miRNA signature of unfolded protein response in H9c2 rat cardiomyoblasts
© Read et al.; licensee BioMed Central Ltd. 2014
Received: 30 July 2014
Accepted: 11 September 2014
Published: 19 September 2014
Glucose and oxygen deprivation during ischemia is known to affect the homeostasis of the endoplasmic reticulum (ER) in ways predicted to activate the unfolded protein response (UPR). Activation of UPR signalling due to ER stress is associated with the development of myocardial infarction (MI). MicroRNAs (miRNAs) are key regulators of cardiovascular development and deregulation of miRNA expression is involved in the onset of many cardiovascular diseases. However, little is known about the mechanisms regulating the miRNA expression in the cardiovascular system during disease development and progression. Here we performed genome-wide miRNA expression profiling in rat cardiomyoblasts to identify the miRNAs deregulated during UPR, a crucial component of ischemia.
We found that expression of 86 microRNAs changed significantly during conditions of UPR in H9c2 cardiomyoblasts. We found that miRNAs with known function in cardiomyoblasts biology (miR-206, miR-24, miR-125b, miR-133b) were significantly deregulated during the conditions of UPR in H9c2 cells. The expression of miR-7a was upregulated by UPR and simulated in vitro ischemia in cardiomyoblasts. Further, ectopic expression of miR-7a provides resistance against UPR-mediated apoptosis in cardiomyoblasts. The ample overlap of miRNA expression signature between our analysis and different models of cardiac dysfunction further confirms the role of UPR in cardiovascular diseases.
This study demonstrates the role of UPR in deregulating the expression of miRNAs in MI. Our results provide novel insights about the molecular mechanisms of deregulated miRNA expression during the heart disease pathogenesis.
KeywordsUnfolded protein response ER stress MicroRNAs Myocardial infarction Mir-7a Apoptosis
Physiological or pathological processes that disturb protein folding in the endoplasmic reticulum cause ER stress and activate a set of signalling pathways termed the Unfolded Protein Response (UPR). In the ischemic state the lack of oxygen and nutrients to the heart can cause lasting damage to this vital organ through cardiomyoblasts death. Ischemic conditions are known to affect ER homeostasis in ways predicted to activate the UPR. Activation of UPR signalling due to ER stress is associated with the development of ischemic heart disease. We and others have shown that simulating ischemia or ischemia/reperfusion in cultured neonatal rat or adult mouse ventricular cardiomyocytes can activate numerous features of the UPR.
In mammals, three ER transmembrane proteins, IRE1, ATF6, and PERK, respond to the accumulation of unfolded proteins in the ER lumen. Activation of PERK, IRE1, and ATF6 initiates ER-to-nucleus intracellular signaling cascades collectively termed the UPR. PERK-mediated phosphorylation of eukaryotic translation initiation factor 2 on the alpha subunit (eIF2α) at Ser51 leads to translational attenuation. Whilst phosphorylation of eIF2α inhibits general translation initiation, it paradoxically increases translation of activating transcription factor 4 (ATF4), which induces the transcription of genes involved in restoration of ER homeostasis. The endoribonuclease activity of IRE1 is responsible for the nonconventional splicing of transcription factor XBP1, which controls the transcription of chaperones and genes involved in ER-associated protein degradation (ERAD). In response to ER stress, ATF6 translocates to the Golgi complex and is sequentially cleaved by two proteases. The processed form of ATF6 (the activated transcription factor) subsequently translocates to the nucleus and binds to ATF/cAMP response elements (CRE) and ER stress responsive elements (ERSE-1) to activate target genes. The transcription factor C/EBP homologous protein (CHOP) operates as a downstream component of ER stress pathways and can transcriptionally upregulate expression of BIM (pro-apoptotic member of the BCL-2 family) during conditions of ER stress. Thus, the UPR attempts to restore ER homeostasis by increasing ER biogenesis, decreasing the influx of new proteins into the ER, promoting transport of damaged proteins from the ER to the cytosol for degradation, and upregulating protein folding chaperones. However, if the damage is too severe and ER homeostasis cannot be restored, apoptosis ensues. Recently we have shown that small 20–22-nt RNAs, commonly referred to as microRNAs (miRNAs), play an important role in the regulation of life and death decisions following ER stress.
miRNAs have been shown to be critically involved in control of cell survival and cell death decisions[13–15]. miRNAs are generated from RNA transcripts that are exported into the cytoplasm, where the precursor-miRNA molecules undergo Dicer-mediated processing (removal of the hairpin loop) to generate mature miRNA. The mature miRNAs assemble into RNA-induced silencing complexes (RISCs) and guide the silencing complex to specific mRNA target molecules with the assistance of argonaute proteins. The main function of miRNAs is to direct posttranscriptional regulation of gene expression, typically by binding to the 3’ UTR of cognate mRNAs and inhibiting their translation and/or stability by targeting them for degradation. Several studies have shown global alterations in miRNA-expression profiles during various types of cellular stresses, such as folate deficiency, arsenic exposure, hypoxia, drug treatment and genotoxic stress. Argonaute family member Ago2, a vital component of RISCs, is distributed diffusely in the cytoplasm and redistributes from the cytoplasm to stress granules and processing (P)-bodies upon exposure to stress conditions. Stress-induced enrichment of Ago2 from cytoplasm to P-bodies is dependent on mature miRNAs suggesting a link between miRNAs and cellular stress.
We performed genome-wide miRNA expression profiling in rat cardiomyoblasts during the conditions of UPR. We found that miRNAs (miR-206, miR-24, miR-125b, miR-133b) with known function in cardiomyoblasts biology[20–22] were significantly deregulated during the conditions of UPR in H9c2 cells. The expression of miR-7a was upregulated by UPR and simulated in vitro ischemia in cardiomyoblasts. Further, ectopic expression of miR-7a provides resistance against UPR-mediated apoptosis in cardiomyoblasts. This study demonstrates the role of UPR in deregulating the expression of miRNAs in MI. Our results provide novel insights about the molecular mechanisms of deregulated miRNA expression during the heart disease pathogenesis.
Results and discussion
Differential expression of miRNAs during UPR in H9c2 cells
Regulation of miR-7a expression by glucose deprivation and simulated ischemia
Next we determined the expression of miR-7a in primary culture of adult rat cardiomyoblasts during the conditions of in vitro simulated ischemia. In order to examine the effect of ischemia on the UPR, induction of UPR target genes was determined. Ischemia induced the expression of CHOP, WARS, p58IPK and ERDJ4 (Figure 4C). Thapsigargin and Tunicamycin treatment also caused an increase in the expression of GRP78, HERP, CHOP, WARS and p58IPK (Figure 1), although the level of mRNA induction was higher. Under similar conditions of in vitro simulated ischemia we observed a significant increase in the levels of miR-7a in primary cardiomyoblasts (Figure 4D). Collectively, these data confirmed that exposure of primary cardiomyoblasts to ischemic conditions induces UPR and miR-7a.
miR-7a protects against UPR-induced cell death
A growing body of evidence shows that miRNAs play an important role in heart diseases. Several miRNAs have been implicated in the control of cardiac apoptosis and fibrosis following myocardial ischemia. In this work, we report the extensive genome-wide profiling of miRNA expression in rat cardiomyoblasts during UPR, a crucial component of ischemia. We found that expression of many miRNAs (miR-24, miR-25, miR-7a, miR-103, miR-17-5p, miR-106b, miR-93, miR-206 and miR-133b) changed significantly during conditions of UPR in cardiomyoblasts. A similar alteration in expression level of these miRNAs has been previously reported by different research groups during conditions of idiopathic cardiomyopathy, ischemic cardiomyopathy, dilated cardiomyopathy, cardiac hypertrophy and heart failure[21, 30]. The muscle specific miR-1 and −206 are closely related in terms of expression and function. Both miR-1 and miR-206 are shown to promote myoblast-to-myotube differentiation[30, 32]. By contrast, miR-133 promotes the proliferation of myoblasts and inhibits their differentiation. Further, miR-1 enhances cardiomyoblast apoptosis by targeting the expression of Hsp60 and Hsp70, while miR-133 targets and represses caspase-9 expression to decrease cardiomyoblast apoptosis. The expression of miR-24 is down-regulated during MI and miR-24 regulates cardiomyoblast apoptosis, in part by direct repression of the BH3-only domain–containing protein Bim. Further ectopic expression of miR-24 in a mouse MI model inhibited cardiomyoblast apoptosis, attenuated infarct size, and reduced cardiac dysfunction. We have recently shown that miRNAs belonging to the miR-106b-25 cluster were downregulated during ER stress, in a PERK-dependent manner, and contributes to optimum induction of Bim and ER stress-induced cell death. The ample overlap of microRNA expression signature between our analysis (in ER stress conditions) and different models of cardiac dysfunction further confirms the role of ER stress in cardiovascular diseases.
In the present study we investigated the potential role of miR-7a in ER stress-induced cell death. Previous studies have reported that miR-7a may act as tumour suppressor miRNA where it inhibits cell proliferation and increases cell apoptosis in some cancers. miR-7a is expressed in a ventro-dorsal gradient along the ventricular wall and plays an important role in the determination of the dopaminergic phenotype during postnatal and adult olfactory neurogenesis by repressing Pax6. In addition miR-7a regulates pancreatic β-cell function by regulating the insulin granule exocytosis. miR-7a is an IL-4-responsive gene in macrophages and functions to regulate IL-4-directed fusion of macrophages to form multinucleated giant cell. However, the function of miR-7a in regulating cell fate during conditions of the UPR was not clear. We found that overexpression of miR-7a significantly decreased ER stress-induced cell apoptosis in cardiomyoblasts. The overexpression of miR-7a may protect rat cardiomyoblast against ER stress-induced cell apoptosis during MI. Indeed expression of miR-7a was shown to be upregulated in H9c2 cells after 10 h hypoxia and 2 h reoxygenation and transfection of miR-7a mimic significantly decreased cell apoptosis and cardiac infarct size in a rat I/R injury model. However this is in contrast to previous reports where miR-7a has been shown to promote cancer progression by inhibiting cell proliferation and inducing apoptosis. The miR-7a expression can modulate the activation of ATF4-CHOP signaling pathway during UPR. The overexpression of CHOP promotes apoptosis in several cell lines, whereas CHOP-deficient cells are resistant to ER stress-induced apoptosis. Our results suggest that miR-7a expression abrogates induction of CHOP and thereby provide resistance to ER stress-induced cell death. However, we did not find any binding site for miR-7a in the 3’ UTR of ATF4 or CHOP. Thus most likely the effects of miR-7a on induction of ATF4 and CHOP are indirect. Our results warrant further studies to reveal the mechanism of ATF4-CHOP regulation by miR-7a.
This study demonstrates the role of UPR in deregulating the expression of miRNAs in MI. The expression of miR-7a was upregulated by UPR and simulated in vitro ischemia in cardiomyoblasts. Further, ectopic expression of miR-7a provides resistance against UPR-mediated apoptosis in cardiomyoblasts. The ample overlap of miRNA expression signature between our analysis and different models of cardiac dysfunction further confirms the role of UPR in cardiovascular diseases.
Cell culture and treatments
The embryonic rat cardiac myoblasts H9c2 (ATCC, CRL-1446) was cultured in Dulbecco’s modified Eagle’s medium supplemented with 10% foetal bovine serum, 50 U/ml penicillin and 5 mg/ml streptomycin. To induce ER stress, cells were treated with 1 μM thapsigargin (Tg) or 1 μg/ml tunicamycin (Tm) for the indicated time periods. Glucose deprivation was achieved by changing the serum and glucose-containing DMEM to serum and glucose free-DMEM and (1 mM) 2-deoxyglucose for 24 hours.
Generation of stable H9c2-miR-7a cells
We generated stable H9c2 cells with increased expression levels of miR-7a by using the lentiviral expression vector pLenti-III-Tet-mir (Applied Biological Materials Inc) and puromycin selection (3 μg/ml) for 7 days. This lentivector is designed to induce the expression of GFP and miRNA of interest upon addition of tetracycline.
Nucleofection of H9c2 cells
The pre-miR precursor miRNAs (PM17111) Pre-miR control and (PM10047) Pre-miR-7a were purchased from Ambion. H9c2 cells were transfected with Pre-miR control and Pre-miR-7a by Nucleofection using nucleofactor kit L (Amaxa Nucleofector Technology) following the manufacturer’s instructions. 24 hours post transfection, the cells were treated with tunicamycin and total RNA was isolated at indicated time points.
RNA extraction and real time RT-PCR
Total RNA was isolated using Trizol (Invitrogen) according to the manufacturer’s instructions. Reverse transcription (RT) was carried out with 2 μg RNA and Oligo dT (Invitrogen) using 20 U Superscript II Reverse Transcriptase (Invitrogen). For real-time PCR experiments, cDNA products were mixed with 2 × TaqMan master mix and 20 × TaqMan Gene Expression Assays (Applied Biosystems) and subjected to 40 cycles of PCR in StepOnePlus instrument (Applied Biosystems). Relative expression was evaluated with ΔΔCT method.
miRNA microarray analysis
At 24 h post treatment with Tg or Tm, total RNA was isolated from the cell samples using the Trizol reagent according to the manufacturer’s instructions and quantified using a nanodrop at 260 nm. For both treatments, three independent biological replicates were generated. Briefly, the assay started with 5 μg of total RNA. Each total RNA sample was enriched for miRNAs. A 20 mer control RNA was spiked into each sample followed by labelling and hybridization. The control RNA was computationally and experimentally verified not to cross-hybridize with the probes of any known miRNA transcript. RNA samples were hybridized overnight on a μParaflo microfluidic chip. Each microfluidic chip contained 350 mature miRNAs of Rat as per Sanger miRBase database (Release 11.0). Each miRNA was spotted on the array nine times and for each RNA sample two chips were used. There were 16 sets of control probes on each array. There were >10 positive controls (spike-in controls & 5S). There were >10 negative controls (mismatch control). The background-subtracted signals were used for statistical tests and clustering analysis.
Microarray data analysis
MiRNA microarray data were analyzed by LC Sciences by subtracting the background and normalizing the signals. Blank spaces represent signal values below detection level. A transcript to be listed as detectable must meet at least two conditions: signal intensity higher than 3 × (background standard deviation) and spot CV <0.5. CV is calculated by (standard deviation)/(signal intensity). When repeating probes are present on an array, a transcript is listed as detectable only if the signals from at least 50% of the repeating probes are above detection level. The miRNA microarray data used the total gene signal, which was the average value of repeating spots. During data process, “bad spots” that have signal values deviated more than 50% of average values of repeating spots and/or spot CV larger than 0.5 are discarded. Differentially expressed signals were determine by t-test with p < 0.05.
Isolation of cardiomyoblasts and simulated ischemia
Ventricular cardiomyoblasts were isolated from male Wistar rats by perfusion of hearts with collagenase type II (300 U/mL) and cultured, as previously described. For this purpose adult male rats were euthanized using deep isoflurane (5%) anaesthesia, hearts were rapidly excised, washed with ice-cold 0.9% NaCl and connected to the Langendorff-perfusion system. Anaesthesia depth was monitored by limb withdrawal using toe pinching. To separate cardiomyoblasts from non-cardiac cells, cardiomyoblasts were sedimented by low force and short centrifugations (5 g, 1 min, four times) and finally without centrifugation in medium containing 4% bovine serum albumin. To prevent growth of non-myocytes, medium was supplemented with 10 μmol/L cytosine-β-d-arabinofuranoside. After 1 hour of plating, cells were washed with culture medium (2% foetal calf serum) to remove non-attached cells. A high purity of cardiomyoblast culture (>93%) was confirmed by light microscopy. Third day after preparation cardiomyoblasts were exposed to simulated in vitro ischemia (SI) consisting of glucose-free anoxia at pH 6.4 as previously described. After 3 hours of ischemia, total RNA was isolated and used for further analysis.
TaqMan real-time microRNA PCR
Total RNA was reverse transcribed using the TaqMan miRNA Reverse Transcription Kit and miRNA-specific stem-loop primers (Applied BioSystems) in a small-scale RT reaction (comprised of 0.19 ml of H2O, 1.5 ml of 10X Reverse-Transcription Buffer, 0.15 ml of 100 mM deoxyribonucleotide triphosphates, 1.0 ml of Multiscribe Reverse-Transcriptase (50 U/ml), and 5.0 ml of input RNA (20 ng/ml); components other than the input RNA were prepared as a larger volume master mix), using a Tetrad2 Peltier Thermal Cycler (Bio-Rad, Alpha Technologies Ltd, Wicklow, Ireland) at 16°C for 30 min, 42°C for 30 min and 85°C for 5 min. For miRNAs and snoRNA, 4.0 ml of RT product was combined with 16.0 ml of PCR assay reagents (comprised of 5.0 ml of H2O, 10.0 ml of TaqMan 2X Universal PCR Master Mix, No AmpErase UNG, and 1.0 ml of TaqMan miRNA Assay) to generate a PCR of 20.0 μl of total volume. Real-time PCR was carried out on an Applied BioSystems 7900HT thermocycler at 95°C for 10 min, followed by 40 cycles of 95°C for 15 s and 60°C for 1 min. Data were analyzed with SDS Relative Quantification Software version 2.2.2 (Applied BioSystems.), with the automatic Ct setting for assigning baseline and threshold for Ct determination.
Annexin V staining
Externalization of phosphatidylserine (PS) to the outer leaflet of the plasma membrane of apoptotic cells was assessed with annexin V-PE. Briefly, cells were collected by centrifugation at 350 g, washed once in ice-cold calcium buffer (10 mM HEPES/NaOH, pH 7.4, 140 mM NaCl, 2.5 mM CaCl2), and incubated with annexin V-FITC or with annexin V-PE for 15 minutes on ice. A wash step in calcium buffer was carried out prior to acquisition on a FACSCalibur flow cytometer (Becton Dickinson).
Cells were washed once in ice-cold PBS and lysed in whole cell lysis buffer (20 mM HEPES pH 7.5, 350 mM NaCl, 0.5 mM EDTA, 1 mM MgCl2, 0.1 mM EGTA and 1% NP-40) after stipulated time of treatments and boiled at 95°C with Laemmli’s SDS-PAGE sample buffer for 5 min. Protein concentration was determined by Bradford method. Equal amount (30 μg/lane) of protein samples were run on an SDS polyacrylamide gel. The proteins were transferred onto nitrocellulose membrane and blocked with 5% milk in PBS-0.05%Tween. The membrane was incubated with the primary antibody for cleaved caspase-3 (ISIS, Cat# 9664) or β-Actin (Sigma, Cat# A-5060) for 2 h at room temperature or overnight at 4°C. The membrane was washed 3 times with PBS-0.05% Tween and further incubated in appropriate horseradish peroxidase-conjugated secondary antibody (Pierce) for 90 min. Signals were detected using Western Lightening Plus ECL (Perkin Elmer).
The data are expressed as mean ± S.D. for three independent experiments. Differences between the treatment groups were assessed using two-tailed unpaired student’s t-tests. The values with a p < 0.05 were considered statistically significant.
We are grateful to the Technical Officers and administrative team in Pathology, School of Medicine, NUI, Galway. We would like to thank Maria Ryan for invaluable technical assistance. This publication has emanated from research conducted with the financial support of Health Research Board (grant number HRA_HSR/2010/24) to S.G.
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