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Neddylation of Coro1a determines the fate of multivesicular bodies and biogenesis of extracellular vesicles
Multivesicular bodies (MVBs) fuse with not only the plasma membranes to release extracellular vesicles (EVs) but also lysosomes for degradation. Rab7 participates in the lysosomal targeting of MVBs. However, the proteins on MVB that directly bind Rab7, causing MVB recruitment of Rab7 remain unidenti...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8500273/ https://www.ncbi.nlm.nih.gov/pubmed/34623756 http://dx.doi.org/10.1002/jev2.12153 |
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author | Fei, Xuefeng Li, Zhijie Yang, Diya Kong, Xianghui Lu, Xinliang Shen, Yingying Li, Xu Xie, Shaofang Wang, Jiaoli Zhao, Yongchao Sun, Yi Zhang, Jing Ye, Zhaoming Wang, Jianli Cai, Zhijian |
author_facet | Fei, Xuefeng Li, Zhijie Yang, Diya Kong, Xianghui Lu, Xinliang Shen, Yingying Li, Xu Xie, Shaofang Wang, Jiaoli Zhao, Yongchao Sun, Yi Zhang, Jing Ye, Zhaoming Wang, Jianli Cai, Zhijian |
author_sort | Fei, Xuefeng |
collection | PubMed |
description | Multivesicular bodies (MVBs) fuse with not only the plasma membranes to release extracellular vesicles (EVs) but also lysosomes for degradation. Rab7 participates in the lysosomal targeting of MVBs. However, the proteins on MVB that directly bind Rab7, causing MVB recruitment of Rab7 remain unidentified. Here, we show that Coro1a undergoes neddylation modification at K233 by TRIM4. Neddylated Coro1a is associated with the MVB membrane and facilitates MVB recruitment and activation of Rab7 by directly binding Rab7. Subsequently, MVBs are targeted to lysosomes for degradation in a Rab7‐dependent manner, leading to reduced EV secretion. Furthermore, a decrease in neddylated Coro1a enhances the production of tumour EVs, thereby promoting tumour progression, indicating that neddylated Coro1a is an ideal target for the regulation of EV biogenesis. Altogether, our data identify a novel substrate of neddylation and reveal an unknown mechanism for MVB recruitment of Rab7, thus providing new insight into the regulation of EV biogenesis. |
format | Online Article Text |
id | pubmed-8500273 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85002732021-10-12 Neddylation of Coro1a determines the fate of multivesicular bodies and biogenesis of extracellular vesicles Fei, Xuefeng Li, Zhijie Yang, Diya Kong, Xianghui Lu, Xinliang Shen, Yingying Li, Xu Xie, Shaofang Wang, Jiaoli Zhao, Yongchao Sun, Yi Zhang, Jing Ye, Zhaoming Wang, Jianli Cai, Zhijian J Extracell Vesicles Research Articles Multivesicular bodies (MVBs) fuse with not only the plasma membranes to release extracellular vesicles (EVs) but also lysosomes for degradation. Rab7 participates in the lysosomal targeting of MVBs. However, the proteins on MVB that directly bind Rab7, causing MVB recruitment of Rab7 remain unidentified. Here, we show that Coro1a undergoes neddylation modification at K233 by TRIM4. Neddylated Coro1a is associated with the MVB membrane and facilitates MVB recruitment and activation of Rab7 by directly binding Rab7. Subsequently, MVBs are targeted to lysosomes for degradation in a Rab7‐dependent manner, leading to reduced EV secretion. Furthermore, a decrease in neddylated Coro1a enhances the production of tumour EVs, thereby promoting tumour progression, indicating that neddylated Coro1a is an ideal target for the regulation of EV biogenesis. Altogether, our data identify a novel substrate of neddylation and reveal an unknown mechanism for MVB recruitment of Rab7, thus providing new insight into the regulation of EV biogenesis. John Wiley and Sons Inc. 2021-10-08 2021-10 /pmc/articles/PMC8500273/ /pubmed/34623756 http://dx.doi.org/10.1002/jev2.12153 Text en © 2021 The Authors. Journal of Extracellular Vesicles published by Wiley Periodicals, LLC on behalf of the International Society for Extracellular Vesicles https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Fei, Xuefeng Li, Zhijie Yang, Diya Kong, Xianghui Lu, Xinliang Shen, Yingying Li, Xu Xie, Shaofang Wang, Jiaoli Zhao, Yongchao Sun, Yi Zhang, Jing Ye, Zhaoming Wang, Jianli Cai, Zhijian Neddylation of Coro1a determines the fate of multivesicular bodies and biogenesis of extracellular vesicles |
title | Neddylation of Coro1a determines the fate of multivesicular bodies and biogenesis of extracellular vesicles |
title_full | Neddylation of Coro1a determines the fate of multivesicular bodies and biogenesis of extracellular vesicles |
title_fullStr | Neddylation of Coro1a determines the fate of multivesicular bodies and biogenesis of extracellular vesicles |
title_full_unstemmed | Neddylation of Coro1a determines the fate of multivesicular bodies and biogenesis of extracellular vesicles |
title_short | Neddylation of Coro1a determines the fate of multivesicular bodies and biogenesis of extracellular vesicles |
title_sort | neddylation of coro1a determines the fate of multivesicular bodies and biogenesis of extracellular vesicles |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8500273/ https://www.ncbi.nlm.nih.gov/pubmed/34623756 http://dx.doi.org/10.1002/jev2.12153 |
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