity in PCT
Freshly purified PCTs were incubated in 100μl of choline solution with or without NBTI or hypoxanthine for 30 minutes. Nucleoside transport activity was assayed in choline buffer supplemented with or without NBTI or hypoxanthine, with [3H]-adenosine (2mCi/nmol), and 20 μM of adenosine. The uptake of adenosine was assayed adding 100μl of solution with [3H]-adenosine for 20 seconds at 22°C. Incubation was stopped by washing with 1ml of cold buffer composed of 137 mM choline chloride and 10 mM Tris-Hepes (pH 7.4). Cells were then centrifuged at 12000 x rpm for 5 minutes at 4°C and washed again. After the second wash the pellet was dissolved in 250μl of 0.5M HCOOH. Aliquots were sampled for protein determination and for radioactivity counting.
Adenosine quantification
HK2 cells were cultured at 80% confluence under standard conditions in 6 well plates for 24 h. The medium was then replaced for Tyrode buffer (10mM HEPES, 12mM NaHCO3, 137mM NaCl, 2.7mM KCl, 5mM Glucose and 1mM CaCl2) supplemented with 2.5μM EHNA and 1μM NBTI for 1h. The adenosine content was quantified using derivatization with 2-chloroacetaldehyde and HPLC with fluorometric detection [20]. The values were normalized to the total amount of cellular proteins. For adenosine quantification in plasma of rats, samples of blood were extracted in proportion 3:1 with STOP solution (10mM EDTA, 10mM EGTA, 1 mM dipyridamole and 2.5 μM EHNA) from caudal vein. Plasma samples were deproteinized using 10% TCA, neutralized with 2 N KOH and treated with solution ZN/Ba [10]. Finally, samples were derivatized and quantified as described above.
Protein extracts
Total proteins were extracted with lysis buffer (2% SDS, 10% glycerol, 63.5 mM Tris HCl, pH 6.8) containing Complete Proteinase Inhibitor and 1μg/ml pepstatin (Roche). The proteins were quantified using BCA protein assay kit (Thermo Scientific).
Western blots
Protein extracts (50μg) were fractionated by 10% SDS-PAGE and transferred to PVDF membranes. The blots were washed with wash buffer (PBS1x, 0.05% Tween20), blocked for 1 h with 0.1% BSA, and incubated with primary antibodies anti-fibronectin (SC-56391), anti-α-SMA (SC-130617) or anti-Pro-COL1A2 (SC-8787) from SantaCruz Biotechnology, and anti-ENT1 from Protein Tech (II 337-1-A7). Primary antibodies against adenosine receptors were anti-A1AR from Sigma, anti-A2AAR and anti-A2BAR from Abcam and anti-A3AR from Millipore. The membranes were washed and the primary antibodies were detected using HRP-coupled secondary antibodies. A chemiluminescence procedure was used for the detection of the proteins (Thermo Scientific). The protein levels were expressed as the ratio between the target protein and β-actin or tubulin detected in the same membrane.
siRNA
Adenosine A3 receptor subtype knockdown was achieved in HK2 cells using commercially available and validated short interfering RNAs (siRNA) from Ambion catalogue number AM16708. Cells seeded in 6-well plates (200,000) were transfected with 100 pmol of siRNA using lipofectamine 3000. Following 24 h post-transfection the cells were exposed to transdifferentiation stimuli and the expression of fibronectin was evaluated by western blot.
Immunohistochemistry
Rat and human kidney tissues were fixed in formalin, embedded in paraffinand 5 μm sections were mounted on silanized slides. Immunodetections were performed as described previously [20] using the primary polyclonal anti-ENT1 antibody from Protein Tech (II 337-1-A7) and the monoclonal anti-αSMA (sc130617) and anti-A3AR (sc-13938) from Santa Cruz Biotechnology. The immunosignals were detected using the LSAB+ System–HRP (DakoCytomation).
Results
Diabetes modifies extracellular adenosine metabolism in epithelial tubule cells
In order to characterize the mechanisms that control extracellular levels of adenosine, we analyzed the nucleoside uptake rates mediated by the nucleoside transporters in epithelial tubule cells. Using the epithelial cell line HK2, derived from human proximal tubules, it was determined that the adenosine uptake activity was largely mediated by the equilibrative sodium-independent transporters (ENTs) compared to the negligible activity mediated by the concentrative nucleoside transporters (CNTs). Particular uptake rates mediated by ENT1 or ENT2 subtypes could be individualized through selective inhibition with 1 μM S-(4-nitrobenzyl)-6-thio-inosine (NBTI) or 2 mM hypoxanthine, respectively [30]. Thus, the uptake mediated by the equilibrative nucleoside transporter-1 (ENT1) was far more significant in comparison to the transport activity mediated by ENT2 in these cells (Fig 1A). Further, we mimicked the effects of diabetes in HK2 cells by exposing them to high D-glucose concentrations. Upon exposure of HK2 to 25mM D-glucose, the ENT1-mediated uptake of adenosine decreased by 50% in comparison to 5mM D-glucose (Fig 1A).
A. Total and particular [3H]adenosine transport activities were assayed in HK2 cells. The effect of D-glucose concentration on transport activities was assayed in HK2 cells exposed to 5mM and 25mM for 24h. Total uptake activity mediated by concentrative (CNTs) and equilibrative (ENTs) systems was obtained in transport buffer containing Na+; while ENTs-mediated uptake was determined by using a Na+ free buffer. CNTs component was derived from the difference between total transport activity in Na+ containing buffer minus the transport activity in Na+ free buffer. The graphs depict particular ENT1 mediated nucleoside uptake as the fraction of the transport in Na+ free buffer inhibited by 1μM NBTI, while the ENT2 fraction that was inhibited by 2mM hypoxanthine. Data is expressed as mean ± SD of triplicate measurements from 20 independent assays. * P < 0.05 versus 5mM D-glucose. B. Renal proximal tubules were isolated from vehicle- and STZ-treated rats following 1 and 4 months. The effect of diabetes on sodium-independent transport uptake activities mediated by ENT1 and ENT2, was quantified. Data is expressed as mean ± SD of triplicate measurements for assays using extracts from 5 animals in each group. * P < 0.05 versus control. C. The protein level of ENT1 in tubule extracts was evaluated by western blot. Representative images of western blots using diabetic (db) and control (ctr) rat extracts are shown. The graph depicts the mean ± SD of ratio between immune signals of ENT1 vs tubulin. The ratio in control extracts were normalized to 1. A statistically significant difference was not found. n = 6. D. The extracellular adenosine levels were quantified in the medium of HK2 cells exposed to NBTI, an inhibitor of ENT1 activity. Data is mean ± SD from 5 experiments. * P < 0.05 versus control.
To further assess the consequences of experimental diabetes on adenosine handling, proximal tubules were isolated from healthy and diabetic rats. Following the induction of experimental diabetes in rats, glycemic levels were raised to values around 450 mg/dl, gaining of mass was depressed and the kidney weight relative to the total body weight was increased which is indicative of kidney hypertrophy (Table 1). The progression of renal injury was evidenced by the detection of increasing levels of proteinuria and urea, manifestly higher than controls animals at 4 months post diabetes induction. In addition, nephropathy manifests with increased uric acid levels, a metabolite generated from purines catabolism (Table 1). Furthermore, an extensive abundance of the alpha-smooth muscle actin (α-SMA) was detected in the cortical area of kidney from diabetic rats following four months of diabetes induction (Fig 2A). Therefore, our analyses in tissue samples from rats following 1 and 4 months post diabetes induction represent early and manifest stages of kidney injury respectively.
A. Representative immunohistochemical detection of α-SMA in kidney sections from vehicle- and STZ-treated diabetic rats. The arrows indicate interstitial and periglomerular staining. B. The graph depicts plasmatic adenosine levels in control and diabetic rat groups. * P < 0.05 vs control, n = 6. C. Representative immunohistochemical detection of α-SMA in kidney sections from 8 weeks old ent1-/- and wild type mice. The graphs (A and C) show quantitative results derived from staining analyses of consecutive field from three animals per group using the UN-SCANIT 2.0 software. Values of control or wild type samples were normalized to 1. * P < 0.05 vs control or wild type. Original magnifications 200X.
Adenosine uptake rates were found to be decreased by diabetes in isolated renal tubules due to a lesser ENT1-mediated activity (Fig 1B), despite the fact that the content of ENT1 in rat renal tissues was not altered by experimental diabetes (Fig 1C). Reduction of adenosine uptake mediated by ENT1 was higher than 70% following one (0.230 ± 0.087 vs 0.060 ± 0.039 pmol • μmoles prot-1 • min-1, P value < 0.01) and four (0.200 ± 0.047 vs 0.053 ± 0.019 pmol • μmoles prot-1 • min-1, P value < 0.01) months from diabetes induction (Fig 1B). Remarkably, the consequence of inhibition of ENT1 activity using NBTI resulted in a marked increase in extracellular adenosine levels in HK2 cells (Fig 1D).
Adenosine mediates profibrotic changes in epithelial tubule cells
A pivotal correlation was evidenced between the mark of the α-SMA, a sign of profibrotic cells activation, and the increase of plasma levels of adenosine in diabetic rats (Fig 2B). Pearson correlation value r was 0.7934 with P value < 0.01 (n = 28). Furthermore, kidneys isolated from ent1-/- knockout mice showed higher levels of α-SMA (Fig 2C). Adenosine renal interstitial levels have been found to rise in ent1-/- mice or animals treated with an inhibitor of its activity [21]. Also, when cells were incubated with dipyridamole to block ENT transport activity, profibrotic changes were induced [23]. These observations suggest a link between altered adenosine handling and profibrotic activation that remains to be elucidated.
The cellular effects of adenosine are mediated by the P1 family of purinergic receptors. The four subtypes of adenosine receptors were found at RNA and protein levels in HK2 cells. The exposure of HK2 cells to the general adenosine receptors agonist NECA induced the expression of the profibrotic markers fibronectin, α-SMA and procollagen type I (Fig 3). These effects were similar to those observed using high D-glucose (25mM) or TGF-β, recognized inducers of profibrotic phenotypic transition in epithelial cells (Fig 3).
The induction of profibrotic markers α-SMA, fibronectin and pro-collagen were evaluated by western blot in HK2 cells treated for 24 h with the general agonist of adenosine receptors NECA (5 μM), TGF-β (2 ng/ml) and high D-glucose (25mM). Representative western blots are shown.
To characterize the adenosine receptor subtypes involved in profibrotic activation, HK2 cells were exposed to a set of selective pharmacological antagonists in conjunction with the general agonist NECA. As shown in Fig 4, the induction of fibronectin and α-SMA mediated by NECA can be blocked using MRS1220, the antagonist of adenosine A3 receptor subtype, independent of the concentrations of D-glucose in the medium (Fig 4). In addition, the antagonist of the A1 receptor subtype blocked the induction of markers in cells exposed to 5mM D-glucose but it was unable to reproduce these effects in cells exposed to a high D-glucose environment (Fig 4). Interestingly, the profibrotic activation using TGF-β can be also blocked by MRS1220 in this cell line in both 5 and 25 mM D-glucose conditions (Fig 5A). Further demonstration of the role of the adenosine A3 receptor subtype was obtained from siRNA experiments. In addition to prevent the induction of fibronectin mediated by NECA and high D-glucose (S1 Fig), the knockdown of the A3 receptor subtype prevented HK2 cell transition in 5 and 25 mM D-glucose conditions TGF-β induced (Fig 5B).
The particular adenosine receptor subtype involved in profibrotic activation was recognized by using selective pharmacological antagonists for each receptor subtype, in conjunction with the general agonist NECA (5 μM). The induction of the markers fibronectin (A) and α-SMA (B) in HK2 cells, was evaluated by western blots. Selective antagonists were DPCPX (30nM) for A1, ZM241385 (10nM) for A2A, MRS1754 (50nM) for A2B and MRS1220 for A3 (10nM) receptor subtypes. The upper images show representative western blot detections of marker content in total protein extracts (50 μg) from treated HK2 cells. The blocking effect was assayed in HK2 cell cultures in 5mM (left white bars graphs) or 25mM (right black bars graphs) D-glucose. The graphs represent the mean ± SD of the ratio between immune signals of fibronectin or α-SMA vs β-actin. The ratio in HK2 cells without any pharmacological modulator was normalized to 1. * P < 0.05 versus untreated cells, # P < 0.05 versus NECA, n = 6.
A. The induction of the marker fibronectin was evaluated by western blots in HK2 cells upon exposure to TGF-β. The contribution of a particular adenosine receptor subtype in TGF-β-induced cell activation, was recognized by using selective pharmacological antagonists. Selective antagonists were DPCPX (30nM) for A1, ZM241385 (10nM) for A2A, MRS1754 (50nM) for A2B and MRS1220 for A3 (10nM) receptor subtypes. B. The particular contribution of the adenosine A3 receptor was evidenced by knocking down the expression of the receptor using siRNA (siRNA A3AR). The upper images show representative western blot detections of fibronectin content in total protein extracts (50 μg) from treated HK2 cells. The blocking effect was assayed in HK2 cells cultures 5mM (left white bars graphs) or 25mM (right black bars graphs) D-glucose. The graphs represent the mean ± SD of the ratio between immune signals of fibronectin vs β-actin. The ratio in HK2 cells without TGF-β treatment was normalized to 1. * P < 0.05 versus untreated cells, # P < 0.05 versus TGF-β, n = 5.
In vivo evaluation of an adenosine A3 receptor antagonist in diabetic rats
The examination of the content of the adenosine receptors in HK2 cells by western blot analysis indicates that the total levels were not affected by the exposure of cells to different D-glucose concentrations (Fig 6A). Furthermore, the content of adenosine receptors in purified tubule extracts did not change following 1 or 4 months post diabetes induction in rats (Fig 6B). Therefore, the possibility to be pharmacologically modulated is conceivable. Following one month post diabetes induction, diabetic rats were treated with MRS1220 or vehicle for 4 weeks. Immune staining of α-SMA was significantly reduced in renal cortical tubules from MRS1220-treated animals compared to vehicle-treated diabetic rats (Fig 7). Treatment with the A3 receptor antagonist did not affect the increased plasma adenosine levels in diabetic rats at this stage (data not shown).
A. The effect of D-glucose exposure (24 h) on the protein levels of adenosine receptor subtypes A1, A2A, A2B and A3 in HK2 cells was evaluated by western blot. Representative images of western blots of total protein extracts from cells exposed to 5 and 25 mM D-glucose are shown. B. The effect of STZ-induced diabetes on adenosine A3 receptor content was evaluated by western blot of total protein extracts from tubules isolated from control (ctr) and diabetic (db) rats following 1 or 4 months post-induction. The graphs show quantitative analysis of immune signals. The means in controls were normalized to 1. A: n = 6, B: n = 3.
Diabetic rats were treated with the adenosine A3 receptor antagonist MRS1220 from days 31 to 60 post diabetes induction, A. Representative inmunohistochemical detection of α-SMA in cortical areas of kidney sections from untreated (control), diabetic (vehicle-treated rats) and MRS1220-treated diabetic rats. Original magnifications 400X. B. The graph shows quantitative results derived from staining analyses of consecutive field from three animals per group using the UN-SCANIT 2.0 software. Values of control samples were normalized to 1. * P < 0.05 vs control.
Evaluation of ENT1 and adenosine A3 receptor in human diabetic nephropathy
Whereas, the STZ-treated diabetic rat model permits the early evaluation of moderate kidney injury, human DN progresses with an extensive renal fibrosis. To further evaluate the expression of ENT1 and the adenosine A3 receptor throughout the progression of human diabetic kidney disease, immune detection of both proteins were carried out in biopsies from normal, moderate and advanced kidney injury. Clinical parameters in patients are shown in S1 Table. The distribution of α-SMA was used to show progression of kidney fibrosis in biopsies (Fig 8). In the most severe renal tubule-interstitial fibrosis damage, glomerulosclerosis with low cellularity and loss of tubular structures was evident. The ENT1 expression was mainly restricted to tubular epithelium and some glomerular cells. This pattern was maintained with the progression of renal injury. The adenosine A3 receptor was located in the epithelial tubule cells, glomerular cells and Bowman’s capsule in normal tissue. Along with the lower glomerular cellularity observed in advanced stages of renal injury, both the content of ENT1 and A3AR were decreased in renal glomeruli. In contrast, the tubulointerstitial distribution of the adenosine A3 receptor subtype was shown increased in human biopsies throughout the progression of kidney injury (Fig 8).
A. Immunohistochemical detection of ENT1 and A3 receptor proteins were carried out in human kidney sections from non-diabetic normal tissue and biopsies from diabetic nephropathy patients. Selected images denote representative progressive stages of renal injury probed by the content of α-smooth muscle actin (α-SMA) and pathological analysis. Arrows indicate interstitial distribution of the immune signal. Original magnification 200x. Scale bars 50μm. B. Representative negative control without primary antibody. Quantitative image analyses of immune staining for ENT1 (C) A3AR (D) and α-SMA (E) in human biopsies. The graphs show quantitative results derived from staining analyses in defined areas (at least 5 glomeruli, 10 tubules and 10 interstitium per sample) using the UN-SCANIT 2.0 software. Human biopsies from 9 diabetic nephropathy patient and 3 controls are individualized in S1 Table. Values in normal tissue samples were normalized to 1. * P < 0.05 vs normal.
Discussion
This study is the first show a link between profibrotic activation of renal epithelial tubule cells with the activity of the adenosine A3 receptor in the context of diabetic renal disease. Thus, the purpose of our research was i) to demonstrate the role of high glucose on altered nucleoside handling in proximal tubule epithelial cells, ii) correlate lower nucleoside uptake activity mediated by ENT1 with increased adenosine levels and iii) to connect increased ligand levels with cellular profibrotic effects mediated by low affinity adenosine receptors. We contribute to the emerging notion that implicates a chronic increase of adenosine with fibrotic processes. Indeed, experimental models have associated such elevated levels of nucleoside and adenosine receptor activity with the progress of hepatic, dermal and pulmonary fibrosis, and recently with chronic kidney disease [31–33].
ENT1 is the main nucleosides transporter in proximal tubules [34] and responsible for the basolateral uptake of adenosine [21]. Extensive distribution of ENT1 throughout the kidney indicates that this transporter plays a role in adenosine signaling beyond nucleoside and nucleobase homeostasis [20,35]. While, decreased ENT1 activity, capable of increasing adenosine levels, has been described as renoprotector in an acute kidney injury model using tissue ischemia and reperfusion [21], the chronic reduction of nucleoside uptake could underlay DN pathogenic fibrosis. Certainly, long term hyperglycemia concurs with decreased ENT1 activity and increasing levels of adenosine in our experimental model. In turn, autocrine/paracrine adenosine signaling mediates fibrotic phenotypic changes in epithelial tubule cells. This injurious loop was impeded by knocking down the A3 receptor in HK2 cells and by using a pharmacological antagonist in diabetic rats. These findings suggest that adenosine receptor blockers may be useful as new therapeutic approach.
There are several evidences showing that glucose levels play a role in the control of ENTs activity [30,36–38]. Some reports recognize insulins action of counteracting decreased nucleoside uptake activity imposed by elevated D-glucose, through ENT1 activity rescue and increasing ENT2-mediated transport [30,36–38]. Probably, these facts could link the deficient insulin signaling and hyperglycemia in renal cells with increasing levels of the nucleoside and the pathogenesis of DN. It is worth noting that in glomeruli isolates from diabetic rats, extracellular adenosine levels were considerably increased in comparison to controls however differences were not seen for other adenine nucleotides [22]. Only sodium-independent uptake activity mediated by ENT1 was inhibited. Probably, it became the main engine for increasing extracellular adenosine, despite the fact that slight changes on AMP hydrolyzing activity have been previously described [22].
The particular increase of plasma adenosine levels in DN patients was described in recent years [9,10], linking the progression of renal injury with adenosine signaling. Using diverse experimental models it has been further suggested that adenosine signaling and receptor induction are common pathogenic pathways in chronic kidney injury [33]. Thus, the adenosine deaminase knockout (ada-/-) mice model, exhibiting augmented levels of the nucleoside because of impeded metabolism, shows renal dysfunction and sclerosis. In addition, Dai and collaborators demonstrated that development of renal fibrosis generated in ada-/- animals can be avoided using an A2BAR antagonist [33]. Promising outcomes were also obtained on renal fibrosis in mice caused by angiotensin II or unilateral ureteral obstruction (UUO) [33]. Furthermore, the diabetic glomerular alterations in STZ-treated rats were ameliorated using an antagonist of A2BAR [22], regardless of the recent proposal that A2BAR has a vascular protective effect in a model of DN [39]. Interestingly, it has recently been described the implication of the adenosine A3 receptor subtype in mediating fibrosis in the UUO experimental model [28], so the antagonist LJ-1888 was able to ameliorate tubule-interstitial fibrosis. Consequently, such protective effects of antagonists of low affinity receptors A2B and A3 could come from the inhibition of the pathogenic effects of adenosine differentially occurring in renal cells types since, the induction of the A2B receptor subtype has been related to podocyte cell dysfunction, increased TGF-β release and diabetic glomerulosclerosis [20,22] while here, we showed that the A3 receptor may be associated with profibrotic activation of tubular epithelial cells.
The location of the A3AR subtype in the kidney has not been conclusively determined. We found that the localization of A3AR was widely distributed in epithelial tubule cells. In addition, we detected the A3AR protein in glomerular cells. Pawelczyk et al [40] described that membrane-associated A3AR protein levels increased by 70% in diabetic kidney cortex and decreased by 80% in medulla. Such increase may not be ascribed to proximal tubule cells because we did not observe changes in the receptor content due to diabetes. Notably, the receptor content was extended to tubulointerstitium in biopsies from DN patients with advanced progression of injury. This fact suggests that with the progression of the disease the interstitium was enriched with A3AR positive cells that could direct interstitial fibrosis. One of the mechanisms involved in renal fibrosis is the infiltration of macrophages which secret several cytokines underlying fibroblast activation and myofibroblast generation [41,42]. In this context, the anti-inflammatory effect of A3AR agonists has been previously suggested [43,44]. On the other hand, epithelial proximal tubule cells seem to be capable of transdifferentiate to a primitive mesenchymal phenotype (epithelial to mesenchymal transition, EMT) in response to certain physiological cues, conducted predominantly by TGF-β [45,46]. In essence, has been proposed these cells appear to be capable of altering their morphology, expressing myofibroblastic markers, and migrating through basement membrane into the interstitium, thus joining the pool of activated fibroblasts. It is suggested that EMT contributes up to one-third of the interstitial cells population that produce fibrotic mediators and extracellular matrix [47]. This process has been recognized in biopsies of patients with DN [48] and strong correlations were established between the EMT occurrence, interstitium expansion and collagen deposition [49,50]. In fact, EMT, myofibroblastic transdifferentiation, proteinuria and the decline in renal function are strongly correlated thus, supporting α-SMA immunostaining to monitor renal fibrosis in diabetic patients [49,50]. Thus, the exact source of A3AR positive cells and their role to renal fibrosis remains to be a debate.
Notably, the induction of α-SMA and fibronectin mediated by TGF-β in HK2 cells were blocked by the A3AR antagonist, suggesting a crosstalk between adenosine and the cytokine intracellular signaling. Consequently, it was suggested that the anti-fibrotic effect of the A3AR antagonist LJ-1888 in the presence of TGF-β up-regulation in the UUO rats kidneys, may account for MAP kinases inactivation [28]. It has been described that the adenosine A1 and A3 receptor subtypes share some signaling properties such as both receptors are coupled to Gi protein and could trigger MAP kinases activation [24,51]. This property could be evident when antagonizing A1 and A3 receptor subtypes, both preventing HK2 cell transdifferentiation under low D-glucose levels. However, the particular signaling property that implicates A3AR with TGF-β mediated profibrotic activation, is a novel topic that remain to be elucidated.
Collectively, our data link the mechanism mediating the increased adenosine levels with the activity of adenosine A3 receptor. This study supports the evaluation of preclinical studies to assess the efficacy of this new alternative for the treatment of DN targeting renal fibrosis.
Supporting Information
S1 Fig. Adenosine A3 receptor knockdown blocks fibronectin induction mediated by NECA and high D-glucose.
A. The content of the adenosine A3 receptor was evaluated by western blot in HK2 cells transfected with commercially available and validated short interfering RNAs (siRNA) from Ambion (catalogue number AM16708). Typically transfection using 100 pmol of selective siRNA decreased A3AR by 80%. B. The induction of the EMT marker fibronectin was evaluated by western blot in HK2 cells upon exposure to NECA (5μM) and 5mM (control) or 25mM (HG) D-glucose. The particular contribution of the A3AR was evidenced by knocking down the expression of the receptor using siRNA (siRNA A3). The graph represents the mean ± SD of the ratio between immune signals of fibronectin vs tubulin. The ratio in HK2 cells in 5mM D-glucose treatment was normalized to 1. # P < 0.05 versus NECA or HG, n = 6.
https://doi.org/10.1371/journal.pone.0147430.s001
(TIF)
Acknowledgments
We thank technician Genaro Alvear for performing the Masson staining in the kidneys and Amber Philp for language edition.
Author Contributions
Conceived and designed the experiments: RSM MPA CQ CO. Performed the experiments: CK CV CJ SA GP MMDE WG CO. Analyzed the data: RSM MPA MMDE CQ CO. Contributed reagents/materials/analysis tools: RSM MPA MMDE CQ CO. Wrote the paper: RSM MPA CQ MMDE.
References
- 1. Yach D, Stuckler D, Brownell KD. Epidemiologic and economic consequences of the global epidemics of obesity and diabetes. Nat Med. 2006;12:62–66. pmid:16397571
- 2. Gross JL, De Azevedo MJ, Silveiro SP, Canani LH, Caramori ML, Zelmanovitz T. Diabetic nephropathy: diagnosis, prevention, and treatment. Diab Care. 2005;28:164–176.
- 3. American Diabetes Association. Standards of medical care in diabetes. Diab Care. 2010;33:S11–S61.
- 4. Gaede P, Lund-Andersen H, Parving HH, Pedersen O. Effect of a multifactorial intervention on mortality in type 2 diabetes. N Engl J Med. 2008;358:580–591. pmid:18256393
- 5. De Boer IH, Rue TC, Hall YN, Heagerty PJ, Weiss NS, Himmelfarb J. Temporal trends in the prevalence of diabetic kidney disease in the United States. JAMA. 2011;305:2532–2539. pmid:21693741
- 6. Nath KA. The tubulointerstitium in progressive renal disease. Kidney Int. 1998;54:992–994. pmid:9734628
- 7. Simonson MS. Phenotypic transitions and fibrosis in diabetic nephropathy. Kidney Int. 2007;71:846–854. pmid:17342177
- 8. Hills C, Squires P. TGF-β1-Induced Epithelial-to-Mesenchymal Transition and Therapeutic Intervention in Diabetic Nephropathy. Am J Nephrol. 2010;31:68–74. pmid:19887790
- 9. Xia JF, Hu P, Liang QL, Zou TT, Wang YM, Luo GA. Correlations of creatine and six related pyrimidine metabolites and diabetic nephropathy in Chinese type 2 diabetic patients. Clin Biochem. 2010;43:957–962. pmid:20510896
- 10. Xia JF, Liang QL, Liang XP, Wang YM, Hu P, Li P, et al. Ultraviolet and tandem mass spectrometry for simultaneous quantification of 21 pivotal metabolites in plasma from patients with diabetic nephropathy. J Chromatogr B Analyt Technol Biomed Life Sci. 2009;877:1930–1936. pmid:19501555
- 11. Quezada C, Alarcón S, Jaramillo C, Muñoz D, Oyarzún C, San Martín R. Targeting adenosine signaling to treatment of diabetic nephropathy. Curr Drug Targets. 2013;14:490–496. pmid:23316933
- 12. Mubagwa K, Flameng W. Adenosine, adenosine receptors and myocardial protection: an updated overview. Cardiovasc Res. 2001;52:25–39. pmid:11557231
- 13. Ackley MA, Governo RJ, Cass CE, Young JD, Baldwin SA, King AE. Control of glutamatergic neurotransmission in the rat spinal dorsal horn by the nucleoside transporter ENT1. J Physiol. 2003;548:507–517. pmid:12611914
- 14. Sonoki K, Iwase M, Iino K, Ichikawa K, Yoshinari M, Ohdo S, et al. Dilazep and fenofibric acid inhibit MCP-1 mRNA expression in glycoxidized LDL-stimulated human endothelial cells. Eur J Pharmacol 2003;475:139–147. pmid:12954370
- 15. Gadalla AE, Pearson T, Currie AJ, Dale N, Hawley SA, Sheehan M, et al. AICA riboside both activates AMP-activated protein kinase and competes with adenosine for the nucleoside transporter in the CA1 region of the rat hippocampus. J Neurochem. 2004;88:1272–1282. pmid:15009683
- 16. Choi DS, Cascini MG, Mailliard W, Young H, Paredes P, McMahon T, et al. The type 1 equilibrative nucleoside transporter regulates ethanol intoxication and preference. Nat Neurosci. 2004;7:855–861. pmid:15258586
- 17. Riksen NP, Rongen GA, Boers GH, Blom HJ, Van den Broek PH, Smits P. Enhanced cellular adenosine uptake limits adenosine receptor stimulation in patients with hyperhomocysteinemia. Arterioscler Thromb Vasc Biol. 2005;25:109–114. pmid:15539618
- 18. Carrier EJ, Auchampach JA, Hillard CJ. Inhibition of an equilibrative nucleoside transporter by cannabidiol: a mechanism of cannabinoid immunosuppression. Proc Natl Acad Sci USA. 2006;103:7895–7900. pmid:16672367
- 19. Farías M, San Martín R, Puebla C, Pearson JD, Casado JF, Pastor-Anglada M, et al. Nitric oxide reduces adenosine transporter ENT1 gene (SLC29A1) promoter activity in human fetal endothelium from gestational diabetes. J Cell Physiol. 2006;208:451–460. pmid:16688763
- 20. Roa H, Gajardo C, Troncoso E, Fuentealba V, Escudero C, Yáñez A, et al. Adenosine mediates transforming growth factor-beta 1 release in kidney glomeruli of diabetic rats. FEBS Lett. 2009;583:3192–3198. pmid:19737558
- 21. Grenz A, Bauerle JD, Dalton JH, Ridyard D, Badulak A, Tak E, et al. Equilibrative nucleoside transporter 1 (ENT1) regulates postischemic blood flow during acute kidney injury in mice. J Clin Invest. 2012;122:693–710. pmid:22269324
- 22. Cárdenas A, Toledo C, Oyarzún C, Sepúlveda A, Quezada C, Guillén-Gómez E, et al. Adenosine A2B receptor-mediated VEGF induction promotes diabetic glomerulopathy. Lab Invest. 2013;93:135–144. pmid:23069939
- 23. Guillén-Gómez E, Pinilla-Macua I, Pérez-Torras S, Choi DS, Arce Y, Ballarín JA, et al. New role of the human equilibrative nucleoside transporter 1 (hENT1) in epithelial-to-mesenchymal transition in renal tubular cells. J Cell Physiol. 2012;227:1521–1528. pmid:21678404
- 24. Fredholm BB, IJzerman AP, Jacobson KA, Linden J, Müller CE. International Union of Basic and Clinical Pharmacology. LXXXI. Nomenclature and classification of adenosine receptors-an update. Pharmacol Rev. 2011;63:1–34. pmid:21303899
- 25. Awad AS, Huang L, Ye H, Duong ET, Bolton WK, Linden J, et al. Adenosine A2A receptor activation attenuates inflammation and injury in diabetic nephropathy. Am J Physiol Renal Physiol. 2006;290: F828–837. pmid:16332931
- 26. Faulhaber-Walter R, Chen L, Oppermann M, Kim SM, Huang Y, Hiramatsu N, et al. Lack of A1 adenosine receptors augments diabetic hyperfiltration and glomerular injury. J Am Soc Nephrol. 2008;19: 722–730. pmid:18256360
- 27. Vallon V, Schroth J, Satriano J, Blantz RC, Thomson SC, Rieg T. Adenosine A1 receptors determine glomerular hyperfiltration and the salt paradox in early streptozotocin diabetes mellitus. Nephron Physiol. 2009;111:30–38.
- 28. Lee J, Hwang I, Lee JH, Lee HW, Jeong LS, Ha H. The selective A3AR antagonist LJ-1888 ameliorates UUO-induced tubulointerstitial fibrosis. Am J Pathol. 2013;183:1488–1497. pmid:24001475
- 29. Vinay P, Gougoux A, Lemieux G. Isolation of a pure suspension of rat proximal tubules. Am J Physiol. 1981;241: F403–411. pmid:6119031
- 30. Muñoz G, San Martín R, Farias M, Cea L, Vecchiola A, Casanello P, et al. Insulin restores glucose inhibition of adenosine transport by increasing the expression and activity of the equilibrative nucleoside transporter 2 in human umbilical vein endothelium. J Cell Physiol. 2006;209:826–835. pmid:16924660
- 31. Sun CX, Zhong H, Mohsenin A, Morschl E, Chunn JL, Molina JG, et al. Role of A2B adenosine receptor signaling in adenosine dependent pulmonary inflammation and injury. J Clin Invest. 2006;116:2173–2182. pmid:16841096
- 32. Peng Z, Fernandez P, Wilder T, Yee H, Chiriboga L, Chan ES, et al. Ecto-5'-nucleotidase (CD73)-mediated extracellular adenosine production plays a critical role in hepatic fibrosis. FASEB. 2008;J 22:2263–2272.
- 33. Dai Y, Zhang W, Wen J, Zhang Y, Kellems RE, Xia Y. A2B adenosine receptor-mediated induction of IL-6 promotes CKD. J Am Soc Nephrol. 2011;22:890–901. pmid:21511827
- 34. Govindarajan R, Bakken AH, Hudkins KL, Lai Y, Casado FJ, Pastor-Anglada M, et al. In situ hybridization and immunolocalization of concentrative and equilibrative nucleoside transporters in the human intestine, liver, kidneys, and placenta. Am J Physiol Regul Integr Comp Physiol. 2007;293:R1809–1822. pmid:17761511
- 35. Damaraju VL, Elwi AN, Hunter C, Carpenter P, Santos C, Barron CG, et al. Localization of broadly selective equilibrative and concentrative nucleoside transporters, hENT1 and hCNT3, in human kidney. Am J Physiol Renal Physiol. 2007;293:F200–211. pmid:17409283
- 36. Sakowicz M, Szutowicz A, Pawelczyk T. Insulin and glucose induced changes in expression level of nucleoside transporters and adenosine transport in rat T lymphocytes. Biochem Pharmacol. 2004;68:1309–1320. pmid:15345320
- 37. Pawelczyk T, Podgorska M, Sakowicz M. The effect of insulin on expression level of nucleoside transporters in diabetic rats. Mol Pharmacol. 2003;63:81–88. pmid:12488539
- 38. Westermeier F, Salomón C, González M, Puebla C, Guzmán-Gutiérrez E, Cifuentes F, et al. Insulin restores gestational diabetes mellitus-reduced adenosine transport involving differential expression of insulin receptor isoforms in human umbilical vein endothelium. Diabetes. 2011;60:1677–1687. pmid:21515851
- 39. Tak E, Ridyard D, Kim JH, Zimmerman M, Werner T, Wang XX, et al. CD73-Dependent Generation of Adenosine and Endothelial AdoRA2B Signaling Attenuate Diabetic Nephropathy. J Am Soc Nephrol. 2014;25:547–563. pmid:24262796
- 40. Pawelczyk T, Grden M, Rzepko , Sakowicz M, Szutowicz A. Region-specific alterations of adenosine receptors expression level in kidney of diabetic rat. Am J Pathol. 2005;167:315–325. pmid:16049319
- 41. Qi W, Chen X, Poronnik P, Pollock CA. The renal cortical fibroblast in renal tubulointerstitial fibrosis. Int J Biochem Cell Biol. 2006;38:1–5. pmid:16230044
- 42. Boor P, Ostendorf T, Floege J. Renal fibrosis: novel insights into mechanisms and therapeutic targets. Nat Rev Nephrol. 2010;6:643–656. pmid:20838416
- 43. Jacobson KA, Gao ZG. Adenosine receptors as therapeutic targets. Nat Rev Drug Discov. 2006;5:247–264. pmid:16518376
- 44. Haskó G, Linden J, Cronstein B, Pacher P. Adenosine receptors: therapeutic aspects for inflammatory and immune diseases. Nat Rev Drug Discov. 2008;7:759–770. pmid:18758473
- 45. Yang J, Liu Y. Dissection of key events in tubular epithelial to myofibroblast transition and its implications in renal interstitial fibrosis. Am J Pathol. 2001;159:1465–1475. pmid:11583974
- 46. Hills CE, Squires PE. TGF-beta1-induced epithelial-to-mesenchymal transition and therapeutic intervention in diabetic nephropathy. Am J Nephrol. 2010;31:68–74. pmid:19887790
- 47. Iwano M, Plieth D, Danoff TM, Xue C, Okada H, Neilson E. Evidence that fibroblasts derive from epithelium during tissue fibrosis. J Clin Invest. 2002;110:341–350. pmid:12163453
- 48. Rastaldi MP, Ferrario F, Giardino L, Dell'Antonio G, Grillo C, Grillo P, et al. Epithelial–mesenchymal transition of tubular epithelial cells in human renal biopsies. Kidney Int. 2002;62:137–146. pmid:12081572
- 49. Essawy M, Soylemezoglu O, Muchaneta-Kubara EC, Shortland J, Brown CB, Al Nahas AM. Myofibroblasts and the progression of diabetic nephropathy. Nephrol Dial Transplant. 1997;12:43–50. pmid:9027772
- 50. Pedagogos E, Hewitson T, Fraser I, Nicholls K, Becker G. Myofibroblasts and arteriolar sclerosis in human diabetic nephropathy. Am J Kidney Dis. 1997;29:912–918. pmid:9186078
- 51. Schulte G, Fredholm BB. The intracellular signaling from adenosine receptors to mitogen-activated protein kinases. Cell Signal. 2003;15:813–827. pmid:12834807