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WAVE facilitates polarized E-cadherin transport
Cadherin dynamics drive morphogenesis, while defects in cadherin polarity contribute to diseases, including cancers. However, the forces polarizing cadherin membrane distribution are not well understood. We previously showed that WAVE-dependent branched actin polarizes cadherin distribution and sugg...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10162425/ https://www.ncbi.nlm.nih.gov/pubmed/36947190 http://dx.doi.org/10.1091/mbc.E22-08-0322 |
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author | Cordova-Burgos, Luigy Rao, Deepti Egwuonwu, Joshua Borinskaya, Sofya Sasidharan, Shashikala Soto, Martha |
author_facet | Cordova-Burgos, Luigy Rao, Deepti Egwuonwu, Joshua Borinskaya, Sofya Sasidharan, Shashikala Soto, Martha |
author_sort | Cordova-Burgos, Luigy |
collection | PubMed |
description | Cadherin dynamics drive morphogenesis, while defects in cadherin polarity contribute to diseases, including cancers. However, the forces polarizing cadherin membrane distribution are not well understood. We previously showed that WAVE-dependent branched actin polarizes cadherin distribution and suggested that one mechanism is protein transport. While previous studies suggested that WAVE is enriched at various endocytic organelles, the role of WAVE in protein traffic is understudied. Here we test the model that WAVE regulates cadherin by polarizing its transport. In support of this model we show that 1) endogenously tagged WAVE accumulates in vivo at several endocytic organelles, including recycling endosomes and at the Golgi; 2) likewise, cadherin protein accumulates at recycling endosomes and the Golgi; 3) loss of WAVE components reduces cadherin accumulation at apically directed RAB-11–positive recycling endosomes and increases accumulation at the Golgi. In addition, live imaging illustrates that dynamics and velocity of recycling endosomes enriched for RAB-11::GFP and RFP::RME-1 are reduced in animals depleted of WAVE components and RAB-11::GFP movements are misdirected, suggesting that WAVE powers and directs their movements. This in vivo study demonstrates the importance of WAVE in promoting polarized transport in epithelia and supports a model that WAVE promotes cell–cell adhesion and polarity by promoting cadherin transport. |
format | Online Article Text |
id | pubmed-10162425 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-101624252023-06-26 WAVE facilitates polarized E-cadherin transport Cordova-Burgos, Luigy Rao, Deepti Egwuonwu, Joshua Borinskaya, Sofya Sasidharan, Shashikala Soto, Martha Mol Biol Cell Articles Cadherin dynamics drive morphogenesis, while defects in cadherin polarity contribute to diseases, including cancers. However, the forces polarizing cadherin membrane distribution are not well understood. We previously showed that WAVE-dependent branched actin polarizes cadherin distribution and suggested that one mechanism is protein transport. While previous studies suggested that WAVE is enriched at various endocytic organelles, the role of WAVE in protein traffic is understudied. Here we test the model that WAVE regulates cadherin by polarizing its transport. In support of this model we show that 1) endogenously tagged WAVE accumulates in vivo at several endocytic organelles, including recycling endosomes and at the Golgi; 2) likewise, cadherin protein accumulates at recycling endosomes and the Golgi; 3) loss of WAVE components reduces cadherin accumulation at apically directed RAB-11–positive recycling endosomes and increases accumulation at the Golgi. In addition, live imaging illustrates that dynamics and velocity of recycling endosomes enriched for RAB-11::GFP and RFP::RME-1 are reduced in animals depleted of WAVE components and RAB-11::GFP movements are misdirected, suggesting that WAVE powers and directs their movements. This in vivo study demonstrates the importance of WAVE in promoting polarized transport in epithelia and supports a model that WAVE promotes cell–cell adhesion and polarity by promoting cadherin transport. The American Society for Cell Biology 2023-04-11 /pmc/articles/PMC10162425/ /pubmed/36947190 http://dx.doi.org/10.1091/mbc.E22-08-0322 Text en © 2023 Cordova-Burgos et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial-Share Alike 4.0 International Creative Commons License. |
spellingShingle | Articles Cordova-Burgos, Luigy Rao, Deepti Egwuonwu, Joshua Borinskaya, Sofya Sasidharan, Shashikala Soto, Martha WAVE facilitates polarized E-cadherin transport |
title | WAVE facilitates polarized E-cadherin transport |
title_full | WAVE facilitates polarized E-cadherin transport |
title_fullStr | WAVE facilitates polarized E-cadherin transport |
title_full_unstemmed | WAVE facilitates polarized E-cadherin transport |
title_short | WAVE facilitates polarized E-cadherin transport |
title_sort | wave facilitates polarized e-cadherin transport |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10162425/ https://www.ncbi.nlm.nih.gov/pubmed/36947190 http://dx.doi.org/10.1091/mbc.E22-08-0322 |
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