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The multiple roles of Rab9 in the endolysosomal system
The small GTPase Rab9 has long been described as a protein that mediates endosome-to-trans-Golgi Network (TGN) transport, and specifically mannose-6-phospate receptor (MPR) recycling. However, studies have challenged this view by showing that Rab9 also is connected to sorting pathways toward the end...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4988448/ https://www.ncbi.nlm.nih.gov/pubmed/27574541 http://dx.doi.org/10.1080/19420889.2016.1204498 |
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author | Kucera, Ana Bakke, Oddmund Progida, Cinzia |
author_facet | Kucera, Ana Bakke, Oddmund Progida, Cinzia |
author_sort | Kucera, Ana |
collection | PubMed |
description | The small GTPase Rab9 has long been described as a protein that mediates endosome-to-trans-Golgi Network (TGN) transport, and specifically mannose-6-phospate receptor (MPR) recycling. However, studies have challenged this view by showing that Rab9 also is connected to sorting pathways toward the endolysosomal compartments. We recently characterized the spatio-temporal dynamics of Rab9 and, by using live cell imaging, we showed that it enters the endosomal pathway together with CI-MPR at the transition stage between early, Rab5-positive, and late, Rab7a-positive, endosomes. More so, the Rab9 constitutively active mutant, Rab9Q66L, accumulates on late endosomes and promotes carrier formation at the TGN. Here, we discuss our findings in light of previous reports on Rab9 in the retrograde transport pathway. |
format | Online Article Text |
id | pubmed-4988448 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-49884482016-08-29 The multiple roles of Rab9 in the endolysosomal system Kucera, Ana Bakke, Oddmund Progida, Cinzia Commun Integr Biol Article Addendum The small GTPase Rab9 has long been described as a protein that mediates endosome-to-trans-Golgi Network (TGN) transport, and specifically mannose-6-phospate receptor (MPR) recycling. However, studies have challenged this view by showing that Rab9 also is connected to sorting pathways toward the endolysosomal compartments. We recently characterized the spatio-temporal dynamics of Rab9 and, by using live cell imaging, we showed that it enters the endosomal pathway together with CI-MPR at the transition stage between early, Rab5-positive, and late, Rab7a-positive, endosomes. More so, the Rab9 constitutively active mutant, Rab9Q66L, accumulates on late endosomes and promotes carrier formation at the TGN. Here, we discuss our findings in light of previous reports on Rab9 in the retrograde transport pathway. Taylor & Francis 2016-07-22 /pmc/articles/PMC4988448/ /pubmed/27574541 http://dx.doi.org/10.1080/19420889.2016.1204498 Text en © 2016 The Author(s). Published with license by Taylor & Francis. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. |
spellingShingle | Article Addendum Kucera, Ana Bakke, Oddmund Progida, Cinzia The multiple roles of Rab9 in the endolysosomal system |
title | The multiple roles of Rab9 in the endolysosomal system |
title_full | The multiple roles of Rab9 in the endolysosomal system |
title_fullStr | The multiple roles of Rab9 in the endolysosomal system |
title_full_unstemmed | The multiple roles of Rab9 in the endolysosomal system |
title_short | The multiple roles of Rab9 in the endolysosomal system |
title_sort | multiple roles of rab9 in the endolysosomal system |
topic | Article Addendum |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4988448/ https://www.ncbi.nlm.nih.gov/pubmed/27574541 http://dx.doi.org/10.1080/19420889.2016.1204498 |
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