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Conserved N- and C-terminal motifs of PAD-1 are required to inhibit extracellular vesicle release

Cells release extracellular vesicles (EVs) carrying cargos that can influence development and disease, but the mechanisms that govern EV release by plasma membrane budding are poorly understood. We previously showed that the Dopey protein PAD-1 inhibits EV release from the plasma membrane in C. eleg...

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Detalles Bibliográficos
Autores principales: Pitts, Lauren R, Nguyen, Alexander T, Wehman, Ann M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Caltech Library 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520342/
https://www.ncbi.nlm.nih.gov/pubmed/36188098
http://dx.doi.org/10.17912/micropub.biology.000625
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author Pitts, Lauren R
Nguyen, Alexander T
Wehman, Ann M
author_facet Pitts, Lauren R
Nguyen, Alexander T
Wehman, Ann M
author_sort Pitts, Lauren R
collection PubMed
description Cells release extracellular vesicles (EVs) carrying cargos that can influence development and disease, but the mechanisms that govern EV release by plasma membrane budding are poorly understood. We previously showed that the Dopey protein PAD-1 inhibits EV release from the plasma membrane in C. elegans . However, PAD-1 is large, and the domains required to regulate EV release were unknown. Here, we reveal that the conserved N-terminal EWAD motif and C-terminal leucine zippers are required to inhibit EV release from the plasma membrane. Revealing a role for these domains is an important first step to identifying how EV release is regulated.
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spelling pubmed-95203422022-09-30 Conserved N- and C-terminal motifs of PAD-1 are required to inhibit extracellular vesicle release Pitts, Lauren R Nguyen, Alexander T Wehman, Ann M MicroPubl Biol New Finding Cells release extracellular vesicles (EVs) carrying cargos that can influence development and disease, but the mechanisms that govern EV release by plasma membrane budding are poorly understood. We previously showed that the Dopey protein PAD-1 inhibits EV release from the plasma membrane in C. elegans . However, PAD-1 is large, and the domains required to regulate EV release were unknown. Here, we reveal that the conserved N-terminal EWAD motif and C-terminal leucine zippers are required to inhibit EV release from the plasma membrane. Revealing a role for these domains is an important first step to identifying how EV release is regulated. Caltech Library 2022-09-14 /pmc/articles/PMC9520342/ /pubmed/36188098 http://dx.doi.org/10.17912/micropub.biology.000625 Text en Copyright: © 2022 by the authors https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle New Finding
Pitts, Lauren R
Nguyen, Alexander T
Wehman, Ann M
Conserved N- and C-terminal motifs of PAD-1 are required to inhibit extracellular vesicle release
title Conserved N- and C-terminal motifs of PAD-1 are required to inhibit extracellular vesicle release
title_full Conserved N- and C-terminal motifs of PAD-1 are required to inhibit extracellular vesicle release
title_fullStr Conserved N- and C-terminal motifs of PAD-1 are required to inhibit extracellular vesicle release
title_full_unstemmed Conserved N- and C-terminal motifs of PAD-1 are required to inhibit extracellular vesicle release
title_short Conserved N- and C-terminal motifs of PAD-1 are required to inhibit extracellular vesicle release
title_sort conserved n- and c-terminal motifs of pad-1 are required to inhibit extracellular vesicle release
topic New Finding
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520342/
https://www.ncbi.nlm.nih.gov/pubmed/36188098
http://dx.doi.org/10.17912/micropub.biology.000625
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