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Under Pressure: the Differential Requirements for Actin during Yeast and Mammalian Endocytosis

Key features of clathrin-mediated endocytosis have been conserved across evolution. However, endocytosis in Saccharomyces cerevisiae is completely dependent on a functional actin cytoskeleton, while actin appears to be less critical in mammalian cell endocytosis. We reveal that the fundamental requi...

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Detalles Bibliográficos
Autores principales: Aghamohammadazadeh, Soheil, Ayscough, Kathryn R.
Formato: Texto
Lenguaje:English
Publicado: 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2875176/
https://www.ncbi.nlm.nih.gov/pubmed/19597484
http://dx.doi.org/10.1038/ncb1918
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author Aghamohammadazadeh, Soheil
Ayscough, Kathryn R.
author_facet Aghamohammadazadeh, Soheil
Ayscough, Kathryn R.
author_sort Aghamohammadazadeh, Soheil
collection PubMed
description Key features of clathrin-mediated endocytosis have been conserved across evolution. However, endocytosis in Saccharomyces cerevisiae is completely dependent on a functional actin cytoskeleton, while actin appears to be less critical in mammalian cell endocytosis. We reveal that the fundamental requirement for actin in early stages of yeast endocytosis is to provide a strong framework to support force generation required to direct the invaginating plasma membrane into the cell against turgor pressure. By providing osmotic support, pressure differences across the plasma membrane were removed and this reduced the requirement for actin-bundling proteins required for normal endocytosis. Conversely, increased turgor pressure in specific yeast mutants correlated with decreased rate of endocytic patch invagination.
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spelling pubmed-28751762010-05-24 Under Pressure: the Differential Requirements for Actin during Yeast and Mammalian Endocytosis Aghamohammadazadeh, Soheil Ayscough, Kathryn R. Nat Cell Biol Article Key features of clathrin-mediated endocytosis have been conserved across evolution. However, endocytosis in Saccharomyces cerevisiae is completely dependent on a functional actin cytoskeleton, while actin appears to be less critical in mammalian cell endocytosis. We reveal that the fundamental requirement for actin in early stages of yeast endocytosis is to provide a strong framework to support force generation required to direct the invaginating plasma membrane into the cell against turgor pressure. By providing osmotic support, pressure differences across the plasma membrane were removed and this reduced the requirement for actin-bundling proteins required for normal endocytosis. Conversely, increased turgor pressure in specific yeast mutants correlated with decreased rate of endocytic patch invagination. 2009-07-13 2009-08 /pmc/articles/PMC2875176/ /pubmed/19597484 http://dx.doi.org/10.1038/ncb1918 Text en
spellingShingle Article
Aghamohammadazadeh, Soheil
Ayscough, Kathryn R.
Under Pressure: the Differential Requirements for Actin during Yeast and Mammalian Endocytosis
title Under Pressure: the Differential Requirements for Actin during Yeast and Mammalian Endocytosis
title_full Under Pressure: the Differential Requirements for Actin during Yeast and Mammalian Endocytosis
title_fullStr Under Pressure: the Differential Requirements for Actin during Yeast and Mammalian Endocytosis
title_full_unstemmed Under Pressure: the Differential Requirements for Actin during Yeast and Mammalian Endocytosis
title_short Under Pressure: the Differential Requirements for Actin during Yeast and Mammalian Endocytosis
title_sort under pressure: the differential requirements for actin during yeast and mammalian endocytosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2875176/
https://www.ncbi.nlm.nih.gov/pubmed/19597484
http://dx.doi.org/10.1038/ncb1918
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