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Rab11 is required for lysosome exocytosis through the interaction with Rab3a, Sec15 and GRAB
Lysosomes are dynamic organelles, capable of undergoing exocytosis. This process is crucial for several cellular functions, namely plasma membrane repair. Nevertheless, the molecular machinery involved in this process is poorly understood. Here, we identify Rab11a and Rab11b as regulators of Ca(2+)-...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8214760/ https://www.ncbi.nlm.nih.gov/pubmed/34100549 http://dx.doi.org/10.1242/jcs.246694 |
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author | Escrevente, Cristina Bento-Lopes, Liliana Ramalho, José S. Barral, Duarte C. |
author_facet | Escrevente, Cristina Bento-Lopes, Liliana Ramalho, José S. Barral, Duarte C. |
author_sort | Escrevente, Cristina |
collection | PubMed |
description | Lysosomes are dynamic organelles, capable of undergoing exocytosis. This process is crucial for several cellular functions, namely plasma membrane repair. Nevertheless, the molecular machinery involved in this process is poorly understood. Here, we identify Rab11a and Rab11b as regulators of Ca(2+)-induced lysosome exocytosis. Interestingly, Rab11-positive vesicles transiently interact with lysosomes at the cell periphery, indicating that this interaction is required for the last steps of lysosome exocytosis. Additionally, we found that the silencing of the exocyst subunit Sec15, a Rab11 effector, impairs lysosome exocytosis, suggesting that Sec15 acts together with Rab11 in the regulation of lysosome exocytosis. Furthermore, we show that Rab11 binds the guanine nucleotide exchange factor for Rab3a (GRAB) as well as Rab3a, which we have previously described to be a regulator of the positioning and exocytosis of lysosomes. Thus, our study identifies new players required for lysosome exocytosis and suggest the existence of a Rab11–Rab3a cascade involved in this process. |
format | Online Article Text |
id | pubmed-8214760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-82147602021-06-22 Rab11 is required for lysosome exocytosis through the interaction with Rab3a, Sec15 and GRAB Escrevente, Cristina Bento-Lopes, Liliana Ramalho, José S. Barral, Duarte C. J Cell Sci Research Article Lysosomes are dynamic organelles, capable of undergoing exocytosis. This process is crucial for several cellular functions, namely plasma membrane repair. Nevertheless, the molecular machinery involved in this process is poorly understood. Here, we identify Rab11a and Rab11b as regulators of Ca(2+)-induced lysosome exocytosis. Interestingly, Rab11-positive vesicles transiently interact with lysosomes at the cell periphery, indicating that this interaction is required for the last steps of lysosome exocytosis. Additionally, we found that the silencing of the exocyst subunit Sec15, a Rab11 effector, impairs lysosome exocytosis, suggesting that Sec15 acts together with Rab11 in the regulation of lysosome exocytosis. Furthermore, we show that Rab11 binds the guanine nucleotide exchange factor for Rab3a (GRAB) as well as Rab3a, which we have previously described to be a regulator of the positioning and exocytosis of lysosomes. Thus, our study identifies new players required for lysosome exocytosis and suggest the existence of a Rab11–Rab3a cascade involved in this process. The Company of Biologists Ltd 2021-06-08 /pmc/articles/PMC8214760/ /pubmed/34100549 http://dx.doi.org/10.1242/jcs.246694 Text en © 2021. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Escrevente, Cristina Bento-Lopes, Liliana Ramalho, José S. Barral, Duarte C. Rab11 is required for lysosome exocytosis through the interaction with Rab3a, Sec15 and GRAB |
title | Rab11 is required for lysosome exocytosis through the interaction with Rab3a, Sec15 and GRAB |
title_full | Rab11 is required for lysosome exocytosis through the interaction with Rab3a, Sec15 and GRAB |
title_fullStr | Rab11 is required for lysosome exocytosis through the interaction with Rab3a, Sec15 and GRAB |
title_full_unstemmed | Rab11 is required for lysosome exocytosis through the interaction with Rab3a, Sec15 and GRAB |
title_short | Rab11 is required for lysosome exocytosis through the interaction with Rab3a, Sec15 and GRAB |
title_sort | rab11 is required for lysosome exocytosis through the interaction with rab3a, sec15 and grab |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8214760/ https://www.ncbi.nlm.nih.gov/pubmed/34100549 http://dx.doi.org/10.1242/jcs.246694 |
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