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      Lgr5-Positive Supporting Cells Generate New Hair Cells in the Postnatal Cochlea

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          Summary

          The prevalence of hearing loss after damage to the mammalian cochlea has been thought to be due to a lack of spontaneous regeneration of hair cells, the primary receptor cells for sound. Here, we show that supporting cells, which surround hair cells in the normal cochlear epithelium, differentiate into new hair cells in the neonatal mouse following ototoxic damage. Using lineage tracing, we show that new hair cells, predominantly outer hair cells, arise from Lgr5-expressing inner pillar and third Deiters cells and that new hair cell generation is increased by pharmacological inhibition of Notch. These data suggest that the neonatal mammalian cochlea has some capacity for hair cell regeneration following damage alone and that Lgr5-positive cells act as hair cell progenitors in the cochlea.

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          Highlights

          • Hair cells regenerate after damage to the neonatal mouse cochlea

          • Generation of hair cells is increased by inhibition of Notch

          • Hair cells regenerate by transdifferentiation with minimal proliferation

          • Regenerated hair cells arise from Lgr5-positive supporting cells

          Abstract

          Although hair cells, the primary receptor cells for sound, had been thought to be incapable of regeneration, Edge and colleagues find that supporting cells, which surround hair cells in the normal cochlear epithelium, include a subset of Lgr5-expressing cells that act as progenitor cells, differentiating into hair cells in the neonatal mouse after damage.

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          Most cited references34

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          Prestin is the motor protein of cochlear outer hair cells.

          The outer and inner hair cells of the mammalian cochlea perform different functions. In response to changes in membrane potential, the cylindrical outer hair cell rapidly alters its length and stiffness. These mechanical changes, driven by putative molecular motors, are assumed to produce amplification of vibrations in the cochlea that are transduced by inner hair cells. Here we have identified an abundant complementary DNA from a gene, designated Prestin, which is specifically expressed in outer hair cells. Regions of the encoded protein show moderate sequence similarity to pendrin and related sulphate/anion transport proteins. Voltage-induced shape changes can be elicited in cultured human kidney cells that express prestin. The mechanical response of outer hair cells to voltage change is accompanied by a 'gating current', which is manifested as nonlinear capacitance. We also demonstrate this nonlinear capacitance in transfected kidney cells. We conclude that prestin is the motor protein of the cochlear outer hair cell.
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            Wnt signalling induces maturation of Paneth cells in intestinal crypts.

            Wnt signalling, which is transduced through beta-catenin/TCF4, maintains the undifferentiated state of intestinal crypt progenitor cells. Mutational activation of the pathway initiates the adenomacarcinoma sequence. Whereas all other differentiated epithelial cells migrate from the crypt onto the villus, Paneth cells home towards the source of Wnt signals--that is, the crypt bottom. Here, we show that expression of a Paneth gene programme is critically dependent on TCF4 in embryonic intestine. Moreover, conditional deletion of the Wnt receptor Frizzled-5 abrogates expression of these genes in Paneth cells in the adult intestine. Conversely, adenomas in Apc-mutant mice and colorectal cancers in humans inappropriately express these Paneth-cell genes. These observations imply that Wnt signals in the crypt can separately drive a stem-cell/progenitor gene programme and a Paneth-cell maturation programme. In intestinal cancer, both gene programmes are activated simultaneously.
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              Notch inhibition induces cochlear hair cell regeneration and recovery of hearing after acoustic trauma.

              Hearing loss due to damage to auditory hair cells is normally irreversible because mammalian hair cells do not regenerate. Here, we show that new hair cells can be induced and can cause partial recovery of hearing in ears damaged by noise trauma, when Notch signaling is inhibited by a γ-secretase inhibitor selected for potency in stimulating hair cell differentiation from inner ear stem cells in vitro. Hair cell generation resulted from an increase in the level of bHLH transcription factor Atoh1 in response to inhibition of Notch signaling. In vivo prospective labeling of Sox2-expressing cells with a Cre-lox system unambiguously demonstrated that hair cell generation resulted from transdifferentiation of supporting cells. Manipulating cell fate of cochlear sensory cells in vivo by pharmacological inhibition of Notch signaling is thus a potential therapeutic approach to the treatment of deafness. Copyright © 2013 Elsevier Inc. All rights reserved.
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                Author and article information

                Contributors
                Journal
                Stem Cell Reports
                Stem Cell Reports
                Stem Cell Reports
                Elsevier
                2213-6711
                20 February 2014
                20 February 2014
                11 March 2014
                : 2
                : 3
                : 311-322
                Affiliations
                [1 ]Department of Otology and Laryngology, Harvard Medical School, Boston, MA 02115, USA
                [2 ]Eaton-Peabody Laboratory, Massachusetts Eye and Ear Infirmary, Boston, MA 02114, USA
                [3 ]Program in Speech and Hearing Bioscience and Technology, Division of Health Sciences and Technology, Harvard and MIT, Cambridge, MA 02139, USA
                [4 ]Massachusetts General Hospital Center for Regenerative Medicine, Boston, MA 02114, USA
                Author notes
                []Corresponding author albert_edge@ 123456meei.harvard.edu
                Article
                S2213-6711(14)00025-3
                10.1016/j.stemcr.2014.01.008
                3964281
                24672754
                6bbe5b04-958e-49de-ac50-9e0ac38a859c
                © 2014 The Authors
                History
                : 21 July 2013
                : 16 January 2014
                : 17 January 2014
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