- 1Molecular Medicine Group, Robarts Research Institute, Western University, London, ON, Canada
- 2Huazhong University of Science and Technology, Wuhan, China
Editorial on the Research Topic
MiRNAs as pivotal components of ncRNA networks associated with CNS injuries and neurodegeneration, and their therapeutic potential
Since miRNA discovery 30 years ago, studies have been focused on understanding miRNA mechanisms of action and biogenesis, as well as the pathways they regulate and their potential role in diagnosis and therapy of different diseases (Dexheimer and Cochella, 2020; Diener et al., 2022; Matulic et al., 2022; Rani and Sengar, 2022). Many studies have revealed alterations in the expression of miRNAs under different physiological and pathological conditions, supporting their participation in all cellular processes (Deveale et al., 2021). Evidence shows that miRNAs respond to different environmental stimuli, such as cellular stress and viral infections, regulating gene expression in different cell types and organisms (Gebert and Macrae, 2019; Deveale et al., 2021). The high stability and rapid expression of miRNAs compared to other RNA species make them ideal candidates in charge of the fine-tuning of mRNA and protein levels, and ultimately of the cellular response to diverse clues (Campos-Melo et al., 2022). These characteristics and the regulatory networks that miRNAs establish interacting with other non-coding RNAs (ncRNAs) such as long non-coding RNAs (lncRNAs) and circular RNAs (circRNAs), are critical for neuronal function, death, and survival and are increasingly recognized as associated with human neurological disorders, such as neurodegeneration, spinal cord injury, and stroke (Yamamura et al., 2018; Nuzziello and Liguori, 2019; Xu et al., 2021; Khan et al., 2022; Li et al., 2022; Silvestro and Mazzon, 2022).
This Research Topic clusters five articles from experts interested in in silico and in vitro miRNA characterization, miRNA functional interactions with other ncRNA molecules, and potential therapeutic roles of miRNAs in neurological diseases. Mégret et al. reviewed the main families of machine learning methods for the analysis of miRNA regulation in neurodegenerative disorders. The authors argue that the challenge in system-level studies to analyze the role of miRNA regulation in neurodegenerative diseases is due to problems of insufficient and inhomogeneous data and in the accuracy of system-level modeling. The authors propose shape analysis of complex omics data as a promising approach to construct improved models of high-level precision in matching miRNA-mRNA profiles in neurodegeneration.
Liang et al. reviewed mesenchymal stem cells (MSC)-derived exosomal miRNAs and its potential applications as therapeutic tools. This group of miRNAs downregulates the expression of several genes such as IRAK1, TRAF6, C/EBPβ IRF5, TLR4, and MAPK6, which induces polarization of macrophages from M1 to M2 phenotype and promotes nerve function recovery. These miRNAs are proposed to provide better therapeutic opportunities for spinal cord injury (SCI) than MSC transplantation.
Thousands of miRNA sequences hitherto have been published in miRbase (Plotnikova et al., 2019) (https://www.mirbase.org/), however, the big majority of them still require experimental validation. In this topic, two novel miRNAs encoded in the urokinase receptor gene (uPAR) gene Plaur which is associated with nerve regeneration, were identified and characterized by Rysenkova et al.. MiRNAs Plaur-miR1-3p and Plaur-miR1-5p, were described to be expressed in mouse brains and target Mef2D, a gene that encodes a protein that regulates gene expression in embryogenesis and brain architecture maintenance, and contributes to the regulation of neuronal apoptosis, neurogenesis, and differentiation.
In recent years, several articles have studied regulatory networks and interactions between miRNAs and other ncRNAs in vitro and in vivo. Both, lncRNAs and circRNAs function as miRNA sponges or decoys altering the availability of miRNAs and their downstream regulatory effects (Liu and Chen, 2022; Sharma et al., 2023; Tang et al., 2023). For this Research Topic, Lan et al. reviewed lncRNAs that are involved in Alzheimer's disease (AD). LncRNAs modulate the transcription of target genes in cis or in trans, and mRNA stability and processing, by regulating the assembly of multi-molecular complexes. This article reviews evidence that lncRNAs contribute to the pathogenesis of AD by regulating tau hyperphosphorylation, Aβ plague formation, mitochondrial and synaptic function, neuroinflammation, and neuronal apoptosis.
Finally, Zhang et al. extensively reviewed the role of circRNAs, covalently closed ncRNAs, in acute central nervous system (CNS) injuries, such as traumatic brain injury (TBI) and SCI. The authors described circRNAs expressed in neuronal injury as beneficial or detrimental for neural cell function and survival. Details of the function of different circRNAs involved in cerebellar ataxia, ischemic stroke, subarachnoid hemorrhage, and brain injury are included, showing evidence of the neuroprotective function of circRNAs through inhibition of inflammation and suppression of apoptosis, promotion of angiogenesis, and reduction of excitotoxicity and oxidative stress, among others. Mechanisms of action of circRNAs in acute CNS injuries are discussed, including their role in regulating miRNA performance.
From viruses to humans, the regulatory role of miRNAs and their wiring networks with other ncRNAs is only beginning to be elucidated. Beyond the experimental characterization of most miRNAs, we need to understand where, when, and how miRNAs exert their actions over specific targets in the cell. This is particularly relevant in animals because the partial base pairing between the miRNA seed region and 3′UTR sequences creates a high repertoire of targets. Studies of spatiotemporal expression and function of miRNAs and their ncRNA partners within subcellular compartments, in different tissue cell types, and ultimately in the whole organism, will allow the understanding of the importance of genome regulation by miRNAs and their link to human diseases of the CNS.
Author contributions
DC-M conceived and wrote the manuscript. CD and LZ reviewed and approved the final article. All authors contributed to the article and approved the submitted version.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
References
Campos-Melo, D., Hawley, Z. C. E., Mclellan, C., and Strong, M. J. (2022). “Chapter 7 - MicroRNA turnover and nuclear function,” in MicroRNA, ed J. Xiao (Academic Press), 109–141. doi: 10.1016/B978-0-323-89774-7.00026-1
Deveale, B., Swindlehurst-Chan, J., and Blelloch, R. (2021). The roles of microRNAs in mouse development. Nat. Rev. Genet. 22, 307–323. doi: 10.1038/s41576-020-00309-5
Dexheimer, P. J., and Cochella, L. (2020). MicroRNAs: from mechanism to organism. Front. Cell. Dev. Biol. 8, 409. doi: 10.3389/fcell.2020.00409
Diener, C., Keller, A., and Meese, E. (2022). Emerging concepts of miRNA therapeutics: from cells to clinic. Trends Genet. 38, 613–626. doi: 10.1016/j.tig.2022.02.006
Gebert, L. F. R., and Macrae, I. J. (2019). Regulation of microRNA function in animals. Nat. Rev. Mol. Cell Biol. 20, 21–37. doi: 10.1038/s41580-018-0045-7
Khan, I., Preeti, K., Fernandes, V., Khatri, D. K., and Singh, S. B. (2022). Role of MicroRNAs, aptamers in neuroinflammation and neurodegenerative disorders. Cell. Mol. Neurobiol. 42, 2075–2095. doi: 10.1007/s10571-021-01093-4
Li, S., Lei, Z., and Sun, T. (2022). The role of microRNAs in neurodegenerative diseases: a review. Cell Biol. Toxicol. 1–31. doi: 10.1007/s10565-022-09761-x
Liu, C. X., and Chen, L. L. (2022). Circular RNAs: characterization, cellular roles, and applications. Cell 185, 2016–2034. doi: 10.1016/j.cell.2022.04.021
Matulic, M., Grskovic, P., Petrovic, A., Begic, V., Harabajsa, S., and Korac, P. (2022). miRNA in molecular diagnostics. Bioengineering 9, 459. doi: 10.3390/bioengineering9090459
Nuzziello, N., and Liguori, M. (2019). The MicroRNA centrism in the orchestration of neuroinflammation in neurodegenerative diseases. Cells 8, 1193. doi: 10.3390/cells8101193
Plotnikova, O., Baranova, A., and Skoblov, M. (2019). Comprehensive analysis of human microRNA-mRNA interactome. Front. Genet. 10, 933. doi: 10.3389/fgene.2019.00933
Rani, V., and Sengar, R. S. (2022). Biogenesis and mechanisms of microRNA-mediated gene regulation. Biotechnol. Bioeng. 119, 685–692. doi: 10.1002/bit.28029
Sharma, U., Kaur Rana, M., Singh, K., and Jain, A. (2023). LINC00324 promotes cell proliferation and metastasis of esophageal squamous cell carcinoma through sponging miR-493-5p via MAPK signaling pathway. Biochem. Pharmacol. 207, 115372. doi: 10.1016/j.bcp.2022.115372
Silvestro, S., and Mazzon, E. (2022). MiRNAs as Promising Translational Strategies for Neuronal Repair and Regeneration in Spinal Cord Injury. Cells 11, 2177. doi: 10.3390/cells11142177
Tang, C., Deng, Y., Shao, S., Guo, Y., Yang, L., Yan, Y., et al. (2023). Long noncoding RNA UCA1 promotes the expression and function of P-glycoprotein by sponging miR-16-5p in human placental BeWo cells. FASEB J. 37, e22657. doi: 10.1096/fj.202201051R
Xu, Y., Hu, Y., Xu, S., Liu, F., and Gao, Y. (2021). Exosomal microRNAs as potential biomarkers and therapeutic agents for acute ischemic stroke: new expectations. Front. Neurol. 12, 747380. doi: 10.3389/fneur.2021.747380
Keywords: miRNA, ncRNAs (non-coding RNAs), neurodegeneration, spinal cord injury, lncRNAs (long non-coding RNAs), circRNAs
Citation: Campos-Melo D, Droppelmann CA and Zhu LQ (2023) Editorial: MiRNAs as pivotal components of ncRNA networks associated with CNS injuries and neurodegeneration, and their therapeutic potential. Front. Mol. Neurosci. 16:1166943. doi: 10.3389/fnmol.2023.1166943
Received: 15 February 2023; Accepted: 22 February 2023;
Published: 13 March 2023.
Edited and reviewed by: Jean-Marc Taymans, Institut National de la Santé et de la Recherche Médicale (INSERM), France
Copyright © 2023 Campos-Melo, Droppelmann and Zhu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Danae Campos-Melo, ZG1hcmliZWwmI3gwMDA0MDt1d28uY2E=