MicroRNAs and the regulation of fibrosis

Authors

  • Xiaoying Jiang,

    1.  Department of Genetics and Molecular Biology, School of Medicine, Xi’an Jiaotong University, Shaanxi, China
    2.  NIHR Translational Research Facility in Respiratory Medicine Group, School of Translational Medicine, Stopford Building, University of Manchester, UK
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  • Eleni Tsitsiou,

    1.  NIHR Translational Research Facility in Respiratory Medicine Group, School of Translational Medicine, Stopford Building, University of Manchester, UK
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  • Sarah E. Herrick,

    1.  NIHR Translational Research Facility in Respiratory Medicine Group, School of Translational Medicine, Stopford Building, University of Manchester, UK
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  • Mark A. Lindsay

    1.  NIHR Translational Research Facility in Respiratory Medicine Group, School of Translational Medicine, Stopford Building, University of Manchester, UK
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Xiaoying Jiang, Department of Genetics and Molecular Biology, Medical College of Xi’an Jiaotong University, 76 Yanta West Road, Xi’an 710061, Shaanxi, China
Fax: +86 2987864621
Tel: +86 2982657013
E-mail: jiangxy@mail.xjtu.edu.cn

Abstract

MicroRNAs (miRNAs) are small, noncoding RNAs of 18–25 nucleotides that are generally believed to either block the translation or induce the degradation of target mRNA. miRNAs have been shown to play fundamental roles in diverse biological and pathological processes, including cell proliferation, differentiation, apoptosis and carcinogenesis. Fibrosis results from an imbalance in the turnover of extracellular matrix molecules and is a highly debilitating process that can eventually lead to organ dysfunction. A growing body of evidence suggests that miRNAs participate in the fibrotic process in a number of organs including the heart, kidney, liver and lung. In this review, we summarize our current understanding of the role of miRNAs in the development of tissue fibrosis and their potential as novel drug targets.

Abbreviations
CTGF

connective tissue growth factor

ECM

extracellular matrix

ERK

extracellular regulated kinase

FGF

fibroblast growth factor

HSC

hepatic stellate cell

miRNA

microRNA

MMP

matrix metalloproteinase

MRE

miRNA-recognition element

PI3K

phosphoinositol 3-kinase

PTEN

phosphatase and tension homolog

TGF-β

transforming growth factor-β

TNF-α

tumor necrosis factor-α

Introduction

MicroRNA (miRNA)-mediated RNA interference has been identified as a novel mechanism that regulates gene expression at the translational level [1,2]. These short RNA sequences of 20–23 nucleotides are produced by the processing of full-length mRNA-like transcripts known as primary miRNAs [3,4]. These larger primary miRNA transcripts undergo enzymatic cleavage by the RNase III Drosha to produce precursor miRNAs of ∼70 nucleotides. These are then transported to the cytoplasm where they are further processed by another RNase III enzyme, dicer, to produce double-stranded RNAs of 21–23 nucleotides. One strand, the mature miRNA, is then loaded into the RNA-induced silencing complex where it is believed to either repress mRNA translation or reduce mRNA stability following imperfect binding between the miRNA and the miRNA-recognition elements (MRE) within the 3′-UTR of target genes. Specificity of the miRNA is thought to be primarily mediated by the ‘seed’ region that is localized between residues 2 and 8 at the 5′ end [5–7].

In most circumstances, miRNAs are believed to either repress mRNA translation or reduce mRNA stability following imperfect binding between the miRNA and the MREs within the 3′-UTR of target genes. The specificity of the miRNA guide strand is thought to be mediated by the ‘seed’ region localized between residues 2 and 8 at the 5′ end [5–7], and the specificity also appears to be influenced by additional factors such as the presence of, and cooperation between, multiple MREs [8,9], the spacing between MREs [9,10], proximity to the stop codon [9], the position within the 3′-UTR [9], the AU composition [9] and the target mRNA secondary structure [11]. However, recent studies have also suggested that miRNAs might enhance mRNA translation in nonproliferating or amino-acid starved cells. Thus, serum starvation and cell-cycle arrest was shown to increase tumor necrosis factor-α (TNF-α) release by a mechanism that involved the binding of miRNA-369-3 to the AU-rich elements within the 3′-UTR of TNF-α and the interaction between two miRNA-induced silencing complex-associated proteins, Ago 2 and fragile-X-mental-retardation-related protein 1 (FXR1) [12,13]. In similar studies, Orom et al. [14] have demonstrated that miRNA-10a increases ribosomal protein expression following amino acid starvation and in response to cellular stress. In this case, the action of miRNA-10a was shown to be mediated through binding within the 5′-UTR (and not the 3′-UTR) of mRNA at regions immediately downstream of the regulatory 5′-TOP motif [14]. It therefore appears that although miRNAs predominately repress translation through binding within the 3′-UTR of target mRNA, individual miRNAs might also increase mRNA translation and bind regions within the 5′-UTR.

There is now overwhelming evidence that miRNAs regulate diverse biological processes including cell proliferation, differentiation and apoptosis, and that aberrant miRNA expression/action can lead to the development of multiple diseases. Fibrosis is characterized by the excess deposition of extracellular matrix (ECM) components, which is the end result of an imbalance of metabolism of the ECM molecule. Irregularities in multiple pathways involved in tissue repair and inflammation can lead to the development of fibrosis. Collagens are the predominant ECM proteins, while other ECM proteins such as fibronectins, elastin and fibrillins also have an important role in the development of fibrosis [15]. Fibrosis is likely to result from both an increased synthesis and decreased degradation of ECM components. In particular, matrix metalloproteinases (MMPs) that degrade the ECM may be up-regulated, while their inhibitors, tissue inhibitor of metalloproteinases, may be down-regulated. Collagens are synthesized by many cell types, but mainly by mesenchymal cells, including fibroblasts. Following tissue injury, fibroblasts differentiate into myofibroblasts and, often, persistent activation of the myofibroblast phenotype with a resistance to apoptosis ensures the development of fibrosis. A number of profibrotic mediators have been identified, and transforming growth factor-β (TGF-β) is proposed to play a central role in many fibrotic conditions. Extensive tissue remodeling and fibrosis can ultimately lead to failure of a number of organs. Although current treatments typically target the inflammatory response, the mechanism of fibrosis is poorly understood and there are few effective therapies. For these reasons, and knowing the multitude of pathways that miRNAs can affect, it is envisaged that investigating the roles of miRNAs in fibrosis could not only advance our understanding of the pathogenesis of this common condition, but might also provide new targets for therapeutic intervention. In this regard, we have reviewed the growing body of evidence which suggests that miRNAs are involved in the process of fibrosis in several organs, including heart, lung, kidney and liver (Fig. 1).

Figure 1.

 Overview of the role of miRNAs in fibrosis.

miRNA and cardiac fibrosis

Cardiac fibroblasts are the most numerous cell type in the heart and are central to the regulation of cardiac ECM metabolism [16]. Excess deposition of ECM components in the heart is associated with numerous cardiovascular diseases, including hypertension, myocardial infarction and cardiomyopathy, and there is now accumulating evidence that implicates miRNAs in the modulation of these conditions [17–21].

The overall importance of miRNAs was shown by Da Costa Martins et al. [22], who reported that conditional deletion of dicer (an enzyme that is central to miRNA metabolism) in the mouse myocardium resulted in cardiomyocyte hypertrophy and remarkable ventricular fibrosis. Subsequent articles have helped to clarify the roles of individual miRNAs in cardiac fibrosis. Using in situ hybridization, Thum et al. [23] found that miR-21 was selectively expressed in cardiac fibroblasts and that miR-21 expression was greatly enhanced in the failing heart in human, mice and rats. Subsequent mechanistic studies of rat cardiac fibroblasts showed that increased miR-21 expression enhanced extracellular regulated kinase (ERK) signaling by targeting the down-regulation of the ERK inhibitor, sprouty homolog 1 (Spry1). In turn, this promoted fibroblast survival and fibroblast growth factor (FGF) secretion, leading to fibroblast proliferation and ECM/collagen deposition in vitro [23]. Significantly, in vivo silencing of miR-21 using an ‘antagomir’ was shown to reduce cardiac ERK kinase activity and inhibit interstitial fibrosis and cardiac dysfunction in a mouse mode of cardiac hypertrophy induced by overloaded pressure [23]. Increased expression of miR-21 has also been demonstrated in the infarct zone of hearts subjected to ischemia-reperfusion, especially in cardiac fibroblasts [24]. Under these circumstances, increased miR-21 expression was shown to target the down-regulation of phosphatase and tension homolog (PTEN), which negatively regulates the phosphoinositol 3-kinase (PI3K)-Akt signaling pathway [24]. The subsequent activation of the PI3K-Akt pathway increased the expression of matrix metalloproteinase-2, which is known to degrade ECM and permit the infiltration of fibroblasts [24].

The miR-29 family has also been implicated in cardiac fibrosis following a report showing down-regulation of the miR-29 family members (miR-29a, miR-29b and miR-29c) in the border zone of murine and human hearts during myocardial infarction [25]. This study also showed down-regulation of miR-149 and increased expression of miR-21, miR-214 and miR-223, although the functional consequences of these changes are unknown. Multiple target genes of the miR-29 family were identified, including ECM proteins such as collagens, fibrillins and elastin, and it was speculated that TGF-β-mediated down-regulation of miR-29 would enhance fibrosis. This was confirmed by demonstrating decreased collagen expression in cultured mouse cardiac fibroblasts transfected with miR-29b mimics and increased collagen expression in mouse liver, kidney and heart following the administration of a cholesterol-modified inhibitor by tail vein injection [25].

Connective tissue growth factor (CTGF) is known to be a potent inducer of tissue fibrosis in multiple tissues, including the heart. Interestingly, Duisters et al. [26] have shown that miR-133 and miR-30 target the down-regulation of CTGF expression in cultured rat cardiomyocytes and fibroblasts. Investigations using rodent models of cardiac hypertrophy and samples from patients with left ventricular hypertrophy showed a reduction in miR-30 and miR-133 expression that was inversely correlated with CTGF, collagen and fibrosis levels [26]. The potential importance of miR-133 has been underlined by reports that miR-133-a1 and miR-133-a2 knockout mice develop severe fibrosis and heart failure [27] and by studies showing that miR-133 and miR-590 are down-regulated in a canine model of nicotine-induced atrial interstitial fibrosis [28,29]. Interestingly, mechanistic studies in the canine models and in cultured atrial fibroblasts have shown that the protective actions of miR-133 and miR-590 are mediated through targeting the down-regulation of TGF-β1 and TGF-β receptor type II, respectively [29].

Finally, van Rooij et al. [30] have demonstrated that mice containing a miR-208 deletion, unlike wild-type mice, did not exhibit cardiomyocyte hypertrophy or fibrosis in response to aortic banding and transgenic expression of activated calcineurin. Although deletion of miR-208 was shown to attenuate expression of the β-myosin heavy chain in heart tissue, the mechanism by which miR-208 impacts on the fibrotic process is unknown.

miRNAs and pulmonary fibrosis

Pulmonary fibrosis is characterized by excessive deposition of collagen and other ECM proteins within the pulmonary interstitium and is commonly associated with the up-regulation of TGF-β [31]. Little is known regarding the role of miRNAs in lung fibrosis, although a recent report by Pottier et al. [32], using human lung fibroblasts, has shown that miR-155 expression was increased following treatment with TNF-α and interleukin-1β and reduced following treatment with TGF-β. Mechanistic studies indicated that increased expression of miR-155 down-regulates the production of keratinocyte growth factor (KGF, FGF-7) and increases fibroblast migration by inducing caspase-3 expression. Studies using a bleomycin-induced mouse model of lung fibrosis confirmed that the up-regulation of miR-155 was correlated with the degree of lung fibrosis in C57BL/6 and BALB/c mice [32].

miRNAs and hepatic fibrosis

Fibrosis is a common outcome of chronic hepatic diseases (including viral hepatitis, alcohol abuse and metabolic diseases) and can ultimately lead to liver cirrhosis and hepatic failure. Hepatic stellate cells (HSCs) are believed to be the main matrix-producing cells in the liver. Following multiple injurious agents and/or exposure to inflammatory cytokines, activated HSCs lose their lipid droplets, migrate to injured sites and are transformed into myofibroblast-like cells that secrete large amounts of ECM leading finally to liver fibrosis [33].

A number of reports have demonstrated an important role of miRNAs during the activation of HSCs. Thus, measurement of the changes in miRNA expression in activated rat HSCs identified 12 up-regulated miRNAs (miR-874, -29c*, -501, -349, -325-5p, -328, -138, -143, -207, -872, -140, 193) and nine down-regulated miRNAs (miR-341, -20b-3p, -15b, -16, -375, -122, -146a, -92b, -126) [34]. Interestingly, over-expression of miR-16 and miR-15b was shown to inhibit HSC proliferation and induce apoptosis through down-regulation of the mitochondrial-associated anti-apoptotic protein, Bcl-2, leading to activation of caspases 3, 8 and 9 [35,36]. In contrast to these studies, a second miRNA expression profile performed in activated rat HSCs showed increased expression of miR-27a and miR-27b [37]. In this case, inhibition of miR-27a and miR-27b reverted activated HSC back to a quiescent state, a process that was mediated by preventing the increase in expression of the miR-27a/b target, retinoid X receptor α [37]. These findings show that miRNAs play a significant role in the progression of liver fibrogenesis via HSC activation.

Steatohepatitis resulting from chronic alcoholic abuse or metabolic syndrome is a common liver disease that usually precedes liver fibrosis [38]. Using two mice models of alcoholic and nonalcoholic steatohepatitis, Dolganiuc et al. [38] has shown changed expression of five miRNAs: miR-705 and miR-1224 were up-regulated in both groups, whilst miR-182, miR-183 and miR-199a-3p were down-regulated in the alcoholic group but up-regulated in the nonalcoholic group. At the present time, the role of these miRNAs in the development of steatohepatitis is unknown.

As with cardiac fibrosis, reduced expression of miR-29a and miR-29b has been demonstrated during activation of primary rat HSCs, in biopsies of patients with hepatitis C virus infection and in a rat model of fibrosis induced by bile-duct ligation. This indicates that the miR-29 family might also have an anti-fibrogenic function in the liver, a suggestion that is supported by functional studies showing decreased collagen synthesis in HSCs following over-expression of miR-29 [39].

miRNAs and renal fibrosis

Renal fibrosis involving excessive deposition of ECM in the kidney, is a common response to chronic kidney diseases, including many kinds of nephritis, nephropathy and other nephritic diseases, which eventually leads to irreversible renal failure [40]. Diabetic nephropathy is a common complication of diabetes and also provides a good model with which to study renal fibrosis, showing progressive fibrosis in the renal glomerulus and tubulo-interstitial region that correlates with the decline of renal function [41].

Kato et al. [42] have reported that miR-192 was up-regulated in the glomeruli of type 1 and type 2 diabetic mice and in cultured mesangial cells treated with TGF-β1. They found that TGF-β1-induced miR-192 expression in mesangial cells increased the expression of collagen 1α2 by down-regulating Zeb2, an E-box repressor [42]. In a subsequent report, this group showed that down-regulation of Zeb2 resulted in increased expression of miR-216a and miR-217. This also contributed to increased collagen production and the development of diabetic nephropathy through the down-regulation of PTEN and the subsequent activation of Akt (Fig. 1) [43]. Increased expression of miR-377 is also thought to regulate the expression of fibronectin, which accumulates in diabetic nephropathy. Expression of miR-377 was up-regulated in mouse models of diabetic nephropathy and in cultured human and mouse mesangial cells treated with high concentrations of glucose and TGF-β1 [44]. Increased expression of fibronectin was shown to result from the miR-377-mediated down-regulation of p21-activated kinase and superoxide dismutase [44].

Conclusion

As outlined in this review, there is now increasing evidence that miRNAs regulate fibrosis in multiple organs including the heart, lung, kidney and liver (Fig. 1). In particular, a number of miRNAs, such as the miR-21 and miR-29 families, are emerging as common regulators of fibrosis in multiple tissues and can be divided into two groups: those that regulate the differentiation into fibrotic cells (i.e. miR-21) and those that directly target the translation of ECM components (i.e. miR-29). As there are few treatment options for fibrosis, modulation of miRNAs using either antisense strands that block their activity or over-expression from viral or plasmid vectors, has been proposed as a potentially novel therapeutic approach [45,46]. Significantly, a number of reports discussed in this review have demonstrated the feasibility of this approach in preclinical mouse models of fibrosis. Thus, van Rooij et al. [25] has shown that inhibiting miR-29 using cholesterol-conjugated antisense strands increased collagen expression in mouse liver, kidney and heart, whilst Thum et al. [23] used a similar approach to demonstrate that inhibition of miR-21 prevents interstitial fibrosis and cardiac hypertrophy in a mouse model of heart infarction. However, future developments will be crucially dependent upon understanding the function and mechanisms of action of these fibrotic miRNAs.

Acknowledgements

This work was supported by the Chinese Government Academic Exchange Programme (X.J.), National Institute of Health Research (E.T.) and the Wellcome Trust (grant no.: 076111; M.A.L.).

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