Cargando…

Microtopographical guidance of macropinocytic signaling patches

In fast-moving cells such as amoeba and immune cells, dendritic actin filaments are spatiotemporally regulated to shape large-scale plasma membrane protrusions. Despite their importance in migration, as well as in particle and liquid ingestion, how their dynamics are affected by micrometer-scale fea...

Descripción completa

Detalles Bibliográficos
Autores principales: Honda, Gen, Saito, Nen, Fujimori, Taihei, Hashimura, Hidenori, Nakamura, Mitsuru J., Nakajima, Akihiko, Sawai, Satoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8685668/
https://www.ncbi.nlm.nih.gov/pubmed/34876521
http://dx.doi.org/10.1073/pnas.2110281118
_version_ 1784617878354395136
author Honda, Gen
Saito, Nen
Fujimori, Taihei
Hashimura, Hidenori
Nakamura, Mitsuru J.
Nakajima, Akihiko
Sawai, Satoshi
author_facet Honda, Gen
Saito, Nen
Fujimori, Taihei
Hashimura, Hidenori
Nakamura, Mitsuru J.
Nakajima, Akihiko
Sawai, Satoshi
author_sort Honda, Gen
collection PubMed
description In fast-moving cells such as amoeba and immune cells, dendritic actin filaments are spatiotemporally regulated to shape large-scale plasma membrane protrusions. Despite their importance in migration, as well as in particle and liquid ingestion, how their dynamics are affected by micrometer-scale features of the contact surface is still poorly understood. Here, through quantitative image analysis of Dictyostelium on microfabricated surfaces, we show that there is a distinct mode of topographical guidance directed by the macropinocytic membrane cup. Unlike other topographical guidance known to date that depends on nanometer-scale curvature sensing protein or stress fibers, the macropinocytic membrane cup is driven by the Ras/PI3K/F-actin signaling patch and its dependency on the micrometer-scale topographical features, namely PI3K/F-actin–independent accumulation of Ras-GTP at the convex curved surface, PI3K-dependent patch propagation along the convex edge, and its actomyosin-dependent constriction at the concave edge. Mathematical model simulations demonstrate that the topographically dependent initiation, in combination with the mutually defining patch patterning and the membrane deformation, gives rise to the topographical guidance. Our results suggest that the macropinocytic cup is a self-enclosing structure that can support liquid ingestion by default; however, in the presence of structured surfaces, it is directed to faithfully trace bent and bifurcating ridges for particle ingestion and cell guidance.
format Online
Article
Text
id pubmed-8685668
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher National Academy of Sciences
record_format MEDLINE/PubMed
spelling pubmed-86856682022-01-06 Microtopographical guidance of macropinocytic signaling patches Honda, Gen Saito, Nen Fujimori, Taihei Hashimura, Hidenori Nakamura, Mitsuru J. Nakajima, Akihiko Sawai, Satoshi Proc Natl Acad Sci U S A Biological Sciences In fast-moving cells such as amoeba and immune cells, dendritic actin filaments are spatiotemporally regulated to shape large-scale plasma membrane protrusions. Despite their importance in migration, as well as in particle and liquid ingestion, how their dynamics are affected by micrometer-scale features of the contact surface is still poorly understood. Here, through quantitative image analysis of Dictyostelium on microfabricated surfaces, we show that there is a distinct mode of topographical guidance directed by the macropinocytic membrane cup. Unlike other topographical guidance known to date that depends on nanometer-scale curvature sensing protein or stress fibers, the macropinocytic membrane cup is driven by the Ras/PI3K/F-actin signaling patch and its dependency on the micrometer-scale topographical features, namely PI3K/F-actin–independent accumulation of Ras-GTP at the convex curved surface, PI3K-dependent patch propagation along the convex edge, and its actomyosin-dependent constriction at the concave edge. Mathematical model simulations demonstrate that the topographically dependent initiation, in combination with the mutually defining patch patterning and the membrane deformation, gives rise to the topographical guidance. Our results suggest that the macropinocytic cup is a self-enclosing structure that can support liquid ingestion by default; however, in the presence of structured surfaces, it is directed to faithfully trace bent and bifurcating ridges for particle ingestion and cell guidance. National Academy of Sciences 2021-12-07 2021-12-14 /pmc/articles/PMC8685668/ /pubmed/34876521 http://dx.doi.org/10.1073/pnas.2110281118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Honda, Gen
Saito, Nen
Fujimori, Taihei
Hashimura, Hidenori
Nakamura, Mitsuru J.
Nakajima, Akihiko
Sawai, Satoshi
Microtopographical guidance of macropinocytic signaling patches
title Microtopographical guidance of macropinocytic signaling patches
title_full Microtopographical guidance of macropinocytic signaling patches
title_fullStr Microtopographical guidance of macropinocytic signaling patches
title_full_unstemmed Microtopographical guidance of macropinocytic signaling patches
title_short Microtopographical guidance of macropinocytic signaling patches
title_sort microtopographical guidance of macropinocytic signaling patches
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8685668/
https://www.ncbi.nlm.nih.gov/pubmed/34876521
http://dx.doi.org/10.1073/pnas.2110281118
work_keys_str_mv AT hondagen microtopographicalguidanceofmacropinocyticsignalingpatches
AT saitonen microtopographicalguidanceofmacropinocyticsignalingpatches
AT fujimoritaihei microtopographicalguidanceofmacropinocyticsignalingpatches
AT hashimurahidenori microtopographicalguidanceofmacropinocyticsignalingpatches
AT nakamuramitsuruj microtopographicalguidanceofmacropinocyticsignalingpatches
AT nakajimaakihiko microtopographicalguidanceofmacropinocyticsignalingpatches
AT sawaisatoshi microtopographicalguidanceofmacropinocyticsignalingpatches