Journal of Cardiology Study & Research Category: Clinical Type: Review Article

Microrna Associated with Generation, Development, and Maintenance of Atrial Fibrillation

Fei Peng1, Hui Gong1*, Lubna Nadeem2*, Lingyun Zhang3 and Guoxiong Xu3*
1 Department Of Internal Medicine, Division Of Cardiology, Jinshan Hospital, Shanghai, China
2 Lunenfeld Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Canada
3 Center Laboratory, Jinshan Hospital, Fudan University, Shanghai, China

*Corresponding Author(s):
Hui Gong
Department Of Internal Medicine, Division Of Cardiology, Jinshan Hospital, Shanghai, China
Lubna Nadeem
Lunenfeld Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Canada
Guoxiong Xu
Center Laboratory, Jinshan Hospital, Fudan University, Shanghai, China

Received Date: Jun 10, 2014
Accepted Date: Aug 19, 2014
Published Date: Sep 02, 2014


MicroRNAs (miRNAs) are a class of small non-coding RNAs, playing important roles in the regulation of the cardiovascular function. MiRNAs are associated with the generation, development, and maintenance of atrial fibrillation through the regulation of the gene expression on targets of ion channels, transporters, calcium binding proteins, extracellular matrix proteins, and other factors. Understanding the relationship between miRNAs and atrial fibrillation is critical to identifying the diagnostic markers, prognosis and therapeutic targets.


Atrial fibrillation; Electrical remodeling; Gene regulation; MicroRNA; Structural remodeling


AF - Atrial Fibrillation
Ang II - Angiotensin II
APD - Action Potential Duration
AT1-R - Angiotensin II Type 1 Receptor
CACNA1C - Calcium Channel Voltage-Dependent L Type Alpha 1C Subunit
CACNB1 - Calcium Channel Voltage-Dependent Beta 1 Subunit
CaMKII - Calcium/Calmodulin-Dependent Protein Kinase II
COL1A1 - Collagen Type I Alpha 1
COL3A1 - Collagen Type III Alpha 1
CTGF - Connective Tissue Growth Factor
DGCR8 - DiGeorge Syndrome Critical Region 8
ERK1/2 - Extracellular Signal-Regulated Kinase1/2
ECM - Extracellular Matrix
ERP - Effective Refractory Period
GJA1 - Gap Junction Alpha 1 Protein
ICa2+ - Intracellular Calcium Current
IK1 - Inward Rectifier Potassium Current
KCNJ2 - Inwardly-Rectifying Channel, Subfamily J, Member 2
KCNN3 - Potassium intermediate/small conductance calcium-activated channel subfamily N member 3
LOX - Lysyl Oxidase
MAPK - Mitogen-Activated Protein Kinase
miR or miRNA - MicroRNA
mRNA - Messenger RNA
NF-?B - Nuclear Factor-?B
PDCD4 - Programmed Cell Death 4
PP2A - Protein Phosphatase
PTEN - Phosphatase and Tensin Homology
RAAS - Renin-Angiotensin-Aldosterone System
Rac1 - Ras-Related C3 Botulinum Toxin Substrate 1
RISC - miRNA-Induced Silencing Complex
RNA - Ribonucleic Acid
RNase - Ribonuclease
RyR2 - Ryanodine Receptor Type 2
SK3 - Small-Conductance Calcium-Activated Potassium Channel 3
Spry1 - Sprouty Homolog 1
TGF-ß - Transforming growth factor-ß
TGF-ßRII - TGF-ß Receptor Type II
THRAP1 - Thyroid Hormone-Associated Protein 1
UTR - Untranslated Region


Atrial Fibrillation (AF) is the most common sustained arrhythmia which affects quality of life drastically [1]. The incidence of AF is 16.8% and 7.6% in men and women, respectively [2]. AF can cause and exacerbate heart failure. Also it is a significant risk factor for ischemic stroke [3,4] and therefore a major cause of cardiovascular morbidity and mortality [5]. Although a copious body of both basic and clinical research exists on AF, not all of the specific pathophysiological mechanisms of the generation, development and maintenance of AF are fully understood. Evidence shows that multiple factors are involved in the generation and development of AF. These factors include oxidative stress, systemic inflammation, autonomic imbalance, endocrine disorders, early electrical remodeling, such as shortened atrial Effective Refractory Period (ERP) and Action Potential Duration (APD) [6], and late mechanical remodeling, such as cardiac hypertrophy and myocardial fibrosis [7]. Recently a few studies have unveiled that miRNAs expression and/or deregulation can influence the generation, development and maintenance of AF. This review focuses on the current understanding about the role and function of miRNAs in AF.


MiRNAs are highly conserved, non-coding endogenous and single-stranded RNAs, which bind to the 3'-Untranslated Regions (UTRs) of target mRNAs to regulate the expression of target genes [8]. MiRNA-mediated post transcriptional gene regulation involves the degradation of the target mRNA or the suppression of its translation depending upon the sequence complementarity between the miRNA seed-sequence and the 3'-UTR of the target mRNA. Partial binding between seed sequence and target mRNA results in the repression of translation, whereas extensive pairing complementarity leads to the degradation of target mRNA [9-11].

The multiple-to-multiple relationship between miRNAs and their targets is recognised [12]. In such relationships one miRNA can target several genes and similarly several miRNAs or a miRNA cluster can target one single gene. Generally, the biological processes of miRNA biogenesis include four steps. First, generation/transcription of primary transcript called primary-miRNA (pri-miRNA) is mediated by RNA Polymerase II in the nucleus [9], which is then polyadenylated and capped by 7-methylguanosine [13]. Second, the pri-miRNA is cleaved by Drosha, a Ribonuclease (RNase) III enzyme, with its co-activator partner, DGCR8 (DiGeorge Syndrome Critical Region 8, a microprocessor complex unit) to form precursor miRNA (pre-miRNA) [14,15]. The third step involves the cytosol export of pre-miRNA by the protein Exportin 5/Ran-GTP complex [16] and further cleavage into a mature miRNA by Dicer, another RNase III enzyme [14]. In the fourth and the last step, the double-stranded mature miRNA is dissociated and incorporated into the miRNA-Induced Silencing Complex (RISC) which then targets complementary mRNAs [15,17] (Figure 1). Typically, miRNA expression is time and tissue type-specific [18].

Figure 1: Biogenesis and function of miRNA.

The nucleus primary-miRNAs (pri-miRNA) are transcribed from long miRNA genes mediated by RNA polymerase II and cleaved by the Ribonuclease III (RNase III) endonuclease Drosha with its partner DGCR8 to turn into precursor-miRNAs (pre-miRNA), which then move from the nucleus to the cytoplasm where the cytoplasmic enzyme Dicer further cleaves the pre-miRNA into double-stranded mature miRNA. The mature miRNAs are incorporated into the RNA-Induced Silencing Complex (RISC). A mature miRNA binds to its target mRNA at 3'-UTR, leading to mRNA degradation or transcriptional repression.

MiRNAs are associated with many physiological processes: embryonic development, cell proliferation, differentiation, apoptosis, autophagy, and tissue or organ formation and remodeling. Especially in the heart, miRNAs play a vital role in angiogenesis, fibrosis, myocardial cells regeneration, and cardiac remodeling and therefore considered to be strong potential tools for the diagnosis and treatment of heart related diseases [9,19-21]. MiRNAs can affect cardiomyocyte excitability and conductivity by the regulation of ion channels permeability, transporters and associated regulatory proteins which can lead to different forms of arrhythmias [22]. The expression of miRNA spectrum in atrial tissue is significantly different in mitral stenosis patients with AF compared with healthy subjects [23]. AF alters the miRNA expression profiles of the left atria of mitral stenosis patients [24], suggesting that miRNA may be involved in the generation and development of AF. In fact, AF is a complex pathology, involving both primary electrical and structure factors. Different miRNA families are associated with different aspects of AF (Table1).

miRNA Target Function Possible role in AF Reference
miR-1 KCNJ2 GJA1 RyR2 Abnormal Ca2+ handling Atrial electrical remodeling [25]
miR-19 CTGF Extracellular matrix, myocardial fibrosis Atrial structural remodeling [26]


MMP-2 expression increase, extracellular matrix, myocardial fibrosis Atrial structural remodeling [27,28]
miR-26 KCNJ2 IK1 increase Atrial electrical remodeling [29]
miR-29 COL1A1 COL3A1 Collagen secretion, inflammation Atrial structural remodeling [30]
miR-30 Ang II Myocardial hypertrophy Atrial structural remodeling [31]
miR-133 ERK1/2 TGF- ß1 TGF-ßRII Myoblast proliferation, myogenesis Atrial structural remodeling [32,33]
miR-155 AT1-R Endothelial dysfunction, vascular remodeling, inflammation Atrial structural remodeling [34]
miR-208 THRAP1 myostatin Myocardial hypertrophy Atrial structural remodeling [35]
miR-328 CACNA1C CACNB1 Ica2+ reduction Atrial electrical remodeling [36]
miR-499 KCNN3 Abnormal Ca2+ handling Atrial electrical remodeling [37]
miR-590 TGF- ß1 TGF-ßRII Collagen content increase Atrial structural remodeling [33]
Table 1: Different miRNAs with potential roles in atrial fibrillation.
Atrial Fibrillation (AF) is characterized by atrial electrical remodeling and structural remodeling.


The mechanisms of AF are complex, but recent studies have shown that miRNAs contribute to the generation and regulation of AF in several ways (Figure 2). For example, miRNAs can induce cardiac immune/inflammatory response [38,39] and affect ion channels as well as structural and electrical remodeling including intracellular calcium overload [40]. These, in turn, can result in shortening of the action potential ERP and APD, which is conducive to the formation of reentry [4].

Figure 2: MiRNAs associated with atrial fibrillation.

Two mechanisms generate and develop atrial fibrillation by making substrate more prone to reentry. MiR-1, miR-26, miR-328 and miR-499 regulate atrial electrical remodeling through the modulation of ion channel (IK1, Ica2+) activity and expression. MiR-19, miR-21, miR-29, miR-30, miR-133, miR-155, miR-208 and miR-590 result in the increase of collagen secretion and extracellular matrix deposition which leads to atrial structural remolding. IK1, inward rectifier potassium current. Ica2+, intracellular calcium current.

miR-29: Role in cardiac immune response

MiR-29 has a crucial role in the generation and development of AF. The down-regulation of miR-29 can induce the fibrosis of the liver [41] and lung [42] and can also cause aneurysms [43]. The risk of AF prevalence is increased by 30% with celiac disease [44]. Overall, inflammation and chronic inflammatory diseases, such as psoriasis, also increase the risk of AF [45]. Therefore, AF is partially moderated by the humoral and systemic inflammatory response induced by local fibrosis. The miR-29 family (miR-29a, miR-29b and miR-29c) is expressed in T and B cells, dendritic cells and thymic epithelial cells, which play a regulatory role in the adaptive immune pathway [46]. Multiple biopsy specimens in left atria with AF have shown lymphocytic myocarditis in 66% of patients and noninflammatory localized cardiomyopathy in 17% of patients [47]. In the canine model of AF, miR-29b was found to target Collagen-1A1 (COL1A1), Collagen-3A1 (COL3A1) and fibrilin [30], which are the prime markers of tissue remodeling. Moreover, the serum level of miR-29b is reduced in patients with AF by 54%, strongly implicating its contribution towards this ailment. The pro-inflammatory factors like Transforming Growth Factor-ß (TGF-ß) [48] and Nuclear Factor-?B (NF-?B) are reported to be the upstream regulators of miR-29 [49].

miR-26, miR-328 and miR-499: Role in regulation of ion channels

The miR-26 family (miR-26a-1, miR-26a-2 and miR-26b) can increase susceptibility to AF by altering the inward rectifier potassium current (IK1). IK1 is the major potassium current of myocardial repolarization, which partially regulate cell excitability and APD. The lower expression of miR-26 in patients with AF and murine atrial tissue induces KIR2.1 and KCNJ2 expression and shortens APD [29], suggesting that the downregulation of miRNA-26 promotes the formation of AF. MiR-26 activates T cell nuclear factor. An elevated T cell nuclear factor in atrial tissue, in turn, reduces the expression of miR-26, leading to the increase in inward rectifier current.

MiR-328 is involved in a variety of physiological and pathological processes of tissue organization, such as the formation of senile dementia [50], primary biliary cirrhosis [51] and chronic bladder pain syndrome [52]. AF is a characterized by abnormal excitability via myocardial calcium overload (e.g. the outflow rate of calcium ions), potentiating the development and maintenance of AF [53]. It has been reported that miR-328 plays an essential role in development of AF [54]. Through microarray analysis, a recent study has shown a 3.5 fold increase in the miR-328 level in eight week samples from a right atrial tachyarrhythmia canine model compared with control. It has also been shown that overexpression of miR-328 increases the susceptibility of animals towards AF, whereas blocking its expression through chemicals or gene knockdown reduces it. In-silico analysis has revealed that calcium channel regulatory genes, such as CACNA1C and CACNB1 (L-type calcium channels a1c and ß1 subunit, respectively), are the targets of miR-328 [36]. MiR-328-mediated inhibition of the L-type calcium channels results in shortening of the action potential duration enhancing the risk of AF development [55]. Furthermore, the expression of miR-328 was found to have a positive correlation with left atrial diameter, suggesting that miR-328 plays a central role in atrial electrical activity.

Mir-499 has been recently shown to target KCNN3 which encodes the small-conductance Ca2+-activated K+ channel 3 (SK3) and potentially contribute to the electrical remodeling event in AF [37].

miR-1 and miR-133: role in regulation of Ca2+ cycling

Mir-1 and miR-133 are two major muscle-specific miRNAs whose deregulation has been associated with the extrasystolic spontaneous Ca2+ release from sarcoplasmic reticulum and the generation of arrythmogenesis after depolarization [22,56]. Increased occurrence of spontaneous Ca2+ release at the molecular level was found to be due the dissociation of Ryanodine Receptors (RyR2s) with the Protein Phosphatase (PP2A) resulting in increased phosphorylation of RyR2s. In canine model of heart failure, high levels of miR-1 and miR-133 were found to be correlated with the down regulation of the regulatory and catalytic subunits (B56a and B56ß) of PP2A and the subsequent increase in Calcium/Calmodulin-dependent protein kinase II (CaMKII) mediated RyR2 hyperphosphorylation resulting in Ca2+ release [57].


AF is maintained by a variety of factors. For example, local atrial structural remodeling (atrial dilatation, tissue fibrosis and scarring etc.) contributes to the formation of reentry substrate resulting in the abnormalities of the atrial internal electrical conduction. The miRNA-mediated regulation of the Connective Tissue Growth Factor (CTGF), Lysyl Oxidase (LOX) and Renin-Angiotensin-Aldosterone System (RAAS) results in atrial collagen deposition and fibrosis, leading to the maintenance of AF [58].
miR-21 and miR-590: Role in Collagen Deposition
MiR-21 is involved in a variety of cancers and participates in tumor cell apoptosis, invasion and metastasis [59]. In the cardiovascular system, however, miR-21 leads to atrial fibrosis and structural remodeling and increases the risk and duration of AF [60]. MiR-21 has shown to increase the risk of AF. The Phosphatase and Tensin homolog gene (PTEN) has been identified as a miR-21 target gene. The PTEN-Akt pathway participates in Extracellular Matrix (ECM) remodeling in atria through MMP2 regulation which leads to atrial fibrosis [27,28]. A recent study has identified another target of miR-21 called Sprouty homolog 1 (Spry1) jointly involved in the regulation of atrial fibrosis [58]. The lower Spry1 level activates the Mitogen-Activated Protein Kinase (MAPK) signaling pathway, increases the number of fibers, and promotes the secretion of growth factors, leading to myocardial fibrosis and tissue remodeling [61,62]. Angiotensin II (Ang II)-induced factors, such as Ras-related C3 botulinum toxin substrate 1 (Rac1), CTGF and LOX, decrease the level of miR-21 resulting in increased Spry1 level in atrial tissue which affects electrical conduction and atrial structure remodeling [26,58]. In mice with increasing age, transgenic cardiac overexpression of Rac1 results in spontaneous AF and fibrosis. However, the inhibition of the expression of miR-21 can effectively prevent atrial fibrosis, reducing associated risk factors for AF.

MiR-590 has recently been correlated with AF due to its role in reducing collagen production and deposition, which is a significant source of atrial fibrosis. In nicotine induced canine models, collagen content was found to be significantly increased, coincident with an increase in TGF-ß/TGF-ßRII and a decrease in miR-590 levels [33].
miR-155 and miR-19: Role in activation of renin-angiotensin-aldosterone system
MiR-155 can target the 3'-mRNA of Ang II Type 1 Receptor (AT1-R) and inhibit AT1-R activation. Endothelial dysfunction, vascular remodeling, and inflammation are prevented by miR-155, which slows down the changes in cardiac structure and reduces the progression of AF [34]. MiR-155 levels in atrial tissue may be reduced in patients with AF, causing AT1-R activation, and in turn leading to a series of changes in cardiac structure and myocardial tension.

It has been shown that in the newborn mouse cardiomyocyte, the high level of miR-19b significantly reduces Ang II-induced CTGF expression, decreases the accumulation of atrial ECM, and prevents atrial fibrosis [26].
miR-133 and miR-590: Role in regulation of myogenesis and atrial remodeling
MiR-133 (miR-133a and miR-133b) is involved in myoblast proliferation and differentiation. Through the next generation sequencing (Solexa), both miR133a and miR-133b were found to be upregulated during myogenesis. In C2C12 myoblasts, miR-133a and miR-133b were found to inhibit proliferation and promote differentiation by regulating ERK1/2 phosphorylation. Fibroblast Growth Factor 1 (FGF1) and PP2Ac (PP2Aca and PP2Acb) are reported to be the potential targets of miR-133a/b [32]. Several studies have reported that the down-regulation of miR-133 was observed in chronic cases of AF [33,63]. Corresponding study of the upregulation of TGF-ß and TGF-ßRII in canine model of AF confirms that TGF-ß and TGF-ßRII are miR-133 targets in atrial fibroblasts [33].
miR-30 and miR-208: Role in myocardial hypertrophy/atrial fibrosis
Atrial fibrosis is characterized by the structural alteration and hypertrophy of cardiac myocytes. Recently dysregulated autophagy has been implicated as a leading cause of myocardial hypertrophy. In the rat model of cardiac hypertrophy, a group has reported the upregulation of an autophagy related gene beclin-1 and a corresponding decrease in the expression of miR-30 in cardiac tissue [31]. Moreover CTGF, a key pro-fibrotic protein, was also found to be a target of miR-30 in rodent model of heart disease [64], implicating a negative regulatory role of miR-30 in the maintenance of AF.

MiR-208 is mainly expressed in cardiac tissue and this family consists of miR-208a and miR-208b encoded by the intron of a cardiac muscle Myosin heavy chain gene (Myh6) and ß-cardiac muscle Myosin heavy chain gene (Myh7), respectively [65]. Thyroid Hormone-Associated Protein 1 (THRAP1) and myostatin, both of which are negative regulators of muscle hypertrophy, are reported targets of miR-208 family. Transgenic expression of miR-208 in murine heart has proven hypertrophic to the cardiac tissue due to decreased expression of THRAP1 and myostatin and is sufficient to induce arrhythmias [35].


AF is a common clinical arrhythmia, but the mechanisms are not yet fully understood. MiRNAs assist in regulation, generation, development and maintenance of AF via modulations in ion channels, receptors and extracellular matrix proteins. Some miRNAs implicated in AF have potential for use as biomarkers and drug targets [66]. For example, serum miR-21 and miR-29 can be used as a noninvasive method for detecting AF and inhibition of miR-21 may prevent myocardial fibrosis to reduce the risk of AF. However, our current knowledge about miRNA and its contribution towards AF is still limited and therefore, learning more about miRNAs will provide new insights into their mechanisms of action and help us in determining effective treatment targets [67]. Data from different studies show that some miRNAs are causative while others have protective effect for AF depending upon their targets. For example, some are pro-fibrotic while others are anti-fibrotic. Similarly, some are pro-arrythmatic whereas others are anti-arrythmatic. Nevertheless, we can identify the deregulated ones to be associated with the disease development and/or maintainance and use them as biomarkers, at least, for that ailment. Future research in this direction is needed, including gathering of larger data sets from animal models and in-depth analysis of the role of miRNAs in the pathogenesis of AF. The definitive function of a particular miRNA can however be evaluated by the knockdown studies, after which the therapeutic potential could be assessed. The functional analysis through miRNA overexpression and their knockdown through anti-miRNA oligos can provide insight about their role in the pathogenesis and/or maintenance of a particular disease. This will help in the development of clinical trials to test miRNA-based therapeutic drugs. In case of AF there is substantial evidence regarding the role of miRNAs in the development and maintenance of the disease. Thus, the beneficial effect of using miRNA for AF seems to hold a lot of promise for future treatments and therapies.


This work was supported by grants from National Natural Science Foundation of China (81272880), the Shanghai Committee of Science and Technology (124119b1300), Shanghai Municipal Health Bureau (2012-186) and a start-up fund of research from Jinshan Hospital (2012-2) to GX.


The authors have nothing to disclose.


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Citation: Peng F, Gong H, Nadeem L, Zhang L, Xu G (2014) Microrna Associated With Generation, Development, and Maintenance of Atrial Fibrillation. J Cardiol Stud Res 1: 003.

Copyright: © 2014  Fei Peng, 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.

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