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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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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. |
format | Online Article Text |
id | pubmed-6874589 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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