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Developmental profiling of microRNAs in the human embryonic inner ear
Due to the extreme inaccessibility of fetal human inner ear tissue, defining of the microRNAs (miRNAs) that regulate development of the inner ear has relied on animal tissue. In the present study, we performed the first miRNA sequencing of otic precursors in human specimens. Using HTG miRNA Whole Tr...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786302/ https://www.ncbi.nlm.nih.gov/pubmed/29373586 http://dx.doi.org/10.1371/journal.pone.0191452 |
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author | Chadly, Duncan M. Best, Jennifer Ran, Cong Bruska, Małgorzata Woźniak, Witold Kempisty, Bartosz Schwartz, Mark LaFleur, Bonnie Kerns, B. J. Kessler, John A. Matsuoka, Akihiro J. |
author_facet | Chadly, Duncan M. Best, Jennifer Ran, Cong Bruska, Małgorzata Woźniak, Witold Kempisty, Bartosz Schwartz, Mark LaFleur, Bonnie Kerns, B. J. Kessler, John A. Matsuoka, Akihiro J. |
author_sort | Chadly, Duncan M. |
collection | PubMed |
description | Due to the extreme inaccessibility of fetal human inner ear tissue, defining of the microRNAs (miRNAs) that regulate development of the inner ear has relied on animal tissue. In the present study, we performed the first miRNA sequencing of otic precursors in human specimens. Using HTG miRNA Whole Transcriptome assays, we examined miRNA expression in the cochleovestibular ganglion (CVG), neural crest (NC), and otic vesicle (OV) from paraffin embedded (FFPE) human specimens in the Carnegie developmental stages 13–15. We found that in human embryonic tissues, there are different patterns of miRNA expression in the CVG, NC and OV. In particular, members of the miR-183 family (miR-96, miR-182, and miR-183) are differentially expressed in the CVG compared to NC and OV at Carnegie developmental stage 13. We further identified transcription factors that are differentially targeted in the CVG compared to the other tissues from stages 13–15, and we performed gene set enrichment analyses to determine differentially regulated pathways that are relevant to CVG development in humans. These findings not only provide insight into the mechanisms governing the development of the human inner ear, but also identify potential signaling pathways for promoting regeneration of the spiral ganglion and other components of the inner ear. |
format | Online Article Text |
id | pubmed-5786302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-57863022018-02-09 Developmental profiling of microRNAs in the human embryonic inner ear Chadly, Duncan M. Best, Jennifer Ran, Cong Bruska, Małgorzata Woźniak, Witold Kempisty, Bartosz Schwartz, Mark LaFleur, Bonnie Kerns, B. J. Kessler, John A. Matsuoka, Akihiro J. PLoS One Research Article Due to the extreme inaccessibility of fetal human inner ear tissue, defining of the microRNAs (miRNAs) that regulate development of the inner ear has relied on animal tissue. In the present study, we performed the first miRNA sequencing of otic precursors in human specimens. Using HTG miRNA Whole Transcriptome assays, we examined miRNA expression in the cochleovestibular ganglion (CVG), neural crest (NC), and otic vesicle (OV) from paraffin embedded (FFPE) human specimens in the Carnegie developmental stages 13–15. We found that in human embryonic tissues, there are different patterns of miRNA expression in the CVG, NC and OV. In particular, members of the miR-183 family (miR-96, miR-182, and miR-183) are differentially expressed in the CVG compared to NC and OV at Carnegie developmental stage 13. We further identified transcription factors that are differentially targeted in the CVG compared to the other tissues from stages 13–15, and we performed gene set enrichment analyses to determine differentially regulated pathways that are relevant to CVG development in humans. These findings not only provide insight into the mechanisms governing the development of the human inner ear, but also identify potential signaling pathways for promoting regeneration of the spiral ganglion and other components of the inner ear. Public Library of Science 2018-01-26 /pmc/articles/PMC5786302/ /pubmed/29373586 http://dx.doi.org/10.1371/journal.pone.0191452 Text en © 2018 Chadly et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Chadly, Duncan M. Best, Jennifer Ran, Cong Bruska, Małgorzata Woźniak, Witold Kempisty, Bartosz Schwartz, Mark LaFleur, Bonnie Kerns, B. J. Kessler, John A. Matsuoka, Akihiro J. Developmental profiling of microRNAs in the human embryonic inner ear |
title | Developmental profiling of microRNAs in the human embryonic inner ear |
title_full | Developmental profiling of microRNAs in the human embryonic inner ear |
title_fullStr | Developmental profiling of microRNAs in the human embryonic inner ear |
title_full_unstemmed | Developmental profiling of microRNAs in the human embryonic inner ear |
title_short | Developmental profiling of microRNAs in the human embryonic inner ear |
title_sort | developmental profiling of micrornas in the human embryonic inner ear |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786302/ https://www.ncbi.nlm.nih.gov/pubmed/29373586 http://dx.doi.org/10.1371/journal.pone.0191452 |
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