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Targeting of endoplasmic reticulum-associated proteins to axons and dendrites in rotavirus-infected neurons
To analyze sorting and compartmentalization of molecules in neuronal endomembranes, the distribution of endogenous proteins associated with the endoplasmic reticulum (ER), intermediate compartment, the Golgi apparatus in cultures of dorsal root ganglion (DRG), and hippocampal neurons was compared wi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science Inc.
1998
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126376/ https://www.ncbi.nlm.nih.gov/pubmed/9671265 http://dx.doi.org/10.1016/S0361-9230(98)00013-6 |
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author | Weclewicz, Katarzyna Svensson, Lennart Kristensson, Krister |
author_facet | Weclewicz, Katarzyna Svensson, Lennart Kristensson, Krister |
author_sort | Weclewicz, Katarzyna |
collection | PubMed |
description | To analyze sorting and compartmentalization of molecules in neuronal endomembranes, the distribution of endogenous proteins associated with the endoplasmic reticulum (ER), intermediate compartment, the Golgi apparatus in cultures of dorsal root ganglion (DRG), and hippocampal neurons was compared with that of newly synthesized ER-associated rotavirus proteins. The endogenous ER-retained immunoglobulin heavy chain binding protein, protein disulfide isomerase, and a peptide containing the KDEL amino acid sequence appeared in the soma and dendrites up to their first branching, but not in axons. However, two other endogenous ER-associated proteins, calreticulin and calnexin, occurred in axons as well as in the somatodendritic domains. The ER-associated rotavirus proteins, VP7 and NSP4, were widely distributed in cell bodies and dendrites. The former appeared also in axons and its localization partially overlapped with that of calreticulin and calnexin. One intermediate compartment protein, ER-Golgi-intermediate compartment-protein-53 (ERGIC-53), extended beyond the first division of the dendrites and did not, as the small guanosine 5′-triphosphate (GTP)-binding protein rab2, appear in axons. The location of rab2 to small vesicles was distinct from that of rotavirus VP7. Cis/medial Golgi cistern proteins were restricted to the cell bodies and proximal dendrites. This study emphasizes the marked heterogeneity in the targeting to axons and dendrites of proteins associated with ER and intermediate compartments. Therefore, the composition of axonal ER-retained molecules differs from that in the soma and this variation may reflect differences in functions between the ER compartments. Viral proteins are useful reporters for such heterogeneities and rotavirus VP7 may be a tool to reveal sorting signals for targeting of vesicular proteins to axons via a nonclassical Golgi-independent mechanism. Such signals may also determine viral targeting to different regions of the brain. |
format | Online Article Text |
id | pubmed-7126376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1998 |
publisher | Elsevier Science Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71263762020-04-08 Targeting of endoplasmic reticulum-associated proteins to axons and dendrites in rotavirus-infected neurons Weclewicz, Katarzyna Svensson, Lennart Kristensson, Krister Brain Res Bull Original Articles To analyze sorting and compartmentalization of molecules in neuronal endomembranes, the distribution of endogenous proteins associated with the endoplasmic reticulum (ER), intermediate compartment, the Golgi apparatus in cultures of dorsal root ganglion (DRG), and hippocampal neurons was compared with that of newly synthesized ER-associated rotavirus proteins. The endogenous ER-retained immunoglobulin heavy chain binding protein, protein disulfide isomerase, and a peptide containing the KDEL amino acid sequence appeared in the soma and dendrites up to their first branching, but not in axons. However, two other endogenous ER-associated proteins, calreticulin and calnexin, occurred in axons as well as in the somatodendritic domains. The ER-associated rotavirus proteins, VP7 and NSP4, were widely distributed in cell bodies and dendrites. The former appeared also in axons and its localization partially overlapped with that of calreticulin and calnexin. One intermediate compartment protein, ER-Golgi-intermediate compartment-protein-53 (ERGIC-53), extended beyond the first division of the dendrites and did not, as the small guanosine 5′-triphosphate (GTP)-binding protein rab2, appear in axons. The location of rab2 to small vesicles was distinct from that of rotavirus VP7. Cis/medial Golgi cistern proteins were restricted to the cell bodies and proximal dendrites. This study emphasizes the marked heterogeneity in the targeting to axons and dendrites of proteins associated with ER and intermediate compartments. Therefore, the composition of axonal ER-retained molecules differs from that in the soma and this variation may reflect differences in functions between the ER compartments. Viral proteins are useful reporters for such heterogeneities and rotavirus VP7 may be a tool to reveal sorting signals for targeting of vesicular proteins to axons via a nonclassical Golgi-independent mechanism. Such signals may also determine viral targeting to different regions of the brain. Elsevier Science Inc. 1998-07-01 1998-07-06 /pmc/articles/PMC7126376/ /pubmed/9671265 http://dx.doi.org/10.1016/S0361-9230(98)00013-6 Text en Copyright © 1998 Elsevier Science Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Original Articles Weclewicz, Katarzyna Svensson, Lennart Kristensson, Krister Targeting of endoplasmic reticulum-associated proteins to axons and dendrites in rotavirus-infected neurons |
title | Targeting of endoplasmic reticulum-associated proteins to axons and dendrites in rotavirus-infected neurons |
title_full | Targeting of endoplasmic reticulum-associated proteins to axons and dendrites in rotavirus-infected neurons |
title_fullStr | Targeting of endoplasmic reticulum-associated proteins to axons and dendrites in rotavirus-infected neurons |
title_full_unstemmed | Targeting of endoplasmic reticulum-associated proteins to axons and dendrites in rotavirus-infected neurons |
title_short | Targeting of endoplasmic reticulum-associated proteins to axons and dendrites in rotavirus-infected neurons |
title_sort | targeting of endoplasmic reticulum-associated proteins to axons and dendrites in rotavirus-infected neurons |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126376/ https://www.ncbi.nlm.nih.gov/pubmed/9671265 http://dx.doi.org/10.1016/S0361-9230(98)00013-6 |
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