A Motor-Driven Mechanism for Cell-Length Sensing

Size homeostasis is fundamental in cell biology, but it is not clear how large cells such as neurons can assess their own size or length. We examined a role for molecular motors in intracellular length sensing. Computational simulations suggest that spatial information can be encoded by the frequen...

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Main Authors: Ida Rishal, Naaman Kam, Rotem Ben-Tov Perry, Vera Shinder, Elizabeth M.C. Fisher, Giampietro Schiavo, Mike Fainzilber
Format: Article
Language:English
Published: Elsevier 2012-06-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124712001386
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spelling doaj-3dd069deda0f46e58c881986091e936e2020-11-25T00:46:48ZengElsevierCell Reports2211-12472012-06-011660861610.1016/j.celrep.2012.05.013A Motor-Driven Mechanism for Cell-Length SensingIda Rishal0Naaman Kam1Rotem Ben-Tov Perry2Vera Shinder3Elizabeth M.C. Fisher4Giampietro Schiavo5Mike Fainzilber6Department of Biological Chemistry, Weizmann Institute of Science, 76100 Rehovot, IsraelDepartment of Biological Chemistry, Weizmann Institute of Science, 76100 Rehovot, IsraelDepartment of Biological Chemistry, Weizmann Institute of Science, 76100 Rehovot, IsraelDepartment of Chemical Research Support, Weizmann Institute of Science, 76100 Rehovot, IsraelDepartment of Neurodegenerative Disease and MRC Centre for Neuromuscular Diseases, Institute of Neurology, University College London, London WC1N 3BG, UKMolecular Neuropathobiology Laboratory, Cancer Research UK London Research Institute, Lincoln's Inn Fields Laboratories, London WC2A 3PX, UKDepartment of Biological Chemistry, Weizmann Institute of Science, 76100 Rehovot, Israel Size homeostasis is fundamental in cell biology, but it is not clear how large cells such as neurons can assess their own size or length. We examined a role for molecular motors in intracellular length sensing. Computational simulations suggest that spatial information can be encoded by the frequency of an oscillating retrograde signal arising from a composite negative feedback loop between bidirectional motor-dependent signals. The model predicts that decreasing either or both anterograde or retrograde signals should increase cell length, and this prediction was confirmed upon application of siRNAs for specific kinesin and/or dynein heavy chains in adult sensory neurons. Heterozygous dynein heavy chain 1 mutant sensory neurons also exhibited increased lengths both in vitro and during embryonic development. Moreover, similar length increases were observed in mouse embryonic fibroblasts upon partial downregulation of dynein heavy chain 1. Thus, molecular motors critically influence cell-length sensing and growth control. http://www.sciencedirect.com/science/article/pii/S2211124712001386
collection DOAJ
language English
format Article
sources DOAJ
author Ida Rishal
Naaman Kam
Rotem Ben-Tov Perry
Vera Shinder
Elizabeth M.C. Fisher
Giampietro Schiavo
Mike Fainzilber
spellingShingle Ida Rishal
Naaman Kam
Rotem Ben-Tov Perry
Vera Shinder
Elizabeth M.C. Fisher
Giampietro Schiavo
Mike Fainzilber
A Motor-Driven Mechanism for Cell-Length Sensing
Cell Reports
author_facet Ida Rishal
Naaman Kam
Rotem Ben-Tov Perry
Vera Shinder
Elizabeth M.C. Fisher
Giampietro Schiavo
Mike Fainzilber
author_sort Ida Rishal
title A Motor-Driven Mechanism for Cell-Length Sensing
title_short A Motor-Driven Mechanism for Cell-Length Sensing
title_full A Motor-Driven Mechanism for Cell-Length Sensing
title_fullStr A Motor-Driven Mechanism for Cell-Length Sensing
title_full_unstemmed A Motor-Driven Mechanism for Cell-Length Sensing
title_sort motor-driven mechanism for cell-length sensing
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2012-06-01
description Size homeostasis is fundamental in cell biology, but it is not clear how large cells such as neurons can assess their own size or length. We examined a role for molecular motors in intracellular length sensing. Computational simulations suggest that spatial information can be encoded by the frequency of an oscillating retrograde signal arising from a composite negative feedback loop between bidirectional motor-dependent signals. The model predicts that decreasing either or both anterograde or retrograde signals should increase cell length, and this prediction was confirmed upon application of siRNAs for specific kinesin and/or dynein heavy chains in adult sensory neurons. Heterozygous dynein heavy chain 1 mutant sensory neurons also exhibited increased lengths both in vitro and during embryonic development. Moreover, similar length increases were observed in mouse embryonic fibroblasts upon partial downregulation of dynein heavy chain 1. Thus, molecular motors critically influence cell-length sensing and growth control.
url http://www.sciencedirect.com/science/article/pii/S2211124712001386
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