MicroRNA modulation of lipid metabolism and oxidative stress in cardiometabolic diseases (original) (raw)

. Author manuscript; available in PMC: 2014 Sep 1.

Abstract

The regulation of cholesterol metabolism is one of the most studied biological processes since its first isolation from gallstones in 1784. High levels of plasma low-density lipoprotein (LDL) cholesterol and reduced levels of plasma high-density lipoprotein (HDL) cholesterol are widely recognized as major risk factors of cardiovascular disease. An imbalance in the production of reactive oxygen species (ROS) can oxidize LDL particles increasing the levels of the highly pro-atherogenic oxidized LDLs (ox-LDLs). Furthermore, under pathological scenarios, numerous molecules can function as pro-oxidants, such as iron or high-glucose levels. In addition to the classical mechanisms regulating lipid homeostasis, recent studies have demonstrated the important role of microRNAs (miRNAs) as regulators of lipoprotein metabolism, its oxidative derivatives and redox balance. Here, we summarize the recent findings in the field, highlighting the contribution of some miRNAs in lipid and oxidative-associated pathologies. We also discuss how therapeutic intervention of miRNAs may be a promising strategy to decrease LDL, increase HDL and ameliorate lipid and oxidative related disorders, including atherosclerosis, non-alcoholic fatty liver disease (NAFLD) and metabolic syndrome.

INTRODUCTION

MiRNAs have emerged as crucial and widely distributed post-transcriptional regulators of gene expression in the majority of biological processes, ranging from housekeeping functions to environmental stress responses [1–4]. In contrast with the high conservation of protein-coding genes between species, miRNAs appear to be an important factor in increasing the complexity of organisms, as mammalian genomes transcribe over an order of magnitude more non-coding RNAs than worms or flies [5]. MiRNAs are transcribed in the nucleus mainly by RNA polymerase II as long primary miRNAs (pri-miRNA) of 500–3000 bp that show a stem-loop hairpin structure. The pri-miRNA undergoes maturation by the sequential action of the Drosha/Pasha complex in the nucleus [6] and Dicer in the cytoplasm [7, 8]. After the pri-miRNA is processed, the mature miRNA (25–21 nt) is incorporated into the RNA-induced silencing complex (RISC) and binds preferentially to the 3´ untranslated region (3´UTR) of the mRNA target genes. Of note, a single miRNA modulates multiple genes often within the same biochemical pathway or interconnected nodes in regulatory networks and can help confer the robustness of biological processes by reinforcing transcriptional programs and attenuating dysregulated transcripts.

Regulation of miRNA function is involved in the pathogenesis of human diseases including cancer, metabolic disorders, cardiovascular diseases and neurological dysfunctions [9]. Here we review the role of miRNAs in regulating lipid metabolism, oxidative stress and cardiovascular diseases, including atherosclerosis. We will also discuss how modulating miRNA expression might be a promising therapy to combat atherosclerotic vascular disease and related dyslipidemias.

1. MiRNA regulation of Cholesterol metabolism

Cholesterol is an essential component of cell membranes and is required for vital processes [10, 11]. An excess of plasma cholesterol leads to its accumulation in the artery wall promoting atherosclerosis, the main cause of death in the Western and developing countries [12]. Cholesterol levels are maintained through a tightly regulated and complex mechanism that includes de novo biosynthesis, internalization of exogenous cholesterol and efflux of its excessive levels. All of these processes are controlled by miRNAs.

MiR-122

MiR-122 was one of the first miRNAs described in humans due to its abundance in the liver. This conserved liver-specific miRNA constitutes 70% of the total miRNA pool in this organ [13, 14], while it is absent in other tissues. Several observations underline the importance of miR-122 in liver biology and disease. First, antisense-mediated inhibition of miR-122 in mice leads to the induction of genes that are normally repressed in adult liver [15], suggesting that this miRNA is important for hepatocyte differentiation. Second, anti-miR-122 therapy in mice and non-human primates results in a significant reduction of plasma cholesterol and triglyceride levels. These effects on lipid metabolism have been associated with the modulation of genes involved in cholesterol synthesis including 3-hydroxy-3-methylglutaryl-CoA synthase 1 (HMGCS1), 3-hydroxy-3-methylglutaryl-CoA reductase (HMGCR), 7-dehydrocholesterol reductase (DHCR7), and squalene epoxidase (SQLE) [15]. However, none of these genes are direct miR-122 targets and thus the mechanism underlying these effects remains unclear. Some of these observations have been recently confirmed in miR-122 deficient mouse models [16]. Specifically, miR-122 liver-specific knockout and miR-122 germline knockout mice have a significant reduction (~30%) of total serum cholesterol and triglyceride levels [17, 18]. Mechanistically, Tsai and colleagues found that the absence of miR-122 results in a significant reduction of the microsomal transfer protein (MTTP) expression, thereby decreasing very low-density lipoprotein (VLDL) secretion from the liver [17] (Figure 1). Together, these observations suggest that absence of miR-122 results in hypolipidemia through reduction of hepatic cholesterol synthesis and VLDL secretion.

Figure 1. Schematic overview of miRNAs involved in lipid metabolism and ROS.

Figure 1

Different miRNAs are grouped in boxes and /or representative organs in which they target lipid metabolism regulators. Biological processes in which they are involved are also shown. ↑ indicates activation, ⊤ indicates inhibition.

miR-33/miR-33*

Different groups among us have recently identified miR-33a and miR-33b as intronic miRNAs located within the sterol regulatory element binding factor 2 (Srebf2) and Srebf1 genes [19–21]. In humans, miR-33a and miR-33b are co-transcribed with their host genes and regulate HDL biogenesis and cholesterol efflux by targeting ATP-binding cassette A1 (ABCA1) and ABCG1, and the endolysosomal transport protein, Niemann-Pick C1 (NPC1) [19–21]. These results were later confirmed genetically in miR-33 deficient mice [22]. In addition to ABCA1 and ABCG1, miR-33 also regulates the expression of two canalicular transporters, ATP-binding cassette, sub-family B (MDR/TAP), member 11 (ABCB11) and aminophospholipid transporter class I type 8B member 1 (ATP8B1), which regulate bile acid secretion [23]. Moreover, Li et al. have recently discovered that miR-33a also regulates the cytochrome P450, family 7, subfamily A, polypeptide 1 (CYP7A1), the rate-limiting enzyme in the synthesis of bile acid from cholesterol [24]. Altogether, these findings suggest that miR-33 is a key player in regulating several steps of the reverse cholesterol transport (RCT), including HDL biogenesis, macrophage cholesterol efflux and bile acid secretion (Figure 1 and Table 1). MiR-33a and miR-33b also contribute to the regulation of fatty acid metabolism, modulating the expression of carnitine palmitoyltransferase 1A (CPT1A), carnitine O-octanyl transferase (CROT), and hydroxyacyl-CoA dehydrogenase-3-ketoacyl-CoA thiolase-enoyl-CoA hydratase (trifunctional protein) β-subunit (HADHB) [25, 26]. CPT1a, CROT and HADHB regulate the transport and degradation of fatty acids in the mitochondria and the overexpression of miR-33 in human hepatic cells results in a significant decrease of fatty acid oxidation [25, 26]. In addition to lipid metabolism, miR-33 also regulates insulin sensitivity and hepatic glucose production by targeting the insulin receptor substrate 2 (IRS2) and glucose-6-phosphatase (G6PC) and phosphoenolpyruvate carboxykinase (PKC1), respectively [25,27].

Table 1.

Summary of the prototypical functions of miRNAs in lipid metabolism and oxidative stress.

miRNA Target mRNA Regulatory effect References
Lipid metabolism
miR-122 ?, MTTP ↑ Cholesterol synthesis (LDL)↑ VLDL secretion [17]
miR-33 ABCA1 ↓ Cholesterol efflux [19]
CROTCPT1HADHB ↓ Fatty acid biosynthesis [25, 26]
CYP7A1ABCB11ATP8B1 ↓ Bile acid synthesis and secretion [23]
IRS2G6PC ↓ Insulin signaling [25, 27]
PCK1 ↓ Glucose metabolism [27]
miR-758, miR-106b, miR144 ABCA1 ↓ Cholesterol Efflux [32–35]
miR-125a, miR-455 SR-BI ↓ Cholesterol metabolism and Steroidogenesis [39]
miR-185, miR-96, miR-223 SR-BI ↓ Cholesterol metabolism and Steroidogenesis [40]
miR-1, miR-206, miR-613 LXRα ↓ Lipogenesis [43, 44]
miR-143, miR-371miR-378/378* CRAT, MED13 ↑ Adipogenesis [45–47]
miR-27a/b, miR-369-5p, miR-130 ANGPTL3GPAM, FABP4 ↓ Adipogenesis [46, 48, 49]
Oxidative stress
miR-125a/b-5p ECE-1ORP-9 Anti-inflammatory [56, 57]
miR-365 BCL-2 Pro-inflammatory [58]
Let-7 BCL-XL Pro-inflammatory [59]
miR-222/221 eNOS Endothelial homeostasis [60]
miR-92a eNOSKLF2KLF4 Endothelial homeostasis [61]
miR-21 eNOSPTENPPAR-a Anti-apoptotic Pro-inflammatory [62]
miR-34, miR-217 SIRT-1 Pro-apoptotic Endothelial senescence [63–65]
miR-633 PPAR-a Monocyte adhesion [69]
miR-146a TLR4KLF-4 Anti-inflammatory VSMC proliferation Neointimal hyperplasia [73, 79]
miR-9 PPAR-γ Anti-inflammatory [74]
miR-27* a/b NF-κB Anti-inflammatory [75–80]
Let-7g LOX-1 Monocyte adhesion [84]
miR-29b DNMT3b Plaque instability [86]
miR-210 ISCU Oxidative response to hypoxia [87–88]
miR-122 HFEHJV Oxidative stress [89]

During miRNA biosynthesis, the passenger strand (also designated as 3p or *) is often rapidly degraded and has no effect on gene expression, but in certain miRNAs, such as miR-33 [28], the Dicer generated duplex (miRNA/miRNA*) gives rise to both “5p” and “3p” mature active miRNAs. Interestingly, we have recently demonstrated that miR-33* shares a similar target network to that of miR-33 and directly represses target genes in human hepatic and macrophage cell lines. Importantly, miR-33* overexpression reduces fatty acid oxidation in hepatocytes. Altogether, these data suggest that miR-33 regulates lipid metabolism through both arms of the miR-33/miR-33* duplex [28].

Anti-miR-33 therapy: a promising approach for treating cardiometabolic diseases

Human epidemiological studies show a strong inverse association between HDL plasma levels and coronary heart disease (CHD), which led several groups to study the potential benefit of anti-miR-33 therapy in preventing atherosclerosis progression and promoting plaque regression in murine models of atherosclerosis. In the first study, Rayner and colleagues demonstrated that 2’-O-methoxyethyl (2´F/MOE) modified anti-miR33 therapy enhances the regression of atherosclerosis in Ldlr−/− mice by increasing circulating HDL-C levels and RCT. Antagonism of miR-33 in mice also reduces lipid and monocyte/macrophage accumulation in atherosclerotic plaques, thereby reducing inflammation. Another interesting finding of this study is the preferential localization of 2’F/MOE anti-miR-33 oligonucleotides in foam cells, which results in a significant derepression of miR-33 target genes, including Abca1. In addition to reduced macrophage accumulation in atherosclerotic plaques from Ldlr−/− mice treated with anti-miR-33 oligonucleotides, the inhibition of miR-33 also decreases the expression of proinflammatory and pro-oxidant genes, including inducible nitric oxide synthase (Nos2) and tumor necrosis factor alpha (Tnf). Even though these results suggest that miR-33 may increase inflammation, other studies have found the opposite results [29]. Indeed, overexpression of miR-33 reduces the expression of the receptor interacting protein 140 (RIP-140), which is a transcriptional co-activator of NF-κB-responsive genes [29].

In addition to the atherosclerosis regression studies, other groups have examined the efficacy of anti-miR-33 therapy during the progression of atherosclerosis. In our study, we found that 2’F/MOE modified anti-miR-33 therapy was effective in an atherosclerosis progression model. We observed a significant reduction in atherosclerotic plaque size in mice treated with miR-33 ASOs. Importantly, the circulating HDL levels were very similar but the cholesterol efflux capacity of HDL isolated from mice treated with miR-33 ASOs was significantly higher compared to HDL isolated from Ctrl-ASO treated mice [30]. We also observed that mice treated with anti-miR-33 oligonucleotides have a significantly higher expression of ABCA1, matrix metallopeptidase (MMP-2), collagen type I alpha 1 (COL1A-1) and COL3A-1 in the aorta. These results suggest that the anti-atherogenic effect of long-term anti-miR-33 therapy is independent of plasma HDL levels. In contrast, Marquart and colleagues have recently reported that anti-miR-33 therapy using locked nucleic acid (LNA) modified oligonucleotides fails to increase circulating HDL levels and to slow the progression of atherosclerosis in Ldlr−/− mice fed a Western diet (WD). These unexpected results might be explained by the different chemistry employed in the oligonucleotide modification, as well as by the reduced hepatic miR-33 levels observed in mice fed a WD. Finally, Horie and colleagues assessed the progression of atherosclerosis in miR-33/ApoE−/− double mutant mice [31]. Similar to the results observed in our study, miR-33 genetic deficiency results in a significant reduction in atherosclerotic plaque formation. However, the authors also found increased levels of circulating HDL in miR-33 null mice, suggesting that the anti-atherogenic effect of miR-33 deficiency might be mediated by increasing plasma HDL and RCT.

Other miRNAs that regulate ABCA1 expression

In addition to miR-33 and miR-122, other miRNAs have also been described to participate in lipid metabolism. MiR-758 and miR-106 have been shown to regulate ABCA1 expression at the post-transcriptional level in hepatocytes, macrophages and neuronal cells [32, 33]. MiR-758 is an intergenic miRNA which is down-regulated after cholesterol loading in macrophages and in the liver of mice fed a high-fat diet [32]. MiR-106 also regulates ABCA1 levels and miR-106 overexpression significantly decreases ABCA1 levels and impairs cellular cholesterol efflux in neuronal cells [33]. In addition to these miRNAs, miR-144 has also been recently reported to regulate lipid metabolism by modulating ABCA1 expression [34, 35]. Ramirez et al showed that ABCA1 is post-transcriptionally regulated by miR-144 in vitro and in vivo (Figure 1 and Table 1). MiR-144 over-expression inhibits ABCA1 expression in human and mouse cell lines, thereby attenuating cholesterol efflux to APOA1. Most importantly, delivery of miR-144 mimics to mice inhibits hepatic ABCA1 expression and reduces circulating HDL levels. Conversely, miR-144 silencing in mice increases hepatic ABCA1 expression and plasma HDL levels. Thus, miR-144 appears to regulate both macrophage cholesterol efflux and HDL biogenesis in the liver. We also reported that liver X receptor (LXR) activation increases miR-144 in macrophages, human hepatic cells and mouse livers and that ABCA1 is a target of LXR-induced miR-144. These data reveal how an inducible miRNA controls a negative feedback loop to ensure a tight regulation of cholesterol homeostasis [34]. In a second report, Vallim and colleagues described a novel pathway that links the activation of nuclear farnesoid X receptor (FXR) to the induction of hepatic miR-144 expression. They use both gain-of-function and loss-of-function experiments to demonstrate that changes in hepatic miR-144 levels are sufficient to regulate hepatic ABCA1 expression and plasma HDL levels. They also identify functional FXR response elements (FXREs) in the miR-144 promoter, consistent with direct FXR regulation [35].

SR-BI regulation by miRNAs

In addition to promoting cellular cholesterol efflux, HDL particles deliver cholesterol esters to the liver through the scavenger receptor class B type I (SR-BI) for excretion [36]. SR-BI is expressed mostly in liver and other steroidogenic cells such as adrenal glands, ovary and testis, where SR-BI delivers the bulk of the cholesterol substrate needed for steroidogenesis, the biological process that synthesizes steroid hormones [37, 38]. MiR-125a-5p and miR-455 have been recently described to regulate SR-BI expression by direct targeting [39] (Figure 1). Importantly, miR-125a and miR-455 overexpression inhibits SR-BI-mediated selective HDL uptake and SR-BI-supported steroid hormone synthesis and accordingly, anti-miR-125a and anti-miR-455 treatment stimulate both processes. In this study, in vitro treatment of primary rat granulosa cells with cyclic AMP (cAMP) or in vivo treatment of rat adrenals with adrenocorticotropic hormone (ACTH) decreased the expression of miR-125a, miR-125b, and miR-455 and reciprocally increased SR-BI expression. Most recently, Wang and colleagues have identified miR-185, miR-96 and miR-223 as important regulators of SR-BI expression and HDL uptake [40]. MiR-185, miR-96 and miR-223 overexpression in Hep-G2 cells inhibits SR-BI expression and decreases HDL uptake. Interestingly, miR-96 and miR-185 levels correlate inversely with SR-BI expression in the liver of ApoE knockout mice fed a high-fat diet [40]. These data suggest that miR-185, miR-96 and miR-223 may be involved in a novel type of regulation of hepatic SR-BI and cholesterol metabolism.

Other miRNAs that regulate lipid metabolism

Several recent reports have identified novel miRNAs that regulate lipid metabolism including miR-1, miR-206, miR-378/378*, miR-27a/b. Two independent studies have addressed the role of several miRNAs inhibiting LXRα expression post-transcriptionally. LXR is a ligand-activated nuclear receptor playing an important role in the transcriptional regulation of lipid metabolism [41]. LXR activation induces the expression of lipogenic genes such as SREBP1c, fatty acid synthase (FAS), carbohydrate responsive element-binding protein (ChREBP) and acetyl-CoA carboxylase (ACC) [42]. In the first study, Zhong and colleagues demonstrate that miR-1 and miR-206 regulate lipogenesis by repressing LXRα expression, thereby decreasing lipogenic gene expression and lipid droplet accumulation in human hepatic cell lines [43] (Figure 1). Using a similar approach, Zhong et al. found that miR-613 also inhibits lipogenesis by suppressing genes involved in lipid synthesis, including SREBP1c, FAS, ChREBP and ACC [44]. Altogether, these observations suggest that the regulation of lipid metabolism by LXRs is also controlled by LXR-induced miRNAs.

There are many other more miRNAs involved in lipid metabolism such as miR-143, miR-371 and miR-378/miR-378* that have been described to promote adipogenesis [45–47] (Figure 1). In contrast, miR-27a, miR-27b, miR-369-5p and miR-130 negatively regulate adipocyte differentiation [46, 48, 49] (Figure 2). Interestingly, miR-27b is highly expressed in the liver of mice fed a high-fat diet [48] and regulates the expression of several key lipid-metabolism genes, including angiopoietin-like 3 (ANGPTL3) and glycerol-3-phosphate acyltransferase (GPAM) [48].

Figure 2. Overview of the potential roles of miRNAs in atherosclerosis.

Figure 2

A schematic picture of the pathological scenario in the atherosclerotic plaque. Boxes represent different biological processes implicated in atherosclerotic disease, such as inflammation, monocyte extravasation, apoptosis, oxidative stress or extracellular miRNAs. MiRNAs can modulate either positively or negatively several of these processes. ↑ indicates activation, ⊤ indicates inhibition.

In summary, miRNAs seem to be modulating post-transcriptionally several processes involved in cholesterol metabolism and, in general, lipid metabolism. It is clear that deeper knowledge of miRNA mechanistic functions could open new opportunities for the therapeutic treatment of lipid-related-diseases.

2. Atherosclerosis, cholesterol and reactive oxygen species (ROS)

There are a growing number of studies that demonstrate the importance of miRNAs in regulating the biology of the human atherosclerotic plaque (Figure 2 and Table 1). Furthermore, miRNA expression profiles comparing atherosclerotic plaques versus healthy arteries or plaques from symptomatic and asymptomatic subjects have been performed [50–52]. Even though these studies provide useful information about the genetic changes of human atherosclerotic plaques, they usually fail to decipher the specific source (cellular and/or area of the plaque) and the molecular mechanisms that underlie the role of these miRNAs. New techniques, such as laser capture microdissection, could help to elucidate the specific commitment of a single miRNA in oxidative stress or lipid metabolism inside a specific cell type and/or in the particular communication established by the plaque milieu [53].

ROS, endothelial cell activation and atherosclerosis

The initial stage of atherosclerotic plaque development is characterized by the infiltration and retention of LDL in the artery wall [54]. LDL particles are subsequently modified and oxidized leading to the accumulation of oxidized LDL particles (ox-LDLs) in the arterial intima. Ox-LDLs generated by mediation of ROS are a major trigger for atheroma plaque formation and development because these modified LDLs are significantly more potent than native LDLs in promoting endothelial dysfunction, one of the first steps leading to plaque formation [55]. In this regard, ox-LDL-regulated expression of miR-125a/b-5p has been shown to control endothelin-1 levels, which has an important role as one of the most potent vasoconstrictive peptides in endothelial cells (ECs) [56, 57]. Moreover, miR-365 and let-7c also regulates EC functions in response to ox-LDLs by targeting the pro-survival molecules B–Cell lymphome 2 (BCL-2) and B–Cell lymphome extra-large (BCL-XL), respectively [58, 59].

Nitric oxide (NO) bioavailabilty is another factor that regulates ROS levels in the artery wall. An imbalance in NO levels potentiates a dysregulation in ROS metabolism resulting in oxidative stress. NO levels are regulated by the nitric oxide synthases (NOS) and among them, endothelial nitric oxide synthase (eNOS) is a key player in cardiovascular diseases. The expression of this enzyme is downregulated at the post-transcriptional level by miRNAs, including miR-222/221and miR-92a [60, 61]. In contrast, miR-21 upregulates eNOS activity and protects against apoptosis through targeting of its antagonist phosphatase and tensin homologue (PTEN) [62]. Other miRNAs have also been shown to regulate EC functions in response to oxidative stress, including miR-34a and miR-217. Both miRNAs regulate SIRT1 signaling [63–65]. SIRT-1 controls EC function against oxidative stress through different mechanisms, such as the increase in NO bioavailability and promotion of mitochondrial biogenesis, thereby augmenting anti-oxidant defenses and preventing senescence [66].

In the atherosclerotic process, endothelial dysfunction and excessive ROS boost the expression of adhesion molecules, inflammatory cytokines and chemotactic factors promoting leucocyte adhesion and transmigration [67]. As a consequence, migrated leukocytes inside the neointima engulf ox-LDLs and enhance macrophage and foam cell differentiation [68]. In this scenario, miR-633 and miR-21 stimulate monocyte adhesion to the endothelium during oscillatory flow by targeting peroxisome proliferator-activated receptor α (PPARα) [69, 70], whereas miR-92a is downregulated during laminar shear flow and upregulates the atheroprotective KLF2 [61] and the pro-inflammatory KLF4 [71]. On the other hand, miR-125a-5p and miR-155 inhibit lipid uptake and the inflammatory responses in ox-LDL-stimulated monocytes/macrophages [72]. Similar effects occur through the action of miR-146a, which hampers ox-LDL uptake and the inflammatory response through targeting toll-like receptor 4 (TLR4) and as a consequence, the inhibition of its downstream signaling cascade [73]. Other miRNAs, such as miR-9, regulates the expression of peroxisome proliferator-activated receptor δ (PPARδ) in human monocytes, negatively affecting the inflammatory response [74].

ROS can also modulate miRNA levels in monocytes/macrophages. In this regard, oxidative stress downregulates miR-27a* and miR-27b* expression in RAW264.7 cells [75]. Both miRNAs inhibit the nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) response induced by lipopolysacharide (LPS). Altogether these results demonstrate that miRNAs regulates ROS production and that ROS production also regulates miRNA expression.

ROS, Vascular Smooth Muscle Cells and atherogenesis

Vascular smooth muscle cells (VSMCs) are mainly involved in the regulation of blood pressure due to contractile tonus. Nonetheless, during atheroma formation both biochemical and mechanical signals promote reprogramming of these stromal cells, switching them from a contractile to a phagocyte-like phenotype [76]. These responses also include changes in migration, proliferation, secretion of proteases and finally apoptosis [77]. VSMCs, apoptosis and secretion of proteolityc enzymes are determinants of plaque instability, rupture and thrombosis when the haemo/necro/lipidic core is exposed to the bloodstream. Indeed, the lipid rich core is six times more thombogenic than any other component from the plaque [78]. The phenotypic changes suffered by VSMCs in the plaque can be modulated by miRNAs, such as miR-27 or miR-146a, among others [79]. MiR-27 has been shown to participate in mostly all known processes that take place in atherosclerosis including inflammation, lipid metabolism, oxidative stress, insulin resistance and type 2 diabetes [80]. MiR-146a controls VSMC functions by regulating the expression of the anti-proliferative KLF4, promoting VSMC proliferation in vitro and neointimal hyperplasia in vivo [79]. Similar to miR-210 and miR-21, miR-146 has also been reported to be dysregulated in human atherosclerotic plaques, while miR-21 is responsible for protecting VSMCs against oxidative stress-induced apoptosis [51, 81].

Cholesterol can promote VSMC transdifferentiation to macrophage-like cells, thereby enhancing the lipid pool in the plaque [76]. One of the mechanisms that allows the ox-LDLs to be engulfed is through the lectin-like oxidized LDL receptor 1 (LOX-1) in VSMCs. As a consequence of this uptake, the production of reactive species is increased in the vasculature [82, 83]. Let-7g has been shown to modulate the uptake of ox-LDL through LOX-1, as well as VSMC apoptosis and ROS production, which is dependent on NADPH activity [84]. Furthermore, ox-LDLs can upregulate miR-29b levels which results in an increased synthesis of metallopeptidase 2/9 (MMP2/9), thus favoring plaque instability through reduction of collagen content [85]. Accordingly, it was recently shown that miR-29 mediates the down-regulation of extracellular matrix proteins, thereby promoting plaque rupture or aneurysm formation [86].

Iron metabolism, ROS and atherogenesis

Other molecules present at high levels in the thrombogenic plaque, such as iron, are also involved in oxidative processes in atherosclerosis and are modulated by miRNAs. Iron metabolism is essential for cell survival since it is needed for the action of several enzyme complexes (i.e. ribonucleotide reductase and cytochrome P450). Nevertheless, when there is an imbalance in iron metabolism homeostasis and its levels are increased, it can promote ROS production through the FENTON reaction. Several miRNAs have been shown to regulate iron homeostasis, such as miR-210. MiR-210 has recently been described to regulate the activity of prototypical iron-sulfur scaffold protein (ISCU) controlling mitochondrial metabolism and free radical response in response to hypoxia [87, 88]. Recently, it has also been shown that miR-122 regulates systemic iron homeostasis by repressing the target genes hemochromatosis (HFE) and hemojuvelin (HJV) [89]. These mRNAs encode activators of the hormone hepcidin, which regulates iron availability and mice with reduced miR-122 levels suffer from iron deficiency [89]. MiR-122 inhibition also decreases the basic leucine zipper transcription factor 1 (BACH1) and increases heme oxygenase-1 (HO-1), a key cytoprotective enzyme with antioxidant properties repressed by BACH1 [90]. These data suggest that therapeutic targeting of miR-122 and upregulation of HO-1 may represent a new strategy for cytoprotection.

Atherosclerosis is a complex disease in which different interactions between various cell types and molecules in the vessel wall have been described. New players, such as red blood cells (RBCs) and iron content, are being highlighted to regulate lipid oxidation/accumulation and the redox status in the atheroma, besides the well-known participants such as ECs, VSMCs or monocytes/macrophages. Elevated levels of LDLs and their oxidation are believed to trigger atherosclerosis and the accumulation of modified species of lipids inside the intima is a hallmark of plaque development and instability. For example, oxidized lipids can be stored inside the cell as ceroids, or aggregates of protein and lipids typical of human plaques, which colocalize with intra- and extracellular iron content [91]. In atherosclerotic plaques, heme/iron groups are increased up to 17 times and have been reported to alter cholesterol efflux and oxidative stress in macrophages [91]. Thus, modulators of these processes, in which lipids and ROS are involved, are of high interest in research and potential targets in vascular therapeutics. While we have already revised numerous scientific findings regarding miRNA modulation of lipid metabolism and redox homeostasis, most of these recent and exciting findings still must be clearly elucidated as a single miRNA (e.g. miR-146a) can exert different functions depending on the cell type in which it is expressed. Furthermore, a single mRNA target can be regulated by several miRNAs. In addition, the complex network of communications established by the cellular milieu in the atherosclerotic plaque requires further studies to reach a therapeutic decision in atherosclerosis.

3. Circulating miRNAs

While the idea of intercellular communication through small vesicles containing mixtures of proteins and nucleic acids was proposed over 30 years ago [92], the presence of cell-type specific miRNAs in these particles has only recently been reported. Cells can selectively package certain miRNAs and are actively secreted into the blood in membrane-derived vesicles [93, 94], lipoproteins, such as HDL [95], and AGO2 ribonucleoprotein complexes [96]. Specifically, circulating miRNAs have recently been shown to be very stable in the plasma and have been implicated in vascular diseases [97, 98]. Despite this, the diagonostic and prognostic properties of these miRNAs are still highly controversial [99]. These extracellular miRNAs have become a focus of attention because of their potential as novel disease biomarkers. Among others, cardiovascular diseases, such as atherosclerosis are characterized by differential plasma miRNA profiles compared with healthy populations [97, 100, 101]. Circulating miRNAs are biologically active since recipient cells show altered gene expression [102, 103]. HDL particles are also able to deliver miRNAs to recipient cells. Interestingly, the miRNA profiles of HDL particles are different in healthy people than in subjects with familial hypercholesterolemia [95]. These interactions can be performed in several different fashions and miRNAs can serve as bridges of communication between cells in the vasculature. In recent studies, it has been shown that extracellular vesicles secreted by shear-stressed ECs enriched in miR-126 or miR-143/145 are engulfed by VSMCs thereby regulating target-gene expression in host cells [104, 105]. Conversely, increased proliferation of ECs can be achieved by exogenous miRNAs secreted by other cells from the vasculature, such as monocytes [103].

Therefore, a new potential role for miRNAs as a possible form of intercellular communication like hormones can be considered. There is increasing interest in the knowledge of the mechanisms that control miRNA extracellular export, cell-specific targeting and recognition machinery. In this regard, the physiological “_in vivo_” roles have to be definitively established; therefore, it is likely that future research on secreted miRNAs will open new therapeutic approaches for cardiovascular disease treatment.

CONCLUSIONS

There is a tremendous interest in the therapeutic application of miRNA inhibitors and miRNA mimics to treat lipid-related disorders. The high conservation of miRNA sequences between species suggests that the biological pathways modulated by miRNAs might also be conserved, making them attractive research targets with potential therapeutic applications. One of the better-studied miRNAs that illustrates this phenomenon is miR-33. Nonetheless, caution should be taken before translating data from murine models to human therapies. A good example derives from miR-33b, which is absent in the mouse genome. Additionally, a given miRNA can be predicted to regulate several hundred genes, in the same way that a gene can be regulated by more than one miRNA. Thus, the contribution of each miRNA in modulating its target gene expression levels will be determined by the relative abundance of each miRNA in different tissues and the biological stimuli that regulates their expression. Therefore, it seems likely that a combination therapy might improve the prognosis for patients with cardiovascular disease.

HIGHLIGHTS.

ACKNOWLEDGMENTS

This work was supported by grants from the National Institutes of Health R01HL107953 and R01HL106063 (to C.F.-H.). N.R. is supported by the Ministerio de Educación (Programa Nacional de Movilidad de Recursos Humanos del Plan Nacional de I-D+i 2008-2011). Figures were produced using Servier Medical Art (www.servier.com).

Footnotes

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DISCLOSURES

C.F.-H has patents on the use of miRNA-33 inhibitors.

References