DSpace Repository

YAP MEDIATES HAIR CELL REGENERATION IN BALANCE ORGANS OF CHICKENS, BUT LATS KINASES SUPPRESS ITS ACTIVITY IN MICE

Show simple item record

dc.contributor.author Rudolf, Mark A.
dc.contributor.author Andreeva, Anna
dc.contributor.author Kozlowski, Mikolaj M.
dc.contributor.author Kim, Christina E.
dc.contributor.author Moskowitz, Bailey A.
dc.contributor.author Anaya-Rocha, Alejandro
dc.contributor.author Kelley, Matthew W.
dc.contributor.author Corwin, Jeffrey T.
dc.date.accessioned 2021-09-16T04:56:26Z
dc.date.available 2021-09-16T04:56:26Z
dc.date.issued 2020-05-13
dc.identifier.citation Rudolf, M. A., Andreeva, A., Kozlowski, M. M., Kim, C. E., Moskowitz, B. A., Anaya-Rocha, A., Kelley, M. W., & Corwin, J. T. (2020). YAP Mediates Hair Cell Regeneration in Balance Organs of Chickens, But LATS Kinases Suppress Its Activity in Mice. The Journal of Neuroscience, 40(20), 3915–3932. https://doi.org/10.1523/jneurosci.0306-20.2020 en_US
dc.identifier.issn 0270-6474
dc.identifier.uri https://doi.org/10.1523/JNEUROSCI.0306-20.2020
dc.identifier.uri https://www.jneurosci.org/content/40/20/3915
dc.identifier.uri http://nur.nu.edu.kz/handle/123456789/5784
dc.description.abstract Loss of sensory hair cells causes permanent hearing and balance deficits in humans and other mammals, but for nonmammals such deficits are temporary. Nonmammals recover hearing and balance sensitivity after supporting cells proliferate and differentiate into replacement hair cells. Evidence of mechanical differences between those sensory epithelia and their supporting cells prompted us to investigate whether the capacity to activate YAP, an effector in the mechanosensitive Hippo pathway, correlates with regenerative capacity in acceleration-sensing utricles of chickens and mice of both sexes. After hair cell ablation, YAP accumulated in supporting cell nuclei in chicken utricles and promoted regenerative proliferation, but YAP remained cytoplasmic and little proliferation occurred in mouse utricles. YAP localization in supporting cells was also more sensitive to shape change and inhibition of MST1/2 in chicken utricles than in mouse utricles. Genetic manipulations showed that in vivo expression of the YAP-S127A variant caused robust proliferation of neonatal mouse supporting cells, which produced progeny that expressed hair cell markers, but proliferative responses declined postnatally. Expression of YAP-5SA, which more effectively evades inhibitory phosphorylation, resulted in TEAD-dependent proliferation of striolar supporting cells, even in adult utricles. Conditional deletion of LATS1/2 kinases abolished the inhibitory phosphorylation of endogenous YAP and led to striolar proliferation in adult mouse utricles. The findings suggest that damage overcomes inhibitory Hippo signaling and facilitates regenerative proliferation in nonmammalian utricles, whereas constitutive LATS1/2 kinase activity suppresses YAP-TEAD signaling in mammalian utricles and contributes to maintaining the proliferative quiescence that appears to underlie the permanence of sensory deficits. Key words: hair cell; Hippo; LATS; regeneration; utricle; YAP en_US
dc.language.iso en en_US
dc.publisher Society for Neuroscience en_US
dc.relation.ispartofseries Journal of Neuroscience;13 May 2020, 40 (20) 3915-3932; DOI: https://doi.org/10.1523/JNEUROSCI.0306-20.2020
dc.rights Attribution-NonCommercial-ShareAlike 3.0 United States *
dc.rights.uri http://creativecommons.org/licenses/by-nc-sa/3.0/us/ *
dc.subject hair cell en_US
dc.subject Hippo en_US
dc.subject LATS en_US
dc.subject regeneration en_US
dc.subject utricle en_US
dc.subject YAP en_US
dc.subject Type of access: Open Access en_US
dc.title YAP MEDIATES HAIR CELL REGENERATION IN BALANCE ORGANS OF CHICKENS, BUT LATS KINASES SUPPRESS ITS ACTIVITY IN MICE en_US
dc.type Article en_US
workflow.import.source science


Files in this item

The following license files are associated with this item:

This item appears in the following Collection(s)

Show simple item record

Attribution-NonCommercial-ShareAlike 3.0 United States Except where otherwise noted, this item's license is described as Attribution-NonCommercial-ShareAlike 3.0 United States