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CYRI proteins: controllers of actin dynamics in the cellular ‘eat vs walk’ decision

Cells use actin-based protrusions not only to migrate, but also to sample their environment and take up liquids and particles, including nutrients, antigens and pathogens. Lamellipodia are sheet-like actin-based protrusions involved in sensing the substratum and directing cell migration. Related str...

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Detalles Bibliográficos
Autor principal: Machesky, Laura M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10212538/
https://www.ncbi.nlm.nih.gov/pubmed/36892409
http://dx.doi.org/10.1042/BST20221354
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author Machesky, Laura M.
author_facet Machesky, Laura M.
author_sort Machesky, Laura M.
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description Cells use actin-based protrusions not only to migrate, but also to sample their environment and take up liquids and particles, including nutrients, antigens and pathogens. Lamellipodia are sheet-like actin-based protrusions involved in sensing the substratum and directing cell migration. Related structures, macropinocytic cups, arise from lamellipodia ruffles and can take in large gulps of the surrounding medium. How cells regulate the balance between using lamellipodia for migration and macropinocytosis is not yet well understood. We recently identified CYRI proteins as RAC1-binding regulators of the dynamics of lamellipodia and macropinocytic events. This review discusses recent advances in our understanding of how cells regulate the balance between eating and walking by repurposing their actin cytoskeletons in response to environmental cues.
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spelling pubmed-102125382023-05-26 CYRI proteins: controllers of actin dynamics in the cellular ‘eat vs walk’ decision Machesky, Laura M. Biochem Soc Trans Review Articles Cells use actin-based protrusions not only to migrate, but also to sample their environment and take up liquids and particles, including nutrients, antigens and pathogens. Lamellipodia are sheet-like actin-based protrusions involved in sensing the substratum and directing cell migration. Related structures, macropinocytic cups, arise from lamellipodia ruffles and can take in large gulps of the surrounding medium. How cells regulate the balance between using lamellipodia for migration and macropinocytosis is not yet well understood. We recently identified CYRI proteins as RAC1-binding regulators of the dynamics of lamellipodia and macropinocytic events. This review discusses recent advances in our understanding of how cells regulate the balance between eating and walking by repurposing their actin cytoskeletons in response to environmental cues. Portland Press Ltd. 2023-04-26 2023-03-09 /pmc/articles/PMC10212538/ /pubmed/36892409 http://dx.doi.org/10.1042/BST20221354 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . Open access for this article was enabled by the participation of the University of Cambridge in an all-inclusive Read & Publish agreement with Portland Press and the Biochemical Society under a transformative agreement with JISC.
spellingShingle Review Articles
Machesky, Laura M.
CYRI proteins: controllers of actin dynamics in the cellular ‘eat vs walk’ decision
title CYRI proteins: controllers of actin dynamics in the cellular ‘eat vs walk’ decision
title_full CYRI proteins: controllers of actin dynamics in the cellular ‘eat vs walk’ decision
title_fullStr CYRI proteins: controllers of actin dynamics in the cellular ‘eat vs walk’ decision
title_full_unstemmed CYRI proteins: controllers of actin dynamics in the cellular ‘eat vs walk’ decision
title_short CYRI proteins: controllers of actin dynamics in the cellular ‘eat vs walk’ decision
title_sort cyri proteins: controllers of actin dynamics in the cellular ‘eat vs walk’ decision
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10212538/
https://www.ncbi.nlm.nih.gov/pubmed/36892409
http://dx.doi.org/10.1042/BST20221354
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