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Neurogenesis of medium spiny neurons in the nucleus accumbens continues into adulthood and is enhanced by pathological pain

In mammals, most adult neural stem cells (NSCs) are located in the ventricular–subventricular zone (V-SVZ) along the wall of the lateral ventricles and they are the source of olfactory bulb interneurons. Adult NSCs exhibit an apico-basal polarity; they harbor a short apical process and a long basal...

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Autores principales: García-González, Diego, Dumitru, Ionut, Zuccotti, Annalisa, Yen, Ting-Yun, Herranz-Pérez, Vicente, Tan, Linette Liqi, Neitz, Angela, García-Verdugo, José Manuel, Kuner, Rohini, Alfonso, Julieta, Monyer, Hannah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8589654/
https://www.ncbi.nlm.nih.gov/pubmed/32612250
http://dx.doi.org/10.1038/s41380-020-0823-4
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author García-González, Diego
Dumitru, Ionut
Zuccotti, Annalisa
Yen, Ting-Yun
Herranz-Pérez, Vicente
Tan, Linette Liqi
Neitz, Angela
García-Verdugo, José Manuel
Kuner, Rohini
Alfonso, Julieta
Monyer, Hannah
author_facet García-González, Diego
Dumitru, Ionut
Zuccotti, Annalisa
Yen, Ting-Yun
Herranz-Pérez, Vicente
Tan, Linette Liqi
Neitz, Angela
García-Verdugo, José Manuel
Kuner, Rohini
Alfonso, Julieta
Monyer, Hannah
author_sort García-González, Diego
collection PubMed
description In mammals, most adult neural stem cells (NSCs) are located in the ventricular–subventricular zone (V-SVZ) along the wall of the lateral ventricles and they are the source of olfactory bulb interneurons. Adult NSCs exhibit an apico-basal polarity; they harbor a short apical process and a long basal process, reminiscent of radial glia morphology. In the adult mouse brain, we detected extremely long radial glia-like fibers that originate from the anterior–ventral V-SVZ and that are directed to the ventral striatum. Interestingly, a fraction of adult V-SVZ-derived neuroblasts dispersed in close association with the radial glia-like fibers in the nucleus accumbens (NAc). Using several in vivo mouse models, we show that newborn neurons integrate into preexisting circuits in the NAc where they mature as medium spiny neurons (MSNs), i.e., a type of projection neurons formerly believed to be generated only during embryonic development. Moreover, we found that the number of newborn neurons in the NAc is dynamically regulated by persistent pain, suggesting that adult neurogenesis of MSNs is an experience-modulated process.
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spelling pubmed-85896542021-11-23 Neurogenesis of medium spiny neurons in the nucleus accumbens continues into adulthood and is enhanced by pathological pain García-González, Diego Dumitru, Ionut Zuccotti, Annalisa Yen, Ting-Yun Herranz-Pérez, Vicente Tan, Linette Liqi Neitz, Angela García-Verdugo, José Manuel Kuner, Rohini Alfonso, Julieta Monyer, Hannah Mol Psychiatry Article In mammals, most adult neural stem cells (NSCs) are located in the ventricular–subventricular zone (V-SVZ) along the wall of the lateral ventricles and they are the source of olfactory bulb interneurons. Adult NSCs exhibit an apico-basal polarity; they harbor a short apical process and a long basal process, reminiscent of radial glia morphology. In the adult mouse brain, we detected extremely long radial glia-like fibers that originate from the anterior–ventral V-SVZ and that are directed to the ventral striatum. Interestingly, a fraction of adult V-SVZ-derived neuroblasts dispersed in close association with the radial glia-like fibers in the nucleus accumbens (NAc). Using several in vivo mouse models, we show that newborn neurons integrate into preexisting circuits in the NAc where they mature as medium spiny neurons (MSNs), i.e., a type of projection neurons formerly believed to be generated only during embryonic development. Moreover, we found that the number of newborn neurons in the NAc is dynamically regulated by persistent pain, suggesting that adult neurogenesis of MSNs is an experience-modulated process. Nature Publishing Group UK 2020-07-01 2021 /pmc/articles/PMC8589654/ /pubmed/32612250 http://dx.doi.org/10.1038/s41380-020-0823-4 Text en © The Author(s), under exclusive licence to Springer Nature Limited 2020, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
García-González, Diego
Dumitru, Ionut
Zuccotti, Annalisa
Yen, Ting-Yun
Herranz-Pérez, Vicente
Tan, Linette Liqi
Neitz, Angela
García-Verdugo, José Manuel
Kuner, Rohini
Alfonso, Julieta
Monyer, Hannah
Neurogenesis of medium spiny neurons in the nucleus accumbens continues into adulthood and is enhanced by pathological pain
title Neurogenesis of medium spiny neurons in the nucleus accumbens continues into adulthood and is enhanced by pathological pain
title_full Neurogenesis of medium spiny neurons in the nucleus accumbens continues into adulthood and is enhanced by pathological pain
title_fullStr Neurogenesis of medium spiny neurons in the nucleus accumbens continues into adulthood and is enhanced by pathological pain
title_full_unstemmed Neurogenesis of medium spiny neurons in the nucleus accumbens continues into adulthood and is enhanced by pathological pain
title_short Neurogenesis of medium spiny neurons in the nucleus accumbens continues into adulthood and is enhanced by pathological pain
title_sort neurogenesis of medium spiny neurons in the nucleus accumbens continues into adulthood and is enhanced by pathological pain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8589654/
https://www.ncbi.nlm.nih.gov/pubmed/32612250
http://dx.doi.org/10.1038/s41380-020-0823-4
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