Self-organizing actin patterns shape membrane architecture but not cell mechanics

Cell-free studies have demonstrated how collective action of actin-associated proteins can organize actin filaments into dynamic patterns, such as vortices, asters and stars. Using complementary microscopic techniques, we here show evidence of such self-organization of the actin cortex in living HeL...

Full description

Bibliographic Details
Main Authors: Fritzsche, M, Li, D, Colin-York, H, Chang, V, Moeendarbary, E, Felce, J, Sezgin, E, Charras, G, Betzig, E, Eggeling, C
Format: Journal article
Language:English
Published: Springer Nature 2017
_version_ 1826286278847496192
author Fritzsche, M
Li, D
Colin-York, H
Chang, V
Moeendarbary, E
Felce, J
Sezgin, E
Charras, G
Betzig, E
Eggeling, C
author_facet Fritzsche, M
Li, D
Colin-York, H
Chang, V
Moeendarbary, E
Felce, J
Sezgin, E
Charras, G
Betzig, E
Eggeling, C
author_sort Fritzsche, M
collection OXFORD
description Cell-free studies have demonstrated how collective action of actin-associated proteins can organize actin filaments into dynamic patterns, such as vortices, asters and stars. Using complementary microscopic techniques, we here show evidence of such self-organization of the actin cortex in living HeLa cells. During cell adhesion, an active multistage process naturally leads to pattern transitions from actin vortices over stars into asters. This process is primarily driven by Arp2/3 complex nucleation, but not by myosin motors, which is in contrast to what has been theoretically predicted and observed in vitro. Concomitant measurements of mechanics and plasma membrane fluidity demonstrate that changes in actin patterning alter membrane architecture but occur functionally independent of macroscopic cortex elasticity. Consequently, tuning the activity of the Arp2/3 complex to alter filament assembly may thus be a mechanism allowing cells to adjust their membrane architecture without affecting their macroscopic mechanical properties.
first_indexed 2024-03-07T01:41:24Z
format Journal article
id oxford-uuid:96f6eba1-1c59-49a4-96d5-0c19c5f3b5ef
institution University of Oxford
language English
last_indexed 2024-03-07T01:41:24Z
publishDate 2017
publisher Springer Nature
record_format dspace
spelling oxford-uuid:96f6eba1-1c59-49a4-96d5-0c19c5f3b5ef2022-03-26T23:56:30ZSelf-organizing actin patterns shape membrane architecture but not cell mechanicsJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:96f6eba1-1c59-49a4-96d5-0c19c5f3b5efEnglishSymplectic Elements at OxfordSpringer Nature2017Fritzsche, MLi, DColin-York, HChang, VMoeendarbary, EFelce, JSezgin, ECharras, GBetzig, EEggeling, CCell-free studies have demonstrated how collective action of actin-associated proteins can organize actin filaments into dynamic patterns, such as vortices, asters and stars. Using complementary microscopic techniques, we here show evidence of such self-organization of the actin cortex in living HeLa cells. During cell adhesion, an active multistage process naturally leads to pattern transitions from actin vortices over stars into asters. This process is primarily driven by Arp2/3 complex nucleation, but not by myosin motors, which is in contrast to what has been theoretically predicted and observed in vitro. Concomitant measurements of mechanics and plasma membrane fluidity demonstrate that changes in actin patterning alter membrane architecture but occur functionally independent of macroscopic cortex elasticity. Consequently, tuning the activity of the Arp2/3 complex to alter filament assembly may thus be a mechanism allowing cells to adjust their membrane architecture without affecting their macroscopic mechanical properties.
spellingShingle Fritzsche, M
Li, D
Colin-York, H
Chang, V
Moeendarbary, E
Felce, J
Sezgin, E
Charras, G
Betzig, E
Eggeling, C
Self-organizing actin patterns shape membrane architecture but not cell mechanics
title Self-organizing actin patterns shape membrane architecture but not cell mechanics
title_full Self-organizing actin patterns shape membrane architecture but not cell mechanics
title_fullStr Self-organizing actin patterns shape membrane architecture but not cell mechanics
title_full_unstemmed Self-organizing actin patterns shape membrane architecture but not cell mechanics
title_short Self-organizing actin patterns shape membrane architecture but not cell mechanics
title_sort self organizing actin patterns shape membrane architecture but not cell mechanics
work_keys_str_mv AT fritzschem selforganizingactinpatternsshapemembranearchitecturebutnotcellmechanics
AT lid selforganizingactinpatternsshapemembranearchitecturebutnotcellmechanics
AT colinyorkh selforganizingactinpatternsshapemembranearchitecturebutnotcellmechanics
AT changv selforganizingactinpatternsshapemembranearchitecturebutnotcellmechanics
AT moeendarbarye selforganizingactinpatternsshapemembranearchitecturebutnotcellmechanics
AT felcej selforganizingactinpatternsshapemembranearchitecturebutnotcellmechanics
AT sezgine selforganizingactinpatternsshapemembranearchitecturebutnotcellmechanics
AT charrasg selforganizingactinpatternsshapemembranearchitecturebutnotcellmechanics
AT betzige selforganizingactinpatternsshapemembranearchitecturebutnotcellmechanics
AT eggelingc selforganizingactinpatternsshapemembranearchitecturebutnotcellmechanics