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Open Access

Peer-reviewed

Research Article

HDL protects against myocardial ischemia reperfusion injury via miR-34b and miR-337 expression which requires STAT3

  • Sarah Pedretti,

    Roles Data curation, Formal analysis, Investigation, Methodology, Writing – original draft

    Affiliation Department of Medical Specialties-Endocrinology, Diabetology, Hypertension and Nutrition, University of Geneva, Geneva, Switzerland

    ⨯
  • Marie-Claude Brulhart-Meynet,

    Roles Data curation, Investigation, Methodology

    Affiliation Department of Medical Specialties-Endocrinology, Diabetology, Hypertension and Nutrition, University of Geneva, Geneva, Switzerland

    ⨯
  • Fabrizio Montecucco,

    Roles Data curation, Funding acquisition, Investigation, Methodology, Resources

    Affiliations First Clinic of Internal Medicine, Department of Internal Medicine, University of Genoa School of Medicine, Genoa, Italy, IRCCS AOU San Martino—IST, Genoa, Genoa, Italy, Centre of Excellence for Biomedical Research (CEBR), University of Genoa, Genoa, Italy

    ⨯
  • Sandrine Lecour,

    Roles Conceptualization, Funding acquisition, Resources

    Affiliation Hatter Institute for Cardiovascular Research in Africa, Department of Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa

    ⨯
  • Richard W. James,

    Roles Conceptualization, Funding acquisition, Investigation, Project administration, Resources, Supervision

    Affiliation Department of Medical Specialties-Endocrinology, Diabetology, Hypertension and Nutrition, University of Geneva, Geneva, Switzerland

    ⨯
  • Miguel A. Frias

    Roles Conceptualization, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Supervision, Validation, Writing – original draft, Writing – review & editing

    Miguel.Frias@unige.ch

    Affiliations Department of Medical Specialties-Endocrinology, Diabetology, Hypertension and Nutrition, University of Geneva, Geneva, Switzerland, Division of Laboratory Medicine, Diagnostics Department, Geneva University Hospitals, Geneva, Switzerland

    ⨯

Abstract

Purpose

High density lipoprotein (HDL) protects against myocardial infarction via mechanisms that remain unclear. STAT3 (signal transducer and activator of transcription 3) plays a key role in HDL-induced cardioprotection. In the heart, microRNAs (miRNAs) are involved in ischemia reperfusion injury. We therefore investigated whether the cardioprotective effect of HDL modulates miRNAs as a downstream target of STAT3 activation.

Methods

STAT3 cardiomyocyte deficient mice (STAT3-KO) and wildtype littermates (STAT3-WT) were submitted to left coronary ligature and reperfused (IR) with or without injection of HDL. Infarct size (IS) was determined and cardiac miRNA expression was evaluated after reperfusion in sham, IR and IR+HDL hearts by microarray analysis.

In vitro, neonatal rat ventricular cardiomyocytes were submitted to hypoxia with or without HDL incubation. Cell viability and miRNA expression were analysed.

Results

In vivo, HDL reduced IS from 40.5±4.3% to 24.4±2.1% (p<0.05) in STAT3-WT mice. HDL failed to protect in STAT3-KO mice. In STAT3-WT mice, both miR-34b and miR-337 were increased in IR compared to sham and IR+HDL groups (p<0.05). These miRNAs were not modulated in STAT3-KO mice. In vitro, incubation with HDL improved cell viability against hypoxia (p<0.05). The expression of miR-34b and miR-337 was increased by hypoxia and reduced by HDL treatment (p<0.05). In cardiomyocytes transfected with miRNA mimics, HDL failed to improve cell viability against hypoxia.

Conclusions

Our study, performed both in vivo and in vitro, delineates a novel cardioprotective signalling pathway activated by HDL, involving STAT3-mediated decrease of miR-34b and miR-337 expression.

Citation: Pedretti S, Brulhart-Meynet M-C, Montecucco F, Lecour S, James RW, Frias MA (2019) HDL protects against myocardial ischemia reperfusion injury via miR-34b and miR-337 expression which requires STAT3. PLoS ONE 14(6): e0218432. https://doi.org/10.1371/journal.pone.0218432

Editor: Ferenc Gallyas Jr., University of PECS Medical School, HUNGARY

Received: September 24, 2018; Accepted: June 3, 2019; Published: June 20, 2019

Copyright: © 2019 Pedretti et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Data Availability: All relevant data are within the manuscript and its Supporting Information files. The other data (results of miRNA affymetrix analysis) can be found in the Gene Expression Omnibus repository, accession number: GSE124176.

Funding: The present study was supported by the Swiss National Science Foundation (SNSF grant 31-135221 to R.W.J. and SNSF grant 310030_152639 to F.M.) and Fondation Prévot, Jubiläumsstiftung SwissLife and Fondation pour la lutte contre le cancer et investigations médico-biologiques (M.A.F.). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Competing interests: The authors have declared that no competing interests exist.

Introduction

Historically, high density lipoproteins (HDL) have been identified as a strong negative predictor of cardiovascular events. Their beneficial effect on the cardiovascular system was attributed, in the first instance, to their ability to facilitate cholesterol excretion [1]. Recent evidence attributes more widespread, beneficial actions to the HDL particle, such as antioxidant, anti-inflammatory and anti-apoptotic actions on vascular cells [2]. The direct actions of HDL on the heart have not been extensively investigated although experimental data show that HDL protects from ischemia reperfusion injury (IR) [3,4], hypoxia [5,6], and apoptosis induced by doxorubicin, a potent anti-cancer drug with cardiotoxic side effects [7]. In previous publications, we demonstrated that the protective effect of HDL against oxidative stress and IR is mediated via the activation of the Survivor Activating Factor Enhancement (SAFE) pathway which involves the activation of intracellular signalling factors including Tumour Necrosis Factor alpha (TNFα) and Signal Transducer and Activator of Transcription 3 (STAT3) [6,8]. In the heart, STAT3 has been shown to be beneficial and plays a pro-survival role. Multiple studies including ours have demonstrated the anti-apoptotic role of STAT3 in cardiac conditioning [9].

MicroRNAs (miRNAs) are non-coding sequences of 20–22 nucleotides that can modulate the expression of several genes simultaneously. miRNAs are involved in multiple actions that modulate cell homeostasis. In the heart, miRNAs modulate the response during IR to promote cell survival [10]. Recently, several research groups have reported the involvement of some miRNAs in the pathophysiology of myocardial infarction [11,12]. Additionally, some miRNAs have been shown to be involved in myocardial ischemic conditioning [13]. Despite the research into signalling pathways involving miRNAs during conditioning regulation, the role of STAT3 in miRNAs’ regulation has not been investigated. Most of the studies on STAT3 and miRNA regulation are in cancer cells. While some miRNAs have been demonstrated to directly target STAT3 expression [14], only a few studies showed that STAT3 can modulate target miRNA [15]. Interestingly the HDL particle has been shown to contain miRNAs and transports them to several different cell types [16,17]. This leads to the regulation of the expression of target mRNA [17]. In patients, the miRNA profile of HDL is modified under pathophysiological conditions such as familial hypercholesterolemia and coronary artery disease (myocardial infarction, stable and unstable angina) [16,18]. However, little is known about the effect of HDL treatment on cardiac miRNA expression and potential consequences for protection against IR.

In this study, we evaluated whether HDL protects against IR injury by modulating the miRNA expression as a downstream target of STAT3 activation.

Materials and methods

Animals

The investigation conforms to the Guide for the Care and Use of Laboratory Animals published by the US National Institutes of Health (NIH Publication No. 85–23, revised 1996) and has been approved by local ethical committee of the Geneva University Medical School (GE12/3891). Animals were housed and treated in accordance with the Guide for Care and Use of laboratory Animals Eighth Edition, published by the US National Institute of Health Publication. Cardiomyocyte specific STAT3-deficient mice (STAT3-KO) and their wildtype littermates (STAT3-WT) from a C57BL/6 genetic background were obtained from the University of Cape Town (South Africa) as previously described [19]. Male mice aged 12–16 weeks and neonatal Wistar rats (obtained from the University Medical Centre (CMU) animal facility, Medical Faculty, University of Geneva, Geneva, Switzerland.) were used in this study. Mice had ad libitum access to water and food (standard diet) and were entrained in a 12 hour light and 12 hour dark cycle. Mouse genotype determined the group attribution; the mice were distributed in the group sequentially.

HDL isolation

HDL (d = 1.063–1.21g/mL) were isolated by cumulative flotation ultracentrifugation as previously described [20] from a plasma pool provided by healthy volunteers (recruited from the University staff). The volunteers gave written, informed consent in accordance with local ethical committee requirements. After isolation, HDL were dialyzed against phosphate buffered saline containing ethylenediaminetetraacetic acid (EDTA) (0.1mM) and stored at 4°C.

In vivo ischemia reperfusion (IR)

IR was achieved through ligation of the left anterior descending (LAD) coronary artery as described in detail previously [21]. In brief, IRI was analysed after ligation of the left anterior descending (LAD) coronary artery. Mice were anaesthetized with 4% isoflurane, intubated and mechanical ventilation performed (150μl, 120 breaths/min) using a rodent respirator (model 683; Harvard Apparatus). Anaesthesia was maintained with 2% isoflurane delivered in 100% O2 through the ventilator. A thoracotomy was performed and an 8–0 prolene suture was passed under the left anterior descending (LAD) coronary artery. After 45min ischemia, LAD coronary artery occlusion was released and reperfused for 8 or 24h. The mouse was injected with the analgesic buprenorphine (0.1 mg/kg mouse body weight, one subcutaneous injection 30min before the intervention and another 8h after the intervention) and was monitored during the first and 8h after the surgery. Approximately 10% of the mice used in this study died during the experiments; from them approximately 90–95% died during or just after the surgery (option stated and approved by the ethical committee). The mice that survived more than one hour after surgery recovered well and did not showed significant, severe signs of illness following the procedures. As stated, the mice were monitored and if they showed signs of illness (abundant bleeding or dyspnea), they were immediately euthanized under anaesthesia ketamine-xylazine (120mg/kg and 16mg/kg, respectively). After 24h reperfusion the mice were re-anaesthetized with ketamine-xylazine (120mg/kg and 16mg/kg, respectively) and the LAD coronary artery was re-occluded. Evan’s blue dye 2% (Sigma) was injected to delineate the in vivo area at risk (AAR). The hearts were harvested, rinsed with PBS, sliced into 5–6 sections and stained with triphenyltetrazolium chloride (TTC 1%) to allow quantification of infarct size. The different zones were determined using a computerized planimetric technique (MetaMorph v6.0, Universal Imaging Corporation) and IS was expressed in percentage of AAR (I/AAR). We paid particular attention to the quantification of the different areas; each slice was carefully evaluated, as it is known that Evans blue can precipitate out of solution on a subsequent addition of TTC and prone to smearing during slicing, resulting in an ambiguous border definition and could therefore explain some small blue staining on the white area [22]. HDL (100μg protein/g mouse) were injected intravenously (retro-orbital) 1min before reperfusion.

Microarray analysis

Cardiac miRNA expression was evaluated in 3 different treatment groups (sham, IR and IR+HDL). After 8h of reperfusion mice were re-anaesthetized and hearts (full ventricle to avoid any bias) collected and frozen. Frozen heart tissues were powdered using liquid nitrogen. Total RNA was extracted using miRNeasy Mini kits (Qiagen) and quantified using Qubit 2.0 (Invitrogen). RNA samples were subjected to microarray analysis using GeneChip miRNA 2.0 Arrays (Affymetrix) which measured 3163 mouse probesets (1908 mature miRNA and 1255 pre-miRNA probesets).

miRNA expression by quantitative PCR

RNA extracted from the in vivo experiments, as well as RNA extracted from cardiomyocytes following hypoxia, was reverse transcribed using the miRCURY Locked Nucleic Acid (LNA) Universal Reverse Transcription (RT) microRNA PCR, Polyadenylation and cDNA synthesis kit (Exiqon). cDNA was diluted 80x and assayed in 10μl PCR reactions according to the protocol. The amplification was performed in a LightCycler 480 Real-Time PCR System (Roche) in 96-well plates. The amplification curves were analyzed using the Roche LightCycler software, both for determination of Cp (by the 2nd derivative method) and for melting curve analysis. Primers for mmu-miR-34b (cat n°205086 MIMAT0004581, also valid for rno), mmu-miR-337 (cat n°205184 MIMAT0004644), rno-miR-337 (cat n°2103270 MIMAT0017035) and U6 (cat n° 203907) as housekeeping gene were used (Exiqon).

Cell culture

Experiments involving animals were approved by the local Animal Ethics Committee (University of Geneva). Neonatal male and female (1 to 2-day-old) Wistar rats were euthanized by decapitation and right ventricles rapidly excised and washed in Hank’s Balanced Salt Solution (HBSS) (Sigma, H9394). Ventricles were then sliced in half and incubated in 50ml of 0.5% trypsin (Sigma, 59418C) at 4ºC overnight with shaking. Trypsin was neutralized with 20ml Dulbecco’s Modified Eagle Medium (DMEM) (Invitrogen 31885023, glucose 1g/L) containing 10% fetal calf serum (FCS) (Biochrom,S0415) and 1% penstrep (Gibco, 15140122) at 37ºC as described in detail previously [23].

Hypoxia protocol

Before hypoxic exposure, cell medium was replaced by modified Tyrode’s solution (in mM: NaCl 136.9, KCl 2.68, Na2HPO4.12H2O 8.1, KH2PO4 1.47, CaCl2 0.9, MgCl2 .6H2O 0.49; pH 7.2). Cardiomyocytes were placed in an anaerobic hypoxia chamber containing 5% CO2 and 95% N2 at 37°C for 7h. For normoxic treatment, cells were maintained in DMEM medium at 37°C in a culture incubator with 5% CO2. Treated cardiomyocytes were exposed to HDL (400μg protein/ml) during hypoxia.

Measurement of cell viability

Following hypoxia, cells were loaded with 0.04% trypan blue and cell viability was immediately analysed using a light microscope. The number of viable (unstained) and non-viable (blue stained) cardiomyocytes in 3 random microscopic fields was recorded, with at least 30 cells counted in each field. Cell viability was normalized to the normoxic control.

Small interfering RNA (siRNA) transfection

Lipofectamine RNAiMAX (Invitrogen) was used to transfect STAT3 siRNA or nonspecific siRNA control into cardiomyocytes according to the recommendations of the manufacturer (Life Technologies). Cells were treated with 50pmol of specific siRNA. After overnight transfection, the complexes were removed, and fresh medium containing 10% FCS was added. STAT3 mRNA expression was analysed using the following procedure: total RNA was extracted (NucleoSpin RNA, Macherey-Nagel) and reverse transcribed using the manufacturers’ protocols. Real-time PCR was performed on a Light-Cycler480II (Roche). Primers to detect STAT3 were (sense) cagcctgtctgcagagttca and (anti-sense) aaggtgatcaggtgcagctc and for housekeeping gene 9S were (sense) ctccggaacaaacggtgaggt and (anti-sense) tccagcttcatcttgccctc.

miR-34b/miR-337 mimics and miR-34b/miR-337 antimiRs transfection

Cardiomyocytes were seeded in petri dishes. Then, miR-34b and miR-337 mimics (Qiagen) (6nM each) or miR-34b and miR-337 antimiRs (Qiagen) (6nM each) were transfected into cells using HiPerFect Transfection Reagent (Qiagen). After overnight transfection, complexes were removed, and fresh medium containing 10% FCS was added. All stars Negative Control siRNA (12nM) (Qiagen) was used as a negative control. This concentration used was comparable to the one used in other studies [24,25]. The expression of miR-34b and miR-337was evaluated by qPCR and showed that both miRNA concentrations were increased in the presence of mimics (n = 8) (S1 Table). The magnitude of changes observed likely exceeded physiological ranges but the concentrations at which endogenous miRNAs are considered pathophysiologic remain unknown to this day.

Statistical analysis

Data are expressed as mean ± the standard error of the mean (SEM). Comparisons were performed by two-way ANOVA analysis (miRNA microarray and RNA sequencing analysis) and by Student t-test (one-way paired and unpaired) when applicable. p<0.05 was accepted as significantly different.

Results

In vivo HDL protects the heart from IR injury via STAT3

In order to evaluate the role of STAT3 in the cardioprotective role of HDL in vivo, mice were submitted to the IR protocol and infarct size was analysed in STAT3-WT and STAT3-KO mice. After 45min of ischemia followed by 24h reperfusion, HDL significantly reduced IS (p<0.05) in STAT3-WT mice hearts but failed to protect in STAT3-KO mice (Fig 1A and 1C). The AAR/V area was similar between the 4 groups (Fig 1B and 1C).

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Fig 1. In vivo HDL protects the heart from IR injury via STAT3 activation.

Mice were submitted to LAD occlusion for 45min and hearts were reperfused for 24h. Mice were injected or not (IR) with HDL (HDL) one minute before reperfusion. A) Quantification of infarct size (I) expressed in % of area at risk (AAR). B) Quantification of AAR per ventricle surface (V). C) Representative images of TTC stained middle heart sections of control or treated mice. Data are mean ± SEM, n = 6–8, *: p<0.05 vs IR.

https://doi.org/10.1371/journal.pone.0218432.g001

In vivo HDL regulates specific miRNAs during IR injury

As a next step, we analysed whether HDL can modulate the expression of miRNA in IR conditioning. The operated mice were divided in 3 groups; sham operated, IR and IR+HDL mice. After 45min of ischemia followed by 8h reperfusion, global miRNA expression was analysed by microarray. In STAT3-WT mice, 15 miRNAs were upregulated and 1 was decreased (p value<0.05 and fold change>2) following IR compared to operated sham mice. Among these potential targets, the expression of miR-34b and miR-337 was significantly changed (p<0.05) when treated with HDL. The expression of miR-34b and miR-337 was increased (fold change 2.22 and 2.21, respectively) in STAT3-WT mice hearts. HDL treatment decreased the expression of both miRNAs (fold change -1.90 and -2.62, respectively). In contrast, the expression of these miRNAs was not modified between conditions in STAT3-KO mice (Fig 2).

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Fig 2. In vivo HDL regulates specific miRNAs during IR injury.

Mice were sham operated (sham) or submitted to LAD occlusion for 45min and hearts were reperfused for 8h (IR). HDL was injected or not one min before reperfusion. miRNA was isolated from total heart and miRNA expression assessed by microarray analysis after 8h of reperfusion in in vivo mouse hearts using GeneChip miRNA 2.0 Arrays. A) miRNA expression significant change (p<0.05) between sham and IR group (Heatmap representation). B) Expression of miR-34b and miR-337 (boxplot representation). n = 3. *: p<0.05 vs sham, #: p<0.05 vs IR.

https://doi.org/10.1371/journal.pone.0218432.g002

These observations were confirmed by qPCR which showed that the expression of miR-34b (Fig 3A) and miR-337 (Fig 3B) was increased by IR (2.26±0.35 and 1.59±0.24, respectively) and reduced by HDL (1.26±0.15 and 0.91±0.10, respectively) in STAT3-WT mice hearts. In contrast, the absence of STAT3 was associated with a significant increase in miR-34b (p = 0.01) and miR-337 (p = 0.03) already in the sham operated animals (Fig 3A and 3B). Subsequent treatment had no significant impact on miRNA levels (Fig 3A and 3B), as observed by qPCR analysis.

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Fig 3. In vivo HDL regulates miR-34b and miR-337 during IR injury.

Mice were sham operated (sham) or submitted to LAD occlusion for 45min and hearts were reperfused for 8h (IR). HDL was injected or not one min before reperfusion. miRNA was isolated from total heart. A) miR-34b and B) miR-337 expression was measured by qPCR and normalized to U6 expression. Data are mean ± SEM, n = 6–9, *: p<0.05 vs sham, #: p<0.05 vs hypoxia. The difference between sham STAT3-WT and STAT3-KO is significant (p<0.05).

https://doi.org/10.1371/journal.pone.0218432.g003

HDL improves cell survival against hypoxia and regulates specific miRNAs during hypoxia

In order to understand the role of these miRNAs in cardiomyocyte survival, we used a model of neonatal rat cardiomyocytes. In these cells, the exposure to hypoxia decreased cell survival from 100% (normoxia) to 75.0±5.3%. HDL treatment restored survival to 95.2±2.8% (Fig 4A).

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Fig 4. HDL improves cell survival against hypoxia and regulates specific miRNAs during hypoxia.

Cardiomyocytes were incubated in Tyrode solution, submitted to 7h hypoxia and treated during hypoxia with HDL. A) Cell viability, B) miR-34b and C) miR-337 expression. Results are expressed in percentage of normoxia. Data are mean ± SEM, n = 8–10, *: p<0.05 vs normoxia, #: p<0.05 vs hypoxia.

https://doi.org/10.1371/journal.pone.0218432.g004

The expression of miR-34b and miR-337 was evaluated in these conditions. Exposure to 7h of hypoxia increased the expression of miR-34b (Fig 4B) and miR-337 (Fig 4C) by approximately 5 and 3 times, respectively. Incubation with HDL significantly reduced the expression of both miRNAs to a level similar to normoxia.

HDL improves cell survival against hypoxia via STAT3 and miRNA expression

The specific role of STAT3 was also evaluated using specific STAT3 siRNA. Treatment with STAT3 siRNA showed a 94.0±2.6% reduction in STAT3 mRNA expression (S1 Fig). these cells transfected either with control siRNA or STAT3 siRNA, exposure to 7h of hypoxia decreased cell survival by 30%. Although HDL treatment protected from cell death in control siRNA transfected cells, HDL failed to restore cell survival in cardiomyocytes transfected with STAT3 siRNA (Fig 5A).

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Fig 5. HDL improves cell survival against hypoxia via STAT3 and miRNA expression.

Cardiomyocytes transfected with control or STAT3 siRNA were incubated in Tyrode solution, submitted to 7h hypoxia and treated during hypoxia with HDL. A) Cell viability, B) miR-34b and C) miR-337 expression. Results are expressed in percentage of normoxia. Data are mean ± SEM, n = 3–7, *: p<0.05 vs normoxia, #: p<0.05 vs hypoxia.

https://doi.org/10.1371/journal.pone.0218432.g005

Additionally, the expression of miR-34b and miR-337 was altered in the cardiomyocytes transfected with STAT3 siRNA. Correspondingly, HDL lost its effect and failed to modulate the expression of these miRNAs (Fig 5B and 5C).

miR-34b and miR-337 expression influence cell survival

The role of these miRNAs in the hypoxic insult was further evaluated using specific mimics and antimiRs. In order to mimic optimally the situation of hypoxia a mix of both miR-34b and miR-337 mimics or miR-34b and miR-337 antimiRs was used. Exposure to hypoxia of cells transfected with the mix of mimics diminished cell survival by approximately 30%. In these cells, HDL lost its protective capacity (Fig 6A). Conversely cardiomyoytes transfected with a mix of antimiRs were protected against the deleterious insult of hypoxia independently of the HDL treatment (Fig 6B).

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Fig 6. miR-34b and miR-337 expression influences cell survival.

Cell viability after 7h of hypoxia in neonatal rat cardiomyocytes treated with negative control, miR-34b and miR-337 mimics (A) or antimiRs (B). Results are expressed in percentage of normoxia. Data are mean ± SEM, n = 5, *: p<0.05 vs normoxia, #: p<0.05 vs hypoxia.

https://doi.org/10.1371/journal.pone.0218432.g006

Discussion

The main findings in our study strongly suggest that HDL confers protection against IR via the can modulation of the expression of miRNAs. In addition, our data show that this modulation by HDL is mediated via the activation of the pro-survival protein STAT3 whose role in HDL-mediated protection has previously been demonstrated in details [6–8].

HDL is a major negative predictor for cardiovascular events. New evidence has demonstrated that HDL has more widespread beneficial effects beyond its role in reverse cholesterol transport [2]. These beneficial effects appear to act via a direct interaction with cells. Although the mechanisms by which HDL can affect cell function remain to be fully elucidated, several studies showed that HDL is capable of influencing a number of intracellular signalling cascades involved in multiple cell survival processes. Little is known concerning the direct effect of HDL in the heart. A few studies, including our own, demonstrated that HDL protects the heart against stress [4–7,21]. However, the precise mechanisms of action have not been fully delineated, underlining the need to expand our understanding on the interaction between HDL and the heart. In our present study, we used human HDL in rodent models. The use of human HDL in rodent models is commonly reported in the literature and has been experimented without any evidence of problems [4,26–30]. Similarly, several studies have used transgenic mice expressing human apoA1, which is the major protein content in HDL particle [31–33]. In order to ensure that HDL derived from different species act in a similar manner in our model, we performed in vitro experiments and showed that both human and murine HDL exerted similar effects on cell death (S2 Fig) as well as on ERK1/2 phosphorylation (S3 Fig) in endothelial cells.

In this study, we evaluated HDL impact on miRNA expression under conditions of IR. The use of the microarray approach allows an objective analysis of the expression of miRNA modulated by IR and HDL treatment in vivo. It revealed miRNAs whose expression was modulated by IR compared to sham-treated mice. Among these miRNAs, only a few were affected by HDL treatment compared to those in IR. The analysis highlighted the expression of 2 miRNAs: miR-34b and miR-337. These experiments were extended in vitro. Similar to the data obtained in vivo, in cultured cardiomyocytes hypoxia induced an increase in miR-34b and miR-337 expression. Experiments using mimics and anti-miRNAs strongly support a role in cell survival under ischemia. Our data demonstrate that a decrease in the expression of these miRNA induced by HDL treatment could improve cardiac cell survival. The potential effect of HDL on miRNAs was only investigated in IR protocol as a particle able to trigger cardioprotective effects. It would also be of interest to explore the regulation of miRNAs following a treatment of HDL in hearts not subjected to IR. In endothelial cells, Tabet et al [34] demonstrated that HDL altered endothelial cell miRNA levels with significant differential miRNA following a treatment with native HDL (3 in total; 1 down: miR-339-5p; 2 up: miR-223 and miR-577).

Our previous publications underlined the role of STAT3 in the protective effect of HDL [6,7]. We also demonstrated that, in the heart, HDL induces the serine phosphorylation of STAT3 after 5 min of stimulation in vitro, ex vivo and in vivo [8,9,21]. Sekine et al. [35] and Feuerborn et al. [36] confirmed a similar effect in prostate cancer DU145 cells and in RAW264.7 murine macrophages, respectively.

In the present study, we used specific cardiomyocyte STAT3 knockout mice to confirm in vivo the role of STAT3 in the HDL-induced cardioprotection cardioprotective effects, therefore supporting our previous work conducted in an isolated heart model [6]. Furthermore, we now demonstrate that STAT3 plays a role in the modulation of the expression of miR-34b and miR-337 in vivo. These results were confirmed in vitro where STAT3 siRNA transfected cardiomyocytes were not protected by HDL treatment. Interestingly, in sham treated animals, absence of STAT3 was associated with a significant increase in both miRNAs (Fig 3A and 3B).

Although the precise role of these specific miRNAs has not been investigated in myocardial IR, Bernardo and colleagues investigated the role of the miR-34 family in the heart submitted to stress [37]. Under conditions of myocardial infarction, the miR-34 family is upregulated whereas inhibition improves heart function. Unfortunately, global inhibition of miR-34a, b and c was used, thus not allowing the evaluation of the specific role of miR-34b in this response [37]. According to our data, miR-34b could play an important role in the effect of miR-34 family. In cardiac studies, miR-34b is associated with congenital disease [38] and is dysregulated in patients with diabetic ischemic heart failure [39]. miR-337 is increased in plasma from coronary artery disease patients compared to control subjects [40] and its expression is modulated in the regenerative process of neonatal ventricular cells [41]. Unfortunately, its role in these different pathologies was not investigated. It should be noted that most of the knowledge on these miRNAs comes from cancer studies. In tumoral cells, miR-337 suppresses cell proliferation, migration, and invasion in human pancreatic cancer cell lines [42] and senescence in human colorectal cancer cells [43]. miR-34b is downregulated in prostate cancer cells, in colonic tumours, gastric carcinogenesis, pancreatic cancer metastasis [44–47] and is correlated with higher lymph node metastasis [48]. Additionally induction of its expression induces cell death in ovarian cancer cells [49]. While an increase of miR-337 expression induced cell death, a decrease in miR-34b expression seems to improve cell survival. This is therefore in agreement with our data. Likewise, miR-34b is upregulated in neuronal PC12 cells exposed to sevoflurane preconditioning [50], suggesting that an increase in miR-34b expression could be protective in neuronal cells. Comparing these studies with our own is difficult, given the different cell type and different pathophysiological conditions.

Thus, our data suggest a new role for these miRNAs in the heart, a role that HDL can beneficially influence by modulating their expression.

There is a growing body of evidence demonstrating that miRNAs are closely associated with the STAT3 signalling pathway. Modulation of STAT3 expression essentially influenced cell survival. Although most of these data have been obtained from cancer cells [14], a few articles described the link between miRNA and STAT3 in cardiac tissue. Among these articles, only one study shows that reduction of STAT3 levels can modulate miRNA expression. More precisely, knock-down of STAT3 increased miR-199a expression and subsequent impairment of the ubiquitin-proteasome system [15]. In the other studies, STAT3 was targeted by miR-17, miR-21 in cardiomyocytes [51,52] and miR-351 in endothelial cells [53]. The reduction of STAT3 protein expression impaired cell survival. In the present study, we therefore highlight a novel aspect on the role of STAT3 in HDL-induced cardioprotection by demonstrating the influence of HDL-activated STAT3 on the expression of miR-34b and miR-337.

Our data identify a novel pathway by which HDL can protect the heart from IR injury with the modulation of miR-337 and miR-34b expression as critical downstream target of STAT3 (see Fig 7). It is, to our knowledge, the first study to demonstrate a role for HDL in modulating miRNA expression following IR. This novel aspect of HDL action in the heart expands our understanding in the cardioprotective effects of HDL. Combination of these protective influences underlines the therapeutic potential of HDL in the heart.

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Fig 7. Proposed mechanism of HDL cardioprotection against IR injury occurring via a STAT3-dependent decrease of miR-34b and miR-337 expression.

https://doi.org/10.1371/journal.pone.0218432.g007

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