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Heterogeneity in the regenerative abilities of central nervous system axons within species: why do some neurons regenerate better than others?
Some neurons, especially in mammalian peripheral nervous system or in lower vertebrate or in vertebrate central nervous system (CNS) regenerate after axotomy, while most mammalian CNS neurons fail to regenerate. There is an emerging consensus that neurons have different intrinsic regenerative capabi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034288/ https://www.ncbi.nlm.nih.gov/pubmed/31823869 http://dx.doi.org/10.4103/1673-5374.270298 |
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author | Rodemer, William Hu, Jianli Selzer, Michael E. Shifman, Michael I. |
author_facet | Rodemer, William Hu, Jianli Selzer, Michael E. Shifman, Michael I. |
author_sort | Rodemer, William |
collection | PubMed |
description | Some neurons, especially in mammalian peripheral nervous system or in lower vertebrate or in vertebrate central nervous system (CNS) regenerate after axotomy, while most mammalian CNS neurons fail to regenerate. There is an emerging consensus that neurons have different intrinsic regenerative capabilities, which theoretically could be manipulated therapeutically to improve regeneration. Population-based comparisons between “good regenerating” and “bad regenerating” neurons in the CNS and peripheral nervous system of most vertebrates yield results that are inconclusive or difficult to interpret. At least in part, this reflects the great diversity of cells in the mammalian CNS. Using mammalian nervous system imposes several methodical limitations. First, the small sizes and large numbers of neurons in the CNS make it very difficult to distinguish regenerating neurons from non-regenerating ones. Second, the lack of identifiable neurons makes it impossible to correlate biochemical changes in a neuron with axonal damage of the same neuron, and therefore, to dissect the molecular mechanisms of regeneration on the level of single neurons. This review will survey the reported responses to axon injury and the determinants of axon regeneration, emphasizing non-mammalian model organisms, which are often under-utilized, but in which the data are especially easy to interpret. |
format | Online Article Text |
id | pubmed-7034288 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-70342882020-03-09 Heterogeneity in the regenerative abilities of central nervous system axons within species: why do some neurons regenerate better than others? Rodemer, William Hu, Jianli Selzer, Michael E. Shifman, Michael I. Neural Regen Res Review Some neurons, especially in mammalian peripheral nervous system or in lower vertebrate or in vertebrate central nervous system (CNS) regenerate after axotomy, while most mammalian CNS neurons fail to regenerate. There is an emerging consensus that neurons have different intrinsic regenerative capabilities, which theoretically could be manipulated therapeutically to improve regeneration. Population-based comparisons between “good regenerating” and “bad regenerating” neurons in the CNS and peripheral nervous system of most vertebrates yield results that are inconclusive or difficult to interpret. At least in part, this reflects the great diversity of cells in the mammalian CNS. Using mammalian nervous system imposes several methodical limitations. First, the small sizes and large numbers of neurons in the CNS make it very difficult to distinguish regenerating neurons from non-regenerating ones. Second, the lack of identifiable neurons makes it impossible to correlate biochemical changes in a neuron with axonal damage of the same neuron, and therefore, to dissect the molecular mechanisms of regeneration on the level of single neurons. This review will survey the reported responses to axon injury and the determinants of axon regeneration, emphasizing non-mammalian model organisms, which are often under-utilized, but in which the data are especially easy to interpret. Wolters Kluwer - Medknow 2019-12-10 /pmc/articles/PMC7034288/ /pubmed/31823869 http://dx.doi.org/10.4103/1673-5374.270298 Text en Copyright: © Neural Regeneration Research http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Review Rodemer, William Hu, Jianli Selzer, Michael E. Shifman, Michael I. Heterogeneity in the regenerative abilities of central nervous system axons within species: why do some neurons regenerate better than others? |
title | Heterogeneity in the regenerative abilities of central nervous system axons within species: why do some neurons regenerate better than others? |
title_full | Heterogeneity in the regenerative abilities of central nervous system axons within species: why do some neurons regenerate better than others? |
title_fullStr | Heterogeneity in the regenerative abilities of central nervous system axons within species: why do some neurons regenerate better than others? |
title_full_unstemmed | Heterogeneity in the regenerative abilities of central nervous system axons within species: why do some neurons regenerate better than others? |
title_short | Heterogeneity in the regenerative abilities of central nervous system axons within species: why do some neurons regenerate better than others? |
title_sort | heterogeneity in the regenerative abilities of central nervous system axons within species: why do some neurons regenerate better than others? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034288/ https://www.ncbi.nlm.nih.gov/pubmed/31823869 http://dx.doi.org/10.4103/1673-5374.270298 |
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