Gene expression analysis of forskolin treated basilar papillae identifies microRNA181a as a mediator of proliferation.

Auditory hair cells spontaneously regenerate following injury in birds but not mammals. A better understanding of the molecular events underlying hair cell regeneration in birds may allow for identification and eventually manipulation of relevant pathways in mammals to stimulate regeneration and res...

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Main Authors: Corey S Frucht, Mohamed Uduman, Jamie L Duke, Steven H Kleinstein, Joseph Santos-Sacchi, Dhasakumar S Navaratnam
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-07-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2901389?pdf=render
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spelling doaj-e7fce3417f88418a8c56a0b6768e13b82020-11-25T01:00:26ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-07-0157e1150210.1371/journal.pone.0011502Gene expression analysis of forskolin treated basilar papillae identifies microRNA181a as a mediator of proliferation.Corey S FruchtMohamed UdumanJamie L DukeSteven H KleinsteinJoseph Santos-SacchiDhasakumar S NavaratnamAuditory hair cells spontaneously regenerate following injury in birds but not mammals. A better understanding of the molecular events underlying hair cell regeneration in birds may allow for identification and eventually manipulation of relevant pathways in mammals to stimulate regeneration and restore hearing in deaf patients.Gene expression was profiled in forskolin treated (i.e., proliferating) and quiescent control auditory epithelia of post-hatch chicks using an Affymetrix whole-genome chicken array after 24 (n = 6), 48 (n = 6), and 72 (n = 12) hours in culture. In the forskolin-treated epithelia there was significant (p<0.05; >two-fold change) upregulation of many genes thought to be relevant to cell cycle control and inner ear development. Gene set enrichment analysis was performed on the data and identified myriad microRNAs that are likely to be upregulated in the regenerating tissue, including microRNA181a (miR181a), which is known to mediate proliferation in other systems. Functional experiments showed that miR181a overexpression is sufficient to stimulate proliferation within the basilar papilla, as assayed by BrdU incorporation. Further, some of the newly produced cells express the early hair cell marker myosin VI, suggesting that miR181a transfection can result in the production of new hair cells.These studies have identified a single microRNA, miR181a, that can cause proliferation in the chicken auditory epithelium with production of new hair cells.http://europepmc.org/articles/PMC2901389?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Corey S Frucht
Mohamed Uduman
Jamie L Duke
Steven H Kleinstein
Joseph Santos-Sacchi
Dhasakumar S Navaratnam
spellingShingle Corey S Frucht
Mohamed Uduman
Jamie L Duke
Steven H Kleinstein
Joseph Santos-Sacchi
Dhasakumar S Navaratnam
Gene expression analysis of forskolin treated basilar papillae identifies microRNA181a as a mediator of proliferation.
PLoS ONE
author_facet Corey S Frucht
Mohamed Uduman
Jamie L Duke
Steven H Kleinstein
Joseph Santos-Sacchi
Dhasakumar S Navaratnam
author_sort Corey S Frucht
title Gene expression analysis of forskolin treated basilar papillae identifies microRNA181a as a mediator of proliferation.
title_short Gene expression analysis of forskolin treated basilar papillae identifies microRNA181a as a mediator of proliferation.
title_full Gene expression analysis of forskolin treated basilar papillae identifies microRNA181a as a mediator of proliferation.
title_fullStr Gene expression analysis of forskolin treated basilar papillae identifies microRNA181a as a mediator of proliferation.
title_full_unstemmed Gene expression analysis of forskolin treated basilar papillae identifies microRNA181a as a mediator of proliferation.
title_sort gene expression analysis of forskolin treated basilar papillae identifies microrna181a as a mediator of proliferation.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2010-07-01
description Auditory hair cells spontaneously regenerate following injury in birds but not mammals. A better understanding of the molecular events underlying hair cell regeneration in birds may allow for identification and eventually manipulation of relevant pathways in mammals to stimulate regeneration and restore hearing in deaf patients.Gene expression was profiled in forskolin treated (i.e., proliferating) and quiescent control auditory epithelia of post-hatch chicks using an Affymetrix whole-genome chicken array after 24 (n = 6), 48 (n = 6), and 72 (n = 12) hours in culture. In the forskolin-treated epithelia there was significant (p<0.05; >two-fold change) upregulation of many genes thought to be relevant to cell cycle control and inner ear development. Gene set enrichment analysis was performed on the data and identified myriad microRNAs that are likely to be upregulated in the regenerating tissue, including microRNA181a (miR181a), which is known to mediate proliferation in other systems. Functional experiments showed that miR181a overexpression is sufficient to stimulate proliferation within the basilar papilla, as assayed by BrdU incorporation. Further, some of the newly produced cells express the early hair cell marker myosin VI, suggesting that miR181a transfection can result in the production of new hair cells.These studies have identified a single microRNA, miR181a, that can cause proliferation in the chicken auditory epithelium with production of new hair cells.
url http://europepmc.org/articles/PMC2901389?pdf=render
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