MicroRNA-1 upregulation promotes myocardiocyte proliferation and suppresses apoptosis during heart development

Introduction

Congenital heart disease (CHD) is one of the most common birth defects in humans worldwide, occurring in ~7–8% of infants born annually (1). Improved surgical treatments have decreased the mortality of children with CHD, but not all infants with CHD survive to adulthood (2,3). The mechanism of heart development is complex, and involves multiple genetic and environmental factors in its regulation (4). Therefore, investigations of relevant target genes and microRNAs (miRNAs) are important to fully comprehend the mechanism of heart development and to provide therapeutic targets for treatment of CHD in children.

miRNAs are endogenous non-coding RNAs of 20–22 nucleotides in length that have diverse functions in biological processes at the transcriptional or post-transcriptional level, by targeting the 3′-UTR of genes (5). Previous studies have revealed that miRNAs are involved in the development of the heart, including cardiomyocyte differentiation, cell cycle and the conducting system of the heart (6,7). The muscle-specific miR-1 has been reported to be important in heart development. For example, miR-1 transcription is affected by the regulation of myogenic differentiation 1 (MyoD), myocyte enhancer factor (Mef), and serum response factor (SRF) (8). High levels of miR-1 expression in mice lead to cardiomyocyte cell cycle arrest at an early stage and attenuated cell proliferation (9,10). The mouse teratoma-derived P19 cells are pluripotent, and thus can be differentiated into cardiomyocytes, skeletal muscle cells and neurons, allowing the application of P19 cells in cell replacement therapy and myocardial tissue engineering (11,12). Although several studies have reported significant roles of miR-1 in regulating heart development in mice and in human cells, few have explored the possible role of miR-1 in regulating the heart development in P19 cells.

The present study aimed to investigate the role of miR-1 in heart development and to reveal a possible mechanism of action. Endogenous expression of miR-1 was assessed in P19 cells, as was the effect of miR-1 overexpression on the biological processes of P19 differentiated cardiomyocytes. In addition, the effect of miR-1 overexpression on cell viability and cell apoptosis-related protein expression was examined.

Materials and methods

Cell culture and cell differentiation

P19 cells (American Type Culture Collection, Manassas, VA, USA) were cultured in Gibco α-modified Eagle's medium (α-MEM; Thermo Fisher Scientific, Inc., Waltham, MA, USA) supplemented with 10% Gibco fetal bovine serum (FBS; Thermo Fisher Scientific, Inc.), 100 U/ml penicillin, and 100 µg/ml streptomycin at 37°C in 5% CO2.

For the cardiac differentiation assay (13), 1×106 cells/ml P19 cells were plated onto 10 cm bacterial dishes in 15 ml α-MEM containing 1% dimethyl sulphoxide (DMSO; Sigma-Aldrich; Merck Millipore, Darmstadt, Germany), 10% FBS, 100 U/ml penicillin, and 100 µg/ml streptomycin at 37°C in 5% CO2. Following 96 h of incubation, cells were transferred onto 6 cm bacterial dishes and cultured in α-MEM containing 10% FBS for another 6 days of incubation.

Cell transfection

The miRNA mimic (Gene ID: 100314077; Sangon Biotech Co., Ltd., Shanghai, China) was transfected into the differentiated P19 cells using the Lipofectamine® 2000 protocol (Thermo Fisher Scientific, Inc.). Cells transfected with the scrambled RNA (catalog no. CS7005; Sangon Biotech, Co., Ltd.) were used as the control.

Cell proliferation assay

Cell proliferation ability was assessed using the 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyltetrazolium bromide (MTT) assay, as previously described (14). Briefly, following transfection for 24 h, 5×103 cells were seeded into 96-well plates. Following 24 h of incubation, cells cultured at 37°C were centrifuged at 4,000 × g for 5 min, and the supernatant was removed. MTT (20 µl) was added into the cells and then cultured for another 4 h. Finally, 150 µl DMSO was mixed with the cells for 10 min to stop the reaction at room temperature. Absorbance of cells in each well was observed at 570 nm with an absorption spectrophotometer (Olympus Corporation, Tokyo, Japan).

Cell apoptosis assay

Apoptotic cells were measured using flow cytometry following staining with the Annexin V-FITC apoptosis kit (Invitrogen; Thermo Fisher Scientific, Inc.), according to the manufacturer's protocol. Briefly, following transfection for 36 h, cells were cultured in fresh serum-free α-MEM medium for 12 h. Then total cells were harvested and washed 3 times with PBS buffer, followed by resuspension in the kit staining buffer. Then, 5 µl of Annexin V-FITC and 5 µl of propidium iodide (PI) were added into the cells at room temperature for 10 min. Mixtures were analyzed using FACS can flow cytometry (BD Biosciences, Franklin Lakes, NJ, USA). The number of early-stage apoptotic cells (Annexin V+ and PI− cells) was then analyzed.

Reverse transcription-quantitative polymerase chain reaction (RT-qPCR)

Extraction of total RNA from cells was performed using TRIzol reagent (Invitrogen; Thermo Fisher Scientific, Inc.), according to the manufacturer's protocol. The extracted RNA was treated with RNase-free Dnase I (Promega Corporation, Madison, WI, USA) to remove the contaminating DNA, and concentration and purity were measured using SMA 400 UV-VIS (Merinton, Shanghai, China). Purified RNA dissolved in nuclease-free water at a concentration of 0.5 µg/µl was used for cDNA synthesis with the PrimerScript 1st Strand cDNA Synthesis kit (Invitrogen; Thermo Fisher Scientific, Inc.). Expression of targets was analyzed using an ABI 7900 (PE Applied Biosystems; Thermo Fisher Scientific, Inc.) and the SYBR ExScript RT-PCR kit (Takara Biotechnology Co., Ltd., Dalian, China). GAPDH was selected as the internal control for target gene expression, U6 small nuclear RNA (U6) was used as the internal control for the miRNA expression. Primers used for target amplification are listed in Table I (15).

Table I. Primers used for target amplification.

Table I.

Primers used for target amplification.

Gene target	Sequence (5′-3′)
GAPDH	F-GGGTGGAGCCAAACGGGTC
	R-GGAGTTGCTGTTGAAGTCGCA
GATA4	F-CCTGCGGCCTCTACATGA
	R-AGGGTCTCACCAGCAGGA
Nkx2-5	F-CCTGCGGCCTCTACATGA
	R-AGGGTCTCACCAGCAGGA
Hand2	F-TACCAGCTACATCGCCTACCT
	R-TCACTGCTTGAGCTCCAGGG
Caspase-3	F-TACCCTGAAATGGGCTTGTGT
	R-GTTAACACGAGTGAGGATGTG
miR-1	F-GTAGGCACCTGAAATGGAA
	R-TTGATGGTGCCTACAGTACAT
U6	F-CGCTTCACGAATTTGCGTGTCAT
	R-AACGCTTCACGAATTTGCGT

[i] F, forward; R, reverse; GATA4, GATA binding protein 4; Nkx2-5, NK2 homeobox 5; Hand2, heart and neural crest derivatives expressed transcript 2; miR-1, microRNA-1; U6, U6 small nuclear RNA.

Western blotting

Cells were lysed with radioimmunoprecipitation assay buffer at 4°C for 5 min (RIPA; Sangon Biotech Co., Ltd.) containing phenylmethylsulfonyl fluoride (PMSF; Sigma-Aldrich; Merck Millipore), and then were centrifuged at 4,000 × g at 4°C for 10 min. Protein concentration was detected using a bicinchoninic acid assay kit (Pierce; Thermo Fisher Scientific, Inc.). For western blotting, total protein (30 µl) was subjected to 12% SDS-PAGE, followed by transfer onto a polyvinylidenefluoride (PVDF) membrane. The PVDF membranes were blocked with TBS/0.1% Tween-20 (TBST) buffer containing 5% non-fat milk at room temperature for 1 h. Then the membranes were incubated with rabbit primary antibodies against heart and neural crest derivatives expressed 2 (Hand 2; 1:100; catalog no. ab10131; Abcam, Cambridge, MA, USA), caspase-3 (1:100; catalog no. ab2171), cleaved caspase-3 (1:100; catalog no. ab13585) or GAPDH (1:100; catalog no. ab8245) obtained from Invitrogen; Thermo Fisher Scientific, Inc., overnight at 4°C, then horseradish-peroxidase labeled goat anti-rat secondary antibody (catalog no. ab7097; 1:1,000; Abcam) at room temperature for 1 h. Finally, the PVDF membranes were washed 3 times with TBST buffer for 10 min each wash. Signals were detected following incubation with a chromogenic substrate using an enhanced chemiluminescence kit (Sigma-Aldrich; Merck Millipore). GAPDH served as the internal control.

Statistical analysis

Data are presented as the mean ± standard deviation of 3 independent replicates. Statistical analysis between two groups was performed using a t-test, whereas the multiple comparisons were analyzed by post-hoc tests that followed one-way analysis of variance. All significant differences were analyzed using SPSS 19.0 statistical software (IBM SPSS, Armonk, NY, USA). P<0.05 was considered to indicate a statistically significant difference.

Results

Cell differentiation of P19 cells

Firstly, successful differentiation of P19 cells into cardiomyocytes was established. Following treatment with DMSO, mRNA expression levels of the cardiomyocyte differentiation markers GATA binding protein 4 (GATA4; Fig. 1A) and NK2 homeobox 5 (Nkx2-5; Fig. 1B) were analyzed. The results demonstrated that the relative mRNA expression levels for GATA4 and Nkx2-5 in the cells increased in a time-dependent manner for the whole duration of the 10 days of differentiation treatment, compared with that at day 0 (Fig. 1). However, their levels in the undifferentiated P19 cells were not significantly different to t=0 at days 5 and 10 (P>0.05; Fig. 1). These results demonstrated that the P19 cells were successfully differentiated into cardiomyocytes in the present study.

Figure 1. Cell differentiation for P19 cells. mRNA expression levels for (A) GATA4 and (B) Nkx2-5 were measured at 0, 5 and 10 days following differentiation treatment in P19 cells by reverse transcription-quantitative polymerase chain reaction, with GAPDH as an internal control. Untreated, undifferentiated cells were used as a control. **P<0.01 and ***P<0.001, with comparisons indicated by lines. GATA4, GATA binding protein 4; Nkx2-5, NK2 homeobox 5; ns, no significant difference.

miR-1 expression in differentiated P19 cells

Endogenous miR-1 mRNA expression was significantly decreased in differentiated P19 cells compared with undifferentiated cells (P<0.05; Fig. 2A). Following transfection of differentiated cells with siRNAs, miR-1 mimic and scramble, for 24 h, miR-1 mRNA expression was analyzed to verify whether the transfection experiment was successful. The results demonstrated that miR-1 mRNA levels were significantly increased following transfection with the miR-1 mimic, compared with both transfected cells and cells transfected with control scrambled RNA (P<0.05; Fig. 2B).

Figure 2. Expression of miR-1 in P19 cells. Expression was analyzed by reverse transcription-quantitative polymerase chain reaction, with U6 small nuclear RNA as the internal control. (A) Expression of endogenous miR-1 in differentiated P19 cells relative to undifferentiated cells. (B) Expression of miR-1 in differentiated P19 cells transfected with either scrambled RNA or miR-1 mimics relative to untransfected control cells. *P<0.05, with comparisons indicated by lines. miR-1, microRNA-1; ns, not significant.

miR-1 overexpression increases P19 cell viability

To assess the effect of miR-1 overexpression on cell viability, viable cells were measured by MTT assay (Fig. 3). The results demonstrated that the number of viable cells was increased in a time-dependent manner in the P19 cells transfected with miR-1 mimic compared with the cells transfected with scrambled RNA control (P<0.01; Fig. 3), suggesting that miR-1 overexpression may promote P19 cell proliferation.

Figure 3. Effects of miR-1 overexpression on differentiated P19 cell viability. Differentiated P19 cells were transfected with either scrambled RNA or miR-1 mimics, and cell viability was assessed by MTT assay. miR-1, microRNA-1. **P<0.01, ***P<0.001 vs. control cells transfected with scramble RNA.

miR-1 overexpression suppresses P19 cell apoptosis

To assess the effect of miR-1 overexpression on cell apoptosis in differentiated P19 cells, apoptotic cells were measured using an Annexin V-FITC labeling assay (Fig. 4). The mean percentage of early-stage apoptotic cells was significantly decreased when miR-1 was overexpressed (6.13%), compared with the untransfected or scrambled RNA-transfected control cells (14.2 and 12.3%, respectively; P<0.01; Fig. 4).

Figure 4. Effect of miR-1 overexpression on apoptosis in differentiated P19 cells. Differentiated P19 cells were untransfected, or transfected with either scrambled RNA or with miR-1 mimics, and apoptosis was measured by Annexin V-FITC/PI staining and flow cytometry. (A) Representative images from the flow cytometry analysis. (B) Quantification of early-stage apoptotic cells. **P<0.01, with comparisons indicated by lines. miR-1, microRNA-1; FITC, fluorescein isothiocyanate; PI, propidium iodide.

Effect of miR-1 overexpression on Hand2 and caspase-3 expression

In order to investigate the possible mechanism of miR-1 in cardiomyocytes, expression of Hand2 and caspase-3 proteins was analyzed in differentiated P19 cells following transfection with miR-1 mimic and scrambled RNA. Hand2 protein expression levels were significantly increased by miR-1 overexpression, compared with the untransfected cells and cells transfected with scrambled RNA (P<0.01; Fig. 5A). By contrast, caspase-3 cleavage was significantly decreased by miR-1 overexpression, compared with the untransfected cells and cells transfected with scrambled RNA (P<0.05; Fig. 5B).

Figure 5. Effect of miR-1 overexpression on Hand2 and caspase-3 protein expression levels. Differentiated P19 cells were untransfected, or transfected with scrambled RNA or with miR-1 mimics. (A) Hand2 protein expression and (B) caspase-3 protein activity was assessed by western blot, with quantification relative to GAPDH. *P<0.05 and **P<0.01, with comparisons indicated by lines. miR-1, microRNA-1; Hand2, heart and neural crest derivatives expressed transcript 2.

Discussion

Previous studies have demonstrated the importance of miRNAs in the regulation of heart development, including miR-1 and miR-133 (16), however, few studies have explored the potential role of miR-1 in P19 differentiated cardiomyocytes. In the present study, expression of miR-1 was evaluated in cardiomyocyte-differentiated and undifferentiated P19 cells, and its effect on the viability and apoptosis of cardiomyocyte-differentiated P19 cells was examined.

In agreement with previous studies (17–20), the present study confirmed that following treatment of P19 cells with DMSO, mRNA expression levels of the GATA4 and Nkx2-5 differentiation markers were significantly increased compared with untreated P19 cells (Fig. 1), indicating that P19 cells were successfully induced towards cardiomyocyte differentiation. When the differentiated P19 cells were examined, a significant decrease in endogenous miR-1 expression was observed compared with the undifferentiated cells (Fig. 2), suggesting an association between miR-1 expression levels and P19 cell differentiation state. The expression of miR-1 in P19 cells has not been previously reported. However, Thomson et al (21) demonstrated that miR-1 and miR-133 were involved in the regulation of P19 embryonal teratocarcinoma at the post-transcriptional level. The current study suggests that abnormal expression of miR-1 may be associated with the cardiomyocyte differentiation of P19 cells.

Consequently, the effect of miR-1 overexpression on cell viability and apoptosis in cardiomyocyte-differentiated P19 cells was assessed. miR-1 upregulation in skeletal muscle has been demonstrated to be positively correlated with muscle proliferation and differentiation (22). By contrast, miR-1 results in suppressed cardiomyocyte apoptosis by targeting HSP60 and caspase-9 (9). Similarly, lung cancer cell apoptosis is suppressed by upregulation of miR-1 (23). In the present study, cardiomyocyte-differentiated P19 cell viability was increased while apoptosis was suppressed by miR-1 overexpression, suggesting that miR-1 may be important in cardiac cell development by regulating proliferation and apoptosis.

The current study demonstrated that miR-1 overexpression resulted in increased Hand2 expression but decreased caspase-3 cleavage in cardiomyocyte-differentiated P19 cells (Fig. 5). Hand2 is asymmetrically expressed in the developing ventricular chambers and is important in cardiac morphogenesis (24). Yelon et al (25) demonstrated that Hand2 served parallel roles to cell proliferation and apoptosis in the heart development of zebrafish, and Olson (26) demonstrated that Hand2 was preferentially expressed in the derivative of the heart field. Hence, it was hypothesized that miR-1 upregulation may contribute to cardiac differentiation in P19 cells. Caspase-3 is a cell apoptosis executor and its high expression indicates a high percentage of apoptotic cells (27,28). Izarra et al (16) demonstrated that miR-1 overexpression results in reduced cell apoptosis in pluripotent stem cells during cardiac differentiation. In addition, Shan et al (29) demonstrated that caspase-3 levels are decreased by miR-1 upregulation in a rat model of myocardial infarction. The present study indicates that miR-1 suppresses cell apoptosis in cardiomyocyte-differentiated P19 cells by decreasing caspase-3 cleavage.

In conclusion, the present study revealed that miR-1 regulates heart development through the cell proliferation and apoptosis processes, by increasing Hand2 expression and suppressing caspase-3 cleavage in cardiomyocyte-differentiated P19 cells. The present study may provide a theoretical basis for the role of miR-1 in regulating cardiomyocytes development and may indicate miR-1 as a potential target in the therapeutic treatment of CHD in infants. Further experimental studies are required to fully understand the mechanism of miR-1 in the regulation of the P19 cells and the heart development.

References