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Dynamic Notch signalling regulates neural stem cell state progression in the Drosophila optic lobe

BACKGROUND: Neural stem cells generate all of the neurons and glial cells in the central nervous system, both during development and in the adult to maintain homeostasis. In the Drosophila optic lobe, neuroepithelial cells progress through two transient progenitor states, PI and PII, before transfor...

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Autores principales: Contreras, Esteban G., Egger, Boris, Gold, Katrina S., Brand, Andrea H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251220/
https://www.ncbi.nlm.nih.gov/pubmed/30466475
http://dx.doi.org/10.1186/s13064-018-0123-8
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author Contreras, Esteban G.
Egger, Boris
Gold, Katrina S.
Brand, Andrea H.
author_facet Contreras, Esteban G.
Egger, Boris
Gold, Katrina S.
Brand, Andrea H.
author_sort Contreras, Esteban G.
collection PubMed
description BACKGROUND: Neural stem cells generate all of the neurons and glial cells in the central nervous system, both during development and in the adult to maintain homeostasis. In the Drosophila optic lobe, neuroepithelial cells progress through two transient progenitor states, PI and PII, before transforming into neuroblasts. Here we analyse the role of Notch signalling in the transition from neuroepithelial cells to neuroblasts. RESULTS: We observed dynamic regulation of Notch signalling: strong activity in PI progenitors, low signalling in PII progenitors, and increased activity after neuroblast transformation. Ectopic expression of the Notch ligand Delta induced the formation of ectopic PI progenitors. Interestingly, we show that the E3 ubiquitin ligase, Neuralized, regulates Delta levels and Notch signalling activity at the transition zone. We demonstrate that the proneural transcription factor, Lethal of scute, is essential to induce expression of Neuralized and promote the transition from the PI progenitor to the PII progenitor state. CONCLUSIONS: Our results show dynamic regulation of Notch signalling activity in the transition from neuroepithelial cells to neuroblasts. We propose a model in which Lethal of scute activates Notch signalling in a non-cell autonomous manner by regulating the expression of Neuralized, thereby promoting the progression between different neural stem cell states. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13064-018-0123-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-62512202018-11-29 Dynamic Notch signalling regulates neural stem cell state progression in the Drosophila optic lobe Contreras, Esteban G. Egger, Boris Gold, Katrina S. Brand, Andrea H. Neural Dev Research Article BACKGROUND: Neural stem cells generate all of the neurons and glial cells in the central nervous system, both during development and in the adult to maintain homeostasis. In the Drosophila optic lobe, neuroepithelial cells progress through two transient progenitor states, PI and PII, before transforming into neuroblasts. Here we analyse the role of Notch signalling in the transition from neuroepithelial cells to neuroblasts. RESULTS: We observed dynamic regulation of Notch signalling: strong activity in PI progenitors, low signalling in PII progenitors, and increased activity after neuroblast transformation. Ectopic expression of the Notch ligand Delta induced the formation of ectopic PI progenitors. Interestingly, we show that the E3 ubiquitin ligase, Neuralized, regulates Delta levels and Notch signalling activity at the transition zone. We demonstrate that the proneural transcription factor, Lethal of scute, is essential to induce expression of Neuralized and promote the transition from the PI progenitor to the PII progenitor state. CONCLUSIONS: Our results show dynamic regulation of Notch signalling activity in the transition from neuroepithelial cells to neuroblasts. We propose a model in which Lethal of scute activates Notch signalling in a non-cell autonomous manner by regulating the expression of Neuralized, thereby promoting the progression between different neural stem cell states. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13064-018-0123-8) contains supplementary material, which is available to authorized users. BioMed Central 2018-11-22 /pmc/articles/PMC6251220/ /pubmed/30466475 http://dx.doi.org/10.1186/s13064-018-0123-8 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Contreras, Esteban G.
Egger, Boris
Gold, Katrina S.
Brand, Andrea H.
Dynamic Notch signalling regulates neural stem cell state progression in the Drosophila optic lobe
title Dynamic Notch signalling regulates neural stem cell state progression in the Drosophila optic lobe
title_full Dynamic Notch signalling regulates neural stem cell state progression in the Drosophila optic lobe
title_fullStr Dynamic Notch signalling regulates neural stem cell state progression in the Drosophila optic lobe
title_full_unstemmed Dynamic Notch signalling regulates neural stem cell state progression in the Drosophila optic lobe
title_short Dynamic Notch signalling regulates neural stem cell state progression in the Drosophila optic lobe
title_sort dynamic notch signalling regulates neural stem cell state progression in the drosophila optic lobe
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251220/
https://www.ncbi.nlm.nih.gov/pubmed/30466475
http://dx.doi.org/10.1186/s13064-018-0123-8
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