Vincristine alleviates adriamycin-induced nephropathy through stabilizing actin cytoskeleton
© The Author(s) 2017
Received: 12 November 2016
Accepted: 13 December 2016
Published: 3 January 2017
Antimicrotubule agent vincristine (VCR) has long been known as an alternative treatment for frequent relapse nephrotic syndrome and steroid-dependent nephrotic syndrome (SDNS). However, the mechanism is unknown. Here we found that VCR at a dosage much lower than that as an antimicrotubule agent can alleviate adriamycin (ADR)-induced proteinuria and podocyte foot process effacement. In cultured podocytes, VCR prevents ADR-induced actin fiber disorganization. In both in vitro and in vivo models, VCR suppresses ADR-induced overexpression of α3β1 integrin and focal adhesion kinase (FAK). These data suggest that VCR may relieve ADR-induced nephropathy through inhibiting injury-induced activation of integrin outside-in signaling to prevent actin cytoskeleton remodeling. Hence, our work reveals a novel role of VCR in regulating actin fiber assembly and provides first evidence on the therapeutic mechanism of VCR on nephrotic syndrome.
KeywordsNephrotic syndrome Vincristine Actin cytoskeleton Focal adhesion kinase Integrin
Minimal change nephrotic syndrome (MCNS) is a common renal disease in childhood. Although about 90% of children with MCNS respond to prednisone treatment, nearly 30% of them have frequent relapses or develop steroid-dependent nephrotic syndrome. Steroid toxicity following repeated steroid treatment demands alternative treatments in those patients . However, current corticosteroid-sparing agents prescribed for children with frequent relapse nephrotic syndrome and SDNS have their own shortcomings, such as high frequent relapses after levamisol or mycophenolic acid discontinuing, risk for infertility after repeated courses of alkylating agents and nephrotoxicity of calcinurin inhibitors . Therefore, it is necessary to search for alternative treatments for patients with frequent relapse nephrotic syndrome and SDNS.
Vincristine (VCR) is a vinca alkaloid that has played an important role in chemotherapy of malignant diseases for 3 decades. The beneficial effects of VCR in nephrotic syndrome associated with hematological malignancy have been noted for many years . But these therapies were consisted of a combination of VCR, sterioids and other cytotoxic agents and it was unclear whether the remission of nephrotic syndrome was directly related to VCR. Goonasekera et al. reported two cases of primary focal segmental glomerulosclerosis (FSGS) that responded to VCR alone . Given those reports, we once treated 12 SDNS patients with intravenous VCR, all of whom had previously completed at least one 8-week course of cyclophosphamide but still had frequent relapses. Results showed that VCR treatment in a subset of children with challenging SDNS could not only relieve proteinuria but also reduce relapse frequency. Moreover, side effects were minimal in most cases . It indicates that VCR may be a valuable alternative treatment for idiopathic nephrotic syndrome patients. However, it’s not clear how VCR relieves symptoms of nephrotic syndrome.
Here we demonstrated that VCR could decrease proteinuria in ADR nephropathy rats after 2-week treatment and relieve hypoalbuminemia and hypercholesterolemia after 4-week treatment. Consistently, VCR rescued podocyte foot process effacement induced by ADR. VCR treatment could stabilize actin cytoskeleton structure and rescue the morphology of ADR-injured podocytes. Molecular analyses indicate that the therapeutic effect of VCR may be mediated by inhibiting the pathological overexpression of α3β1 integrin and FAK in ADR-induced nephropathy.
ADR nephropathy rat model and treatment with VCR
ADR nephropathy was induced in male SD rats weighing 200 ± 20 g by tail vein injection with single dose of ADR (7.5 mg/kg body weight, dissolved in 0.9% NaCl) . As normal control group, rats were injected with equal volume of 0.9% NaCl. Four weeks later, ADR nephropathy rats were divided in two groups. One group was injected with VCR 0.2 mg/kg body weight twice per week for 4 weeks. The other group was injected with equal volume of 0.9% NaCl. Urine was collected from each rat in metabolic cage to determine 24 h protein level. It was done weekly after ADR injection for the first two weeks and then once for every two weeks. Blood samples were obtained in chloral hydrate anaesthetized rats at 2, 4 and 8 weeks after ADR injection. Plasma was extracted for serum albumin and cholesterol measurement.
Podocyte cell culture
Immortalized mouse podocyte cell line was kindly provided by Professor Jianghua Chen (The First Affiliated Hospital of Zhejiang University, School of Medicine). The immortalized podocytes were cultured for 5 days at 33 °C in 5% CO2 under permissive condition [RPMI 1640 (Sigma) with 10% fetal bovine serum (Gibco), 10U/ml of recombinant mouse γ-interferon (Peprotech) and 100U/ml penicillin/streptomycin (Gibco) on type I collagen (Sigma)-coated BD dishes]. They were subsequently cultured at 37 °C in 5% CO2 under restrictive condition (permissive condition without γ-IFN) to induce differentiation. It took 12–14 days to induce differentiation. After podocytes were well-differentiated, they were incubated with 0.5 µM ADR to induce cell injury. For VCR treatment group, 5 nM VCR was added 1 h after ADR injury. Cells were further cultured for 24 h before the following processes.
F-actin immunofluoresence staining
100 nM working stock of Actin-stain™ 488 phalloidin was prepared by diluting 3.5 μl of 14 μM labeled stock phalloidin (Cytoskeleton) into 500 μl of PBS. Cells were gently washed by PBS after removing culture media at room temperature (RT). After 3.7% paraformaldehyde (PFA) fixation, cells were rinsed once with PBS and permeabilized by 0.5% Triton X-100/PBS. Cells were rinsed once with PBS and then 100 nM Actin-stain™ 488 phalloidin was incubated with cells at RT in dark for 30 min. After washing three times in PBS, cells were counter-stained by DAPI. Images were obtained with DM6000 upright microscope (Leica). Fifty high magnification fields from each sample were randomly chosen for the measurement of cell area and actin fiber number. All the analyses were done with Image-Pro Plus. Three separate experiments for each group were analyzed.
Total RNA was extracted from the podocytes and kidney cortex with Trizol (Invitrogen). 1ug total RNA from each sample was reverse transcribed with PrimeScript RT Kit (TaKaRa) to synthesize cDNA. Next, 1ul cDNA was used for PCR amplification with SYBR Green PCR Master Mix (TaKaRa). Reactions were performed on a 7900HT Fast Realtime PCR system (ABI). Gapdh was used as internal normalizer for all the examined genes. At least three samples from each group were used for qPCR analysis. Primers were designed using the Primer Express software (Primer Premier 5.0) based on the Gene Bank accession numbers. Primer sequences are:
Gapdh: 5′-CTCATGACCACAGTCCATGC; 5′-CACAATTGGGGGTAGGAACAC; Podocin: 5′-ACCTTTCCATGAGGTGGTAAC; 5′-CTGGATGGCTTTGGACAC Nephrin: 5′-CTTGTTGTCCGATTTGCCCC; 5′-CCTGGGCTGCAGACACATTA; Synaptopodin: 5′-GCTGGAGCTTTGGGCCG; 5′-GTTGAAGAGCTGGACCCCTC; Podocalyxin: 5′-TACATCCAAACCGACAGGCA; 5′-GGCTGTAGTGGTGTGGAGAC; FAK: 5′-ATACACCATGCCCTCAACCAG; 5′-GGTCAAACTGGCGCATTGTT α3-integrin: 5′-ATCCACAGCAATGGGTCCTG; 5′-GGAACAGGTCAACACGGTCT; β1-integrin: 5′-TGTCCTACTGGTCCCGACAT; 5′-TTTTCACCCGTGTCCCACTT
Podocytes and kidney cortex were lysed with RIPA Lysis Buffer (Beyotime) supplemented with protease inhibitor (Sigma) and phosphatase inhibitor (Roche). After determination of protein concentration with BCA protein assay kit (Bio-Rad), 20 µg protein per sample were denatured by boiling at 96 °C for 5 min in sample buffer. Equivalent amounts of protein were loaded and electrophoresed in SDS-PAGE gels. After electrophoresis, gels were transferred to nitrocellulose (NC) filter membranes. Next, membranes were blocked with mouse Anti-FAK (BD Transduction) or anti-phospho-FAK (Tyr397, Millipore) for 2 h. After washing with PBS, membranes were incubated with IRDye 800-conjugated goat anti-rabbit IgG secondary antibody (Rockland) for half an hour. Immunoreactive bands were visualized with a Licor Odyssey Infrared Imaging System (LI-COR Biosciences).
Rats were anaesthetized by chloral hydrate and were sacrificed by cervical vertebrae. Kidneys were removed from the bodies. The kidney cortex were isolated and fixed in 10% neutral buffered formalin for hematoxylin and eosin staining or fixed in 2.5% glutaraldehyde for electron microscopy.
Results were analyzed for statistically significant differences using SPSS 16.0 software. Data were presented as mean ± standard deviation (SD) and tested by one-way ANOVA. p < 0.05 were considered significantly.
VCR ameliorates symptoms of ADR-induced nephropathy and rescues foot process effacement
Starting from 4 weeks after ADR injection, rats in VCR treatment group were administrated with 0.2 mg/kg body weight VCR, which was converted from clinical dosage 1 mg/m2 according to dose conversion between human and rat. At the beginning of VCR treatment, there was no difference in 24 h urine protein level between ADR and VCR group (Fig. 1a). However, 24 h urine protein level decreased significantly after two-week VCR treatment and continued to decrease afterwards (Fig. 1a). Consistently, both serum albumin and cholesterol levels were recovered to normal ranges after 4 weeks’ treatment (Fig. 1b, c). Ultrastructurally, the majority of podocyte foot processes reappeared after 4-week VCR treatment (Fig. 2d). On cellular level, mesangial matrix deposition and cell infiltration in VCR treatment group were also attenuated (Fig. 3d). These data indicates that VCR can rescue effacement of podocyte foot process to ameliorate ADR-induced nephropathy.
Vincristine stabilizes actin cytoskeleton to maintain podocyte morphology in ADR-injured podocytes
VCR functions as an antimicrotubule agent and blocks cell mitosis at high concentration (≥40 nM) . Since the dosage used for nephrotic treatment is much lower than that for cancer treatment, we first tested the effect of VCR on cultured podocytes at lower concentrations (1, 2, 5, 10 and 20 nM). We found that treatment with 1, 2 or 5 nM VCR for 24 h didn’t have any adverse effect on podocyte actin fiber and microtubule cytoskeleton (Fig. 4c and data not shown). Hence, we applied 5 nM VCR to test VCR effect on ADR injured podocyts. Indeed, 5 nM VCR treatment 1 h after ADR injury could stabilize actin fibers and maintain actin cytoskeleton distribution, thereby preventing the shrinkage of podocytes, (Fig. 4d). Quantitative measurements indicated that both the average area and actin fiber number of podocyte decreased significantly (p < 0.05) in ADR injured podocytes compared with the untreated podocytes, while there was no significant difference (p > 0.05) between the untreated and ADR + VCR groups (Fig. 4e, f). These results demonstrate that a low concentration level of VCR can rescue ADR-induced podocyte defect through stabilizing actin fiber formation.
VCR reduces pathological overexpression of α3β1 integrin and FAK in ADR-induced nephropathy
VCR is a well-known antimicrotubule agent that induces tubulin self-association into coiled spiral aggregates to prevent microtubule assembly and therefore block cell mitosis . Hence, it is widely used to treat human cancers . Its beneficial effect on nephrotic syndrome of leukemia patients prompted nephrologists to use VCR as an alternative treatment for nephrotic syndrome . But how VCR relieves nephrotic syndrome is unclear.
Nephrotic disorders with proteinuria are usually caused by marked foot process effacement of podocytes due to actin cytoskeletal disruption . Indeed, we find that VCR can stabilize actin cytoskeleton in ADR-injured podocyte at a low dosage that doesn’t disrupt microtubules. It indicates that VCR has additional effect on cytoskeletons other than microtubule disruption. Interestingly, studies on vincristine resistance in malignant tumors show that expression changes in genes encoding actin cytoskeleton components are associated with the intrinsic and acquired VCR resistance , suggesting a complicated interaction between VCR and actin cytoskeleton. Here, we provide the first evidence indicating that a low concentration of VCR can stabilize actin fibers, although it is unclear whether VCR can directly bind actin fibers or not.
Actin cytoskeleton connects to extracellular matrix through focal adhesion in foot processes, which constitutes an integral component of the glomerular filtration barrier . The maintenance and remodeling of these structures are regulated by integrin outside-in signaling modulated by FAK . Podocyte FAK deletion or inhibition of FAK activation protect against proteinuria and foot process effacement induced by glomerular injury . Our data suggest that the actin fiber-stabilizing effect of VCR may be mediated by suppressing overexpression of α3β1 integrin and FAK in both in vitro and in vivo models. Interestingly, we didn’t note that the level of activated form FAK Y397 was significantly reduced after VCR treatment. It indicates that the reduced FAK expression level, independent of FAK Y397 activation, is sufficient to alleviate proteinuria and foot process effacement. The segregation of FAK overexpression and FAK Y397 phosphorylation is also noted in the activation of cancer cell migration . Our data provide novel insight into the complexity of FAK activation and downstream effect during the pathogenesis of podocyte injury, which requires further investigation. Further clarification of the therapeutic mechanism of VCR would help attract more attention to use it as a cheap and effective alternative treatment for nephrotic syndrome.
steroid-dependent nephrotic syndrome
focal adhesion kinase
minimal change nephrotic syndrome
focal segmental glomerulosclerosis
LY conceived of the study, conducted all the experiments and drafted the manuscript. ZZ designed experiments and finalized the manuscript. YM helped in podocyte culture. YW and HS helped in animal experiments. WZ participated in experimental design and coordination. All authors read and approved the final manuscript.
We thank Mr. Wenfeng Wang, Ms. Xiaoling Zheng, Xiangyang Liu and Jing Wang for technical supports. Our work was supported by Grants 2013CB945302 from MOST, 81170153 and 31371465 from NSFC, XBR2015 from Shanghai HFPC and the Program for Professor of Special Appointment (Eastern Scholar) at Shanghai Institutions of Higher Learning.
The authors declare that they have no competing interests.
Availability of data and materials
The datasets supporting the conclusions of this article are included in the article and available from the corresponding author on request.
Animal care and use in all the experiments were in accordance with the guidelines approved by the Institutional Animal Care and Use Committee of Shanghai Children’s Medical Center.
This work was financially supported by Grants 2013CB945302 from MOST, 81170153 and 31371465 from NSFC, XBR2015 from Shanghai HFPC and the Program for Professor of Special Appointment (Eastern Scholar) at Shanghai Institutions of Higher Learning.
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