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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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.
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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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