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Endocytosis at extremes: Formation and internalization of giant clathrin-coated pits under elevated membrane tension

Internalization of clathrin-coated vesicles from the plasma membrane constitutes the major endocytic route for receptors and their ligands. Dynamic and structural properties of endocytic clathrin coats are regulated by the mechanical properties of the plasma membrane. Here, we used conventional fluo...

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Autores principales: Akatay, Ahmet Ata, Wu, Tianyao, Djakbarova, Umidahan, Thompson, Cristopher, Cocucci, Emanuele, Zandi, Roya, Rudnick, Joseph, Kural, Comert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9532848/
https://www.ncbi.nlm.nih.gov/pubmed/36213118
http://dx.doi.org/10.3389/fmolb.2022.959737
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author Akatay, Ahmet Ata
Wu, Tianyao
Djakbarova, Umidahan
Thompson, Cristopher
Cocucci, Emanuele
Zandi, Roya
Rudnick, Joseph
Kural, Comert
author_facet Akatay, Ahmet Ata
Wu, Tianyao
Djakbarova, Umidahan
Thompson, Cristopher
Cocucci, Emanuele
Zandi, Roya
Rudnick, Joseph
Kural, Comert
author_sort Akatay, Ahmet Ata
collection PubMed
description Internalization of clathrin-coated vesicles from the plasma membrane constitutes the major endocytic route for receptors and their ligands. Dynamic and structural properties of endocytic clathrin coats are regulated by the mechanical properties of the plasma membrane. Here, we used conventional fluorescence imaging and multiple modes of structured illumination microscopy (SIM) to image formation of endocytic clathrin coats within live cells and tissues of developing fruit fly embryos. High resolution in both spatial and temporal domains allowed us to detect and characterize distinct classes of clathrin-coated structures. Aside from the clathrin pits and plaques detected in distinct embryonic tissues, we report, for the first time, formation of giant coated pits (GCPs) that can be up to two orders of magnitude larger than the canonical pits. In cultured cells, we show that GCP formation is induced by increased membrane tension. GCPs take longer to grow but their mechanism of curvature generation is the same as the canonical pits. We also demonstrate that GCPs split into smaller fragments during internalization. Considering the supporting roles played by actin filament dynamics under mechanically stringent conditions that slow down completion of clathrin coats, we suggest that local changes in the coat curvature driven by actin machinery can drive splitting and internalization of GCPs.
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spelling pubmed-95328482022-10-06 Endocytosis at extremes: Formation and internalization of giant clathrin-coated pits under elevated membrane tension Akatay, Ahmet Ata Wu, Tianyao Djakbarova, Umidahan Thompson, Cristopher Cocucci, Emanuele Zandi, Roya Rudnick, Joseph Kural, Comert Front Mol Biosci Molecular Biosciences Internalization of clathrin-coated vesicles from the plasma membrane constitutes the major endocytic route for receptors and their ligands. Dynamic and structural properties of endocytic clathrin coats are regulated by the mechanical properties of the plasma membrane. Here, we used conventional fluorescence imaging and multiple modes of structured illumination microscopy (SIM) to image formation of endocytic clathrin coats within live cells and tissues of developing fruit fly embryos. High resolution in both spatial and temporal domains allowed us to detect and characterize distinct classes of clathrin-coated structures. Aside from the clathrin pits and plaques detected in distinct embryonic tissues, we report, for the first time, formation of giant coated pits (GCPs) that can be up to two orders of magnitude larger than the canonical pits. In cultured cells, we show that GCP formation is induced by increased membrane tension. GCPs take longer to grow but their mechanism of curvature generation is the same as the canonical pits. We also demonstrate that GCPs split into smaller fragments during internalization. Considering the supporting roles played by actin filament dynamics under mechanically stringent conditions that slow down completion of clathrin coats, we suggest that local changes in the coat curvature driven by actin machinery can drive splitting and internalization of GCPs. Frontiers Media S.A. 2022-09-21 /pmc/articles/PMC9532848/ /pubmed/36213118 http://dx.doi.org/10.3389/fmolb.2022.959737 Text en Copyright © 2022 Akatay, Wu, Djakbarova, Thompson, Cocucci, Zandi, Rudnick and Kural. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Molecular Biosciences
Akatay, Ahmet Ata
Wu, Tianyao
Djakbarova, Umidahan
Thompson, Cristopher
Cocucci, Emanuele
Zandi, Roya
Rudnick, Joseph
Kural, Comert
Endocytosis at extremes: Formation and internalization of giant clathrin-coated pits under elevated membrane tension
title Endocytosis at extremes: Formation and internalization of giant clathrin-coated pits under elevated membrane tension
title_full Endocytosis at extremes: Formation and internalization of giant clathrin-coated pits under elevated membrane tension
title_fullStr Endocytosis at extremes: Formation and internalization of giant clathrin-coated pits under elevated membrane tension
title_full_unstemmed Endocytosis at extremes: Formation and internalization of giant clathrin-coated pits under elevated membrane tension
title_short Endocytosis at extremes: Formation and internalization of giant clathrin-coated pits under elevated membrane tension
title_sort endocytosis at extremes: formation and internalization of giant clathrin-coated pits under elevated membrane tension
topic Molecular Biosciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9532848/
https://www.ncbi.nlm.nih.gov/pubmed/36213118
http://dx.doi.org/10.3389/fmolb.2022.959737
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