Introduction
Acute myocardial infarction (AMI) a serious cardiovascular disease and a leading cause of global deaths, which contributes to the occurrence of coronary artery obstruction [
1]. There are approximately 17 million of deaths occurred annually due to cardiovascular diseases, and the AMI-related mortality accounts for about 13% [
2]. It is reported that a number of patients with evolving myocardial infarction die before receiving efficient treatment [
3]. Thus, early and accurate diagnosis is of great importance for the treatment of AMI. Currently, the cardiac troponin I (cTnI) is the preferred diagnostic biomarker for AMI patients, but the elevation of cTnI is also appeared in cases with heart failure, sepsis and chronic kidney diseases, leading to the limited application of cTnI [
4,
5]. Thus, novel diagnostic biomarkers with high accuracy are necessary for AMI patients.
The disease progression of AMI is complex and has reported to related with vascular endothelial injury and inflammatory responses [
6]. The normal vascular endothelium can sustain the fluid shear stress, while the injury in vascular endothelial cells triggers cardiovascular diseases [
7]. To evaluate the endothelial injury degree, some biomarkers have been identified, including cTnI, heart-type fatty acid-binding protein (H-FABP) and von Willebrand factor (vWF). The sustained inflammatory response following AMI could contribute to left ventricular dysfunction and remodeling [
8], leading to the strategies that attenuate inflammation become efficient therapeutic approaches to improve the clinical outcomes of AMI patients [
9]. Kruppel-like factor 2 (KLF2) is a key molecule in angiogenesis and vascular formation [
10] and plays a pivotal role in the regulation of endothelial proliferation in AMI [
11,
12]. A study by Liu et al. has reported that KLF2 mediates the effect of miR-92a on endothelial injury in AMI rats [
12]. In addition, KLF2 serves an important regulator in the expression of anti-inflammatory genes, thereby involving in the pathogenesis of cardiovascular diseases [
13]. These aforementioned researches inspire us to identify novel molecules that related with KLF2 to improve AMI treatment.
According to the bioinformatic prediction by miRanda (
http://www.microrna.org/microrna/home.do), we found a complementary sequence of microRNA-32-5p (miR-32-5p) at the 3′-untranslated region (3′-UTR) of KLF2. Numerous microRNAs (miRNAs) have been investigated in cardiovascular diseases [
14,
15]. The aberrant expression of miRNAs has been determined as diagnostic biomarkers or therapeutic targets in the progression of AMI [
16]. miR-32-5p has been reported to modulate the viability of vascular smooth muscle cells and play as a biomarker of coronary artery calcification [
17]. In addition, the regulatory effect of miR-32-5p on inflammatory responses has been found in macrophages infected by
Mycobacterium tuberculosis [
18] and rats with neuropathic pain [
19]. As a potential upstream regulator of KLF2, the role of miR-32-5p in endothelial activation remains unclear.
To improve the diagnosis and therapy of AMI, this study sought to verify the effect of miR-32-5p on endothelial cell proliferation, assess the relationship of miR-32-5p with endothelial injury and inflammation in AMI patients and evaluate its diagnostic accuracy.
Materials and methods
Cell culture
Human umbilical vein endothelial cells (HUVECs) were purchased from the Cell Bank of the Chinese Academy of Sciences (Shanghai, China) and cultured in endothelial growth medium (Gibco, CA, USA) at 37 °C in a humidified atmosphere with 5% CO2.
Patients and sample collection
A total of 88 AMI patients were enrolled from Qingdao Jiaozhou Central Hospital between 2015 and 2017, and 50 age- and gender-matched healthy volunteers were recruited as controls at a same time period. None of the patients had received any therapy before blood sampling, and the healthy individuals had no medical history of cardiovascular diseases. The diagnosis of AMI was performed in accordance with the universal definition of myocardial infarction [
20]. Venous blood was collected from the participants immediately after admission to hospital and centrifuged to isolate serum samples for subsequent analyses. The experimental procedures of this study were approved by the Ethics Committee of Qingdao Jiaozhou Central Hospital, and an informed consent was received from each participant. The demographic and clinical characteristics of the patients and healthy subjects were listed in Table
1, and there were no statistical differences in age, gender, body mass index (BMI), history of smoking, hypertension, hyperlipidaemia, diabetes mellitus between the AMI patients and healthy controls (all
P > 0.05), while the AMI patients had a higher atherogenic index (AI) than the healthy individuals (
P < 0.001).
Table 1Demographic and clinical characteristics of the research cohort
Age (years, mean ± SD) | 60.82 ± 18.13 | 60.81 ± 17.35 | 0.997 |
Gender (male/female, % of male) | 29 / 21, 58.0% | 48 / 40, 54.5% | 0.694 |
BMI (kg/m2, mean ± SD) | 24.31 ± 2.83 | 25.25 ± 2.88 | 0.064 |
Smoking (n, %) | 26, 52.0% | 46, 52.3% | 0.975 |
Hypertension (n, %) | 28, 56.0% | 47, 53.4% | 0.769 |
Hyperlipidaemia (n, %) | 25, 50.0% | 46, 52.3% | 0.797 |
Diabetes mellitus (n, %) | 14, 28.0% | 27, 30.7% | 0.740 |
AI (mean ± SD) | 1.84 ± 0.56 | 6.49 ± 1.68 | <0.001 |
RNA extraction and quantitative real-time PCR (qRT-PCR)
Total RNA in serum and cells was extracted using TRIzol reagent (Life Technologies, Carlsbad, CA, USA) following the manufacture’s protocol. The purity of RNA was evaluated using a NanoDrop 1000 spectrophotometer (Thermo Scientific, Utah, USA). Reverse transcription was performed from RNA to synthesize cDNA using a TaqMan miRNA RT Kit (Applied Biosystems, Foster City, USA). The expression of miR-32-5p and mRNA of KLF2 was estimated by qRT-PCR using the SYBR green I Master Mix kit (Invitrogen, Carlsbad, CA, USA) on the 7300 Real-Time PCR System (Applied Biosystems, USA) with the following reaction conditions: 95 °C for 10 min, 95 °C for 30 s, 60 °C for 20 s, 72 °C for 15 s, a total of 40 cycles. The relative expression levels of miR-32-5p and KLF2 were calculated using the 2−ΔΔCt method and normalized to U6 and GAPDH, respectively.
Luciferase activity assay
The complementary sequence of miR-32-5p at the 3′-UTR of KLF2 was predicted by the miRanda (
http://www.microrna.org/microrna/home.do). To verify the interaction between miR-32-5p and KLF2, a luciferase reporter assay was performed. The 3′-UTR of KLF2 containing the putative binding sites of miR-32-5p was cloned and inserted into the luciferase reporter vector pmiR-REPORT (Life Technologies, USA). The reporter vectors carried wild type (WT) or mutant type (MT) of KLF2 3′-UTR were co-transfected into HUVECs with miR-32-5p mimic or miR-32-5p inhibitor (GenePharma, Shanghai, China) using Lipofectamine 3000 (Invitrogen, Carlsbad, CA, USA) following the protocols of manufacturers. Twenty-four hours later, the relative luciferase activity was measured using a Luciferase 1000 Assay System (Promega, USA).
CCK-8 assay
To verify whether miR-32-5p was involved in the regulation of endothelial cell proliferation, a Cell Counting Kit-8 (CCK-8; Beyotime, Nantong, China) was used to evaluate the proliferation of HUVECs. HUVECs were transfected with miR-32-5p mimic, miR-32-5p inhibitor or the corresponding negative controls (mimic NC and inhibitor NC) (GenePharma, Shanghai, China) using Lipofectamine 3000 (Invitrogen, Carlsbad, CA, USA) as per the manufacturer’s instruction. At 48 h after cell transfection, HUVECs with a cell density of 3 × 103 cell/well were seeded into 96-well plates and supplemented with CCK-8 reagent at 0, 24, 48, 72 h with further 4 h of incubation. The absorbance at 450 nm of the cell culture was measured by a microplate reader (BioTek Instruments, VT, USA).
Enzyme-linked immunosorbent assay (ELISA)
The serum levels of myocardial damage and endothelial injury biomarkers (cTnI, H-FABP and vWF) and pro-inflammatory cytokines (IL-1β, IL-6 and TNF-α) were examined using the ELISA kit (RayBiotech, GA, USA) following the manufacturers’ instruction.
Statistical analysis
Data were presented as mean ± SD and analyzed using SPSS 18.0 software (SPSS Inc., Chicago, IL) and GraphPad Prism 5.0 software (GraphPad Software, Inc., USA). Comparisons between groups were analyzed using Student’s t test and one-way ANOVA. Correlations of miR-32-5p with endothelial injury markers and pro-inflammatory cytokines were performed using Pearson correlation analysis. Receiver operating characteristic (ROC) curves and area under the curve (AUC) were used to evaluate the diagnostic accuracy of miR-32-5p. A value of P < 0.05 was considered of statistically significant.
Discussion
AMI is one of the leading causes of death worldwide and needs efficient strategies for early diagnosis and therapy. This study sought to explore a novel miRNA molecule that might play a critical role in the pathogenesis of AMI. By bioinformatics and luciferase activity assay, miR-32-5p was predicted and determined as an upstream regulator of KLF2 in HUVECs. Cell viability assay showed that the proliferation of HUVECs was suppressed by the overexpression of miR-32-5p, but was enhanced by the knockdown of miR-32-5p. Further clinical research data indicated that the upregulated expression levels of miR-32-5p in AMI patients were negatively correlated with the increased expression levels of KLF2. The serum miR-32-5p levels were positively correlated with the levels of myocardial damage and endothelial injury markers (cTnI, H-FABP and vWF), pro-inflammatory cytokines (IL-1β, IL-6 and TNF-α) and AI. For the clinical significance evaluation, the ROC curve based on serum expression of miR-32-5p showed a relatively high diagnostic accuracy for miR-32-5p in patients with AMI.
Endothelial function is significantly impaired during the progression of AMI, which could be indicated by the inhibited cell viability [
22]. For the treatment of AMI, the endothelial activation has been considered as an important signal for the therapeutic efficacy [
23], and the explorations of novel molecules that serve as candidate therapeutic targets were performed by investigating the changes in endothelial function [
12]. miRNAs are involved in the regulation of cell proliferation, and some members of them have been determined with pivotal roles in AMI pathogenesis by modulating endothelial cell viability [
12,
22]. For example, Huang et al. reported that miR-103a expression was elevated in AMI patients and involved in the pathogenesis of AMI by regulating the endothelial function, a result manifested by the inhibiting effect of miR-103a on cell proliferation of HUVECs [
24]. Bayoumin et al. gave evidence for miR-532 as a regulator of cardiac endothelial cell proliferation and deduced that miR-532 had a cardioprotective effect against AMI-associated ischemic heart diseases [
22]. Yu et al. investigated the role of miR-133a in AMI patients following radical surgery for gastric cancer, and found that miR-133a expression was increased in AMI patients and the silence of miR-133a in HUVECs led to enhanced cell proliferation, indicating the critical role of miR-133a in the endothelial injury process after AMI [
25]. These aforementioned literatures implied us to identify novel functional miRNAs in AMI progression by focusing on their relationship with endothelial cell function.
KLF2 has been identified as a regulator of endothelial activation with promoting effect on HUVECs viability [
12,
26]. This study used bioinformatics prediction to find that miR-32-5p was a regulator of KLF2 by binding its 3′-UTR. Previous literatures have reported that regulatory effect of miR-32-5p on cell proliferation in cervical cancer cells [
27] and cardiac fibroblast [
28]. However, there was no report regarding to the relationship of miR-32-5p with endothelial cell viability. In the present study, the cell viability results showed that the cell proliferation of HUVECs could be inhibited by the overexpression of miR-32-5p, while was promoted by the knockdown of miR-32-5p, which indicated that miR-32-5p might be involved in endothelial cell viability by targeting KLF2. Furthermore, the expression examination results revealed a significant increase in the expression of miR-32-5p in patients with AMI compared with healthy controls. It is reported that miR-32-5p may serve a critical role in the progression of atherosclerosis by regulating arterial calcification [
17,
29]. In this study, the AI values of AMI patients were significantly high, and we found that the serum levels of miR-32-5p was positively correlated with the AI values, indicating that miR-32-5p might be involved in the development of AMI by regulating the arterial calcification. The subsequent correlation analysis found the positive correlation between miR-32-5p and the endothelial injury biomarkers. Thus, we considered that the elevated expression of miR-32-5p might be involved in the endothelial injury in the pathogenesis of AMI.
After the occurrence of AMI, the left ventricular dysfunction and remodeling can be promoted by the sustained inflammatory responses. KLF2 has been found to regulate some key molecules or signaling involved in inflammation [
30,
31]. As a regulator of KLF2, miR-32-5p has been found to contribute to inflammatory responses in macrophages infected by
Mycobacterium tuberculosis [
18] and rats with neuropathic pain [
19]. Thus, the relationship of miR-32-5p was further analyzed with the serum levels of inflammatory cytokines in AMI patients. The statistical correlation analysis data showed that miR-32-5p was positively correlated with IL-1β, IL-6 and TNF-α, indicating that miR-32-5p might participate the inflammatory responses through regulating KLF2. However, whether miR-32-5p has regulatory effect on the inflammatory responses in AMI was not assessed in this study, warrant further investigations.
There are lots of AMI patients died before receiving hospital therapy, and early diagnosis remains one of the approaches to reduce AMI mortality. The dysregulation of miRNAs in various diseases has attracted increasing attention on their diagnostic value [
32]. In prostate cancer patients, the deregulated expression of miR-32-5p has been identified as a diagnostic biomarker [
33]. Considering the upregulation of miR-32-5p in AMI patient, this study constructed a ROC curve based on miR-32-5p expression levels and showed that serum expression of miR-32-5p had relatively high diagnostic accuracy to distinguish AMI patients from healthy controls. Thus, the elevated serum miR-32-5p might serve as a diagnostic biomarker of AMI. However, the diagnostic potential results of miR-32-5p might be limited by the small sample size of this study. Thus, further investigations with a larger study cohort are needed to confirm the clinical significance and functional role of miR-32-5p in AMI.
Taken together, miR-32-5p is a direct regulator of KLF2 and may be involved in the endothelial injury and inflammatory responses in the pathogenesis of AMI. The elevated serum miR-32-5p expression in AMI patients may serve as a candidate diagnostic biomarker for the screening of AMI patients. This study provides a novel insight into the diagnosis and pathogenesis of AMI, and the strategies to inhibit miR-32-5p may have potentials to improve AMI treatment.
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