Open Access

Icariside II protects cardiomyocytes from hypoxia‑induced injury by upregulating the miR‑7‑5p/BTG2 axis and activating the PI3K/Akt signaling pathway

  • Authors:
    • Dongxia Hu
    • Yong Gu
    • Dan Wu
    • Juanjuan Zhang
    • Qing Li
    • Jun Luo
    • Shaochuan Li
    • Zhen Yuan
    • Bo Zhu
  • View Affiliations

  • Published online on: July 16, 2020     https://doi.org/10.3892/ijmm.2020.4677
  • Pages: 1453-1465
  • Copyright: © Hu et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

Icariside II (ICS II) has been reported to have protective effects against oxidative stress. However, whether ICS II protects cardiomyocytes from myocardial infarction (MI), and the associated underlying mechanisms, remain to be elucidated. Therefore, the current study investigated the effects of ICS II on hypoxia‑injured H9c2 cells, as well as the associated molecular mechanisms. A hypoxic injury model was established to emulate the effects of MI. The effects of ICS II on the proliferation of rat cardiomyocyte H9c2 cells were assessed with cell counting kit‑8 assays. The apoptotic status of the cells was assessed by flow cytometry, and the expression of apoptosis‑related proteins was analyzed by western blotting. A microRNA (miRNA/miR) microarray was used to quantify the differential expression of miRNAs after ICS II treatment, and the levels of miR‑7‑5p were further quantified by reverse transcription‑quantitative PCR. Whether ICS II affected hypoxia‑injured cells via miR‑7‑5p was subsequently examined, and the target of miR‑7‑5p was also investigated by bioinformatics analysis and luciferase reporter assays. The effects of ICS II on the PI3K/Akt pathway were then evaluated by western blot analysis. Hypoxia treatment decreased viability and the migration and invasion abilities of H9c2 cells, and also induced apoptosis. ICS II significantly increased viability and reduced hypoxia‑associated apoptosis. Moreover, ICS II treatment led to the upregulation of miR‑7‑5p, and the protective effects of ICS II were found to rely on miR‑7‑5p. Moreover, BTG anti‑proliferation factor (BTG2) was identified as a direct target of miR‑7‑5p, and overexpression of BTG2 inhibited the protective effects of miR‑7‑5p. Finally, ICS II treatment resulted in the activation of the PI3K/Akt signaling pathway, which is essential for the survival of H9c2 cells under hypoxic conditions. In summary, ICS II reduces hypoxic injury in H9c2 cells via the miR‑7‑5p/BTG2 axis and activation of the PI3K/Akt signaling pathway.

Introduction

Myocardial infarction (MI) as a result of cardiovascular diseases is a leading cause of death and disability world-wide (1). MI caused by temporary or permanent occlusion of the main coronary arteries may lead to a reduction in the blood supply to the cardiac muscle (2). Significant levels of cardiomyocyte apoptosis are an important physiological feature of MI, which can be triggered by hypoxia (3). Ultimately, MI may promote heart failure due to decreased contraction of the myocardium (4). Although the treatment of MI has mark-edly improved, the mortality and morbidity rates are still far from satisfactory (5). Therefore, the identification of potential therapeutic agents against MI, as well as the elucidation of its underlying mechanisms, is critical.

Icariside II (ICS II) is a flavonol glycoside that can be isolated from Herba Epimedii, which has commonly been used in Traditional Chinese Medicine for thousands of years (6). ICS II has been reported to possess anti-inflammatory, antitumor and anti-osteoporotic properties (7). In recent years, ICS II has been found to exert various cardioprotective effects, such as the alleviation of myocardial fibrosis and diabetic cardiomyopathy (8,9). However, the specific roles and related molecular mechanisms of ICS II in hypoxia-induced H9c2 cells remain elusive.

MicroRNAs (miRNAs/miRs) are a group of endogenous, noncoding small RNAs that play important roles in numerous pathological and physiological processes (10). Accumulating evidence has revealed that miRNAs play an essential role in the pathophysiological consequences of MI (11,12), and several potential agents isolated from herbs have been found to exert their pharmacological activities through the regulation of miRNAs (13,14). miR-7-5p is a multifaceted miRNA that participates in the development of various types of cancer (15). It is also able to protect cardiomyocytes against ischemia/reperfusion (I/R) injury by targeting Poly [ADP-ribose] polymerase 1 (16). However, whether miR-7-5p is also involved in regulating the functions of ICS II in MI was previously unknown.

In the current study, H9c2 rat cardiomyocytes were cultured under hypoxic conditions to produce an MI injury model. Then, the effects of ICS II on the hypoxia-induced injury of H9c2 cells, and its possible molecular mechanisms, were investigated. The results indicate that ICS II protects H9c2 cells from hypoxia-induced injury via the regulation of the miR-7-5/BTG anti-proliferation factor (BTG2) axis and the PI3K/Akt signaling pathway.

Materials and methods

Cell culture and treatment

Rat cardiomyocyte H9c2 cells were purchased from the American Type Culture Collection. H9c2 cells were maintained in DMEM (Thermo Fisher Scientific, Inc.) with 10% fetal bovine serum, 100 U/ml penicillin and 100 µg/ml streptomycin (all Gibco; Thermo Fisher Scientific, Inc.) at 37°C (5% CO2) in a humidified atmosphere. To establish the hypoxia-induced injury model, cells were exposed to hypoxic conditions (93% N2, 2% O2 and 5% CO2) for 24 h; cells incubated under normoxic conditions (95% air and 5% CO2) were used as a control. ICS II (purity >98% by HPLC) was purchased from Nanjing Zelang Medical Technology Corporation Ltd. ICS II was dissolved in DMSO (Sigma-Aldrich; Merck KGaA) to a concentration of 10 mM and stored at -80°C. ICS II was diluted with complete medium to achieve the different designated concentrations. Cells were treated with different concentrations of ICSII (2, 4 and 8 µM) at 37°C for 24 h, and then subjected to different types of analysis. LY294002 (Sigma-Aldrich; Merck KGaA), an inhibitor of the PI3K/Akt pathway, was stored at −20°C and diluted in complete medium at a final concentration of 10 µM. Where appropriate, cells were co-treated with LY294002 (10 µM) and ICSII (8 µM) at 37°C for 24 h, and subsequently analyzed experimentally. The same concentration of DMSO was applied to cells as a control. All other routine chemicals were obtained from Sigma.

Transfection

miR-7-5p mimics, miR-7-5p inhibitor and a negative control miR (NC) were all synthesized by Suzhou GenePharma Co., Ltd and used at a concentration of 100 nM. The full-length BTG2 sequence was inserted into a pcDNA 3.1 plasmid (Suzhou GenePharma Co., Ltd.), and the empty vector was used as a negative control. The cells were transfected with the corresponding vectors using Lipofectamine® 2000 (Thermo Fisher Scientific, Inc.) according to the manufacturer's instructions. Reverse transcription-quantitative (RT-q) PCR and western blot analysis were performed to determine transfection efficacy. Subsequent experimentation was performed 24 h after the transfection.

Cell viability assay

The Cell Counting Kit-8 (CCK-8; Beijing Solarbio Science & Technology Co., Ltd.) was used to assess cell viability according to the manufacturer's protocol. H9c2 cells were seeded into 96-well plates at a density of 5×103 cells/well and cultured at 37°C overnight. The cells were then cultured under hypoxic conditions for 24 h (as afore-mentioned), which was followed by a further 24-h incubation at 37°C under normoxic conditions. After reoxygenation, 10 µl CCK-8 solution was added to each well, followed by a 4-h incubation period. The absorbance at 450 nm was measured using a microplate reader (Bio-Rad Laboratories, Inc.).

Cell migration and invasion assays

The migration of H9c2 cells was assessed by chamber migration assays, using two-chamber-Transwell 24-well cell culture plates (Corning, Inc.) with 8-µm polycarbonate filters. Briefly, hypoxic injury was induced in H9c2 cells as aforementioned, following treatment with ISC II where appropriate; the cells were then resuspended in 200 µl serum-free media, and then seeded into the upper chambers of the inserts within a 24-well plate (1×105 cells/well); 500 µl complete medium was added to the lower compartment as a chemoattractant. After culture for 48 h at 37°C, the migrated cells in the lower chamber were fixed with ethanol, stained with crystal violet at room temperature for 5 min, and counted under an inverted light microscope at ×200 magnification (Olympus Corporation). For the invasion assays, the inserts were precoated with Matrigel (BD Biosciences) at room temperature for 1 h. Each experiment was performed in triplicate.

Apoptosis assay

The percentage of apoptotic cells was measured using the FITC-Annexin V Apoptosis Detection kit (BD Bioscience) according to the manufacturer's instructions. The cells were analyzed using a FACScan flow cytometer (BD Bioscience) with FlowJo v10.0.7 software (Tree Star, Inc.).

RNA purification and RT-qPCR

Total RNA was extracted from cells using TRIzol® reagent (Invitrogen; Thermo Fisher Scientific, Inc.) according to the manufacturer's instructions. Reverse transcription of the RNA was performed using the PrimeScript™ RT reagent kit (Takara Biotechnology Co., Ltd.) and qPCR was performed with the TaqMan™ MicroRNA Reverse Transcription kit and TaqMan™ Universal Master Mix (Applied Biosystems; Fisher Scientific, Inc.). GAPDH and U6 were used as internal controls for BTG2 and miR-7-5p, respectively. The reverse transcription primer for miR-7-5p was 5′-GTC GTA TCC AGT GCA GGG TCC GAG GTG CAC TGG ATA CGA CAC AAC AA-3′. The qPCR primers were as follows: miR-7-5p forward, 5′-TGG AAG ACT AGT GAT TTT-3′ and reverse, 5′-CTC AAC TGG TGT CGT G-3; BTG2 forward, 5′-CTG GAG GAG AAC TGG CTG TC-3′ and reverse, 5′-AAA ACA ATG CCC AAG GTC TG-3′; U6 forward, 5′-GCT TCG GCA GCA CAT ATA CTA AAA T-3′ and reverse, 5′-CGC TTC ACG AAT TTG CGT GTC AT-3′; and GAPDH forward, 5′-TGA CCA CAG TCC ATG CCA TC-3′ and reverse, 5′-GAC AAG CTT CCC GTT CTC AG-3′. The qPCR conditions were as following: 30 sec at 94°C, followed by 40 cycles of 5 sec at 94°C, 10 sec at 55°C, 10 sec at 72°C, and a final extension of 10 min at 72°C. The expression levels in tissues and cells were calculated using the 2−ΔΔCq method (17).

miRNA microarray analysis

Total cellular RNA was purified from cells cultured under hypoxic conditions using TRIzol® reagent and the RNeasy mini kit (Qiagen GmbH) according to the manufacturer's instructions. The RNA samples were quantified using a NanoDrop spectrophotometer (NanoDrop Technologies; Thermo Fisher Scientific, Inc.), and then labeled using the miRCURY™ Hy3™/Hy5™ Power labelling kit (Qiagen GmbH). The labelled samples were hybridized to a microarray (NimbleGen Systems, Inc.) for 16-20 h, and the array sections were scanned using the GenePix 4000B micro-array scanner (Axon Instruments). The results were read and analyzed using GenePix Pro V6.0 (Molecular Devices, LLC). A heat map diagram was used to display the data for two-way hierarchical clustering of genes and samples.

Bioinformatic analysis

TargetScan bioinformatics software (www.targetscan.org) was used to predict the potential target of miR-7-5p.

Dual-luciferase reporter assay

A BTG2 3'-unranslated region (UTR) cDNA fragment, which contained the miR-7-5p binding site, was subcloned into a pmirGIO dual luciferase miRNA target expression plasmid (Promega Corporation) to create a luciferase reporter vector (BTG2-wt). A BTG2 3'-UTR that was mutated at the miR-7-5p complementary site was generated (BTG2-mut) using the GeneArt™ Site-directed Mutagenesis System (Thermo Fisher Scientific, Inc.) according to the manufacturer's instructions, and was also inserted into a pmirGIO reporter plasmid. H9c2 cells were subsequently co-transfected with the both reporter plasmid and miR-7-5p mimics or mimic NC, and luciferase activity was subsequently detected using the Dual-luciferase Reporter Assay system (Promega Corporation). Transfection was performed using Lipofectamine® 2000 according to the manufacturer's protocol. Luciferase activity was measured 24 h after transfection and Renilla luciferase activity was used to normalize that of firefly luciferase.

Lactate dehydrogenase (LDH) release detection

The release of LDH was measured using the LDH Cytotoxicity Assay kit (Beyotime Institute of Biotechnology) according to the manufacturer's instructions.

Western blot analysis

Total protein was extracted from cells using RIPA lysis buffer and quantified using the Caspase-3 Assay kit (Fluorometric) (both Beyotime Institute of Biotechnology). Equal amounts of protein (20 µg) were resolved using 12% SDS-PAGE gels and then transferred onto PVDF membranes (EMD Millipore). After blocking with 5% skim milk, the membranes were incubated with primary antibodies overnight at 4°C, which was followed by probing with ant-mouse IgG, HRP-linked antibody (cat. no. 7076) or anti-rabbit HRP-linked antibody (cat. no. 7074) (1:5,000, Cell Signaling Technology, Inc.) at room temperature for 1 h. The protein bands were visualized using an ECL detection system (EMD Millipore), and the intensity of the protein bands was quantified using ImageJ Software (National Institutes of Health). The following primary antibodies were purchased from Cell Signaling Technology, Inc.: Bcl-2 (cat. no. 15071), Bax (cat. no. 14796), GAPDH (cat. no. 5174), caspase-3 (cat. no. 9662), caspase-9 (cat. no. 9502), phosphorylated (p)-PI3K (cat. no. 4228), PI3K (cat. no. 3011), p-Akt (cat. no. 9614) and Akt (cat. no. 2966). The BTG2 antibody (cat. no. ab85051) was purchased from Abcam. All primary antibodies were diluted at a ratio of 1:1,000 in 5% BSA.

Statistical analysis

The data are presented as the means ± standard deviation from three independent repeated experiments. Statistical analysis was performed using GraphPad 7.0 statistical software (GraphPad Software, Inc.), and the significant differences between groups were deter-mined by one-way analysis of variance followed by Tukey's post hoc test. P<0.05 was considered to indicate a statistically significant difference.

Results

Hypoxia induces myocardial injury in H9c2 cells

To produce a hypoxia-induced injury model, H9c2 cells were exposed to hypoxic conditions for 4, 8, 12 and 24 h, and cellular viability was assessed using the CCK-8 assay. As indicated in Fig. 1A, hypoxia reduced the viability of H9c2 cells in a time-dependent manner. The levels of apoptosis were also detected following culture under hypoxic conditions for 24 h and were significantly increased when compared with those of the control group (Fig. 1B). These results were further supported by an LDH assay, which confirmed that hypoxia treatment significantly promoted LDH release (Fig. 1C). Furthermore, compared with the control, hypoxia treatment led to the downregulation of the anti-apoptotic protein Bcl-2, and upregulation of the proapoptotic protein Bax; the cleavage of caspase-3 and -9 was also observed following exposure to hypoxic conditions (Fig. 1D). The migration and invasion abilities of H9c2 cells were also significantly decreased following culture under hypoxic conditions (Fig. 1E and F). Therefore, it was confirmed that hypoxia results in damage to H9c2 cells, and that an in vitro hypoxia cell model was successfully generated.

ICS II protects H9c2 cells from hypoxia-induced injury

The effects of ICS II on hypoxia-induced injury in H9c2 cells were investigated. To determine a suitable dosage, cells were incubated with various concentrations of ICS II (2, 4 and 8 µM) for 24 h, and cell viability was then assessed. As shown in Fig. 2A, there were no significant differences in cell viability among cells treated with different concentrations of ICS II. As 2-8 µM exerted neither pro- nor anti-survival effects on H9c2 cells under normoxic conditions, 8 µM was selected as the dose of ICS II for subsequent experiments.

The protective effects of ICS II on H9c2 cells under hypoxic conditions were then investigated. CCK-8 assay results indicated that the hypoxia-induced decrease in cell viability was notably mitigated by ICS II pretreatment (P<0.01; Fig. 2B). Similarly, the hypoxia-induced increase in apoptosis was significantly reversed (P<0.001; Fig. 2C), and hypoxia-induced LDH release was significantly inhibited (P<0.01; Fig. 2D) by ICS II pretreatment. Western blot analysis revealed that hypoxia induced alterations in Bax, Bcl-2, cleaved caspase-3 and -9, and that these results were significantly reversed by ICS II treatment (P<0.05; Fig. 2E). Furthermore, ICS II treatment markedly increased the migration and invasion capacities of H9c2 cells under hypoxic conditions (Fig. 2F and G). These data indicate that ICS II provides protection against hypoxia-associated injury in H9c2 cells.

ICS II attenuates hypoxia-induced injury in H9c2 cells by upregulating miR-7-5p expression

An miRNA chip array was used to determine whether the protective effects of ICS II were exerted via the regulation of miRNAs. In total, 11 upregulated and 11 downregulated miRNAs were identified following ICS II treatment of H9c2 cells under hypoxic conditions, of which miR-7-5p was the most upregulated (Fig. 3A). The levels of miR-7-5p following ICS II treatment were then verified using RT-qPCR. The results showed that treatment with ICS II markedly increased miR-7-5p expression (Fig. 3B), indicating the involvement of miR-7-5p in the protective effects of ICS II. To investigate the role of miR-7-5p in this setting, miR-7-5p mimics and inhibitors were transfected into H9c2 cells. As indicated in Fig. 3C, miR-7-5p levels were significantly increased following transfection with miR-7-5p mimics (P<0.001), and notably decreased by the miR-7-5p inhibitor (P<0.01) compared with the control cells. The transfected cells were then treated with ICS II prior to exposure to hypoxic conditions. The effects of ICS II pretreatment were significantly abrogated by inhibiting miR-7-5p, which is indicated by decreased cell viability (P<0.01; Fig. 3D), increased apoptosis (P<0.01; Fig. 3E) and increased LDH release (P<0.001; Fig. 3F). Conversely, miR-7-5p mimics enhanced the protective effects of ICS II, showing increased cell viability (P<0.001; Fig. 3C), decreased apoptosis (P<0.01; Fig. 3E) and decreased LDH release (P<0.05; Fig. 3F). Moreover, western blot analysis confirmed that the protective effect of ICS II against hypoxia-induced injury relied on the upregulation of miR-7-5p (Fig. 3G), since caspase-3 cleavage was rescued by inhibiting miR-7-5p in the presence of ICS II under hypoxic conditions. ICS II was also demonstrated to restore the migration and invasive capacities of H9c2 cells under hypoxic conditions via miR-7-5p, since inhibition of miR-7-5p blocked this effect (Fig. 3H). These data indicate that ICS II provides protective effects against hypoxia in H9c2 cells, at least partly via the upregulation of miR-7-5p.

miR-7-5p directly targets BTG2, which reverses the effect of miR-7-5p on H9c2 cells exposed to hypoxic conditions

Using TargetScan, BTG2 was identified as a potential target for miR-7-5p (Fig. 4A, left). Luciferase reporter assays confirmed the association between miR-7-5p and BTG2 (Fig. 4B); the luciferase activity of BTG2-wt was significantly inhibited in miR-7-5p-transfected cells, while that of the BTG2-mut remained unaltered. Furthermore, the mRNA and protein levels of BTG2 were significantly decreased and increased in the miR-7-5p mimic and inhibitor groups, respectively (Fig. 4B and C). These observations suggest a negative regulatory relationship between miR-7-5p and BTG2.

BTG2 was then ectopically expressed to investigate whether miR-7-5p affected hypoxia-induced injury in H9c2 cells via the regulation of BTG2. As indicated in Fig. 4D, western blot analysis showed that the protein level of BTG2 was successfully overexpressed in H9c2 cells via transfection with pcDNA3.1 BTG2 (P<0.001). Further experiments revealed that the effects of miR-7-5p on migration and invasion under hypoxic conditions were blocked by BTG2 overexpression (Fig. 4E). Functional experiments indicated that miR-7-5p overexpression retained cell viability (P<0.001; Fig. 4F), reduced apoptosis (P<0.001; Fig. 4G), reduced LDH release (P<0.001; Fig. 4H), downregulated cleaved caspase-3/-9 and pro-apoptotic Bax, and upregulated Bcl-2 (Fig. 4I) in hypoxia-treated cells. However, the effects of miR-7-5p overexpression on cells treated under hypoxic conditions were obviously abrogated by BTG2 overexpression (P<0.001; Fig. 4F-I). These results indicate that the overexpression of BTG2 reverses the effect of miR-7-5p on hypoxia-treated H9c2 cells.

BTG2 knockdown protects H9c2 cells from hypoxia-induced injury

To further confirm the role of BTG2 in the protective effects of ICS II, siRNAs were used to knock down BTG2 in H9c2 cells. As indicated in Fig. 5A, two siRNAs targeting BTG2 (siBTG2 #1 and #2) were transfected into H9c2 cells for 24 h, which resulted in a significant decrease in BTG2 expression compared with the control group (siCtrl); 24 h post-transfection, H9c2 cells were exposed to hypoxic conditions for another 24 h, and cell viability was assayed. BTG2 knockdown under hypoxic conditions markedly enhanced the viability of H9c2 cells compared with that of the control group (Fig. 5B). Moreover, knockdown of BTG2 successfully reduced apoptosis and LDH release caused by hypoxia (Fig. 5C and D). In addition, western blotting also confirmed that the activation of caspase-3 and -9, the downregulation of Bcl-2 and the upregulation of Bax caused by hypoxia were reversed by BTG2 knockdown. Knocking down BTG2 also restored the migration and invasion abilities of H9c2 cells under hypoxic conditions (Fig. 5F). Taken together, these data suggest that BTG2 may be an important regulator in hypoxia-induced injury of H9c2 cells.

ICS II exerts its protective effect by activating the PI3K/Akt signaling pathway

Mounting evidence indicates that the PI3K/Akt signaling pathway plays an essential protective role in cardiomyoblasts. Therefore, the potential effects of ICS II on the PI3K/Akt signaling pathway were investigated. As indicated in Fig. 5A, p-PI3K and p-Akt levels were notably decreased in H9c2 cells exposed to hypoxic conditions, compared with those of the control group; there was little change in the levels of total PI3K and Akt. Treatment with ICS II or overexpression of miR-7-5p mimics restored the expression of p-PI3K and p-Akt, indicating the activation of the PI3K/Akt signaling pathway (Fig. 6A). However, the phosphorylation levels of PI3K and Akt were decreased in the presence of hypoxia, ICS II and miR-7-5p inhibitor combined (Fig. 6A). These findings indicate that ICS II activates the PI3K/Akt signaling pathway via the upregulation of miR-7-5p under hypoxic conditions. To further investigate the function of the PI3K/Akt signaling pathway in the protective effect of ICS II, cells were treated with LY294002, a specific PI3K/Akt inhibitor. As shown in Fig. 6B, LY294002 successfully inhibited the activation of the PI3K/Akt signaling pathway. LY294002 also abrogated the protective effects of ICS II on the viability of H9c2 cells under hypoxic conditions (Fig. 6C). LY249002 also promoted apoptosis and the release of LDH, which was induced by hypoxia in the presence of ICS II (Fig. 6D and E). Moreover, the activation of caspase-3 and -9, a decrease in Bcl-2 and an increase in Bax caused by hypoxia were also caused by LY294002 (Fig. 6F). Furthermore, the effects of ICS II on the migration and invasion of H9c2 cells under hypoxic conditions could be blocked by LY294002 (Fig. 6G). Collectively, these data suggest that ICS II treatment activates the PI3K/Akt signaling pathway, which is essential for the survival of H9c2 cells under hypoxic conditions.

Discussion

In the present study, the protective effects of ICS II on hypoxia-induced cardiomyocyte injury were investigated, as well as the potential underlying molecular mechanisms. Hypoxic exposure was found to markedly decrease the viability of rat H9c2 cardiomyocytes and to induce apoptosis. ICS II protected H9c2 cells against hypoxia-induced apoptosis and a loss in viability by upregulating the expression of miR-7-5p. In addition, BTG2 was identified as a direct target of miR-7-5p, and its overexpression abrogated the protective effects of miR-7-5p in a hypoxia-induced injury model. Furthermore, ICS II was also shown to activate the PI3K/Akt signaling pathway, which is essential for the survival of H9c2 cells under hypoxic conditions.

ICS II is a flavonol glycoside isolated from Herba Epimedii that has been found to exhibit antitumor, anti-inflammatory, neuroprotective and antidiabetic activities (18-20). However, there are few reports about the effects of ICS II on hypoxia-induced cell injury. A previous study showed that ICS II could attenuate myocardial fibrosis by inhibiting the NF-kB and transforming growth factor-β1/Smad2 signaling pathways (8). Another study indicated that ICS II ameliorated diabetic cardiomyopathy in streptozotocin-induced diabetic rats (9). However, the effects of ICS II on hypoxic-induced cardiomyocyte injury remained elusive. In the present study, hypoxia-induced injury was significantly abrogated by ICS II, presenting with increased viability and reduced apoptosis. In line with previous studies, these findings further confirmed the cardioprotective effects of ICS II.

To elucidate the potential underlying molecular mechanisms of ICS II protection on hypoxia-induced H9c2 cell injury, the relationship between ICS II and miR-7-5p was investigated in hypoxia-treated H9c2 cells. miR-7-5p is a miRNA that is evolutionarily conserved from parasites to mammals. miR-7-5p has been found to act as a tumor suppressor in various types of cancer, such as bladder cancer, pancreatic cancer and melanoma (21-23). Only a few studies have investigated the functions of miR-7-5p in cardiomyopathy, but it has been found to protect cardiomyocytes from I/R-induced injury (16). In addition, a recent study also revealed that the inhibition of miR-7-5p contributed to myocardial I/R injury (24). In line with these reports, the present study revealed that inhibiting miR-7-5p expression notably reversed the protective effects of ICS II in a hypoxia-induced H9c2 cell injury model.

BTG2 is a member of the BTG/TOB gene family (25) that BTG2 has been identified as a tumor suppressor in various cancer types (26). A previous study found that the downregulation of BTG2 via miR-21 could protect cardiomyocytes against doxorubicin-induced apoptosis (27). In the present study, bioinformatics and luciferase gene reporter assays showed that BTG2 was a direct target of miR-7-5p in H9c2 cells. Moreover, BTG2 reversed the protective effect of miR-7-5p on hypoxia-induced injury in H9c2 cells. In addition, BTG2 knockdown emulated the effects of ICS II treatment by providing protective effects to H9c2 cells against hypoxia-induced injury. These findings indicate that BTG2 may be an important regulator in MI, and that the effect of ICS II on the expression of miR-7-5p may also rely on the regulation of BTG2. Notably, it was also found that hypoxia treatment could lead to the upregulation of BTG2 (28); there-fore, further studies are required to further investigate the role of BTG2 in hypoxia.

An abundance of evidence has shown that activation of the PI3K/Akt pathway is able to protect the heart from I/R injury, as well as enhance the survival of cardiomyocytes (29,30). Consistent with the findings of the present study, ICS II activated the Akt signaling pathway and thereby exerted protective effects on osteoblasts (31). However, another study reported that ICS II inhibited the PI3K/Akt signaling pathway in non-small cell lung cancer cells. From the results of the present study, it was proposed that ICS II is able to both activate and inhibit the PI3K/Akt signaling pathway depending on the cell type involved, though further study is required to confirm this hypothesis. In line with a previous study, miR-7-5p was also shown to trigger the activation of the PI3K/Akt signaling pathway (32). Notably, in another recent study, it was shown that silencing BTG2 contributed to the activation of the PI3K/Akt pathway, which is in accordance with the findings of the present study (33).

To the best of our knowledge, the present study was the first to investigate the effects of ICS II on hypoxia-treated H9c2 cells. The results revealed an in vitro protective effect of ICS II on cardiomyocytes. The present study also revealed that miR-7-5p was a downstream factor responsive to ICS II, and that ICS II may protect H9c2 cells from hypoxia-induced injury via the upregulation of miR-7-5p. Furthermore, BTG2 was identified as a direct target gene of miR-7-5p, and BTG2 over-expression reversed the effects of miR-7-5p on hypoxia-treated H9c2 cells, while BTG2s knockdown provided protective effects. Finally, the present study demonstrated that ICS II treatment also led to the activation of the PI3K/Akt pathway, which is essential for the survival of H9c2 cells under hypoxic conditions. More clinical and/or in vivo experimentation is required to support these findings.

Acknowledgments

Not applicable.

Funding

The present study was supported by the key fund of the Jiangxi Science and Technology Bureaucracy (grant no. 20171BBG70016).

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Authors' contributions

DH was involved in the conception of the study and writing the original manuscript draft. YG was involved in study conception and design, and critical revision of the manuscript. DW was involved in study conception and design, and data acquisition. JZ, QL and JL analyzed and interpreted the data and drafted the manuscript. SL took part in data acquisition and revising the manuscript for important intellectual content. ZY and BZ took part in study conception and design, as well as supervision, project administration, funding acquisition and writing (reviewing and editing). All authors read and approved the final manuscript.

Ethics approval and consent to participate

Not applicable.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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October-2020
Volume 46 Issue 4

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Online ISSN:1791-244X

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Copy and paste a formatted citation
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Spandidos Publications style
Hu D, Gu Y, Wu D, Zhang J, Li Q, Luo J, Li S, Yuan Z and Zhu B: Icariside II protects cardiomyocytes from hypoxia‑induced injury by upregulating the miR‑7‑5p/BTG2 axis and activating the PI3K/Akt signaling pathway. Int J Mol Med 46: 1453-1465, 2020.
APA
Hu, D., Gu, Y., Wu, D., Zhang, J., Li, Q., Luo, J. ... Zhu, B. (2020). Icariside II protects cardiomyocytes from hypoxia‑induced injury by upregulating the miR‑7‑5p/BTG2 axis and activating the PI3K/Akt signaling pathway. International Journal of Molecular Medicine, 46, 1453-1465. https://doi.org/10.3892/ijmm.2020.4677
MLA
Hu, D., Gu, Y., Wu, D., Zhang, J., Li, Q., Luo, J., Li, S., Yuan, Z., Zhu, B."Icariside II protects cardiomyocytes from hypoxia‑induced injury by upregulating the miR‑7‑5p/BTG2 axis and activating the PI3K/Akt signaling pathway". International Journal of Molecular Medicine 46.4 (2020): 1453-1465.
Chicago
Hu, D., Gu, Y., Wu, D., Zhang, J., Li, Q., Luo, J., Li, S., Yuan, Z., Zhu, B."Icariside II protects cardiomyocytes from hypoxia‑induced injury by upregulating the miR‑7‑5p/BTG2 axis and activating the PI3K/Akt signaling pathway". International Journal of Molecular Medicine 46, no. 4 (2020): 1453-1465. https://doi.org/10.3892/ijmm.2020.4677