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microRNA-183 is Essential for Hair Cell Regeneration after Neomycin Injury in Zebrafish
PURPOSE: microRNAs (miRNAs) are non-coding RNAs composed of 20 to 22 nucleotides that regulate development and differentiation in various organs by silencing specific RNAs and regulating gene expression. In the present study, we show that the microRNA (miR)-183 cluster is upregulated during hair cel...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Yonsei University College of Medicine
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725352/ https://www.ncbi.nlm.nih.gov/pubmed/29214789 http://dx.doi.org/10.3349/ymj.2018.59.1.141 |
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author | Kim, Chang Woo Han, Ji Hyuk Wu, Ling Choi, Jae Young |
author_facet | Kim, Chang Woo Han, Ji Hyuk Wu, Ling Choi, Jae Young |
author_sort | Kim, Chang Woo |
collection | PubMed |
description | PURPOSE: microRNAs (miRNAs) are non-coding RNAs composed of 20 to 22 nucleotides that regulate development and differentiation in various organs by silencing specific RNAs and regulating gene expression. In the present study, we show that the microRNA (miR)-183 cluster is upregulated during hair cell regeneration and that its inhibition reduces hair cell regeneration following neomycin-induced ototoxicity in zebrafish. MATERIALS AND METHODS: miRNA expression patterns after neomycin exposure were analyzed using microarray chips. Quantitative polymerase chain reaction was performed to validate miR-183 cluster expression patterns following neomycin exposure (500 µM for 2 h). After injection of an antisense morpholino (MO) to miR-183 (MO-183) immediately after fertilization, hair cell regeneration after neomycin exposure in neuromast cells was evaluated by fluorescent staining (YO-PRO1). The MO-183 effect also was assessed in transgenic zebrafish larvae expressing green fluorescent protein (GFP) in inner ear hair cells. RESULTS: Microarray analysis clearly showed that the miR-183 cluster (miR-96, miR-182, and miR-183) was upregulated after neomycin treatment. We also confirmed upregulated expression of the miR-183 cluster during hair cell regeneration after neomycin-induced ototoxicity. miR-183 inhibition using MO-183 reduced hair cell regeneration in both wild-type and GFP transgenic zebrafish larvae. CONCLUSION: Our work demonstrates that the miR-183 cluster is essential for the regeneration of hair cells following ototoxic injury in zebrafish larvae. Therefore, regulation of the miR-183 cluster can be a novel target for stimulation of hair cell regeneration. |
format | Online Article Text |
id | pubmed-5725352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Yonsei University College of Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-57253522018-01-01 microRNA-183 is Essential for Hair Cell Regeneration after Neomycin Injury in Zebrafish Kim, Chang Woo Han, Ji Hyuk Wu, Ling Choi, Jae Young Yonsei Med J Original Article PURPOSE: microRNAs (miRNAs) are non-coding RNAs composed of 20 to 22 nucleotides that regulate development and differentiation in various organs by silencing specific RNAs and regulating gene expression. In the present study, we show that the microRNA (miR)-183 cluster is upregulated during hair cell regeneration and that its inhibition reduces hair cell regeneration following neomycin-induced ototoxicity in zebrafish. MATERIALS AND METHODS: miRNA expression patterns after neomycin exposure were analyzed using microarray chips. Quantitative polymerase chain reaction was performed to validate miR-183 cluster expression patterns following neomycin exposure (500 µM for 2 h). After injection of an antisense morpholino (MO) to miR-183 (MO-183) immediately after fertilization, hair cell regeneration after neomycin exposure in neuromast cells was evaluated by fluorescent staining (YO-PRO1). The MO-183 effect also was assessed in transgenic zebrafish larvae expressing green fluorescent protein (GFP) in inner ear hair cells. RESULTS: Microarray analysis clearly showed that the miR-183 cluster (miR-96, miR-182, and miR-183) was upregulated after neomycin treatment. We also confirmed upregulated expression of the miR-183 cluster during hair cell regeneration after neomycin-induced ototoxicity. miR-183 inhibition using MO-183 reduced hair cell regeneration in both wild-type and GFP transgenic zebrafish larvae. CONCLUSION: Our work demonstrates that the miR-183 cluster is essential for the regeneration of hair cells following ototoxic injury in zebrafish larvae. Therefore, regulation of the miR-183 cluster can be a novel target for stimulation of hair cell regeneration. Yonsei University College of Medicine 2018-01-01 2017-11-29 /pmc/articles/PMC5725352/ /pubmed/29214789 http://dx.doi.org/10.3349/ymj.2018.59.1.141 Text en © Copyright: Yonsei University College of Medicine 2018 http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kim, Chang Woo Han, Ji Hyuk Wu, Ling Choi, Jae Young microRNA-183 is Essential for Hair Cell Regeneration after Neomycin Injury in Zebrafish |
title | microRNA-183 is Essential for Hair Cell Regeneration after Neomycin Injury in Zebrafish |
title_full | microRNA-183 is Essential for Hair Cell Regeneration after Neomycin Injury in Zebrafish |
title_fullStr | microRNA-183 is Essential for Hair Cell Regeneration after Neomycin Injury in Zebrafish |
title_full_unstemmed | microRNA-183 is Essential for Hair Cell Regeneration after Neomycin Injury in Zebrafish |
title_short | microRNA-183 is Essential for Hair Cell Regeneration after Neomycin Injury in Zebrafish |
title_sort | microrna-183 is essential for hair cell regeneration after neomycin injury in zebrafish |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725352/ https://www.ncbi.nlm.nih.gov/pubmed/29214789 http://dx.doi.org/10.3349/ymj.2018.59.1.141 |
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