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Vascular regulation of adult neurogenesis under physiological and pathological conditions

Neural stem cells in the mammalian adult brain continuously produce new neurons throughout life. Accumulating evidence in rodents suggests that various aspects of adult neurogenesis, including the genesis, migration, and maturation of new neurons, are regulated by factors derived from blood vessels...

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Detalles Bibliográficos
Autores principales: Sawada, Masato, Matsumoto, Mami, Sawamoto, Kazunobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955849/
https://www.ncbi.nlm.nih.gov/pubmed/24672424
http://dx.doi.org/10.3389/fnins.2014.00053
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author Sawada, Masato
Matsumoto, Mami
Sawamoto, Kazunobu
author_facet Sawada, Masato
Matsumoto, Mami
Sawamoto, Kazunobu
author_sort Sawada, Masato
collection PubMed
description Neural stem cells in the mammalian adult brain continuously produce new neurons throughout life. Accumulating evidence in rodents suggests that various aspects of adult neurogenesis, including the genesis, migration, and maturation of new neurons, are regulated by factors derived from blood vessels and their microenvironment. Brain injury enhances both neurogenesis and angiogenesis, thereby promoting the cooperative regeneration of neurons and blood vessels. In this paper, we briefly review the mechanisms for the vascular regulation of adult neurogenesis in the ventricular-subventricular zone under physiological and pathological conditions, and discuss their clinical potential for brain regeneration strategies.
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spelling pubmed-39558492014-03-26 Vascular regulation of adult neurogenesis under physiological and pathological conditions Sawada, Masato Matsumoto, Mami Sawamoto, Kazunobu Front Neurosci Neuroscience Neural stem cells in the mammalian adult brain continuously produce new neurons throughout life. Accumulating evidence in rodents suggests that various aspects of adult neurogenesis, including the genesis, migration, and maturation of new neurons, are regulated by factors derived from blood vessels and their microenvironment. Brain injury enhances both neurogenesis and angiogenesis, thereby promoting the cooperative regeneration of neurons and blood vessels. In this paper, we briefly review the mechanisms for the vascular regulation of adult neurogenesis in the ventricular-subventricular zone under physiological and pathological conditions, and discuss their clinical potential for brain regeneration strategies. Frontiers Media S.A. 2014-03-17 /pmc/articles/PMC3955849/ /pubmed/24672424 http://dx.doi.org/10.3389/fnins.2014.00053 Text en Copyright © 2014 Sawada, Matsumoto and Sawamoto. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Sawada, Masato
Matsumoto, Mami
Sawamoto, Kazunobu
Vascular regulation of adult neurogenesis under physiological and pathological conditions
title Vascular regulation of adult neurogenesis under physiological and pathological conditions
title_full Vascular regulation of adult neurogenesis under physiological and pathological conditions
title_fullStr Vascular regulation of adult neurogenesis under physiological and pathological conditions
title_full_unstemmed Vascular regulation of adult neurogenesis under physiological and pathological conditions
title_short Vascular regulation of adult neurogenesis under physiological and pathological conditions
title_sort vascular regulation of adult neurogenesis under physiological and pathological conditions
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955849/
https://www.ncbi.nlm.nih.gov/pubmed/24672424
http://dx.doi.org/10.3389/fnins.2014.00053
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