Potassium bisperoxo (1,10-phenanthroline)oxovanadate suppresses proliferation of hippocampal neuronal cell lines by increasing DNA methyltransferases

Xiao-Li Tian , Shu-Yuan Jiang , Xiao-Lu Zhang , Jie Yang Jun-He Cui Xiao-Lei Liu Ke-Rui Gong, Shao-Chun Yan Chun-Yang Zhang , Guo Shao

1 Biomedicine Research Center, Basic Medical College and Baotou Medical College of Neuroscience Institute, Baotou Medical College, Baotou,Inner Mongolia Autonomous Region, China

2 Inner Mongolia Key Laboratory of Hypoxic Translational Medicine, Baotou Medical College, Baotou, Inner Mongolia Autonomous Region, China

3 Beijing Key Laboratory of Hypoxic Conditioning Translational Medicine, Xuanwu Hospital, Capital Medical University, Beijing, China

4 Department of Oral and Maxillofacial Surgery, University of California San Francsico, San Francisco, CA, USA.

5 Department of Neurosurgery, the First Affiliated Hospital of Baotou Medical College, Baotou, Inner Mongolia Autonomous Region, China

Abstract Bisperoxo (1,10-phenanthroline) oxovanadate (BpV) can reportedly block the cell cycle. The present study examined whether BpV alters gene expression by affecting DNA methyltransferases (DNMTs), which would impact the cell cycle. Immortalized mouse hippocampal neuronal precursor cells (HT22) were treated with 0.3 or 3 μM BpV. Proliferation, morphology, and viability of HT22 cells were detected with an IncuCyte real-time video imaging system or inverted microscope and 3-(4,5-dimethylthiazol-2-yl)-5(3-carboxymethonyphenol)-2-(4-sulfophenyl)-2H-tetrazolium, respectively. mRNA and protein expression of DNMTs and p21 in HT22 cells was detected by real-time polymerase chain reaction and immunoblotting, respectively. In addition, DNMT activity was measured with an enzyme-linked immunosorbent assay. Effects of BpV on the cell cycle were analyzed usingflow cytometry. Results demonstrated that treatment with 0.3 μM BpV did not affect cell proliferation, morphology, or viability; however, treatment with 3 μM BpV decreased cell viability, increased expression of both DNMT3B mRNA and protein, and inhibited the proliferation of HT22 cells; and 3 μM BpV also blocked the cell cycle and increased expression of the regulatory factor p21 by increasing DNMT expression in mouse hippocampal neurons.

Key Words: nerve regeneration; hippocampal neurons; potassium bisperoxo (1,10-phenanthroline) oxovanadate; DNA methyltransferase;p21; HT22 cell; cell cycle; immunoblotting; DNA methylation; neural regeneration

Introduction

Vanadium can adopt multiple oxidation states and different vanadium compounds have arisen as potential drugs for their anti-diabetic, anti-cancer, and anti-parasitic effects(Kioseoglou et al., 2015; Irving and Stoker, 2017; Levina and Lay, 2017). Potassium bisperoxo (1,10-phenanthroline)oxovanadate (BpV), a V5+compound and specific inhibitor of protein tyrosine phosphatases, can arrest the cell cycle and alter neurotransmitter release in nerve cells (Faure et al., 1995; Bieger et al., 2002). Jung and his colleagues reported that vanadium can alter DNA methylation levels of some genes (Jung et al., 2017). DNA methylation, which is governed by methyltransferases (DNMTs), can regulate gene expression to ultimately determine the characteristics of a cell (Bestor, 2000; Rodriguez-Osorio et al., 2010;Taberlay and Jones, 2011). Thus, changes in DNMTs may account for the biological function of vanadium, which can serve as a potential drug. Indeed, changes in DNMT and DNA methylation levels of cell cycle-related genes may be potential mechanisms of As2O3-induced cell cycle arrest (Eyvani et al., 2016). Moreover, DNA methylation patterns can alter expression of some neurotransmitter genes (Alelu-Paz et al., 2014) and DNMT-catalyzed DNA methylation is one mechanism by which gene expression is regulated in the brain (Gibbs et al., 2010; Bettscheider et al., 2012; Zhang et al., 2014; Yu et al., 2017). The aim of this study was to explore whether BpV affects DNMTs, which regulate DNA methylation patterns.

DNA methylation is catalyzed by three active DNMTs(DNMT1, DNMT3A, and DNMT3B) and one non-catalytic accessory protein (DNMT3L). DNA methylation takes place at position five of cytosine residues in CpG islands (Bestor, 2000; Shao et al., 2013; Liu et al., 2017).Establishing specific DNA methylation patterns is important for both normal or abnormal cell processes, such as somatic tissue development and cancer (Okano et al., 1999;Cassinotti et al., 2012; Cheng et al., 2014; Saradalekshmi et al., 2014). DNMTs also play important roles in cell cycle control (Stephens et al., 1996; Xiong et al., 2009; Yang et al., 2017). Fournel et al. (1999) showed that DNMT inhibition upregulated protein levels of p21, a cell cycle regulator. Fang and Lu (2002) reported that p21 may be a key factor in the growth arrest induced in transformed cells.This study explored the effects of BpV on DNMTs and the cell cycle (via detection of p21, a cyclin-dependent kinase inhibitor) in immortalized mouse hippocampal neuronal precursor cells (HT22).

Materials and Methods

Cell culture and treatment with BpV

HT22 cells (National Laboratory of Molecular Oncology,Cancer Institute and Hospital, Chinese Academy of Medical Sciences and the Peking Union Medical College, China)were maintained in our laboratory as previously described(Zhao et al., 2016). Cells were either treated with vehicle(0.1% dimethyl sulfoxide) (Sigma, St. Louis, MO, USA) or BpV (Alexis, San Diego, CA, USA). The pH value of cell culture medium was 7 and BpV is stable in neutral aqueous solution (Matsugo et al., 2015; Chakrabarty and Banerjee,2016).

IncuCyte assays

HT22 cells were seeded in 96-well tissue culture plates at a density of 4000 cells per well. Wells were randomly divided into six groups and cultured for 24 hours before adding BpV at concentrations of 0, 0.3, 3, 30, 300, or 3000 μM (n =3). Cells were cultured for 12 hours and then treated with BpV at various concentrations or 0.1% dimethyl sulfoxide as a control. Cells were monitored and imaged with an IncuCyte FLR, and data were analyzed with IncuCyte Confl uence version 1.5 software (Essen Bioscience, Ann Arbor,MI, USA). All experiments were performed in triplicate.

3-(4,5-Dimethylthiazol-2-yl)-5(3-carboxymethonyphenol)-2-(4-sulfophenyl)-2H-tetrazolium (MTS) assay

Cell viability was measured by MTS assay using a CellTiter 96 Aqueous One Solution Cell Proliferation Assay kit(Promega, Madison, WI, USA). According to the manufacturer's protocol, cells were seeded into 96-well plates and treated with BpV or dimethyl sulfoxide. HT22 cells were seeded into a 96-well plate at a density of 2000 cells per well and cultured in an incubator with 5% CO2and 95% air at 37°C for 24 hours. Different concentrations of BpV or dimethyl sulfoxide were added for 24 hours. MTS was added and detected every half hour. Experiments were performed as previously described by Hwang et al. (2011). Each experiment was conducted in triplicate.

Real time-polymerase chain reaction (PCR)

HT22 cells were cultured to 70% confluence in culture dishes with 5% CO2and 95% air at 37°C. BpV (0.3 or 3 μM) was added for 12 or 24 hours. Total RNA was extracted from HT22 cells with or without BpV treatment using Trizol reagent (Invitrogen, Carlsbad, CA, USA) according to the manufacturer's instructions. The concentration and purity of RNA were determined spectrophotometrically by reading the absorbance at 260 and 280 nm. Aliquots (3 μg)of total RNA were reverse transcribed into cDNA using a commercial kit (Invitrogen). Real time-PCR was conducted in triplicate on an ABI 7900 real-time PCR system using PowerUP SYBR green master mix (Thermo Fisher Scientific,San Jose, CA, USA), a Quant Studio 7 Flex instrument, and fast gene-expression method with the following cycling conditions∶ 95°C for 2 minutes; 40 cycles of 95°C for 30 seconds,59°C for 30 seconds, and 72°C for 30 seconds; followed by 72°C for 2 minutes. Reactions were carried out in triplicate and β-actin gene expression was used as an internal control to normalize variability in expression levels. The results were analyzed by the 2-ΔΔCTvalue method, as previously described(Zhang et al., 2014, 2016). Primers used in this study are shown in Table 1.

Table 1 Primer sequences

Immunoblotting

HT22 cells were cultured to 70% confluence in culture dishes with 5% CO2and 95% air at 37°C. BpV (0.3 or 3 μM)was added for 12 or 24 hours. After harvesting, cells were washed in phosphate-buffered saline before lysing with radioimmunoprecipitation assay buffer (Beyotime Biotechnology, Shanghai, China). Protein concentrations were determined using a bicinchoninic acid protein assay kit(Pierce Biotechnology, Rockford, IL, USA). Equal amounts of protein were separated by 10% sodium dodecyl sulfate polyacrylamide gel electrophoresis and transferred to nitrocellulose membranes (Roche Diagnostics, Indianapolis,IN, USA). Membranes were blocked with 5% nonfat milk before incubation with rabbit polyclonal anti-DNMT1,-DNMT3A, -DNMT3B, or -P21 (a cyclin-dependent kinase inhibitor) (Novus Biologicals, Littleton, CO, USA), and a mouse monocloncal anti-actin antibody (Sigma) (Liu et al.,2017). Primary antibodies were used at a dilution of 1∶1000.Blots were visualized with an enhanced chemiluminescence detection system (Beyotime Biotechnology). Optical densities of bands were quantified using ImageJ 1.8.0 soft-ware (Scion Corporation, Torrance, CA, USA). Western blot data were normalized to β-actin. Cells were harvested and lysed. Protein expression levels of DNMT1, DNMT3A,DNMT3B, and p21 were determined by immunoblotting analysis as previously described by He et al. (2013).

Analysis of cell cycle

HT22 cells were cultured to 70% confluence in culture dishes with 5% CO2and 95% air at 37°C. BpV (0.3 or 3 μM) was added for 12 or 24 hours. Cell cycle distribution was measured with flow cytometry (Becton Dickinson,Franklin Lakes, NJ, USA). Briefly, cells were cultured as previously described, collected, and washed twice in phosphate-buffered saline. Cell pellets were re-suspended in 0.5 mL phosphate-buffered saline andfixed in 4.5 mL 70%ethanol overnight. The following day, cells were centrifuged at 800 × g for 5 minutes and pellets were resuspended in 0.1% Triton X-100 containing 0.2 mg/mL propidium iodide and 0.1 mg/mL RNase A. This was followed by incubation in the dark for 30 minutes at room temperature (Yang et al., 2017). Cells were cultured, fixed, and stained as previously described (Yang et al., 2017). Percentages of cells in each phase of the cell cycle (G0/G1, S, and G2/M) were analyzed using ModFit 3.0 software (Becton Dickinson).Cell percentages were calculated as previously described by Bohmer (1982). Results are reported as percentages of total cells in each phase.

DNMT activity assay

HT22 cells were cultured to 70% confluence in culture dishes with 5% CO2and 95% air at 37°C. BpV (0.3 or 3 μM) was added for 12 or 24 hours. Nuclear proteins were isolated with and EpiQuik nuclear extraction kit (Epigentek,Brooklyn, NY, USA). The reaction was initiated by adding 10 μg of nuclear extracts to the unique, cytosine-rich DNA substrate coated enzyme-linked immunosorbent assay(ELISA) plate provided in the EpiQuik DNMT Activity/Inhibition Assay Ultra Kit (Epigentek), which contains active DNMTs, and incubating for 60 minutes at 37°C. Methylated DNA was recognized by an anti-5-methylcytosine antibody. Amounts of methylated DNA, which is proportional to enzyme activity, were calorimetrically quantified at 450 nm (Yang et al., 2017).

Statistical analysis

Data are expressed as the mean ± SD and were analyzed with SPSS Version 17.0®software (SPSS, Chicago, IL, USA).One-way analysis of variance followed by Tukey's honest significant difference post hoc test was applied for statistical analysis. P ＜ 0.05 was considered statistically significant.

Results

Effect of BpV on cell proliferation and viability

Results of incubation of HT22 cells with BpV at various concentrations from 0.3 μM (0.1 μg/mL) to 3 mM (1 mg/mL) are presented in Figure 1A. A concentration of 0.3 μM BpV did not affect the proliferation of HT22 cells. However,treatment with 3 μM (1 μg/mL) BpV completely arrested cell proliferation. These results indicated that 3 μM was the lowest concentration at which cell proliferation was totally arrested in this study. HT22 cell viability was detected at 12 and 24 hours after BpV treatment with concentrations ranging from 0.3 μM to 3 mM (Figure 1B and C). Lower dosages of BpV (0.3 μM) were unable to remarkably decrease cell viability at 12 or 24 hours after treatment. Moreover, 3 μM BpV decreased cell viability at 24 hours, but showed no significant effect at 12 hours. Therefore, 0.3 μM and 3 μM BpV were used in subsequent experiments.

Effect of BpV on cell morphology

HT22 cells treated with vehicle showed good refraction with sharp and clear membrane borders by light micros-copy (Figure 2). After 12 or 24 hours of exposure to 3 μM BpV, the morphological appearance of HT22 cells was obviously changed, along with a reduction in cell number and increase in cellular debris, indicating reduced cell viability.However, the morphological appearance of cells incubated with 0.3 μM BpV was not obviously changed with regard to cell number or cellular debris.

Influence of BpV on cell cycle

The effect of BpV on cell cycle is shown in Figure 3. BpV at a concentration of 0.3 μM did not markedly affect cell cycle phases. However, incubation with 3 μM BpV for 24 hours arrested the cell cycle in S phase (P ＜ 0.05).

Effect of BpV on DNMT expression levels

HT22 cells were incubated with 0.3 μM or 3 μM BpV for 12 or 24 hours. DNMT1, DNMT3A, and DNMT3B mRNA were significantly increased at 12 and 24 hours (Figure 4AF) with 3 μM BpV. However, with regard to protein levels,only DNMT3B was found to be increased at 24 hours in the 3 μM BpV group (Figure 4M). Notably, 0.3 μM BpV did not produce any significant alterations of DNMT mRNA or protein expression levels (Figure 4).

Influence of BpV on DNMT activity

Total DNMT activities were detected with an EpiQuik DNMT Activity/Inhibition Assay Ultra Kit. At a concentration of 0.3 μM, BpV did not significantly affect DNMT activities. However, at a concentration of 3 μM BpV, DNMT activities were significantly increased at 24 hours (P ＜ 0.05;Figure 4N).

Influence of BpV on p21 expression

Results shown in Figure 5 demonstrate that 3 μM BpV remarkably increased mRNA and protein expression levels of p21 at 24 hours. However, 0.3 μM BpV did not produce any notable alteration in p21 mRNA or protein expression levels (Figure 5).

Discussion

BpV is well known for its protein tyrosine phosphatase inhibitor function, insulin-mimetic properties, and anti-tumor activity (Posner et al., 1994; Bevan et al., 1995; Caron et al., 2008). Additionally, it has effects on nerve cells in animal and cell models. BpV showed neuroprotective effects on the function of primary sensory axons (Nakashima et al., 2008). In addition, it can enhance dopamine release,a neurotransmitter produced by neurons, in PC12 cells(Bieger et al., 2002). In the present study, we explored the effect of BpV on DNMTs in HT22 cells, a mouse hippocampus-derived cell line that is widely used as an in vitro neural cell model. Our results showed that treatment with 3 μM BpV completely blocked the proliferation of HT22 cells. Expression of DNMTs and p21 was increased, and cells were blocked at the S transition of mitosis.

Different concentrations of BpV were administered to neural cells in vitro or in vivo. Cerovac et al. (1999) reported that 0.1 μM BpV was not toxic to the rat neural cell line PC12, and 5-10 μM BpV did not cause a significant amount of death; however, 100 μM BpV was toxic to PC12 cells. Rats infused with 3 or 10 μM BpV exhibited reduced 6-hydroxydopamine-induced neurotoxic injury in rat nigrostriatal neurons (Yang et al., 2007). Similarly, different concentrations of BpV had different effects on HT22 cells∶0.3 μM BpV did not affect proliferation, while 3 μM BpV completely inhibited proliferation. Nevertheless, HT22 cells treated with 3 μM BpV exhibited inhibited proliferation, with fewer cells and more cellular debris.

Inhibition of HT22 cell profileration by BpV may result from cell cycle arrest. We previously reported that the cell cycle of EC109 cells incubated with 100 μM vanadium compound (NaV) was arrested at S phase (Yang et al.,2016). Moreover, the cell cycle progression of neuroblastoma and glioma cells was arrested by BpV at the G2/M phase (Faure et al., 1995). In the present study, HT22 cells were arrested at S phase by 3 μM BpV. Thus, different types of cells may show different sensitivities to BpV, which may arrest cells at different cell cycle phases.

Notably, the cell cycle arrest effect induced by BpV could be caused by reactive oxygen species (Andrezalova et al.,2013). Indeed, Matsugo et al. (2015) reported that peroxidovanadium complexes can generate reactive oxygen species, which may induce upregulation of DNMT expression(Wu and Ni, 2015; Tasdogan et al., 2016; Miozzo et al.,2018). It has also been suggested that Cr(IV)-induced G1 phase arrest may contribute to global hypomethylation (Lou et al., 2013). Notably, silver nanoparticles (AgNPs) can induce G2/M phase arrest and increase DNMT expression in HT22 cells (Mytych et al., 2017). However, the relationship between DNMTs and BpV has not been reported thus far.We proposed that BpV may be similar to Cr(IV) and Ag-NPs, which can induce changes in DNA methylation and DNMT expression to elicit cytotoxic effects. Although we did not detect DNA methylation levels directly, we measured DNMT expression and activity in HT22 cells after BpV treatment and found that BpV may affect the HT22 cell epigenome by increasing levels of DNMT1, DNMT3A,and DNMT3B. Decitabine treatment increased the percentage of cells in G2/M and upregulated p21 expression independent of DNMT1 and DNMT3b in leukemia cells (Jiemjit et al., 2008). As such, DNMT expression and activities may underlie the mechanisms responsible for cell cycle arrest.

Elevated expression of p21 may play a vital role in cellular growth arrest (Yu et al., 2009; Zurlo et al., 2013; Li et al., 2014). After BpV treatment, p21 levels increased, which may contribute to the BpV-mediated anti-proliferative activity observed in our study. We found that both DNMTs and p21 were increased in HT22 cells after treatment with 3 μM BpV. Notably, a GC-rich region has been reported in the human p21 promoter (Prowse et al., 1997; Fang and Lu,2002). Therefore, increased DNMT expression may lead to gene hypermethylation and decreased gene expression.However, Fournel et al. (1999) demonstrated a regulatory link between DNMT and p21 that was independent of DNA methylation. Thus, BpV-induced increases in p21 may not depend on changes of its promoter DNA methylation. Results for p21 were consistent with the findings of Fournel and colleagues (Fournel et al., 1999). Our data support a potential mechanism by which the regulatory link between DNMT and p21 does not rely on changes of p21 DNA methylation.

Figure 1 Proliferation and viability of cells treated with different concentrations of BpV.

Figure 2 Morphological appearance of HT22 cells treated with 0.3 or 3 µM BpV for 12 or 24 hours.

Figure 3 Flow cytometry analysis of the cell cycle in HT22 cells treated with BpV.

Figure 5 BpV increases the expression of p21 (a cyclin-dependent kinase inhibitor) in HT22 cells.

Figure 4 Effect of BpV on expression and activity of DNMTs in HT22 cells across time.

Our results demonstrated that 3 μM BpV remarkably inhibited HT22 cell proliferation, as cells were arrested in S phase; simultaneously, DNMTs were increased. However,the exact mechanism by which BpV induced DNMTs still requires further exploration. In the meantime, BpV may be considered as an agent for activating DNMTs in HT22 cells.

Author contributions:Study concept: GS, CYZ and SCY; experiment implementation: XLT, SYJ, and XLZ; data analysis: JY, JHC and XLL;manuscript preparation: KRG. All authors approved thefinal version of the paper.

Conflicts of interest:The authors declare that there are no conflicts of interest associated with this manuscript.

Financial support:This study was supported by the National Natural Science Foundation of China, No. 81160244, 81360316, 81460283,81660307 (all to GS); the Inner Mongolia Science Foundation of China, No. 2018LH08078 (to GS), 2016MS(LH)0307 (to SYJ); the Baotou Health Foundation, China, No. WSJJ2016008 (to SYJ); the Inner Mongolia Educational Research Foundation, China, No. NJZY207 (to GS),NJZY17243 (to SCY), NJZY17250 (to XLL), NJZY17251 (to SYJ); the Baotou Medical College Foundation, China of No. BYJJ-DF201602,BYJJ-YF201615, BSJJ201617, BYJJ-QM201633, BYJJ-QM201656,BYJJ201502 (to GS); the Science and Technology Planning Project of Baotou of China, No. CX2017-5 (to GS); the National Key R&D Program of China, No. 2017YFC1308405 (to GS). The funding sources had no role in study conception and design, data analysis or interpretation,paper writing or deciding to submit this paper for publication.

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