Panax Notoginseng Ameliorates Podocyte EMT by Targeting the Wnt/β-Catenin Signaling Pathway in STZ-Induced Diabetic Rats.

INTRODUCTION: Epithelial-mesenchymal transition (EMT) may contribute to podocyte dysfunction in diabetic nephropathy (DN). Aiming to identify novel therapeutic options, we investigated the protective effects of Panax notoginseng (PN) on podocyte EMT in diabetic rats and explored its mechanisms.
METHODS: Diabetes was induced in rats with streptozotocin (STZ) by intraperitoneal injection at 55 mg/kg. Diabetic rats were randomly divided into three groups, namely, diabetic rats, diabetic rats treated with beraprost sodium (BPS) at 0.6 mg/kg/d or PN at 0.4 g/kg/d p.o., for 12 weeks. Urinary albumin/creatinine ratio (ACR), biochemical parameters, renal histopathology, and podocyte morphological changes were evaluated. Protein expression of EMT markers (desmin, α-SMA, and nephrin) as well as components of the Wnt/β-catenin pathway (wnt1, β-catenin, and snail) was detected by immunohistochemistry and Western blot, respectively.
RESULTS: In diabetic rats, severe hyperglycemia and albuminuria were detected. Moreover, mesangial expansion and podocyte foot process effacement were found markedly increased in diabetic kidneys. Increased protein expression of wnt1, β-catenin, snail, desmin, and α-SMA, as well as decreased protein expression of nephrin was detected in diabetic kidneys. All these abnormalities found in DN rats were partially restored by PN treatment.
CONCLUSION: PN ameliorated albuminuria and podocyte EMT in diabetic rats partly through inhibiting Wnt/β-catenin signaling pathway. These findings provide experimental arguments for a novel therapeutic option in DN.

Introduction

Diabetic nephropathy is a major cause of end-stage renal disease1 and becomes a global health problem. However, therapeutic strategies for preventing its progression are limited. The morphological abnormalities of DN include mesangial expansion, glomerular endothelial cell injury, glomerular basement membrane thickening, and podocytes depletion.2,3 Podocytes are important functional cells in the glomerulus and cannot regenerate when they suffer from injury. The clinical study demonstrated that podocyte loss contributed to the progression of DN.4 Many studies indicated that podocyte injury played an important role in the development and progression of DN.5–9 Recently, epithelial–mesenchymal transition has been demonstrated to play an important role in renal fibrogenesis.10 Podocyte EMT was also associated with the development of albuminuria in DN.11 Moreover, EMT was a crucial mechanism leading to podocyte depletion and proteinuria in DN.12 Thus, podocytes EMT may contribute to podocyte dysfunction, which represents a novel mechanism leading to DN. This novel discovery may offer promising insights to the development of new therapeutic options for the treatment of DN. It was reported that podocyte depletion was in association with the development of DN.13 Therefore, there is a pressing need for the development of novel and effective interventions for podocyte injury. Panax notoginseng, an edible and medicinal Chinese herb, is widely used in China for physical fitness. PN has been included in the list of health Chinese herbs with drug and food properties announced by the National Health Commission of the People’s Republic of China. Our previous study found that Notoginsenoside R1, one of the major components of PN, ameliorated glucose-induced podocyte adhesive dysfunction and subsequent podocyte detachment.14 Notoginsenoside R1 was also reported to attenuate renal ischemia-reperfusion injury in rats.15 Panax notoginseng saponins, the traditional Chinese medical compound consisting of total saponins from PN, protected against kidney injury in diabetic rats through upregulation of silent information regulator and activation of antioxidant proteins.16 However, the protective effects of PN on podocyte EMT in diabetic rats have not been investigated yet. Thus, this study aimed to investigate the effects of PN on albuminuria and podocyte EMT in diabetic rats. We hypothesized that PN attenuated albuminuria and podocyte EMT in diabetic rats partly through inhibiting Wnt/β-catenin signaling pathway, which will provide a potential new treatment for DN.

Materials and Methods

Materials

Panax notoginseng granule was purchased from Sanjiu Medical & Pharmaceutical Co Ltd (Shenzhen, China, the approval number of the Chinese Pharmaceutical Regulatory Department:1702002S). The total saponin content in PN granule was greater than 3.75%. Beraprost sodium was purchased from Beijing Tide Pharmaceutical Co Limited (Beijing, China). Streptozotocin (STZ) (1000254870) was acquired from Sigma (Sigma, USA). Bicinchoninic acid (BCA) (BL521A) was acquired from Biosharp (Biosharp, China). ECL (BL520A) was acquired from Biosharp (Biosharp, China). Bovine serum albumin (BSA)(4240GR100) was acquired from BioFroxx (BioFroxx, Germany). Nitrocellulose membrane acquired from Millipore (Millipore, USA). Anti-Wnt1 (sc-514531) antibody was purchased from Santa Cruz (Santa Cruz, USA). Anti-Nephrin (PRS2265) antibody was purchased from sigma (Sigma, USA), and the secondary antibodies were purchased from Cell Signaling (Cell Signaling, USA). Antibodies of β-catenin (ab32572), snail (ab53519), desmin (ab15200), α-SMA (ab5694), β-actin (ab8226), α-tubulin (ab7291) and the secondary antibodies (ab6721) were obtained from Abcam (Abcam, USA). Blood glucose meter (ACCU-CHEK, Germany); Automatic biochemistry analyzer (HITACHI 7600-120E, Japan); light microscopy (Leica, Germany); electron microscopy (Philip, Netherlands).

Animal Studies

All animal experiments were performed in accordance with the National Institutes of Health guide for the care and use of laboratory animals. All experimental protocols were approved by the Animal Ethics Committee of Shanghai sixth people’s hospital (laboratory animal permit: SYXK (Shanghai) 2011-0128). Healthy male Sprague-Dawley (SD) rats weighing 180 to 200 g were provided by Experimental Animal Center of our hospital. Animals were fed in room temperature at 23°C. Rats were fed with free water and standard food. Diabetes rats were induced with STZ (55 mg/kg) dissolved in 0.1 M citrate buffer (pH 4.5) by a single intraperitoneal. Three days after STZ injection, the blood glucose (BG) level was measured from the tail vein using a blood glucose meter. Rats with a blood glucose beyond 16.7 mmol/L were considered as diabetic rats. Diabetic rats were then randomly divided into three groups (n=7/each group): (1) diabetic rats (DN); (2) diabetic rats treated with BPS at 0.6 mg/kg/d (DN+BPS); (3) diabetic rats treated with PN at 0.4 g/kg/d (DN+PN). Normal Sprague-Dawley rats were considered as normal control rats (NC). BPS and PN were started after blood glucose beyond 16.7 mmol/L and were treated by oral garage once daily for 12 weeks. Rats were kept in individual metabolic cages for 24 hrs urine collection at the end of 3 and 12 weeks of treatment. Urine was centrifuged at 1500 rpm for 5 mins at 4°C. Whole urine was stored at −80°C. Urinary albumin/creatinine ratio (ACR) was measured by using an automatic biochemistry analyzer. Rats were then anesthetized with pentobarbital sodium and the blood samples were taken through the abdominal aorta for measuring creatinine by using an automatic biochemistry analyzer. All rats were then sacrificed and the kidneys were harvested immediately.

Histological Studies

Tissues were fixed with 10% buffered formalin and embedded in paraffin, cut into 4 μm sections and stained with hematoxylin and eosin (HE) and periodic acid-schiff (PAS). The stained sections were then detected by light microscopy. Glomerular injury was evaluated by mesangial expansion in sections stained with HE and PAS. The sections were then observed independently by two blinded investigators. Glomerular mesangial expansion was scored semi-quantitatively as previously described in the literature.17

Electron Microscopy Studies

The renal cortex was cut into pieces on ice, fixed with 2% glutaraldehyde dissolved in PBS 2 hrs at 4°C and washed twice in the same buffer. The tissue fragments were post-fixed in 1% PBS-buffered OsO4 for 2 hrs at 4°C and washed twice in the same buffer. Dehydrate with different concentration of ethanols. Epoxy propane replacement twice. Saturate with epoxy propane and epoxy resin 618, embedded in epoxy 48 hrs at 60°C. Ultrathin sections were stained with uranyl acetate and lead citrate and examined by electron microscopy. The number of podocyte foot processes present in each micrograph was divided by the total length of GBM regions in each image to determine the average density of podocyte foot processes. The electron microscope photos were evaluated in a blinded fashion.

Western Blot Studies

Kidney cortex was homogenized in lysis buffer on ice with a homogenizer. The supernatants were collected after centrifuging at 10,000 rpm for 10 mins at 4°C. Protein concentration of the supernatants was measured by the BCA kit assay. The whole tissue lysates were mixed with SDS loading buffer (30% Acrylamide, 1 M Tris–HCl6.8, 1.5 M Tris–HCl8.8, 10% SDS, 10% Ammonium persulfate, TEMED, ddH2O). Samples were separated by sodium dodecyl sulfate (SDS)/polyacrylamide gel electrophoresis and electro-transferred to a nitrocellulose membrane. The membranes were blocked with 5% bovine serum albumin in TBST for 1.5 hrs. After washing 5 mins for three times with TBST, the blots were incubated overnight at 4°C with anti-nephrin (1:2000), anti-desmin (1:5000), anti-α-SMA (1:5000), anti-wnt1 (1:1000), anti-β-catenin (1:5000), anti-snail (1:3000), and anti-β-actin (1:5000) and α-tubulin (1:5000) antibodies at the dilutions by 5% bovine serum albumin in TBST. After washing 5 mins for five times with TBST, membranes were incubated with horseradish peroxidase-conjugated secondary antibodies (1:5000) at the dilutions by 5% bovine serum albumin in TBST for 1 hr at room temperature. After washing 5 mins for five times with TBST, protein bands were visualized by ECL. Optical density of the bands was measured by a Bio-Rad gel imaging system. Equality of loading was ensured by using the antibody to β-actin or α-tubulin. Protein expression was quantified as the ratio of specific band to β-actin or α-tubulin.

Immunohistochemistry Studies

Paraffin-embedded of kidney tissues were deparaffinized with rehydrated, xylene, and ethanol. Anti-nephrin (1:200), anti-desmin (1:200), anti-α-SMA (1:200), anti-wnt1 (1:200), anti-β-catenin (1:500) and anti-snail (1:100) antibodies were diluted in 1% BSA, all antibodies were incubated during 45 mins at room temperature. Antigen repaired for 10 mins by boiling water bath. Primary antibodies were diluted in 2% BSA and incubated overnight at 4°C. The secondary antibodies (1:1000) were incubated 60 mins at 37°C. Use diaminobenzidine and hematoxylin staining, and then rinsing, redyeing, dehydration, transparency, and tablet sealing. The immunohistochemical staining in each glomerulus was scored semi-quantitatively as previously described in the literature.18 All slides were observed independently by two blinded investigators.

Statistical Analysis

All data were expressed as mean ± standard error of the mean (SEM). Statistics were conducted by SPSS version 18.0. The significance of differences in continuous variables among groups was tested by one-way analysis of variance (ANOVA) followed by Dunnett’s multiple range test. A P value < 0.05 was considered statistically significant.

Results

Effects of PN on Serum and Urine Levels of Biochemical Markers in Diabetic Rats

The STZ-induced diabetic rats developed severe hyperglycemia and albuminuria. Level of blood glucose in DN, DN+BPS, and DN+PN groups were prominently increased in STZ-induced diabetic rats when compared with control rats (Figure 1A). No significant difference in the level of creatinine were observed between PN treated and untreated diabetic rats, which indicated that PN did not cause apparent toxicity to the kidney (Figure 1B). The diabetic rats showed severe albuminuria when compared with the control rats. However, PN or BPS significantly reduced ACR in diabetic rats at the end of 3 weeks and 12 weeks (Figure 2) of treatment. Thus, PN treatment attenuated albuminuria in diabetic rats.

Figure 1

The level of blood glucose at baseline in rats (A). Effects of PN treatment on serum creatinine (B). PN and BPS were administered once daily by oral garage for 12 weeks. Results were expressed as the mean ± SEM (n = 7). *P<0.05 vs NC.

Abbreviations: NC, control rats; DN, STZ-induced diabetic rats; DN+BPS, DN rats treated with BPS at 0.6 mg/kg/d; DN+PN, DN rats treated with PN at 0.4 g/kg/d.

Figure 2

Effects of PN treatment on urinary albumin/creatinine ratio (ACR) in diabetic rats at the end of 3 weeks and 12 weeks. PN and BPS were administered once daily by oral garage for 12 weeks. Results were expressed as the mean ± SEM (n = 7).*P<0.05 vs NC; #P<0.05 vs DN.

Abbreviations: NC, control rats; DN, STZ-induced diabetic rats; DN+BPS, DN rats treated with BPS at 0.6 mg/kg/d; DN+PN, DN rats treated with PN at 0.4 g/kg/d.

Effects of PN on Renal Histopathology and Podocyte Foot Process Effacement in STZ-Induced Diabetic Rats

Diabetic rats exhibited focal mesangial matrix expansion. However, PN or BPS markedly ameliorated mesangial expansion when compared with untreated STZ-induced diabetic rats (Figure 3). Moreover, PN or BPS also ameliorated podocyte foot process effacement in diabetic rats (Figure 4). These results indicated that PN significantly attenuated renal histopathology and podocyte foot process effacement in diabetic rats.

Figure 3

Effects of PN treatment on mesangial expansion in diabetic rats. Representative hematoxylin and eosin (HE) and periodic acid-schiff (PAS) staining of kidney sections (A)(magnification 400×). Semiquantitative analyses of mesangial expansion detected by HE (B) and PAS (C). PN and BPS were administered once daily by oral garage for 12 weeks. Results were expressed as the mean ± SEM (n = 7). The arrow represents mesangial expansion in diabetic rats glomerular. *P<0.05 vs NC; #P<0.05 vs DN.

Abbreviations: NC, control rats; DN, STZ-induced diabetic rats; DN+BPS, DN rats treated with BPS at 0.6 mg/kg/d; DN+PN, DN rats treated with PN at 0.4 g/kg/d.

Figure 4

Effects of PN treatment on renal podocyte foot process effacement in STZ-induced diabetic rats. Representative electron photomicrographs from each group of rats (A) (magnification 13500×). Quantitative analysis of density of podocyte foot processes (B).

Abbreviations: NC, control rats; DN, STZ-induced diabetic rats; DN+BPS, DN rats treated with BPS at 0.6 mg/kg/d; DN+PN, DN rats treated with PN at 0.4 g/kg/d. PN and BPS were administered once daily by oral garage for 12 weeks. Results were expressed as the mean ± SEM. The arrow represents podocyte foot process effacement in diabetic rats.*P<0.05 vs NC; #P<0.05 vs DN.

Effects of PN on Podocyte EMT in Diabetic Rats

Compared with the control rats, we observed that the protein of nephrin was markedly reduced in diabetic rats. Nevertheless, treatment with PN increased the protein expression of nephrin (Figure 5A) in diabetic rats. Compared with the normal control rats, the protein expression of α-SMA and desmin was increased in diabetic rats. However, DN+PN group showed decreased protein expression of desmin (Figure 5B) and α-SMA (Figure 5C) in diabetic rats. The findings of immunohistochemical staining further confirmed the above findings (Figure 6). Decreased protein expression of nephrin, and increased protein expression of desmin and α-SMA were tested in kidneys from diabetic rats. Furthermore, these abnormalities were restored by treatment with PN. These results demonstrated that PN might ameliorate podocyte EMT in diabetic rats.

Figure 5

Effects of PN treatment on protein expression of nephrin, desmin, and α-SMA in diabetic rats. Representative immunoblots stained for nephrin (A), desmin (B) and α-SMA (C) in the kidney. PN and BPS were administered once daily by oral garage for 12 weeks. Results were expressed as the mean ± SEM. *P<0.05 vs NC; #P<0.05 vs DN.

Abbreviations: NC, control rats; DN, STZ-induced diabetic rats; DN+BPS, DN rats treated with BPS at 0.6 mg/kg/d; DN+PN, DN rats treated with PN at 0.4 g/kg/d.

Figure 6

Effects of PN treatment on nephrin, desmin, and α-SMA expression in diabetic rats detected by immunohistochemistry staining (magnification 400×). Representative photomicrographs of immunostaining for nephrin, desmin, and α-SMA (A) in kidney sections. Semiquantitative analyses of immunostaining for nephrin (B), desmin (C) and α-SMA (D) per glomerulus. PN and BPS were administered once daily by oral garage for 12 weeks. Results were expressed as the mean ± SEM. The arrow represents protein expression of nephrin, desmin, and α-SMA in diabetic rats glomerular.*P<0.05 vs NC; #P<0.05 vs DN.

Abbreviations: NC, control rats; DN, STZ-induced diabetic rats; DN+BPS, DN rats treated with BPS at 0.6 mg/kg/d; DN+PN, DN rats treated with PN at 0.4 g/kg/d.

Effects of PN on Wnt/β-Catenin Signaling Pathway in STZ-Induced Diabetic Kidneys

By Western blot analysis, we found that the protein expression of wnt1, β-catenin, and snail was increased in the renal tissue from STZ-induced diabetic rats when compared with the control rats. Most importantly, PN treatment suppressed protein expression of wnt1 (Figure 7A), β-catenin (Figure 7B) and snail (Figure 7C) in the kidneys from diabetic rats. These findings were further confirmed by the results of immunohistochemistry analysis (Figure 8). We observed that the expression of wnt1, β-catenin, and snail was markedly increased in the renal tissue from diabetic rats when compared with the control rats. However, PN treatment decreased expression of wnt1, β-catenin, and snail in diabetic rats. The above results indicated that the protective effect of PN on podocyte EMT was associated with the inhibition of Wnt/β-catenin signaling pathway in diabetic rats.

Figure 7

Effects of PN treatment on protein expression of wnt1, β-catenin, and snail in diabetic rats. Representative immunoblots stained for wnt1 (A), β-catenin (B) and snail (C) in the kidney. PN and BPS were administered once daily by oral garage for 12 weeks. Results were expressed as the mean ± SEM. *P<0.05 vs NC; #P<0.05 vs DN.

Abbreviations: NC, control rats; DN, STZ-induced diabetic rats; DN+BPS, DN rats treated with BPS at 0.6 mg/kg/d; DN+PN, DN rats treated with PN at 0.4 g/kg/d.

Figure 8

Effects of PN treatment on expression of wnt1, β-catenin, and snail in diabetic rats detected by immunohistochemistry staining (magnification 400×). Representative photomicrographs of immunostaining for wnt1, β-catenin, and snail (A) in kidney sections. Semiquantitative analyses of immunostaining for wnt1 (B), β-catenin (C) and snail (D) per glomerulus. PN and BPS were administered once daily by oral garage for 12 weeks. Results were expressed as the mean ± SEM. The arrow represents protein expression of wnt1, β-catenin, and snail in diabetic rats glomerular.*P<0.05 vs NC; #P<0.05 vs DN.

Abbreviations: NC, control rats; DN, STZ-induced diabetic rats; DN+BPS, DN rats treated with BPS at 0.6 mg/kg/d; DN+PN, DN rats treated with PN at 0.4 g/kg/d.

Discussion

Diabetes mellitus (DM) has become an important global health problem.19 Clinical hallmarks of DN include proteinuria and decline in glomerular filtration rate leading to ESRD.20,21 These functional changes developed a consequence of structural abnormalities, including mesangial expansion and podocyte injury.22,23 Recently, much work has underlined the important role of podocyte in the development and progression of DN.5–9 Thus, podocytes become a promising target for the development of novel treatment for DN.

The novel finding of this study was the discovery of a natural medicine for treatment of DN. We reported that PN ameliorated podocyte dysfunction and EMT partly by inhibiting Wnt/β-catenin signaling pathway in STZ-induced diabetic rats. This conclusion was based upon the following findings: (i) Treatment with PN attenuated the functional and structural abnormalities of DN, such as albuminuria, mesangial expansion, and podocyte foot process effacement; (ii) Treatment with PN ameliorated the protein expression of desmin, α-SMA, and nephrin in diabetic rats. (iii) Treatment with PN significantly inhibited protein expression of wnt1, β-catenin, and snail. Therefore, PN might be a novel drug to attenuate podocyte EMT partly through inhibiting Wnt/β-catenin signaling pathway in diabetic rats. PN is a promising drug candidate for DN according to the results obtained in an animal model of DN.

Beraprost sodium is an orally active prostacyclin (prostaglandin I2; PGI2) analogue. Previous study reported that BPS ameliorated proteinuria and renal histologic lesions in diabetic rats.24 Experimental study documented that BPS had a beneficial effect on DN.25 Recent study demonstrated that BPS attenuated characteristics of metabolic syndrome in obese rats.26 Thus, BPS was used as a positive control in this study to investigate the protective effect of PN on the functional and structural abnormalities of DN. We found that treatment with PN or BPS attenuated the functional and structural abnormalities of DN. The previous study found that the BPS alleviated constriction effect of angiotensin II on efferent glomerular arteriole and attenuated glomerular hyperfiltration, as well as inhibited growth of mesangial cells by platelet-derived growth factor to decrease albuminuria in the patients of incipient DN.27 However, there were different mechanisms of PN and BPS in the treatment of DN. Our study demonstrated that PN protected DN through inhibiting Wnt/β-catenin signaling pathway.

Loss of podocytes by EMT characterizes the early stages of DN. To identify new therapeutic strategies, we firstly investigated the effects of PN on podocyte EMT in diabetic rats. Podocyte injury resulted in abnormal permeability of the GBM, terminally leading to proteinuria.28,29 Importantly, podocyte injury was closely associated with the progression of glomerular diseases.30 Many studies demonstrated that EMT was associated with podocyte loss and proteinuria in DN.31–33 During EMT, podocytes lose the expression of nephrin, while augmenting the expression of desmin and α-SMA.34–36 Taken together, podocyte EMT is recognized to play a crucial role in the development of DN and targeted inhibition of podocyte EMT may provide a new therapeutic approach for DN. In the present study, we observed that α-SMA and desmin expression were increased while nephrin expression was decreased in diabetic rats. Treatment with PN for 12 weeks decreased renal expression of α-SMA and desmin, preserved nephrin expression, as well as ameliorated albuminuria in diabetic rats. These results demonstrated that PN ameliorated podocyte EMT in diabetic rats.

We next investigated the mechanisms underlying the action of PN on podocyte EMT in diabetic rats. Dysfunction of Wnt signaling may contribute to a wide range of pathologies of human diseases.37 Emerging evidence demonstrated that Wnt/β-catenin signaling played a critical role in mediating podocyte dysfunction and albuminuria.38 Wnt signaling pathway was also associated with podocyte injury and dysfunction in DN.39 In vitro study demonstrated that high glucose increased expression of β-catenin and snail and promoted EMT.40 Mounting evidence indicated that Wnt/β-catenin signaling might be a novel therapeutic target for proteinuria kidney disease.41 In the present study, we found that increased protein expression of wnt1, β-catenin, snail, desmin, and α-SMA, as well as decreased protein expression of nephrin, were detected in diabetic rats. All of these abnormalities were restored by PN. These results indicated that the regulatory effect of PN on Wnt/β-catenin signaling pathway might be accountable for its protective effects against podocyte EMT.

Moreover, a systematic review and meta-analysis provided evidence that PN was beneficial to patients with unstable angina pectoris and did not affect blood routine, urine routine, stool routine, as well as liver and renal function.42 In our study, PN had no significant effect on blood glucose, which indicated that the protective effects of PN on albuminuria were independent of lowering blood glucose (data not shown). Furthermore, there was no significant difference in the level of serum creatinine between PN treated and untreated diabetic rats, which indicated that PN did not cause apparent toxicity to the kidney.

STZ-model is one of the widely used animal models of early DN, due to their brief experimental procedure and absence of advanced pathological lesions. But the effects of STZ-induced diabetes are closely dependent on mouse strain and gender, with male mice being more susceptible to STZ-induced diabetes and obvious renal injury compared to their female counterparts.43 STZ selectively leads to damage to the insulin-producing β-cells in the pancreas. Destruction to these cells causes insulin deficiency and impairs normal glucose metabolism,44 which similar to human type 1 diabetes progresses in DN. We will use the type 2 diabetes model to further investigate the protective effects of PN in future studies.

In conclusion, our study demonstrated that PN attenuated albuminuria and podocyte EMT in diabetic rats partly through inhibiting Wnt/β-catenin signaling pathway (Figure 9). These findings highlight a promising novel treatment for DN and other renal diseases that affect podocytes.

Figure 9

Schematic mechanism of PN of ameliorating podocyte EMT by Wnt/β-catenin signaling pathway in STZ-induced diabetic rats.