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Hippocampal neural stem cells facilitate access from circulation via apical cytoplasmic processes
Blood vessels (BVs) are considered an integral component of neural stem cells (NSCs) niches. NSCs in the dentate gyrus (DG(have enigmatic elaborated apical cellular processes that are associated with BVs. Whether this contact serves as a mechanism for delivering circulating molecules is not known. H...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7297534/ https://www.ncbi.nlm.nih.gov/pubmed/32496193 http://dx.doi.org/10.7554/eLife.52134 |
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author | Licht, Tamar Sasson, Esther Bell, Batia Grunewald, Myriam Kumar, Saran Kreisel, Tirzah Ben-Zvi, Ayal Keshet, Eli |
author_facet | Licht, Tamar Sasson, Esther Bell, Batia Grunewald, Myriam Kumar, Saran Kreisel, Tirzah Ben-Zvi, Ayal Keshet, Eli |
author_sort | Licht, Tamar |
collection | PubMed |
description | Blood vessels (BVs) are considered an integral component of neural stem cells (NSCs) niches. NSCs in the dentate gyrus (DG(have enigmatic elaborated apical cellular processes that are associated with BVs. Whether this contact serves as a mechanism for delivering circulating molecules is not known. Here we uncovered a previously unrecognized communication route allowing exclusive direct access of blood-borne substances to hippocampal NSCs. BBB-impermeable fluorescent tracer injected transcardially to mice is selectively uptaken by DG NSCs within a minute, via the vessel-associated apical processes. These processes, measured >30 nm in diameter, establish direct membrane-to-membrane contact with endothelial cells in specialized areas of irregular endothelial basement membrane and enriched with vesicular activity. Doxorubicin, a brain-impermeable chemotherapeutic agent, is also readily and selectively uptaken by NSCs and reduces their proliferation, which might explain its problematic anti-neurogenic or cognitive side-effect. The newly-discovered NSC-BV communication route explains how circulatory neurogenic mediators are 'sensed' by NSCs. |
format | Online Article Text |
id | pubmed-7297534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-72975342020-06-18 Hippocampal neural stem cells facilitate access from circulation via apical cytoplasmic processes Licht, Tamar Sasson, Esther Bell, Batia Grunewald, Myriam Kumar, Saran Kreisel, Tirzah Ben-Zvi, Ayal Keshet, Eli eLife Neuroscience Blood vessels (BVs) are considered an integral component of neural stem cells (NSCs) niches. NSCs in the dentate gyrus (DG(have enigmatic elaborated apical cellular processes that are associated with BVs. Whether this contact serves as a mechanism for delivering circulating molecules is not known. Here we uncovered a previously unrecognized communication route allowing exclusive direct access of blood-borne substances to hippocampal NSCs. BBB-impermeable fluorescent tracer injected transcardially to mice is selectively uptaken by DG NSCs within a minute, via the vessel-associated apical processes. These processes, measured >30 nm in diameter, establish direct membrane-to-membrane contact with endothelial cells in specialized areas of irregular endothelial basement membrane and enriched with vesicular activity. Doxorubicin, a brain-impermeable chemotherapeutic agent, is also readily and selectively uptaken by NSCs and reduces their proliferation, which might explain its problematic anti-neurogenic or cognitive side-effect. The newly-discovered NSC-BV communication route explains how circulatory neurogenic mediators are 'sensed' by NSCs. eLife Sciences Publications, Ltd 2020-06-04 /pmc/articles/PMC7297534/ /pubmed/32496193 http://dx.doi.org/10.7554/eLife.52134 Text en © 2020, Licht et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Licht, Tamar Sasson, Esther Bell, Batia Grunewald, Myriam Kumar, Saran Kreisel, Tirzah Ben-Zvi, Ayal Keshet, Eli Hippocampal neural stem cells facilitate access from circulation via apical cytoplasmic processes |
title | Hippocampal neural stem cells facilitate access from circulation via apical cytoplasmic processes |
title_full | Hippocampal neural stem cells facilitate access from circulation via apical cytoplasmic processes |
title_fullStr | Hippocampal neural stem cells facilitate access from circulation via apical cytoplasmic processes |
title_full_unstemmed | Hippocampal neural stem cells facilitate access from circulation via apical cytoplasmic processes |
title_short | Hippocampal neural stem cells facilitate access from circulation via apical cytoplasmic processes |
title_sort | hippocampal neural stem cells facilitate access from circulation via apical cytoplasmic processes |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7297534/ https://www.ncbi.nlm.nih.gov/pubmed/32496193 http://dx.doi.org/10.7554/eLife.52134 |
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