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A NUMB–EFA6B–ARF6 recycling route controls apically restricted cell protrusions and mesenchymal motility
The endocytic protein NUMB has been implicated in the control of various polarized cellular processes, including the acquisition of mesenchymal migratory traits through molecular mechanisms that have only been partially defined. Here, we report that NUMB is a negative regulator of a specialized set...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123001/ https://www.ncbi.nlm.nih.gov/pubmed/30061108 http://dx.doi.org/10.1083/jcb.201802023 |
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author | Zobel, Martina Disanza, Andrea Senic-Matuglia, Francesca Franco, Michel Colaluca, Ivan Nicola Confalonieri, Stefano Bisi, Sara Barbieri, Elisa Caldieri, Giusi Sigismund, Sara Pece, Salvatore Chavrier, Philippe Di Fiore, Pier Paolo Scita, Giorgio |
author_facet | Zobel, Martina Disanza, Andrea Senic-Matuglia, Francesca Franco, Michel Colaluca, Ivan Nicola Confalonieri, Stefano Bisi, Sara Barbieri, Elisa Caldieri, Giusi Sigismund, Sara Pece, Salvatore Chavrier, Philippe Di Fiore, Pier Paolo Scita, Giorgio |
author_sort | Zobel, Martina |
collection | PubMed |
description | The endocytic protein NUMB has been implicated in the control of various polarized cellular processes, including the acquisition of mesenchymal migratory traits through molecular mechanisms that have only been partially defined. Here, we report that NUMB is a negative regulator of a specialized set of understudied, apically restricted, actin-based protrusions, the circular dorsal ruffles (CDRs), induced by either PDGF or HGF stimulation. Through its PTB domain, NUMB binds directly to an N-terminal NPLF motif of the ARF6 guanine nucleotide exchange factor, EFA6B, and promotes its exchange activity in vitro. In cells, a NUMB–EFA6B–ARF6 axis regulates the recycling of the actin regulatory cargo RAC1 and is critical for the formation of CDRs that mark the acquisition of a mesenchymal mode of motility. Consistently, loss of NUMB promotes HGF-induced cell migration and invasion. Thus, NUMB negatively controls membrane protrusions and the acquisition of mesenchymal migratory traits by modulating EFA6B–ARF6 activity. |
format | Online Article Text |
id | pubmed-6123001 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61230012019-03-03 A NUMB–EFA6B–ARF6 recycling route controls apically restricted cell protrusions and mesenchymal motility Zobel, Martina Disanza, Andrea Senic-Matuglia, Francesca Franco, Michel Colaluca, Ivan Nicola Confalonieri, Stefano Bisi, Sara Barbieri, Elisa Caldieri, Giusi Sigismund, Sara Pece, Salvatore Chavrier, Philippe Di Fiore, Pier Paolo Scita, Giorgio J Cell Biol Research Articles The endocytic protein NUMB has been implicated in the control of various polarized cellular processes, including the acquisition of mesenchymal migratory traits through molecular mechanisms that have only been partially defined. Here, we report that NUMB is a negative regulator of a specialized set of understudied, apically restricted, actin-based protrusions, the circular dorsal ruffles (CDRs), induced by either PDGF or HGF stimulation. Through its PTB domain, NUMB binds directly to an N-terminal NPLF motif of the ARF6 guanine nucleotide exchange factor, EFA6B, and promotes its exchange activity in vitro. In cells, a NUMB–EFA6B–ARF6 axis regulates the recycling of the actin regulatory cargo RAC1 and is critical for the formation of CDRs that mark the acquisition of a mesenchymal mode of motility. Consistently, loss of NUMB promotes HGF-induced cell migration and invasion. Thus, NUMB negatively controls membrane protrusions and the acquisition of mesenchymal migratory traits by modulating EFA6B–ARF6 activity. Rockefeller University Press 2018-09-03 /pmc/articles/PMC6123001/ /pubmed/30061108 http://dx.doi.org/10.1083/jcb.201802023 Text en © 2018 Zobel et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Research Articles Zobel, Martina Disanza, Andrea Senic-Matuglia, Francesca Franco, Michel Colaluca, Ivan Nicola Confalonieri, Stefano Bisi, Sara Barbieri, Elisa Caldieri, Giusi Sigismund, Sara Pece, Salvatore Chavrier, Philippe Di Fiore, Pier Paolo Scita, Giorgio A NUMB–EFA6B–ARF6 recycling route controls apically restricted cell protrusions and mesenchymal motility |
title | A NUMB–EFA6B–ARF6 recycling route controls apically restricted cell protrusions and mesenchymal motility |
title_full | A NUMB–EFA6B–ARF6 recycling route controls apically restricted cell protrusions and mesenchymal motility |
title_fullStr | A NUMB–EFA6B–ARF6 recycling route controls apically restricted cell protrusions and mesenchymal motility |
title_full_unstemmed | A NUMB–EFA6B–ARF6 recycling route controls apically restricted cell protrusions and mesenchymal motility |
title_short | A NUMB–EFA6B–ARF6 recycling route controls apically restricted cell protrusions and mesenchymal motility |
title_sort | numb–efa6b–arf6 recycling route controls apically restricted cell protrusions and mesenchymal motility |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123001/ https://www.ncbi.nlm.nih.gov/pubmed/30061108 http://dx.doi.org/10.1083/jcb.201802023 |
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