Reversal of contractility as a signature of self-organization in cytoskeletal bundles

Bundles of cytoskeletal filaments and molecular motors generate motion in living cells, and have internal structures ranging from very organized to apparently disordered. The mechanisms powering the disordered structures are debated, and existing models predominantly predict that they are contractil...

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Main Author: Martin Lenz
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2020-03-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/51751
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spelling doaj-5c8ff2b266a14a3ca0e0b552e888e6412021-05-05T20:53:41ZengeLife Sciences Publications LtdeLife2050-084X2020-03-01910.7554/eLife.51751Reversal of contractility as a signature of self-organization in cytoskeletal bundlesMartin Lenz0https://orcid.org/0000-0002-2307-1106Université Paris-Saclay, CNRS, LPTMS, Orsay, France; PMMH, CNRS, ESPCI Paris, PSL University, Sorbonne Université, Université de Paris, Paris, FranceBundles of cytoskeletal filaments and molecular motors generate motion in living cells, and have internal structures ranging from very organized to apparently disordered. The mechanisms powering the disordered structures are debated, and existing models predominantly predict that they are contractile. We reexamine this prediction through a theoretical treatment of the interplay between three well-characterized internal dynamical processes in cytoskeletal bundles: filament assembly and disassembly, the attachement-detachment dynamics of motors and that of crosslinking proteins. The resulting self-organization is easily understood in terms of motor and crosslink localization, and allows for an extensive control of the active bundle mechanics, including reversals of the filaments’ apparent velocities and the possibility of generating extension instead of contraction. This reversal mirrors some recent experimental observations, and provides a robust criterion to experimentally elucidate the underpinnings of both actomyosin activity and the dynamics of microtubule/motor assemblies in vitro as well as in diverse intracellular structures ranging from contractile bundles to the mitotic spindle.https://elifesciences.org/articles/51751cytoskeletonmathematical modelingactinmicrotubulesmolecular motors
collection DOAJ
language English
format Article
sources DOAJ
author Martin Lenz
spellingShingle Martin Lenz
Reversal of contractility as a signature of self-organization in cytoskeletal bundles
eLife
cytoskeleton
mathematical modeling
actin
microtubules
molecular motors
author_facet Martin Lenz
author_sort Martin Lenz
title Reversal of contractility as a signature of self-organization in cytoskeletal bundles
title_short Reversal of contractility as a signature of self-organization in cytoskeletal bundles
title_full Reversal of contractility as a signature of self-organization in cytoskeletal bundles
title_fullStr Reversal of contractility as a signature of self-organization in cytoskeletal bundles
title_full_unstemmed Reversal of contractility as a signature of self-organization in cytoskeletal bundles
title_sort reversal of contractility as a signature of self-organization in cytoskeletal bundles
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2020-03-01
description Bundles of cytoskeletal filaments and molecular motors generate motion in living cells, and have internal structures ranging from very organized to apparently disordered. The mechanisms powering the disordered structures are debated, and existing models predominantly predict that they are contractile. We reexamine this prediction through a theoretical treatment of the interplay between three well-characterized internal dynamical processes in cytoskeletal bundles: filament assembly and disassembly, the attachement-detachment dynamics of motors and that of crosslinking proteins. The resulting self-organization is easily understood in terms of motor and crosslink localization, and allows for an extensive control of the active bundle mechanics, including reversals of the filaments’ apparent velocities and the possibility of generating extension instead of contraction. This reversal mirrors some recent experimental observations, and provides a robust criterion to experimentally elucidate the underpinnings of both actomyosin activity and the dynamics of microtubule/motor assemblies in vitro as well as in diverse intracellular structures ranging from contractile bundles to the mitotic spindle.
topic cytoskeleton
mathematical modeling
actin
microtubules
molecular motors
url https://elifesciences.org/articles/51751
work_keys_str_mv AT martinlenz reversalofcontractilityasasignatureofselforganizationincytoskeletalbundles
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