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Axon degeneration: Molecular mechanisms of a self-destruction pathway
Axon degeneration is a characteristic event in many neurodegenerative conditions including stroke, glaucoma, and motor neuropathies. However, the molecular pathways that regulate this process remain unclear. Axon loss in chronic neurodegenerative diseases share many morphological features with those...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3255986/ https://www.ncbi.nlm.nih.gov/pubmed/22232700 http://dx.doi.org/10.1083/jcb.201108111 |
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author | Wang, Jack T. Medress, Zachary A. Barres, Ben A. |
author_facet | Wang, Jack T. Medress, Zachary A. Barres, Ben A. |
author_sort | Wang, Jack T. |
collection | PubMed |
description | Axon degeneration is a characteristic event in many neurodegenerative conditions including stroke, glaucoma, and motor neuropathies. However, the molecular pathways that regulate this process remain unclear. Axon loss in chronic neurodegenerative diseases share many morphological features with those in acute injuries, and expression of the Wallerian degeneration slow (WldS) transgene delays nerve degeneration in both events, indicating a common mechanism of axonal self-destruction in traumatic injuries and degenerative diseases. A proposed model of axon degeneration is that nerve insults lead to impaired delivery or expression of a local axonal survival factor, which results in increased intra-axonal calcium levels and calcium-dependent cytoskeletal breakdown. |
format | Online Article Text |
id | pubmed-3255986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-32559862012-07-09 Axon degeneration: Molecular mechanisms of a self-destruction pathway Wang, Jack T. Medress, Zachary A. Barres, Ben A. J Cell Biol Reviews Axon degeneration is a characteristic event in many neurodegenerative conditions including stroke, glaucoma, and motor neuropathies. However, the molecular pathways that regulate this process remain unclear. Axon loss in chronic neurodegenerative diseases share many morphological features with those in acute injuries, and expression of the Wallerian degeneration slow (WldS) transgene delays nerve degeneration in both events, indicating a common mechanism of axonal self-destruction in traumatic injuries and degenerative diseases. A proposed model of axon degeneration is that nerve insults lead to impaired delivery or expression of a local axonal survival factor, which results in increased intra-axonal calcium levels and calcium-dependent cytoskeletal breakdown. The Rockefeller University Press 2012-01-09 /pmc/articles/PMC3255986/ /pubmed/22232700 http://dx.doi.org/10.1083/jcb.201108111 Text en © 2012 Wang et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Reviews Wang, Jack T. Medress, Zachary A. Barres, Ben A. Axon degeneration: Molecular mechanisms of a self-destruction pathway |
title | Axon degeneration: Molecular mechanisms of a self-destruction pathway |
title_full | Axon degeneration: Molecular mechanisms of a self-destruction pathway |
title_fullStr | Axon degeneration: Molecular mechanisms of a self-destruction pathway |
title_full_unstemmed | Axon degeneration: Molecular mechanisms of a self-destruction pathway |
title_short | Axon degeneration: Molecular mechanisms of a self-destruction pathway |
title_sort | axon degeneration: molecular mechanisms of a self-destruction pathway |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3255986/ https://www.ncbi.nlm.nih.gov/pubmed/22232700 http://dx.doi.org/10.1083/jcb.201108111 |
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