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Open Medicine

formerly Central European Journal of Medicine

Editor-in-Chief: Darzynkiewicz, Zbigniew


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Volume 11, Issue 1

Issues

Volume 10 (2015)

MicroRNAs as regulatory elements in psoriasis

Yuan Liu
  • Department of Dermatovenereology, Tianjin Medical University General Hospital, 154 Anshan Road, Heping District, Tianjin 300052, China
  • Other articles by this author:
  • De Gruyter OnlineGoogle Scholar
/ Quanzhong Liu
  • Corresponding author
  • Department of Dermatovenereology, Tianjin Medical University General Hospital, 154 Anshan Road, Heping District, Tianjin 300052, China
  • Email
  • Other articles by this author:
  • De Gruyter OnlineGoogle Scholar
Published Online: 2016-08-12 | DOI: https://doi.org/10.1515/med-2016-0063

Abstract

Psoriasis is a chronic, autoimmune, and complex genetic disorder that affects 23% of the European population. The symptoms of Psoriatic skin are inflammation, raised and scaly lesions. microRNA, which is short, nonprotein-coding, regulatory RNAs, plays critical roles in psoriasis. microRNA participates in nearly all biological processes, such as cell differentiation, development and metabolism. Recent researches reveal that multitudinous novel microRNAs have been identified in skin. Some of these substantial novel microRNAs play as a class of posttranscriptional gene regulator in skin disease, such as psoriasis. In order to insight into microRNAs biological functions and verify microRNAs biomarker, we review diverse references about characterization, profiling and subtype of microRNAs. Here we will share our opinions about how and which microRNAs are as regulatory in psoriasis.

Keywords: microRNAs; Psoriasis

1 Introduction

Human skin is the outermost bodily barrier; it protects inner organs from stress and hazards [1, 2]. Human skin tends to rapidly repair when injured, although that involves a complex healing process. These functions of skin are maintained by a system of regulatory mechanisms that involves various mediators [3, 4]. Some reports indicate that epigenetic regulatory mechanisms are contributing factors [5].

Skin diseases, including skin cancer and psoriasis, exert more and more severe influence on public health, for example psoriasis, a common skin disease. It characterized by a chronic, autoimmune, and complex genetic disorder. Psoriasis undergoes three different processes of cellular alteration in skin: abnormal differentiation of keratinocyte, hyperproliferation of keratinocyte, and infiltration of immune into the dermis and epidermis [6]. Some common molecular components, genetic alterations of genes that participate in inflammatory pathways, and environmental risks can contribute to the pathogenesis of psoriasis [7,8].

Recent research reveals that microRNAs have an important influence on psoriasis. MicroRNAs (microRNAs) are single-stranded, noncoding, short RNA molecules; they act as regulators of gene expression and play critical roles in nearly all biological processes. One example is the differentiation, development, and metabolism of the human body cell [9,10], which is influenced complementary mRNAs by binding to a target. As recent reports have indicated, expression of distinct microRNAs is upregulated in psoriatic skin compared with healthy skin, and that this process is related to regulation of keratinocyte proliferation and/or differentiation or suppression of T-cell apoptosis in psoriasis [11]. A plethora of microRNAs have been reported to be related to regulation in psoriasis, and different microRNAs can play a vital role at different stages of the disease. For example, miR-31 can modulate inflammatory mediator production and leucocyte infiltration to skin, and thus be present in psoriatic keratinocytes and contribute to psoriatic inflammation [11]. miR-203 is upregulated during keratinocyte differentiation of psoriatic skin by regulating the expression of TNF-a, IL-8, IL-24. Whereas miR-21 can be suppressed during apoptosis, miR-146a is upregulated in Th1 cells from T cells [12]. Thus, an appropriate combination of microRNAs could act as a regulator of psoriasis and thereby could potentially provide biomarker, therapy and diagnostic information.

2 MicroRNAs in skin

MicroRNAs are typically defined as the most abundant small RNAs on pre-microRNA hairpins. More and more diverse variants of microRNAs have been discovered, including canonical and noncanonical microRNAs [13-15], microRNA-like–RNA, [16] and microRNA isoforms [17]. The Drosha and Dicer pathways are the essential differences between canonical and noncanonical. For example, previously discovered noncanonical microRNAs, mirtrons that arise from disbranched intron lariats, serve as substrates for Dicer cleavage [18, 19]. Another less abundant variant of small RNAs, isoforms or isomiRs, that exiss in nearly all sepsis, also act as regular microRNAs [20, 21]. This small RNA regulates the same mRNA target as their companion microRNAs and accompany them to their exclusive target genes [22]. This phenomenon indicates that microRNA-mediated gene expression regulators have robustness and plasticity, and that they have abundant functions complementary to canonical microRNAs [23].

During skin development and cell differentiation, microRNAs play an important role in regulating different signaling pathways by interacting with their target mRNAs. Their regulated targets has been implicated in the pathogenesis of psoriasis [24, 25]. This evidence suggests that microRNA can be participate in early skin development and affect the psoriasis process. When knocking out either Dicer or Dgcr8, severe defects in murine embryonic skin development have emerged, which produce rough skin, body weight loss, defects in hair follicle downgrowth, and abnormal apoptosis [26]. Hyperproliferation that topically appears as a feature of psoriasis has been observed in the Dicer knocked-out epidermis, showing the close relationship between microRNA and epidermal proliferation [27]. Several microRNAs with functions in skin morphogenesis and homeostasis have been studied (Table 1). For example, miR-21 is up-regulated in diseased skin, as well as in psoriasis and squamous cell skin cancer [28]. The miR-199 family is highly expressed in hair follicles, which indicates a potential regulatory function in hair morphogenesis [29]. miR-203 is also upregulated when keratinocytes differentiate, inducing expression of TNF-a, IL-8, IL-24 and suppressing cytokine signaling 3 [30]. In addition, many studies have recognized that several other microRNAs are related to skin development and homeostasis (Table 1). For instance, the miR-200 family and miR-205 have been shown to target ZEB1 and ZEB2 and are highly expressed in normal skin. Downregulation of miR-200 and miR-205 will induce upregulation of ZEB1 and ZEB2 via epithelial-to-mesenchymal transition [31].

Table 1

microRNAs involved in skin development

3 microRNAs in psoriatic skin

Psoriasis, which appears as white silvery scales, is a common skin disease with characteristics of a chronic, autoimmune, and complex genetic disorder. Many factors, both genetic and environmental, can contribute to its emergence. Humans with psoriasis may suffer from hyperproliferation, aberrant differentiation of keratinocytes, loss of the superficial granular layer, and thickening of the cornified envelope. Research over last few years suggests that epigenetic regulatory mechanisms may enable skin regeneration and execution of gene expression in skin. This theory may be applicable to processes of skin repair, regulation of keratinocyte proliferation, differentiation, and migration, along with dermal regeneration and neoangiogenesis [5]. The grainyhead-like 3 (Grhl3/Get1) transcription factor is one of the regulators in epidermal genes that control the expression of specific microRNAs [27]. As one of the most widely studied microRNAs, miR-21 is abundantly expressed in skin [34]. Some records have indicated that it is upregulated in pathological conditions such as psoriasis [35]. When miR-21 is upregulated, the differentiation and hyperplasia are impaired and Grhl3 tends to be down regulated [5]. microRNA-31, one of the most dynamic microRNAs, exists in the skin of psoriatic patients and of mouse models. Transcription of miR-31 will be triggered by activated NF-κB and then promotes the keratinocyte hyperproliferation in psoriasis. When the miR-31 seed sequence is blocked by antagomirs and its effects are tested on an imiquimod (IMQ)-induced psoriasis mouse model, we found that there was a pronounced decrease in acanthosis and dermal cellular infiltration [11]. Furthermore, the majority of the collected data suggest that more and more novel human microRNAs have been detected. For example, miR-4623 acts on TNFRSF1B that is reported existing in psoriatic arthritis [36]. As another intronic, miR-944 is encoded in KPT15, which acts as a downregulator in psoriatic skin [37]. miR-944 contributes to maintaining stemness in skin by located in an intron of p63 [38]. A very special microRNA, miR-203-AS, is identified as a distinct microRNA on the DNA strand at the locus antisense to miR-203 [39]. Another example is miR-103, it also encodes on both antisense and sense strands. As for noncanonical microRNAs and microRNA-like RNAs in psoriatic skin, has-miR-1983 as a t-RNA-derived microRNA expresses in psoriatic and normal human skin [40].

A systematic analysis has revealed that microRNA isoforms originate from diverse tissues and across species [41,42]. For example, 5’-isomiRs (Table 2). miR-142 and miR-233 with high 5’-heterogeneities in human psoriatic lesions is expressed in dendritic cells and neutrophils, respectively [43-45].

Table 2

Some of microRNAs that express aberrantly in human psoriatic skin

4 Summary and future

Although the study of microRNAs in mammalian skin, such as in psoriatic skin, is an early stage, the research has already provided new insights into a novel layer of gene regulation. In the present article, some microRNAs, along with their targets, have been discussed; this provide us increased knowledge of psoriasis mechanisms. Taking miR-203 as an example, it has an essential role in early skin development and a critical role in psoriasis (shown in Table 2). This knowledge gives us hope that we will eventually find an excellent candidate for treatment of psoriasis.

Although the science is incomplete, new threads for future research have emerged. To reveal the etiology of autoimmune skin disorders, psoriasis included, a high-quality and rapid analysis system should be put in place to find the complex genetic networks; this will require a comprehensive profile of the transcriptome. Finding these complex genetic networks bring along another challenge: to integrate the information of genotypic variations. These genotypic variations hold a potential to explore causal genetic variations and then to lead to a connection with disease phenotypes. Furthermore, detailed genetic knowledge of the mechanism behind psoriasis development will be beneficial to developing animal models for research.

No matter how great the challenge, we are optimistic regarding the future of this field and are willing to make efforts to contribute to it. We believe that there is a possible cure for skin-related disease in deeper understanding of small RNA- and microRNA-based therapies.

Acknowledgements

This study was supported by Tianjin Medical University General Hospital Youth Incubation Foundation (ZYYFY2014018)

References

  • [1]

    Fuchs E. Scratching the surface of skin development. Nature 2007; 445: 834-842 Google Scholar

  • [2]

    Martin P. Wound healing–aiming for perfect skin regeneration. Science 1997; 276: 75-81 Google Scholar

  • [3]

    Slominski A, Zbytek B, Nikolakis G, Manna PR, Skobowiat C, Zmijewski M. Steroidogenesis in the skin: implications for local immune functions. J Steroid Biochem Mol Biol 2013; 137: 107-123 Google Scholar

  • [4]

    Slominski A T, Zmijewski M A, Skobowiat C, Zbytek B, Slominski R M, Steketee J D. Sensing the environment: regulation of local and global homeostasis by the skin’s neuroendocrine system. Adv Anat Embryol Cell Biol 2012; 212: 1-115 Google Scholar

  • [5]

    Christopher J. Lewis, Andrei N. Mardaryev, Andrey A, et al. The Epigenetic Regulation of Wound Healing. Wound Healing Society 2014; 3:468-475 Google Scholar

  • [6]

    Aditi C, Aditi R, Swapan S, Raghunath C. Genetic and epigenetic basis of psoriasis pathogenesis. Molecular Immunology 2015; 64:33-323 Google Scholar

  • [7]

    Mee J B, Johnson C M, Morar N, Burslem F, Groves R W. The psoriatic transcriptome closely resembles that induced by interleukin-1 in cultured keratinocytes: dominance of innate immune responses in psoriasis. Am J Pathol 2007; 171: 32-42 Google Scholar

  • [8]

    Zhou X, Krueger J G, Kao M J, Lee E, Du F, et al. Novel mechanisms of T-cell and dendritic cell activation revealed by profiling of psoriasis on the 63,100-element oligonucleotide array. Physiol Genomics 2003; 13: 69-78 Google Scholar

  • [9]

    Roberson E D O, Bowcock A M. Psoriasis genetics: breaking the barrier. Trends Genet 2010;26: 415-423 Google Scholar

  • [10]

    Rongloetti F, Fiorucci C, Parodi A. Psoriasis induced or aggravated by drugs. J Rheumatol 20089; 3: 59-61 Google Scholar

  • [11]

    Sha Y, Zhen Y X, Fang Z L, Ling Y Z, Fang K, et al. NF-kB-induced microRNA-31 promotes epidermal hyperplasia by repressing protein phosphatase 6 in psoriasis. Nature Communications 2015;  CrossrefGoogle Scholar

  • [12]

    Raaby L, Langkilde A, Kjellerup R B, Vinter H, Khatib S H, et al. Changes in mRNA expression precede changes in microRNA expression in lesional psoriatic skin during treatment with adalimumab. British Journal of Dermatology 2015; 173:436-447 Google Scholar

  • [13]

    Berezikov E, Chung W J, Willis J, Cuppen E, Lai EC. Mammalian mirtron genes. Mol Cell 2007; 28: 328-336 Google Scholar

  • [14]

    Castellano L, Stebbing J. Deep sequencing of small RNAs identifies canonical and non-canonical microRNA and endogenous siRNAs in mammalian somatic tissues. Nucleic Acids Res 2013; 41: 3339-3351Google Scholar

  • [15]

    Miyoshi K, Miyoshi T, Siomi H. Many ways to generate microRNAlike small RNAs: non-canonical pathways for microRNA production. Mol Genet Genomics 2010; 284: 95-103 Google Scholar

  • [16]

    Babiarz J E, Ruby J G, Wang Y, Bartel D P, Blelloch R. Mouse ES cells express endogenous shRNAs, siRNAs, and other microprocessor-independent, dicer-dependent small RNAs. Genes Dev 2008; 22: 2773-2785 Google Scholar

  • [17]

    Morin R D, O’Connor M D, Griffith M, Kuchenbauer F, Delaney A, Prabhu AL, et al. Application of massively parallel sequencing to microRNA profiling and discovery in human embryonic stem cells. Genome Res 2008; 18: 610-621 Google Scholar

  • [18]

    Berezikov E, Chung W J, Willis J, Cuppen E, Lai E C. Mammalian mirtron genes. Mol Cell 2007; 28: 328-336 Google Scholar

  • [19]

    Chiang H R, Schoenfeld L W, Ruby J G, Auyeung V C, Spies N, Baek D, et al. Mammalian microRNAs: experimental evaluation of novel and previously annotated genes. Genes Dev 2010; 24: 992-1009 Google Scholar

  • [20]

    Ebhardt H A, Tsang H H, Dai D C, Liu Y, Bostan B, Fahlman R P. Meta-analysis of small RNA-sequencing errors reveals ubiquitous posttranscriptional RNA modifications. Nucleic Acids Res 2009; 37: 2461-2470 Google Scholar

  • [21]

    Xia J, Zhang W. A meta-analysis revealed insights into the sources, conservation and impact of microRNA 5=-isoforms in four model species. Nucleic Acids Res [Epub ahead of print]. Google Scholar

  • [22]

    Wyman S K, Knouf E C, Parkin R K, Fritz B R, Lin D W, Dennis L M, et al. Post-transcriptional generation of microRNA variants by multiple nucleotidyl transferases contributes to microRNA transcriptome complexity. Genome Res 2011; 21: 1450-1461 Google Scholar

  • [23]

    Xia J, Zhang W X. MicroRNAs in normal and psoriatic skin. Physiol Genomics.2014; 46: 113-122 Google Scholar

  • [24]

    Schneider M R. MicroRNAs as novel players in skin development, homeostasis and disease. Br J Dermatol 2012;166: 22-28 Google Scholar

  • [25]

    Sonkoly E, Lovén J, Xu N, Meisgen F, Wei T, Brodin P, et al. MicroRNA-203 functions as a tumor suppressor in basal cell carcinoma. Oncogenesis 1: e3, 2012 Google Scholar

  • [26]

    Yi R, Pasolli H A, Landthaler M, Hafner M, Ojo T, Sheridan R, et al. DGCR8- dependent microRNA biogenesis is essential for skin development. Proc Natl Acad Sci USA 2009; 106: 498-502 Google Scholar

  • [27]

    Andl T, Murchison E P, Liu F, Zhang Y, Yunta G M, Tobias J W, et al. The microRNAprocessing enzyme dicer is essential for the morphogenesis and maintenance of hair follicles. Curr Biol 2006; 16: 1041-1049 Google Scholar

  • [28]

    Ambica B, William G, Diana D, Amelia S H, Elizabeth G, Zhenquan Y, et al. The Grainyhead transcription factor Grhl3/ Get1, suppresses miR-21 expression and tumorigenesis in skin: Modulation of the miR-21 target MSH2 by RNA-binding protein DND1. NIH Public Access 2013:1497-1507 Google Scholar

  • [29]

    Yi R, Carroll D, Pasolli H, Zhang Z, Dietrich F S, Tarakhovsky A. Morphogenesis in skin is governed by discrete sets of differentially expressed microRNAs. Nat Genet 2006; 38: 356-362 Google Scholar

  • [30]

    Yi R, Poy M N, Stoffel M, Fuchs E. A skin microRNA promotes differentiation by repressing “stemness”. Nature 2008; 452: 225-229 Google Scholar

  • [31]

    Gudjonsson J E, Ding J, Johnston A, Tejasvi T, Guzman A M, Nair RP, et al. Assessment of the psoriatic transcriptome in a large sample: additional regulated genes and comparisons with in vitro models. J Invest Dermatol 130: 2010, 1829-1840 Google Scholar

  • [32]

    Antonini D, Russo MT, De Rosa L, Gorrese M, Del Vecchio L. Missero C. Transcriptional repression of miR-34 family contributes to p63-mediated cell cycle progression in epidermal cells. J Invest Dermatol 2010;130: 1249-1257 Google Scholar

  • [33]

    Zhang L, Stokes N, Polak L, Fuchs E. Specific microRNAs are preferentially expressed by skin stem cells to balance self-renewal and early lineage commitment. Cell. Stem Cell 2011;8: 294-308 Google Scholar

  • [34]

    Andl T, Murchison E P, Liu F, Zhang Y, Yunta-Gonzalez M, Tobias JW, et al. The microRNAprocessing enzyme dicer is essential for the morphogenesis and maintenance of hair follicles. Curr Biol. 2006; 16(10):1041-1049 Google Scholar

  • [35]

    Joyce C E, Zhou X, Xia J, Ryan C, Thrash B, Menter A, et al. Deep sequencing of small RNAs from human skin reveals major alterations in the psoriasis microRNAome. Hum Mol Genet. 2011; 20(20):4025-4040 Google Scholar

  • [36]

    Reich K, Hüffmeier U, König IR, Lascorz J, Lohmann J, Wendler J, et al. TNF polymorphisms in psoriasis: association of psoriatic arthritis with the promoter polymorphism TNF-857 independent of the PSORS1 risk allele. Arthritis Rheum 2007; 56: 2056-2064 Google Scholar

  • [37]

    Gudjonsson J E, Ding J, Johnston A, Tejasvi T, Guzman A M, Nair R P, et al Google Scholar

  • [38]

    Assessment of the psoriatic transcriptome in a large sample: additional regulated genes and comparisons with in vitro models. J Invest Dermatol 2010;130: 1829-1840 Google Scholar

  • [39]

    Senoo M, Pinto F, Crum C P, McKeon F. P63 is essential for the proliferative potential of stem cells in stratified epithelia. Cell 2007; 129: 523-536 Google Scholar

  • [40]

    Joyce C E, Zhou X, Xia J, Ryan C, Thrash B, Menter A, et al. Deep sequencing of small RNAs from human skin reveals major alterations in the psoriasis microRNAome. Hum Mol Genet 2011; 20: 4025-4040 Google Scholar

  • [41]

    Xia J, Joyce C E, Bowcock A M, Zhang W. Noncanonical microRNAs and endogenous siRNAs in normal and psoriatic human skin. Hum Mol Genet 2013; 22: 737-748 Google Scholar

  • [42]

    Michal W. microRNA in the control of stem-like phenotype of cancer cells. Open Life Sciences. 2013 ; 8 (10): 931-942 Google Scholar

  • [43]

    Aldona P, Jerzy M, Grazyna C. Eruption of palmoplantar pustular psoriasis in patient treated with anti-androgen therapy for prostate cancer and aggravation of lesions after statin treatment. Open Medicine. 2014; 9 (5): 657-662 Google Scholar

  • [44]

    Sun Y, Varambally S, Maher CA, Cao Q, Chockley P, Toubai T, et al, Targeting of microRNA-142-3p in dendritic cells regulates endotoxin-induced mortality. Blood 2011; 117: 6172-6183Google Scholar

  • [45]

    Gregory P A, Bert A G, Paterson E L, Barry S C, Tsykin A, Farshid G, et al. The miR-200 family and miR-205 regulate epithelial to mesenchymal transition by targeting ZEB1 and SIP1. Nat Cell Biol 2008;10: 593-601 Google Scholar

  • [46]

    Plank M, Maltby S. Targeting translational control as a novel way to treat inflammatory disease: the emerging role of MicroRNAs. Asia-Pacific Journal of Clinical Oncology. 2013; 9 (43): 981-999Google Scholar

About the article

Quanzhong Liu, Tel: 86-022-60363131; Fax:86-022-60363131


Received: 2016-01-13

Accepted: 2016-03-12

Published Online: 2016-08-12

Published in Print: 2016-01-01


Conflict of interest statement

Authors state no conflict of interest.


Citation Information: Open Medicine, Volume 11, Issue 1, Pages 336–340, ISSN (Online) 2391-5463, DOI: https://doi.org/10.1515/med-2016-0063.

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© 2016 Yuan Liu, Quanzhong Liu. This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License. BY-NC-ND 3.0

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