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Identifying MicroRNAs Involved in Degeneration of the Organ of Corti during Age-Related Hearing Loss

MicroRNAs (miRNAs), a class of short non-coding RNAs that regulate the expression of mRNA targets, are important regulators of cellular senescence and aging. We questioned which miRNAs are involved in age-related degeneration of the organ of Corti (OC), the auditory sensory epithelium that transduce...

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Autores principales: Zhang, Qian, Liu, Huizhan, McGee, JoAnn, Walsh, Edward J., Soukup, Garrett A., He, David Z. Z.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3640032/
https://www.ncbi.nlm.nih.gov/pubmed/23646144
http://dx.doi.org/10.1371/journal.pone.0062786
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author Zhang, Qian
Liu, Huizhan
McGee, JoAnn
Walsh, Edward J.
Soukup, Garrett A.
He, David Z. Z.
author_facet Zhang, Qian
Liu, Huizhan
McGee, JoAnn
Walsh, Edward J.
Soukup, Garrett A.
He, David Z. Z.
author_sort Zhang, Qian
collection PubMed
description MicroRNAs (miRNAs), a class of short non-coding RNAs that regulate the expression of mRNA targets, are important regulators of cellular senescence and aging. We questioned which miRNAs are involved in age-related degeneration of the organ of Corti (OC), the auditory sensory epithelium that transduces mechanical stimuli to electrical activity in the inner ear. Degeneration of the OC is generally accepted as the main cause of age-related hearing loss (ARHL), a progressive loss of hearing in individuals as they grow older. To determine which miRNAs are involved in the onset and progression of ARHL, miRNA gene expression in the OC of two mouse strains, C57BL/6J and CBA/J, was compared at three different ages using GeneChip miRNA microarray and was validated by real-time PCR. We showed that 111 and 71 miRNAs exhibited differential expression in the C57 and CBA mice, respectively, and that downregulated miRNAs substantially outnumbered upregulated miRNAs during aging. miRNAs that had approximately 2-fold upregulation included members of miR-29 family and miR-34 family, which are known regulators of pro-apoptotic pathways. In contrast, miRNAs that were downregulated by about 2-fold were members of the miR-181 family and miR-183 family, which are known to be important for proliferation and differentiation, respectively. The shift of miRNA expression favoring apoptosis occurred earlier than detectable hearing threshold elevation and hair cell loss. Our study suggests that changes in miRNA expression precede morphological and functional changes, and that upregulation of pro-apoptotic miRNAs and downregulation of miRNAs promoting proliferation and differentiation are both involved in age-related degeneration of the OC.
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spelling pubmed-36400322013-05-03 Identifying MicroRNAs Involved in Degeneration of the Organ of Corti during Age-Related Hearing Loss Zhang, Qian Liu, Huizhan McGee, JoAnn Walsh, Edward J. Soukup, Garrett A. He, David Z. Z. PLoS One Research Article MicroRNAs (miRNAs), a class of short non-coding RNAs that regulate the expression of mRNA targets, are important regulators of cellular senescence and aging. We questioned which miRNAs are involved in age-related degeneration of the organ of Corti (OC), the auditory sensory epithelium that transduces mechanical stimuli to electrical activity in the inner ear. Degeneration of the OC is generally accepted as the main cause of age-related hearing loss (ARHL), a progressive loss of hearing in individuals as they grow older. To determine which miRNAs are involved in the onset and progression of ARHL, miRNA gene expression in the OC of two mouse strains, C57BL/6J and CBA/J, was compared at three different ages using GeneChip miRNA microarray and was validated by real-time PCR. We showed that 111 and 71 miRNAs exhibited differential expression in the C57 and CBA mice, respectively, and that downregulated miRNAs substantially outnumbered upregulated miRNAs during aging. miRNAs that had approximately 2-fold upregulation included members of miR-29 family and miR-34 family, which are known regulators of pro-apoptotic pathways. In contrast, miRNAs that were downregulated by about 2-fold were members of the miR-181 family and miR-183 family, which are known to be important for proliferation and differentiation, respectively. The shift of miRNA expression favoring apoptosis occurred earlier than detectable hearing threshold elevation and hair cell loss. Our study suggests that changes in miRNA expression precede morphological and functional changes, and that upregulation of pro-apoptotic miRNAs and downregulation of miRNAs promoting proliferation and differentiation are both involved in age-related degeneration of the OC. Public Library of Science 2013-04-30 /pmc/articles/PMC3640032/ /pubmed/23646144 http://dx.doi.org/10.1371/journal.pone.0062786 Text en © 2013 Zhang 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Zhang, Qian
Liu, Huizhan
McGee, JoAnn
Walsh, Edward J.
Soukup, Garrett A.
He, David Z. Z.
Identifying MicroRNAs Involved in Degeneration of the Organ of Corti during Age-Related Hearing Loss
title Identifying MicroRNAs Involved in Degeneration of the Organ of Corti during Age-Related Hearing Loss
title_full Identifying MicroRNAs Involved in Degeneration of the Organ of Corti during Age-Related Hearing Loss
title_fullStr Identifying MicroRNAs Involved in Degeneration of the Organ of Corti during Age-Related Hearing Loss
title_full_unstemmed Identifying MicroRNAs Involved in Degeneration of the Organ of Corti during Age-Related Hearing Loss
title_short Identifying MicroRNAs Involved in Degeneration of the Organ of Corti during Age-Related Hearing Loss
title_sort identifying micrornas involved in degeneration of the organ of corti during age-related hearing loss
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3640032/
https://www.ncbi.nlm.nih.gov/pubmed/23646144
http://dx.doi.org/10.1371/journal.pone.0062786
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