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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...

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Autores principales: Licht, Tamar, Sasson, Esther, Bell, Batia, Grunewald, Myriam, Kumar, Saran, Kreisel, Tirzah, Ben-Zvi, Ayal, Keshet, Eli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
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.
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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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