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NgCAM and VAMP2 reveal that direct delivery and dendritic degradation maintain axonal polarity
Neurons are polarized cells of extreme scale and compartmentalization. To fulfill their role in electrochemical signaling, axons must maintain a specific complement of membrane proteins. Despite being the subject of considerable attention, the trafficking pathway of axonal membrane proteins is not w...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8886818/ https://www.ncbi.nlm.nih.gov/pubmed/34731031 http://dx.doi.org/10.1091/mbc.E21-08-0425 |
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author | Nabb, Alec T. Bentley, Marvin |
author_facet | Nabb, Alec T. Bentley, Marvin |
author_sort | Nabb, Alec T. |
collection | PubMed |
description | Neurons are polarized cells of extreme scale and compartmentalization. To fulfill their role in electrochemical signaling, axons must maintain a specific complement of membrane proteins. Despite being the subject of considerable attention, the trafficking pathway of axonal membrane proteins is not well understood. Two pathways, direct delivery and transcytosis, have been proposed. Previous studies reached contradictory conclusions about which of these mediates delivery of axonal membrane proteins to their destination, in part because they evaluated long-term distribution changes and not vesicle transport. We developed a novel strategy to selectively label vesicles in different trafficking pathways and determined the trafficking of two canonical axonal membrane proteins, neuron–glia cell adhesion molecule and vesicle-associated membrane protein-2. Results from detailed quantitative analyses of transporting vesicles differed substantially from previous studies and found that axonal membrane proteins overwhelmingly undergo direct delivery. Transcytosis plays only a minor role in axonal delivery of these proteins. In addition, we identified a novel pathway by which wayward axonal proteins that reach the dendritic plasma membrane are targeted to lysosomes. These results redefine how axonal proteins achieve their polarized distribution, a crucial requirement for elucidating the underlying molecular mechanisms. |
format | Online Article Text |
id | pubmed-8886818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-88868182022-03-16 NgCAM and VAMP2 reveal that direct delivery and dendritic degradation maintain axonal polarity Nabb, Alec T. Bentley, Marvin Mol Biol Cell Articles Neurons are polarized cells of extreme scale and compartmentalization. To fulfill their role in electrochemical signaling, axons must maintain a specific complement of membrane proteins. Despite being the subject of considerable attention, the trafficking pathway of axonal membrane proteins is not well understood. Two pathways, direct delivery and transcytosis, have been proposed. Previous studies reached contradictory conclusions about which of these mediates delivery of axonal membrane proteins to their destination, in part because they evaluated long-term distribution changes and not vesicle transport. We developed a novel strategy to selectively label vesicles in different trafficking pathways and determined the trafficking of two canonical axonal membrane proteins, neuron–glia cell adhesion molecule and vesicle-associated membrane protein-2. Results from detailed quantitative analyses of transporting vesicles differed substantially from previous studies and found that axonal membrane proteins overwhelmingly undergo direct delivery. Transcytosis plays only a minor role in axonal delivery of these proteins. In addition, we identified a novel pathway by which wayward axonal proteins that reach the dendritic plasma membrane are targeted to lysosomes. These results redefine how axonal proteins achieve their polarized distribution, a crucial requirement for elucidating the underlying molecular mechanisms. The American Society for Cell Biology 2022-01-01 /pmc/articles/PMC8886818/ /pubmed/34731031 http://dx.doi.org/10.1091/mbc.E21-08-0425 Text en © 2022 Nabb and Bentley. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 4.0 International Creative Commons License. |
spellingShingle | Articles Nabb, Alec T. Bentley, Marvin NgCAM and VAMP2 reveal that direct delivery and dendritic degradation maintain axonal polarity |
title | NgCAM and VAMP2 reveal that direct delivery and dendritic degradation maintain axonal polarity |
title_full | NgCAM and VAMP2 reveal that direct delivery and dendritic degradation maintain axonal polarity |
title_fullStr | NgCAM and VAMP2 reveal that direct delivery and dendritic degradation maintain axonal polarity |
title_full_unstemmed | NgCAM and VAMP2 reveal that direct delivery and dendritic degradation maintain axonal polarity |
title_short | NgCAM and VAMP2 reveal that direct delivery and dendritic degradation maintain axonal polarity |
title_sort | ngcam and vamp2 reveal that direct delivery and dendritic degradation maintain axonal polarity |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8886818/ https://www.ncbi.nlm.nih.gov/pubmed/34731031 http://dx.doi.org/10.1091/mbc.E21-08-0425 |
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