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Endocytic turnover of Rab8 controls cell polarization
Adaptation of cell shape and polarization through the formation and retraction of cellular protrusions requires balancing of endocytosis and exocytosis combined with fine-tuning of the local activity of small GTPases like Rab8. Here, we show that endocytic turnover of the plasma membrane at protrusi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358338/ https://www.ncbi.nlm.nih.gov/pubmed/28137756 http://dx.doi.org/10.1242/jcs.195420 |
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author | Vidal-Quadras, Maite Holst, Mikkel R. Francis, Monika K. Larsson, Elin Hachimi, Mariam Yau, Wai-Lok Peränen, Johan Martín-Belmonte, Fernando Lundmark, Richard |
author_facet | Vidal-Quadras, Maite Holst, Mikkel R. Francis, Monika K. Larsson, Elin Hachimi, Mariam Yau, Wai-Lok Peränen, Johan Martín-Belmonte, Fernando Lundmark, Richard |
author_sort | Vidal-Quadras, Maite |
collection | PubMed |
description | Adaptation of cell shape and polarization through the formation and retraction of cellular protrusions requires balancing of endocytosis and exocytosis combined with fine-tuning of the local activity of small GTPases like Rab8. Here, we show that endocytic turnover of the plasma membrane at protrusions is directly coupled to surface removal and inactivation of Rab8. Removal is induced by reduced membrane tension and mediated by the GTPase regulator associated with focal adhesion kinase-1 (GRAF1, also known as ARHGAP26), a regulator of clathrin-independent endocytosis. GRAF1-depleted cells were deficient in multi-directional spreading and displayed elevated levels of GTP-loaded Rab8, which was accumulated at the tips of static protrusions. Furthermore, GRAF1 depletion impaired lumen formation and spindle orientation in a 3D cell culture system, indicating that GRAF1 activity regulates polarity establishment. Our data suggest that GRAF1-mediated removal of Rab8 from the cell surface restricts its activity during protrusion formation, thereby facilitating dynamic adjustment of the polarity axis. |
format | Online Article Text |
id | pubmed-5358338 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53583382017-04-10 Endocytic turnover of Rab8 controls cell polarization Vidal-Quadras, Maite Holst, Mikkel R. Francis, Monika K. Larsson, Elin Hachimi, Mariam Yau, Wai-Lok Peränen, Johan Martín-Belmonte, Fernando Lundmark, Richard J Cell Sci Research Article Adaptation of cell shape and polarization through the formation and retraction of cellular protrusions requires balancing of endocytosis and exocytosis combined with fine-tuning of the local activity of small GTPases like Rab8. Here, we show that endocytic turnover of the plasma membrane at protrusions is directly coupled to surface removal and inactivation of Rab8. Removal is induced by reduced membrane tension and mediated by the GTPase regulator associated with focal adhesion kinase-1 (GRAF1, also known as ARHGAP26), a regulator of clathrin-independent endocytosis. GRAF1-depleted cells were deficient in multi-directional spreading and displayed elevated levels of GTP-loaded Rab8, which was accumulated at the tips of static protrusions. Furthermore, GRAF1 depletion impaired lumen formation and spindle orientation in a 3D cell culture system, indicating that GRAF1 activity regulates polarity establishment. Our data suggest that GRAF1-mediated removal of Rab8 from the cell surface restricts its activity during protrusion formation, thereby facilitating dynamic adjustment of the polarity axis. The Company of Biologists Ltd 2017-03-15 /pmc/articles/PMC5358338/ /pubmed/28137756 http://dx.doi.org/10.1242/jcs.195420 Text en © 2017. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Vidal-Quadras, Maite Holst, Mikkel R. Francis, Monika K. Larsson, Elin Hachimi, Mariam Yau, Wai-Lok Peränen, Johan Martín-Belmonte, Fernando Lundmark, Richard Endocytic turnover of Rab8 controls cell polarization |
title | Endocytic turnover of Rab8 controls cell polarization |
title_full | Endocytic turnover of Rab8 controls cell polarization |
title_fullStr | Endocytic turnover of Rab8 controls cell polarization |
title_full_unstemmed | Endocytic turnover of Rab8 controls cell polarization |
title_short | Endocytic turnover of Rab8 controls cell polarization |
title_sort | endocytic turnover of rab8 controls cell polarization |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358338/ https://www.ncbi.nlm.nih.gov/pubmed/28137756 http://dx.doi.org/10.1242/jcs.195420 |
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