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Neuronal survival in the brain: neuron type-specific mechanisms

Neurogenic regions of mammalian brain produce many more neurons that will eventually survive and reach a mature stage. Developmental cell death affects both embryonically produced immature neurons and those immature neurons that are generated in regions of adult neurogenesis. Removal of substantial...

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Detalles Bibliográficos
Autores principales: Pfisterer, Ulrich, Khodosevich, Konstantin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5386560/
https://www.ncbi.nlm.nih.gov/pubmed/28252642
http://dx.doi.org/10.1038/cddis.2017.64
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author Pfisterer, Ulrich
Khodosevich, Konstantin
author_facet Pfisterer, Ulrich
Khodosevich, Konstantin
author_sort Pfisterer, Ulrich
collection PubMed
description Neurogenic regions of mammalian brain produce many more neurons that will eventually survive and reach a mature stage. Developmental cell death affects both embryonically produced immature neurons and those immature neurons that are generated in regions of adult neurogenesis. Removal of substantial numbers of neurons that are not yet completely integrated into the local circuits helps to ensure that maturation and homeostatic function of neuronal networks in the brain proceed correctly. External signals from brain microenvironment together with intrinsic signaling pathways determine whether a particular neuron will die. To accommodate this signaling, immature neurons in the brain express a number of transmembrane factors as well as intracellular signaling molecules that will regulate the cell survival/death decision, and many of these factors cease being expressed upon neuronal maturation. Furthermore, pro-survival factors and intracellular responses depend on the type of neuron and region of the brain. Thus, in addition to some common neuronal pro-survival signaling, different types of neurons possess a variety of 'neuron type-specific' pro-survival constituents that might help them to adapt for survival in a certain brain region. This review focuses on how immature neurons survive during normal and impaired brain development, both in the embryonic/neonatal brain and in brain regions associated with adult neurogenesis, and emphasizes neuron type-specific mechanisms that help to survive for various types of immature neurons. Importantly, we mainly focus on in vivo data to describe neuronal survival specifically in the brain, without extrapolating data obtained in the PNS or spinal cord, and thus emphasize the influence of the complex brain environment on neuronal survival during development.
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spelling pubmed-53865602017-04-27 Neuronal survival in the brain: neuron type-specific mechanisms Pfisterer, Ulrich Khodosevich, Konstantin Cell Death Dis Review Neurogenic regions of mammalian brain produce many more neurons that will eventually survive and reach a mature stage. Developmental cell death affects both embryonically produced immature neurons and those immature neurons that are generated in regions of adult neurogenesis. Removal of substantial numbers of neurons that are not yet completely integrated into the local circuits helps to ensure that maturation and homeostatic function of neuronal networks in the brain proceed correctly. External signals from brain microenvironment together with intrinsic signaling pathways determine whether a particular neuron will die. To accommodate this signaling, immature neurons in the brain express a number of transmembrane factors as well as intracellular signaling molecules that will regulate the cell survival/death decision, and many of these factors cease being expressed upon neuronal maturation. Furthermore, pro-survival factors and intracellular responses depend on the type of neuron and region of the brain. Thus, in addition to some common neuronal pro-survival signaling, different types of neurons possess a variety of 'neuron type-specific' pro-survival constituents that might help them to adapt for survival in a certain brain region. This review focuses on how immature neurons survive during normal and impaired brain development, both in the embryonic/neonatal brain and in brain regions associated with adult neurogenesis, and emphasizes neuron type-specific mechanisms that help to survive for various types of immature neurons. Importantly, we mainly focus on in vivo data to describe neuronal survival specifically in the brain, without extrapolating data obtained in the PNS or spinal cord, and thus emphasize the influence of the complex brain environment on neuronal survival during development. Nature Publishing Group 2017-03 2017-03-02 /pmc/articles/PMC5386560/ /pubmed/28252642 http://dx.doi.org/10.1038/cddis.2017.64 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ Cell Death and Disease is an open-access journal published by Nature Publishing Group. This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Review
Pfisterer, Ulrich
Khodosevich, Konstantin
Neuronal survival in the brain: neuron type-specific mechanisms
title Neuronal survival in the brain: neuron type-specific mechanisms
title_full Neuronal survival in the brain: neuron type-specific mechanisms
title_fullStr Neuronal survival in the brain: neuron type-specific mechanisms
title_full_unstemmed Neuronal survival in the brain: neuron type-specific mechanisms
title_short Neuronal survival in the brain: neuron type-specific mechanisms
title_sort neuronal survival in the brain: neuron type-specific mechanisms
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5386560/
https://www.ncbi.nlm.nih.gov/pubmed/28252642
http://dx.doi.org/10.1038/cddis.2017.64
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