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Long-term self-renewing stem cells in the adult mouse hippocampus identified by intravital imaging
Neural stem cells (NSCs) generate neurons throughout life in the mammalian hippocampus. However, the potential for long-term self-renewal of individual NSCs within the adult brain remains unclear. We used 2-photon microscopy and followed NSCs that were genetically labeled through conditional recombi...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7116750/ https://www.ncbi.nlm.nih.gov/pubmed/33349709 http://dx.doi.org/10.1038/s41593-020-00759-4 |
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author | Bottes, Sara Jaeger, Baptiste N. Pilz, Gregor-Alexander Jörg, David J. Cole, John Darby Kruse, Merit Harris, Lachlan Korobeynyk, Vladislav I. Mallona, Izaskun Helmchen, Fritjof Guillemot, François Simons, Benjamin D. Jessberger, Sebastian |
author_facet | Bottes, Sara Jaeger, Baptiste N. Pilz, Gregor-Alexander Jörg, David J. Cole, John Darby Kruse, Merit Harris, Lachlan Korobeynyk, Vladislav I. Mallona, Izaskun Helmchen, Fritjof Guillemot, François Simons, Benjamin D. Jessberger, Sebastian |
author_sort | Bottes, Sara |
collection | PubMed |
description | Neural stem cells (NSCs) generate neurons throughout life in the mammalian hippocampus. However, the potential for long-term self-renewal of individual NSCs within the adult brain remains unclear. We used 2-photon microscopy and followed NSCs that were genetically labeled through conditional recombination driven by the regulatory elements of the stem cell-expressed genes GLI Family Zinc Finger 1 (Gli1) or Achaete-scute homolog 1 (Ascl1). Through intravital imaging of NSCs and their progeny, we identify a population of Gli1-targeted NSCs showing long-term self-renewal in the adult hippocampus. In contrast, once activated, Ascl1-targeted NSCs undergo limited proliferative activity before they become exhausted. Using single-cell RNA sequencing, we show that Gli1- and Ascl1-targeted cells have highly similar yet distinct transcriptional profiles, supporting the existence of heterogeneous NSC populations with diverse behavioral properties. Thus, we here identify long-term self-renewing NSCs that contribute to the generation of new neurons in the adult hippocampus. |
format | Online Article Text |
id | pubmed-7116750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
spelling | pubmed-71167502021-06-21 Long-term self-renewing stem cells in the adult mouse hippocampus identified by intravital imaging Bottes, Sara Jaeger, Baptiste N. Pilz, Gregor-Alexander Jörg, David J. Cole, John Darby Kruse, Merit Harris, Lachlan Korobeynyk, Vladislav I. Mallona, Izaskun Helmchen, Fritjof Guillemot, François Simons, Benjamin D. Jessberger, Sebastian Nat Neurosci Article Neural stem cells (NSCs) generate neurons throughout life in the mammalian hippocampus. However, the potential for long-term self-renewal of individual NSCs within the adult brain remains unclear. We used 2-photon microscopy and followed NSCs that were genetically labeled through conditional recombination driven by the regulatory elements of the stem cell-expressed genes GLI Family Zinc Finger 1 (Gli1) or Achaete-scute homolog 1 (Ascl1). Through intravital imaging of NSCs and their progeny, we identify a population of Gli1-targeted NSCs showing long-term self-renewal in the adult hippocampus. In contrast, once activated, Ascl1-targeted NSCs undergo limited proliferative activity before they become exhausted. Using single-cell RNA sequencing, we show that Gli1- and Ascl1-targeted cells have highly similar yet distinct transcriptional profiles, supporting the existence of heterogeneous NSC populations with diverse behavioral properties. Thus, we here identify long-term self-renewing NSCs that contribute to the generation of new neurons in the adult hippocampus. 2021-02-01 2020-12-21 /pmc/articles/PMC7116750/ /pubmed/33349709 http://dx.doi.org/10.1038/s41593-020-00759-4 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Bottes, Sara Jaeger, Baptiste N. Pilz, Gregor-Alexander Jörg, David J. Cole, John Darby Kruse, Merit Harris, Lachlan Korobeynyk, Vladislav I. Mallona, Izaskun Helmchen, Fritjof Guillemot, François Simons, Benjamin D. Jessberger, Sebastian Long-term self-renewing stem cells in the adult mouse hippocampus identified by intravital imaging |
title | Long-term self-renewing stem cells in the adult mouse hippocampus identified by intravital imaging |
title_full | Long-term self-renewing stem cells in the adult mouse hippocampus identified by intravital imaging |
title_fullStr | Long-term self-renewing stem cells in the adult mouse hippocampus identified by intravital imaging |
title_full_unstemmed | Long-term self-renewing stem cells in the adult mouse hippocampus identified by intravital imaging |
title_short | Long-term self-renewing stem cells in the adult mouse hippocampus identified by intravital imaging |
title_sort | long-term self-renewing stem cells in the adult mouse hippocampus identified by intravital imaging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7116750/ https://www.ncbi.nlm.nih.gov/pubmed/33349709 http://dx.doi.org/10.1038/s41593-020-00759-4 |
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