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Mitochondria-enriched protrusions are associated with brain and intestinal stem cells in Drosophila

Brain stem cells stop dividing in late Drosophila embryos and begin dividing again in early larvae after feeding induces reactivation. Quiescent neural stem cells (qNSCs) display an unusual cytoplasmic protrusion that is no longer present in reactivated NSCs. The protrusions join the qNSCs to the ne...

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Autores principales: Endow, Sharyn A., Miller, Sara E., Ly, Phuong Thao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6874589/
https://www.ncbi.nlm.nih.gov/pubmed/31799429
http://dx.doi.org/10.1038/s42003-019-0671-4
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author Endow, Sharyn A.
Miller, Sara E.
Ly, Phuong Thao
author_facet Endow, Sharyn A.
Miller, Sara E.
Ly, Phuong Thao
author_sort Endow, Sharyn A.
collection PubMed
description Brain stem cells stop dividing in late Drosophila embryos and begin dividing again in early larvae after feeding induces reactivation. Quiescent neural stem cells (qNSCs) display an unusual cytoplasmic protrusion that is no longer present in reactivated NSCs. The protrusions join the qNSCs to the neuropil, brain regions that are thought to maintain NSCs in an undifferentiated state, but the function of the protrusions is not known. Here we show that qNSC protrusions contain clustered mitochondria that are likely maintained in position by slow forward-and-backward microtubule growth. Larvae treated with a microtubule-stabilizing drug show bundled microtubules and enhanced mitochondrial clustering in NSCs, together with reduced qNSC reactivation. We further show that intestinal stem cells contain mitochondria-enriched protrusions. The qNSC and intestinal stem-cell protrusions differ from previously reported cytoplasmic extensions by forming stem-cell-to-niche mitochondrial bridges that could potentially both silence genes and sense signals from the stem cell niche.
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spelling pubmed-68745892019-12-03 Mitochondria-enriched protrusions are associated with brain and intestinal stem cells in Drosophila Endow, Sharyn A. Miller, Sara E. Ly, Phuong Thao Commun Biol Article Brain stem cells stop dividing in late Drosophila embryos and begin dividing again in early larvae after feeding induces reactivation. Quiescent neural stem cells (qNSCs) display an unusual cytoplasmic protrusion that is no longer present in reactivated NSCs. The protrusions join the qNSCs to the neuropil, brain regions that are thought to maintain NSCs in an undifferentiated state, but the function of the protrusions is not known. Here we show that qNSC protrusions contain clustered mitochondria that are likely maintained in position by slow forward-and-backward microtubule growth. Larvae treated with a microtubule-stabilizing drug show bundled microtubules and enhanced mitochondrial clustering in NSCs, together with reduced qNSC reactivation. We further show that intestinal stem cells contain mitochondria-enriched protrusions. The qNSC and intestinal stem-cell protrusions differ from previously reported cytoplasmic extensions by forming stem-cell-to-niche mitochondrial bridges that could potentially both silence genes and sense signals from the stem cell niche. Nature Publishing Group UK 2019-11-22 /pmc/articles/PMC6874589/ /pubmed/31799429 http://dx.doi.org/10.1038/s42003-019-0671-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Endow, Sharyn A.
Miller, Sara E.
Ly, Phuong Thao
Mitochondria-enriched protrusions are associated with brain and intestinal stem cells in Drosophila
title Mitochondria-enriched protrusions are associated with brain and intestinal stem cells in Drosophila
title_full Mitochondria-enriched protrusions are associated with brain and intestinal stem cells in Drosophila
title_fullStr Mitochondria-enriched protrusions are associated with brain and intestinal stem cells in Drosophila
title_full_unstemmed Mitochondria-enriched protrusions are associated with brain and intestinal stem cells in Drosophila
title_short Mitochondria-enriched protrusions are associated with brain and intestinal stem cells in Drosophila
title_sort mitochondria-enriched protrusions are associated with brain and intestinal stem cells in drosophila
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6874589/
https://www.ncbi.nlm.nih.gov/pubmed/31799429
http://dx.doi.org/10.1038/s42003-019-0671-4
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