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Evidence of impaired macroautophagy in human degenerative cervical myelopathy
Degenerative cervical myelopathy (DCM) is a common progressive disease of the spinal cord which can cause tetraplegia. Despite its prevalence, few studies have investigated the pathophysiology of DCM. Macroautophagy is a cellular process which degrades intracellular contents and its disruption is th...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9279443/ https://www.ncbi.nlm.nih.gov/pubmed/35831377 http://dx.doi.org/10.1038/s41598-022-15158-x |
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author | Smith, Sam S. Young, Adam M. H. Davies, Benjamin M. Takahashi, Hitoshi Allinson, Kieren S. J. Kotter, Mark R. N. |
author_facet | Smith, Sam S. Young, Adam M. H. Davies, Benjamin M. Takahashi, Hitoshi Allinson, Kieren S. J. Kotter, Mark R. N. |
author_sort | Smith, Sam S. |
collection | PubMed |
description | Degenerative cervical myelopathy (DCM) is a common progressive disease of the spinal cord which can cause tetraplegia. Despite its prevalence, few studies have investigated the pathophysiology of DCM. Macroautophagy is a cellular process which degrades intracellular contents and its disruption is thought to contribute to many neurodegenerative diseases. The present study tests the hypothesis that macroautophagy is impaired in DCM. To address this, we utilised a collection of post-mortem cervical spinal cord samples and investigated seven DCM cases and five human controls. Immunohistochemical staining was used to visualise proteins involved in autophagy. This demonstrated significantly reduced numbers of LC3 puncta in cases versus controls (p = 0.0424). Consistent with reduced autophagy, we identified large aggregates of p62 in four of seven cases and no controls. Tau was increased in two of five cases compared to controls. BCL-2 was significantly increased in cases versus controls (p = 0.0133) and may explain this reduction in autophagy. Increased BCL-2 (p = 0.0369) and p62 bodies (p = 0.055) were seen in more severe cases of DCM. This is the first evidence that autophagy is impaired in DCM; the impairment appears greater in more severe cases. Further research is necessary to investigate whether macroautophagy has potential as a therapeutic target in DCM. |
format | Online Article Text |
id | pubmed-9279443 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-92794432022-07-15 Evidence of impaired macroautophagy in human degenerative cervical myelopathy Smith, Sam S. Young, Adam M. H. Davies, Benjamin M. Takahashi, Hitoshi Allinson, Kieren S. J. Kotter, Mark R. N. Sci Rep Article Degenerative cervical myelopathy (DCM) is a common progressive disease of the spinal cord which can cause tetraplegia. Despite its prevalence, few studies have investigated the pathophysiology of DCM. Macroautophagy is a cellular process which degrades intracellular contents and its disruption is thought to contribute to many neurodegenerative diseases. The present study tests the hypothesis that macroautophagy is impaired in DCM. To address this, we utilised a collection of post-mortem cervical spinal cord samples and investigated seven DCM cases and five human controls. Immunohistochemical staining was used to visualise proteins involved in autophagy. This demonstrated significantly reduced numbers of LC3 puncta in cases versus controls (p = 0.0424). Consistent with reduced autophagy, we identified large aggregates of p62 in four of seven cases and no controls. Tau was increased in two of five cases compared to controls. BCL-2 was significantly increased in cases versus controls (p = 0.0133) and may explain this reduction in autophagy. Increased BCL-2 (p = 0.0369) and p62 bodies (p = 0.055) were seen in more severe cases of DCM. This is the first evidence that autophagy is impaired in DCM; the impairment appears greater in more severe cases. Further research is necessary to investigate whether macroautophagy has potential as a therapeutic target in DCM. Nature Publishing Group UK 2022-07-13 /pmc/articles/PMC9279443/ /pubmed/35831377 http://dx.doi.org/10.1038/s41598-022-15158-x Text en © The Author(s) 2022 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Smith, Sam S. Young, Adam M. H. Davies, Benjamin M. Takahashi, Hitoshi Allinson, Kieren S. J. Kotter, Mark R. N. Evidence of impaired macroautophagy in human degenerative cervical myelopathy |
title | Evidence of impaired macroautophagy in human degenerative cervical myelopathy |
title_full | Evidence of impaired macroautophagy in human degenerative cervical myelopathy |
title_fullStr | Evidence of impaired macroautophagy in human degenerative cervical myelopathy |
title_full_unstemmed | Evidence of impaired macroautophagy in human degenerative cervical myelopathy |
title_short | Evidence of impaired macroautophagy in human degenerative cervical myelopathy |
title_sort | evidence of impaired macroautophagy in human degenerative cervical myelopathy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9279443/ https://www.ncbi.nlm.nih.gov/pubmed/35831377 http://dx.doi.org/10.1038/s41598-022-15158-x |
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