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Extracellular Micro-RNAs in Health and Disease: Basic Science, Biogenesis and Release

DOI: 10.4236/ajmb.2016.61001    4,062 Downloads   4,731 Views   Citations

ABSTRACT

Small non-protein coding micro-RNAs are regularly exported out of cells, both in health and disease. More than ninety percent of extracellular miRNAs are associated with lower-molecular-mass complexes bound to Argonaute 2 (Ago2), nucleophosmin-1 (NPM1) and high density lipoproteins (HDL), whereas the rest (~10%) are membrane-vesicle-encapsulated within exosomes, shedding microvesicles and apoptotic bodies. Regardless of the debate of the nature of circulating miRNA as byproducts of routine cell activities or mediators of cell-cell communication, proper understanding of the molecular behaviors of miRNA in health and disease, is expected to open a new gate for the discovery of new diagnostic tools and possibly therapeutic implementation in the near future.

Received 22 September 2015; accepted 2 January 2016; published 5 January 2016

1. Introduction

Since Victor Ambros and Garry Ruvkun discovered micro-RNA (miRNAs), they revolutionized our understanding of the molecular mechanisms of cell function [1] . Functional studies indicate that miRNAs participate in the regulation of almost every cellular process, and are intrinsically associated with much of human pathology [2] . MiRNAs are endogenously produced, short non-coded RNAs of 21 - 25 nucleotides that are post-transcrip- tional component of gene regulatory network that modulate the precise amounts of proteins expressed in all cell, frequently by mRNA translation repression or less often by mRNA cleavage or degradation [2] [3] .

Recently, it was also shown that mRNA may up-regulate the expression of their target genes as well [4] [5] . It is well documented that a single miRNA can influence hundreds of mRNA gene transcripts and thereby, it has been implicated as a key player in virtually all cell processes [5] - [8] . While the majority of miRNAs are found intra-cellular, a virtual number have been detected outside cells, including various body fluids (i.e. saliva, urine, breast milk, seminal plasma, tears, amniotic fluid, colostrum, bronchial lavage, cerebrospinal fluid, peritoneal fluid, and pleural fluid) from normal individuals [9] .

Cells have protective enzymatic and non-enzymatic mechanisms against oxidative stress [10] targeting reconstitution of normal cell function. However, oxidative stress occurs when the reactive oxygen species (ROS) level overwhelms defensive mechanisms [11] [12] . The produced miRNAs under these different conditions varies accordingly. Furthermore, alterations in the level and composition of these extracellular miRNAs, as part of extracellular RNAs (exRNAs), have been well correlated with disease or injurious conditions [13] - [16] , suggesting that these extracellular miRNAs can be served as diagnostic and prognostic biomarkers. The source of exRNAs can be endogenous or exogenous, including microbes and foods [17] . Recent findings show that exRNA can act as a signaling molecule, communicating with other cells and carrying genetic information from cell to cell throughout the body [1] . Circulating miRNAs are remarkably stable despite high extracellular RNase activity [9] . In addition to packing within extracellular vesicles (EVs) which are impermeable to RNases, extracellular miRNAs are also packaged in some manner to protect them against RNase digestion, through the formation of protein-miRNA complexes [18] .

It is of note here to mention that horizontal gene transfer (HGT) is occurring without genomic integration. Although the study of miRNA is still in the very early stages, current research is exploring the association between various diseases and changes in the type and amount of miRNAs. These diseases include several types of cancer, neurological disorders, heart disease, kidney disease, and more [19] - [22] . This review provides an overview of the properties of extracellular miRNAs, summarizing the current theories regarding extracellular miRNA origin and function, arguing for more compelling translation of circulating miRNAs into clinical practice.

2. Biogenesis of miRNAs (Figure 1)

Non-protein coding RNAs (ncRNAs) have linked this class of nucleic acids with a large panel of biological processes, such as homeostasis, development and carcinogenesis [23] - [25] . Different classes of small RNAs continue to be discovered. There are three major classes of animal ncRNAs; microRNAs (miRNAs), short interfering RNAs (siRNAs), and Piwi-interacting RNAs (piRNAs). MiRNAs are small, non-coding RNAs commonly found intra-cellular in all tissues and function as post-transcriptional component of gene regulators. MiRNAs can be generated in a cell by either canonical pathway or non-canonical pathways [26] - [28] . The canonical pathway is Drosha (an RNase III-like protein)/DGCR8 (DiGeorge syndrome critical region gene 8) and Dicer dependent, while the non-canonical pathway may be independent of Drosha/DGCR8 or Dicer. In both pathways, miRNAs are produced via processing and editing, resulting in the formation of mature, functional miRNAs of 21 - 25 nucleotides. Canonical pathway of miRNA biogenesis is responsible for the production of the majority of the known miRNAs. In the canonical pathway, genes are usually transcribed by RNA polymerase II (Pol II) [29] [30] . Arising from intergenic or intragenic (both exonic and intronic) genomic regions. Of note, while endogenous siRNAs originate from double-stranded (ds) RNA precursors, miRNAs and piRNAs are transcribed as long single-stranded (ss) RNAs. Primary transcripts (pri-miR), fold back to form double stranded hairpin structures which are then subjected to sequential processing; first the precursor molecules (pre-miR), 80 - 120 nucleotides long, are produced in the nucleus by type III endonuclease microprocessor DROSHA and its cofactor DGCRA8, followed by their export to the cytoplasm mediated by EXPORTIN 5.

In the cytoplasm, where they are processed by another type III endonuclease, DICER, into the short “active” molecules (guide strand), while the opposite (passenger) strand is preferentially destroyed [31] [32] . MiRNAs are finally loaded onto a multi-protein complex, called RNA-induced silencing complex (RISC), which includes argonaute (Ago) proteins (in humans four Ago proteins are recognized, Ago 1 - 4), have overlapping roles in RISC formation that mediates mRNA degradation or translational repression.

In recent years, several alternative pathways of miRNA biogenesis are identified [31] [32] . Pre-miRNA mimics, endogenous short hairpin RNA (shRNA), other hairpinstructure or other non-coding RNA, can enter the

Figure 1. Biogenesis and function of microRNA (miRNA). The majority of miRNA are synthesized through the canonical pathway, in which miRNA genes are transcribed via RNA polymerase II to produce pri-miRNA (long transcripts with multiple hairpin loop structures). Pri-miRNAs are processed by the Microprocessor protein complex containing Drosha/DGCR8, resulting in gene- ration of smaller precursor molecules called pre-miRNAs. After exported from the nucleus via Ex- portin-5, the pre-miRNAs are further processed via Dicer in the cytoplasm to generate short, double- stranded miRNAs. The mature miRNA direct RISC (a complex containing ago) to target gene mRNA, resulting in mRNA degradation (miRNA/mRNA with perfect complimentary sequences match in RNA). In the non-canonical pathways, miRNAs can be synthesized in either Drosha/DGCR8 or Dicer independent pathways. The short pre-miRNA like precursor can come from mitron, endo- shRNA or other noncoding RNA. In some special conditions, the precursor can be processed by Ago2 instead of Dicer to be the mature miRNA (Adopted from Qingquing Wei et al., 2013 [67] ).

miRNA biogenesis pathway after direct processing with or without Dicer (non-canonical pathway). The mechanism(s) of piRNA biogenesis remain elusive, and are only found in animals, and specifically in the germline [31] [32] .

Argonaute protein uptake of mature miRNA is thought to stabilize the guide strand, while the passenger strand is preferentially destroyed. Argonaute may preferentially retain miRNAs with many targets over miRNAs with few or no targets, leading to degradation of the non-targeting molecules. This turnover of mature miRNA is needed for rapid changes in miRNA expression profiles [33] . MiRNA biogenesis is critically regulated at the levels of epigenetic modulation, gene transcription and miRNA processing.

Many of the miRNA genes are flanked by promoter regions which are governed by specific transcription factors like Myc, p53, and hypoxia-inducible factor (HIF-1) [26] . These observations suggest that pathological challenges are pivotal in regulation of gene expression of miRNAs. In addition, global miRNA expression can also be modulated by the change of proteins or enzymes involved in miRNA processing, e.g. Drosha, exportin-5, Dicer and Ago [34] .

3. Circulating microRNAs

Circulating extracellular miRNAs are remarkably stable despite high extracellular RNase activity [35] . The membranes of EVs are impermeable to RNases, therefore, attributable to the remarkable stability of vesicle encapsulated miRNA. In addition to packing within EVs, extracellular miRNAs are also packaged in some manner to protect them against RNase digestion, through the formation of protein-miRNA complexes [20] [22] [24] [25] [36] [41] .

Both forms, vesicles encapsulated or protein associated, consistently revealed the presence of miRNA in almost all body fluids. Three different possibilities have been suggested to explain the different mechanisms of miRNA secretion; i) Passive leakage from injured cells or degraded cells of short half-lives, such as platelets, ii) active secretion via Extracellular vesicles (EVs) and iii) associated with lower-molecular-mass complexes [37] - [42] . Secreted miRNAs are also shown to be remarkably stable despite the austere conditions they are subjected to in both the blood stream (RNase digestion) and during handling (e.g. extreme temperatures and pH values) [43] - [48] . It has been demonstrated that EVs-associated miRNAs represent the minority, whereas about 90% of plasma circulating miRNAs are travelling in an AGO-protein-bound form [19] [45] . Similarly, about 99% of miRNAs exported by cells in culture under normal conditions were membrane-vesicle-free and associated with AGO proteins [45] . It is feasible that the differences in isolation protocols for RNAs could account for the discrepancy in the reported distribution of extracellular miRNA between EVs and protein-bound fraction of serum.

3.1. Extracellular Vesicle-Encapsulated miRNA

A major breakthrough was the demonstration that the cargo of EVs included both mRNA and miRNA could be translated into proteins by target cells [47] [48] . Recently, analysis of RNA from EVs demonstrated that EVs contain a large variety of other small noncoding RNA species, including RNA transcripts overlapping with protein-coding regions, repeat sequences, structural RNAs, tRNA fragments, piwi RNA (piRNAs) and small interfering RNAs (siRNAs) [49] [50] . Exosomes are secretory products of endosomal origin, while, microvesicles directly bud from the plasma cell membrane [51] . The mechanism of formation of exosomes is the process of the endosomal pathway, including endocytic vesicles, early endosomes, late endosomes; also known as multivesicular bodies (MVBs) and finally lysosomes [52] . The pathway of multivesicular endosomes (MVEs) that are prone to fuse with lysosomes and predestined for lysosomal degradation, differ from the pathway of secretory MVEs predestined to become secreted as exosomes; i.e. ESCRT-dependent and ESCRT-non-dependent pathways. Endosomal sorting complex responsible for transport (ESCRT) is a four multi-protein complexes assembled within the MVEs: (ESCRT)-0, -I, -II, and -III, with associate accessory proteins (e.g., Alix and VPS4). The ESCRT-0, -I, and -II complexes recognize and sequester ubiquitinated membrane proteins at the endosomal membrane, while the ESCRT-III complex is responsible for membrane budding and actual scission of intraluminal vesicles) ILVs and exosomal release [53] - [55] . An alternative pathway, independent of the ESCRT machinery has also been described, and it includes the ceramide and sphingolipid pathway, in which the enzyme natural sphingomyelinase-2 (nSMase2) is involved inmediation of exosomal release [56] [57] . Exosomes are released by a wide spectrum of cell types and their release appears to be modulated by micro-environmental milieu and influenced by growth factors, heat shock and stress conditions, pH variations and therapy [58] - [60] . The mechanisms by which EVs affect the target cells include transfer/activation of signaling protein receptors or intercellular exchange of proteins and RNAs, which are both recruited to induce phenotypic modulation in the target cells [61] .

3.2. Protein-Associated miRNA

Recently, accumulated data suggest that the majority of circulating miRNAs may not be only confined within extracellular vesicles, but a substantial fraction is also bound to protein complexes, such as high density lipoproteins (HDL), Argonaute-2 (Ago2) and nucleophosmin-1 (NPM-1). HDL bounded miRNA has been reported to be present in the plasma of healthy subjects. The uptake of HDL bounded miRNA seems to be dependent on the interplay between cholesteryl ester of HDL and the cell surface HDL receptor, named scavenger receptor class B, type I (SR-BI) [44] .

Turchinovich and colleagues [43] , showed that the majority of miRNAs found in human plasma, are associated with Ago2 and that the high proportion of Ago-miRNA may represent by-products of dead cells, since Ago-miRNA complexes, which are known to be present within Exosomes, are known to be extremely stable within cells [59] , and it may be derived from vesicles potentially damaged during purification [74] .

These findings raise indeed intriguing questions about whether these miRNAs have a different biological role and source; researchers have proposed that miRNA-protein complexes may be released into circulation as a consequence of cell lysis or necrosis, meaning that if participated in cell-cell communication this might incidentally occur under certain circumstances including cell stress and intra-cytoplasmic accumulation of unfolded or misfolded proteins. Nonetheless, it is believed that the role of these complexes has not been discovered yet.

4. MiRNA Release: Active Sorting or Byproduct of Cell Activity!

Two hypothesizes have been postulated to explain the presence of circulating extracellular miRNA, both, vesicles encapsulated or protein associated. MiRNA release either by the selective sorting system or mere byproduct of cell activity and waste disposal is yet debatable. Accumulating evidence, however, suggests that both theories can be true [43] . The hypothesis of cell activity byproduct has been claimed by the some observations; miRNA remains stable for weeks in cell lysate without enzymatic inhibition (e.g. RNases), which support the notion of simple passive release of miRNA in response to over production and cytoplasmic crowd [42] . Moreover, miRNA produced by several cell lines after three days culture under normal conditions was significantly lower than their parental cells of origin which supports this notion. Besides, the extracellular miRNA production by some cell lines is mainly (>95%) in a protein-associated state [42] . Moreover, apart from crowd and overflow release, yet, no clear indication of either active release of vesicle-free AGO2-miRNA complexes from cells or their uptake by recipient cells in mammals [43] . In contrast, miRNAs entrapped within microvesicles can horizontally transfer gene information to recipient cells, modulate gene expression and trigger functional effects [62] [63] . The exact mechanisms by which cells scission/release EVs containing miRNAs remains incompletely understood; however, the release is multifactorial and modulated particularly by extracellular signals [64] . Microvesicles are released by direct budding from the plasma cell membrane, whereas exosomes release process might be ceramide enzyme nSMase2-dependent or nondependent machinery [65] . However, exosome release is blocked by inhibiting nSMase2 (neutral sphingomyelinase 2) and interestingly, inhibition of nSMase2 actually increases the export of miRNAs by HDL [65] , suggesting two different pathways to exert the same action, meaning, two distinct mechanisms and/or competition in the export pathways. Moreover, the ESCRT-III complex is responsible for membrane budding and actual scission of intraluminal vesicles (ILVs) and exosomal release [53] - [55] . The activation of nSMase2 enzyme and ESCRT-III complex and their involvement in the release of vesicles might be a response to the crowd and overflow proposition. This means that, in case of crowd and overflow, the cell endosomal pathway is unable to cope with the abrupt increase in the need for degradation through the endocytic pathway, hence activation of an alternative pathway to eliminate and secrete these contents outside the cell. Other observations have been supporting the hypothesis of active sorting; high EVs miRNA level than that contained in the parental cells which may be explained by the observation that certain miRNAs can be lost during extraction from samples [66] . The differences in the blood collection protocols willimpact the comparison between extracellular versus intracellular miRNA profiles expressed in different cell types [67] - [71] .

5. Function of miRNA

Each class of small RNAs binds to a member of the Argonaute (Ago) family of proteins. The Argonaute protein family includes eight members (Ago 1 - 4, present in all mammalian cells and Piwi 1 - 4, found in the germ line and hematopoietic stem cells) in the human genome [68] . The siRNAs and miRNAs associate the Ago clade, whereas piRNAs associate the Piwi clade [69] . The Ago protein bound to the small RNA comprises the RNA- induced silencing complex (RISC). The RISCs containing miRNAs are primarily target messenger RNAs (mRNAs) by either complete complementarity causing degradation of the mRNAs or incomplete complementarity, causing translation repression (slowing or preventing mRNA translation) [70] , a combination of the two is hotly debated. However, the balance between repressed and degraded mRNA might play an integral role as post-transcriptional component of gene regulatory network that modulate the precise amounts and type of proteins expressed in cells. MiRNA is a crucial player in gene regulation through different mechanisms of actions mostly controlling gene transcription and translation processes [69] . Recently, miRNA has been also reported to induce histone modifications methylation of the DNA promotor sites and thus, ameliorating the target gene expression [70] .

6. Clinical Applications of Extracellular miRNA

The search for novel, early disease predictors represent a current and a permanent challenge in disease recognition. MiRNAs offer a new class of biologically active molecules that contribute many disease processes [71] . Accumulating evidences showed that circulating extracellular miRNA, both, vesicles encapsulated or protein-associated can serve as disease biomarkers [72] . Some points need to be cleared to maximize the benefit and minimize the pitfalls. Cell contribution in the disease state within the same organ varies among different cells of the same organ. This variability may be attributed to the stress phase, which differs among cells even within the same organ. RNA microarray profiling of intracellular miRNA may only reflect the stress phase of a particular cell. On the other hand, extracellular circulating miRNA represents the final net result of miRNAs that produced by most of involved cells. Besides, vesicles are subjected to shearing force associated with centrifugation and filtration that might alter its miRNA contents [72] . But the possibility of other distant organ miRNA release that might alter the interpretation of the results is still there. Confounding biological and technical factors, such as age or gender of patients as well as storage conditions and processing protocols, are essential in order to judge the value of miRNAs as biomarkers [72] . Besides, identification of a set of extracellular miRNAs rather than single up or down regulated miRNA against intracellular protein microarray would be more reliable biomarker for a specific disease. Recently, not only miRNA are recognized as disease biomarkers, but also miRNAs signatures are increasingly recognized as valuable biomarkers for a differential diagnosis in clinically overlapping diseases such as non-ischemic systolic heart failure versus acute myocardial infarction [73] .

Nishimura N. and his collaborators addressed the combination of miRNA and siRNA in nanoliposomal particles to target oncogenic pathways altered in ovarian cancer. Combined targeting of the Eph pathway using EphA2 -targeting siRNA and the tumor suppressor miR-520d-3p exhibits remarkable therapeutic synergy and enhanced tumor suppression in vitro and in vivo compared with either monotherapy alone [74] .

Recently, miR-423-5p, miR-18b-3p, miR-129-5p, miR-1254, miR-675, and miR-622) were reported to be elevated in patients with heart failure, with miR-423-5p positively correlated with N-terminal pro-brain natriuretic peptide (NT-proBNP) levels and most strongly related to the clinical diagnosis of heart failure [75] . Besides, plasma levels of miR-208b and miR-499 both have been highly associated with AMI. Also, it was demonstrated that measuring miR-1 in plasma is a good approach for blood-based detection of human AMI [76] . Circulating miR-1 is significantly increased in the blood of AMI patients compared to non-AMI subjects and were positively correlated with serum CK-MB (Creatine kinase-MB) [77] .

Kato and collaborators recently show that miR-192 levels increase significantly in glomeruli isolated from streptozotocin-injected diabetic mice as well as diabetic db/db mice, in parallel with increased TGF-𝛽1 and collagen 1a2 (Col1a2) levels [78] . Upregulation of renal miR-192 during diabetic kidney diseases is also found in db/db mice, type 2 diabetes rat, and whole blood samples of type 2 diabetes patients [79] .

7. Conclusions

The fact that diverse diseases in different organ systems (liver, kidney, pancreas, heart, lung and skin) may end with fibrotic changes suggests common pathogenic pathways. These pathways are orchestrated by complex activities within different cells in which specific molecular pathways and gene expression have emerged. These specific molecules are cell specific (relates to the stress phase of cells involved), rather than organ specific. Current researches are exploring the association between various diseases and changes in miRNAs as part of molecular pathways activation. The activation of molecular pathways of cell stress in different diseases seems to be more or less similar regardless the organ involved in a specific disease; resulting in cellular dysfunction, parenchymal scarring and ultimately organ failure. The clinical presentation of any disease can be explained as “functional expression of cell disruption” depending on the cell mass involved in this response.

As all living organisms should have a facility to get rid of their metabolic wastes. Exosomes, microvesicles, apoptotic bodies and protein associated nucleoproteins might be some forms of cell excreta. Two hypothesizes have been postulated to explain the presence of circulating extracellular RNAs, both, vesicles encapsulated or protein associated. RNAs release either by the selective sorting system or mere byproduct of cell activity and waste disposal is yet debatable. Accumulating evidence, however, suggests that both theories can be true. Extracellular nucleoproteins consist of a variety of factors among which miRNA is seemingly of particular importance in response to molecular pathways activation. Yet, we treat most of diseases after the onset of the functional disturbances, while thorough understanding of the molecular cell biology will enable us to diagnose and hence treat cells far before the onset of symptoms and signs by targeting molecular cell disruption in which miRNA is a pivotal player.

The response of cells to stress, which can be physical, chemical or biological stressor(s), is a series of biological events that facilitate and promote counteraction and adaptation to qualify these cells to survive. Cell adaptation can be categorized into five major types including atrophy, hypertrophy, hyperplasia, dysplasia and metaplasia. The adaptation may be physiologic or pathologic. In case of failure of adaptation, cells will proceed to a state of cell death, through undergoing autophagy, apoptosis and necrosis. From cell adaptation to cell death, the process of fibro-genesis is activated to modulate the final anatomical and physiological outcome of the tissue in reaction to stress. Duration, severity and frequency of exposure to stressors are detrimental for the nature of cell response to stress. Correlation between exRNA profiles in various adaptation mechanisms has not yet been thoroughly investigated. This profile will expedite the discovery of complex panel of biomarkers to monitor specific disease states along the complete pathogenic pathway for prediction, initiation, development, diagnosis, progression, regression, and treatment efficacy of the disease.

Acknowledgements

The authors gratefully acknowledge Rashad S. Barsoum, Professor of Internal Medicine and Nephrology, Faculty of Medicine, Cairo University, Egypt, for his unlimited help and support. We wish also to acknowledge Dr. Mayar W.N., Faculty of Medicine; October Six University, whose efforts were behind most of the steps of this work.

Conflict of Interest

We, the authors of this review, declare that there is no conflict of interest that could be perceived as prejudicing impartiality of the research. We fully declare that no financial or other potential conflict of interest.

Conflicts of Interest

The authors declare no conflicts of interest.

Cite this paper

Nassar, W. , El-Ansary, M. , Fayyad, T. and Aziz, M. (2016) Extracellular Micro-RNAs in Health and Disease: Basic Science, Biogenesis and Release. American Journal of Molecular Biology, 6, 1-11. doi: 10.4236/ajmb.2016.61001.

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