Notch signaling represses cone photoreceptor formation through the regulation of retinal progenitor cell states

Abstract Notch signaling is required to repress the formation of vertebrate cone photoreceptors and to maintain the proliferative potential of multipotent retinal progenitor cells. However, the mechanism by which Notch signaling controls these processes is unknown. Recently, restricted retinal proge...

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Main Authors: Xueqing Chen, Mark M. Emerson
Format: Article
Language:English
Published: Nature Publishing Group 2021-07-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-93692-w
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spelling doaj-7619a49ad38c47f59e5abf5ba2cd289d2021-07-18T11:24:31ZengNature Publishing GroupScientific Reports2045-23222021-07-0111111810.1038/s41598-021-93692-wNotch signaling represses cone photoreceptor formation through the regulation of retinal progenitor cell statesXueqing Chen0Mark M. Emerson1Biology PhD Program, The Graduate Center, The City University of New YorkBiology PhD Program, The Graduate Center, The City University of New YorkAbstract Notch signaling is required to repress the formation of vertebrate cone photoreceptors and to maintain the proliferative potential of multipotent retinal progenitor cells. However, the mechanism by which Notch signaling controls these processes is unknown. Recently, restricted retinal progenitor cells with limited proliferation capacity and that preferentially generate cone photoreceptors have been identified. Thus, there are several potential steps during cone genesis that Notch signaling could act. Here we use cell type specific cis-regulatory elements to localize the primary role of Notch signaling in cone genesis to the formation of restricted retinal progenitor cells from multipotent retinal progenitor cells. Localized inhibition of Notch signaling in restricted progenitor cells does not alter the number of cones derived from these cells. Cell cycle promotion is not a primary effect of Notch signaling but an indirect effect on progenitor cell state transitions that leads to depletion of the multipotent progenitor cell population. Taken together, this suggests that the role of Notch signaling in cone photoreceptor formation and proliferation are both mediated by a localized function of Notch in multipotent retinal progenitor cells to repress the formation of restricted progenitor cells.https://doi.org/10.1038/s41598-021-93692-w
collection DOAJ
language English
format Article
sources DOAJ
author Xueqing Chen
Mark M. Emerson
spellingShingle Xueqing Chen
Mark M. Emerson
Notch signaling represses cone photoreceptor formation through the regulation of retinal progenitor cell states
Scientific Reports
author_facet Xueqing Chen
Mark M. Emerson
author_sort Xueqing Chen
title Notch signaling represses cone photoreceptor formation through the regulation of retinal progenitor cell states
title_short Notch signaling represses cone photoreceptor formation through the regulation of retinal progenitor cell states
title_full Notch signaling represses cone photoreceptor formation through the regulation of retinal progenitor cell states
title_fullStr Notch signaling represses cone photoreceptor formation through the regulation of retinal progenitor cell states
title_full_unstemmed Notch signaling represses cone photoreceptor formation through the regulation of retinal progenitor cell states
title_sort notch signaling represses cone photoreceptor formation through the regulation of retinal progenitor cell states
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-07-01
description Abstract Notch signaling is required to repress the formation of vertebrate cone photoreceptors and to maintain the proliferative potential of multipotent retinal progenitor cells. However, the mechanism by which Notch signaling controls these processes is unknown. Recently, restricted retinal progenitor cells with limited proliferation capacity and that preferentially generate cone photoreceptors have been identified. Thus, there are several potential steps during cone genesis that Notch signaling could act. Here we use cell type specific cis-regulatory elements to localize the primary role of Notch signaling in cone genesis to the formation of restricted retinal progenitor cells from multipotent retinal progenitor cells. Localized inhibition of Notch signaling in restricted progenitor cells does not alter the number of cones derived from these cells. Cell cycle promotion is not a primary effect of Notch signaling but an indirect effect on progenitor cell state transitions that leads to depletion of the multipotent progenitor cell population. Taken together, this suggests that the role of Notch signaling in cone photoreceptor formation and proliferation are both mediated by a localized function of Notch in multipotent retinal progenitor cells to repress the formation of restricted progenitor cells.
url https://doi.org/10.1038/s41598-021-93692-w
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