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Journal ArticleDOI

Atoh1 expression defines activated progenitors and differentiating hair cells during avian hair cell regeneration.

Jon Cafaro, +2 more
- 01 Jan 2007 - 
- Vol. 236, Iss: 1, pp 156-170
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TLDR
A role for Atoh1 is suggested in re‐specifying supporting cells and in biasing postmitotic cells toward the hair cell fate during hair cell regeneration in the mature chicken ear.
Abstract
In the avian inner ear, nonsensory supporting cells give rise to new sensory hair cells through two distinct processes: mitosis and direct transdifferentiation. Regulation of supporting cell behavior and cell fate specification during avian hair cell regeneration is poorly characterized. Expression of Atoh1, a proneural transcription factor necessary and sufficient for developmental hair cell specification, was examined using immunofluorescence in quiescent and regenerating hair cell epithelia of mature chickens. In untreated birds, Atoh1 protein was not detected in the auditory epithelium, which is quiescent. In contrast, numerous Atoh1-positive nuclei were seen in the utricular macula, which undergoes continual hair cell turnover. Atoh1-positive nuclei emerged in the auditory epithelium by 15 hr post-ototoxin administration, before overt hair cell damage and supporting cell re-entry into the cell cycle. Subsequently, Atoh1 labeling was seen in 15% of dividing supporting cells. During cell division, Atoh1 was distributed symmetrically to daughter cells, but Atoh1 levels were dramatically regulated shortly thereafter. After cellular differentiation, Atoh1 labeling was confined to hair cells regenerated through either mitosis or direct transdifferentiation. However, Atoh1 expression in dividing progenitors did not necessarily predict hair cell fate specification in daughter cells. Finally, predominant modes of hair cell regeneration varied significantly across the radial axis of the auditory epithelium, with mitosis most frequent neurally and direct transdifferentiation most frequent abneurally. These observations suggest a role for Atoh1 in re-specifying supporting cells and in biasing postmitotic cells toward the hair cell fate during hair cell regeneration in the mature chicken ear. Developmental Dynamics 236:156–170, 2007. © 2006 Wiley-Liss, Inc.

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Citations
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Journal ArticleDOI

Notch Inhibition Induces Cochlear Hair Cell Regeneration and Recovery of Hearing after Acoustic Trauma

TL;DR: It is shown 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.
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Wnt signaling induces proliferation of sensory precursors in the postnatal mouse cochlea

TL;DR: It is suggested that Lgr5 marks sensory precursors and that Wnt signaling can promote their proliferation and provide mechanistic insights into Wnt-responsive progenitor cells during sensory organ development.
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Spontaneous hair cell regeneration in the neonatal mouse cochlea in vivo

TL;DR: It is demonstrated that the neonatal mouse cochlea is capable of spontaneous hair cell regeneration after damage in vivo, which might shed light on the competence of supporting cells to regenerate hair cells and on the factors that promote the survival of newly regenerated hair cells.
Journal ArticleDOI

Notch signaling regulates the extent of hair cell regeneration in the zebrafish lateral line.

TL;DR: A model where Notch signaling limits the number of hair cells produced during regeneration by regulating support cell proliferation is suggested, where proliferative hair cell progenitors are located centrally within the neuromasts, whereas peripheral support cells may have a separate function.
Journal ArticleDOI

Hair cell regeneration in the avian auditory epithelium

TL;DR: Current knowledge about supporting cell properties is reviewed and candidate signaling molecules for regulating supporting cell behavior, in quiescence and after damage are discussed, suggesting they are differentially regulated.
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