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MicroRNAs 218a-5p, 219a-5p, and 221-3p regulate vestibular compensation
Unilateral vestibular deafferentation (UVD) interrupts afferent signals from one side, resulting in an imbalance of the resting activity between bilateral vestibular nuclei. Vestibular compensation is the process of balancing the resting activity to reestablish homeostasis. Here, we investigated mic...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5562769/ https://www.ncbi.nlm.nih.gov/pubmed/28821887 http://dx.doi.org/10.1038/s41598-017-09422-8 |
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author | Chang, Mun Young Park, Sohyeon Choi, Jun Jae Kim, Young-Kook Suh, Myung-Whan Lee, Jun Ho Oh, Seung Ha Park, Moo Kyun |
author_facet | Chang, Mun Young Park, Sohyeon Choi, Jun Jae Kim, Young-Kook Suh, Myung-Whan Lee, Jun Ho Oh, Seung Ha Park, Moo Kyun |
author_sort | Chang, Mun Young |
collection | PubMed |
description | Unilateral vestibular deafferentation (UVD) interrupts afferent signals from one side, resulting in an imbalance of the resting activity between bilateral vestibular nuclei. Vestibular compensation is the process of balancing the resting activity to reestablish homeostasis. Here, we investigated microRNAs (miRNAs) that regulate vestibular compensation using the Sprague–Dawley rat. After determining the progression of vestibular compensation following UVD, microarray analysis was performed and nine miRNAs were selected as candidates. Following validation by quantitative reverse transcription-PCR, three miRNAs remained. We assessed the effect of these miRNAs on vestibular compensation using miRNA oligomers. We compared the results of the rotarod test and 5-bromo-2′-deoxyuridine immunohistochemistry following UVD between the control group and the groups in which the candidate miRNA oligomers were administered. Administration of miR-218a-5p, 219a-5p, and 221-3p oligomers significantly affected vestibular compensation. Target pathway analysis of these miRNAs supported our results. Our findings suggest that the miRNAs 218a-5p, 219a-5p, and 221-3p regulate vestibular compensation. |
format | Online Article Text |
id | pubmed-5562769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55627692017-08-21 MicroRNAs 218a-5p, 219a-5p, and 221-3p regulate vestibular compensation Chang, Mun Young Park, Sohyeon Choi, Jun Jae Kim, Young-Kook Suh, Myung-Whan Lee, Jun Ho Oh, Seung Ha Park, Moo Kyun Sci Rep Article Unilateral vestibular deafferentation (UVD) interrupts afferent signals from one side, resulting in an imbalance of the resting activity between bilateral vestibular nuclei. Vestibular compensation is the process of balancing the resting activity to reestablish homeostasis. Here, we investigated microRNAs (miRNAs) that regulate vestibular compensation using the Sprague–Dawley rat. After determining the progression of vestibular compensation following UVD, microarray analysis was performed and nine miRNAs were selected as candidates. Following validation by quantitative reverse transcription-PCR, three miRNAs remained. We assessed the effect of these miRNAs on vestibular compensation using miRNA oligomers. We compared the results of the rotarod test and 5-bromo-2′-deoxyuridine immunohistochemistry following UVD between the control group and the groups in which the candidate miRNA oligomers were administered. Administration of miR-218a-5p, 219a-5p, and 221-3p oligomers significantly affected vestibular compensation. Target pathway analysis of these miRNAs supported our results. Our findings suggest that the miRNAs 218a-5p, 219a-5p, and 221-3p regulate vestibular compensation. Nature Publishing Group UK 2017-08-18 /pmc/articles/PMC5562769/ /pubmed/28821887 http://dx.doi.org/10.1038/s41598-017-09422-8 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Chang, Mun Young Park, Sohyeon Choi, Jun Jae Kim, Young-Kook Suh, Myung-Whan Lee, Jun Ho Oh, Seung Ha Park, Moo Kyun MicroRNAs 218a-5p, 219a-5p, and 221-3p regulate vestibular compensation |
title | MicroRNAs 218a-5p, 219a-5p, and 221-3p regulate vestibular compensation |
title_full | MicroRNAs 218a-5p, 219a-5p, and 221-3p regulate vestibular compensation |
title_fullStr | MicroRNAs 218a-5p, 219a-5p, and 221-3p regulate vestibular compensation |
title_full_unstemmed | MicroRNAs 218a-5p, 219a-5p, and 221-3p regulate vestibular compensation |
title_short | MicroRNAs 218a-5p, 219a-5p, and 221-3p regulate vestibular compensation |
title_sort | micrornas 218a-5p, 219a-5p, and 221-3p regulate vestibular compensation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5562769/ https://www.ncbi.nlm.nih.gov/pubmed/28821887 http://dx.doi.org/10.1038/s41598-017-09422-8 |
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