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Protrudin functions from the endoplasmic reticulum to support axon regeneration in the adult CNS
Adult mammalian central nervous system axons have intrinsically poor regenerative capacity, so axonal injury has permanent consequences. One approach to enhancing regeneration is to increase the axonal supply of growth molecules and organelles. We achieved this by expressing the adaptor molecule Pro...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645621/ https://www.ncbi.nlm.nih.gov/pubmed/33154382 http://dx.doi.org/10.1038/s41467-020-19436-y |
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author | Petrova, Veselina Pearson, Craig S. Ching, Jared Tribble, James R. Solano, Andrea G. Yang, Yunfei Love, Fiona M. Watt, Robert J. Osborne, Andrew Reid, Evan Williams, Pete A. Martin, Keith R. Geller, Herbert M. Eva, Richard Fawcett, James W. |
author_facet | Petrova, Veselina Pearson, Craig S. Ching, Jared Tribble, James R. Solano, Andrea G. Yang, Yunfei Love, Fiona M. Watt, Robert J. Osborne, Andrew Reid, Evan Williams, Pete A. Martin, Keith R. Geller, Herbert M. Eva, Richard Fawcett, James W. |
author_sort | Petrova, Veselina |
collection | PubMed |
description | Adult mammalian central nervous system axons have intrinsically poor regenerative capacity, so axonal injury has permanent consequences. One approach to enhancing regeneration is to increase the axonal supply of growth molecules and organelles. We achieved this by expressing the adaptor molecule Protrudin which is normally found at low levels in non-regenerative neurons. Elevated Protrudin expression enabled robust central nervous system regeneration both in vitro in primary cortical neurons and in vivo in the injured adult optic nerve. Protrudin overexpression facilitated the accumulation of endoplasmic reticulum, integrins and Rab11 endosomes in the distal axon, whilst removing Protrudin’s endoplasmic reticulum localization, kinesin-binding or phosphoinositide-binding properties abrogated the regenerative effects. These results demonstrate that Protrudin promotes regeneration by functioning as a scaffold to link axonal organelles, motors and membranes, establishing important roles for these cellular components in mediating regeneration in the adult central nervous system. |
format | Online Article Text |
id | pubmed-7645621 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76456212020-11-10 Protrudin functions from the endoplasmic reticulum to support axon regeneration in the adult CNS Petrova, Veselina Pearson, Craig S. Ching, Jared Tribble, James R. Solano, Andrea G. Yang, Yunfei Love, Fiona M. Watt, Robert J. Osborne, Andrew Reid, Evan Williams, Pete A. Martin, Keith R. Geller, Herbert M. Eva, Richard Fawcett, James W. Nat Commun Article Adult mammalian central nervous system axons have intrinsically poor regenerative capacity, so axonal injury has permanent consequences. One approach to enhancing regeneration is to increase the axonal supply of growth molecules and organelles. We achieved this by expressing the adaptor molecule Protrudin which is normally found at low levels in non-regenerative neurons. Elevated Protrudin expression enabled robust central nervous system regeneration both in vitro in primary cortical neurons and in vivo in the injured adult optic nerve. Protrudin overexpression facilitated the accumulation of endoplasmic reticulum, integrins and Rab11 endosomes in the distal axon, whilst removing Protrudin’s endoplasmic reticulum localization, kinesin-binding or phosphoinositide-binding properties abrogated the regenerative effects. These results demonstrate that Protrudin promotes regeneration by functioning as a scaffold to link axonal organelles, motors and membranes, establishing important roles for these cellular components in mediating regeneration in the adult central nervous system. Nature Publishing Group UK 2020-11-05 /pmc/articles/PMC7645621/ /pubmed/33154382 http://dx.doi.org/10.1038/s41467-020-19436-y Text en © The Author(s) 2020 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/. |
spellingShingle | Article Petrova, Veselina Pearson, Craig S. Ching, Jared Tribble, James R. Solano, Andrea G. Yang, Yunfei Love, Fiona M. Watt, Robert J. Osborne, Andrew Reid, Evan Williams, Pete A. Martin, Keith R. Geller, Herbert M. Eva, Richard Fawcett, James W. Protrudin functions from the endoplasmic reticulum to support axon regeneration in the adult CNS |
title | Protrudin functions from the endoplasmic reticulum to support axon regeneration in the adult CNS |
title_full | Protrudin functions from the endoplasmic reticulum to support axon regeneration in the adult CNS |
title_fullStr | Protrudin functions from the endoplasmic reticulum to support axon regeneration in the adult CNS |
title_full_unstemmed | Protrudin functions from the endoplasmic reticulum to support axon regeneration in the adult CNS |
title_short | Protrudin functions from the endoplasmic reticulum to support axon regeneration in the adult CNS |
title_sort | protrudin functions from the endoplasmic reticulum to support axon regeneration in the adult cns |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645621/ https://www.ncbi.nlm.nih.gov/pubmed/33154382 http://dx.doi.org/10.1038/s41467-020-19436-y |
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