Publication Date:
2010-05-21
Description:
Crawling locomotion of eukaryotic cells is achieved by a process dependent on the actin cytoskeleton: protrusion of the leading edge requires assembly of a network of actin filaments, which must be disassembled at the cell rear for sustained motility. Although ADF/cofilin proteins have been shown to contribute to actin disassembly, it is not clear how activity of these locally acting proteins could be coordinated over the distance scale of the whole cell. Here we show that non-muscle myosin II has a direct role in actin network disassembly in crawling cells. In fish keratocytes undergoing motility, myosin II is concentrated in regions at the rear with high rates of network disassembly. Activation of myosin II by ATP in detergent-extracted cytoskeletons results in rear-localized disassembly of the actin network. Inhibition of myosin II activity and stabilization of actin filaments synergistically impede cell motility, suggesting the existence of two disassembly pathways, one of which requires myosin II activity. Our results establish the importance of myosin II as an enzyme for actin network disassembly; we propose that gradual formation and reorganization of an actomyosin network provides an intrinsic destruction timer, enabling long-range coordination of actin network treadmilling in motile cells.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3662466/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉 〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3662466/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wilson, Cyrus A -- Tsuchida, Mark A -- Allen, Greg M -- Barnhart, Erin L -- Applegate, Kathryn T -- Yam, Patricia T -- Ji, Lin -- Keren, Kinneret -- Danuser, Gaudenz -- Theriot, Julie A -- R01AI067712/AI/NIAID NIH HHS/ -- T32GM007276/GM/NIGMS NIH HHS/ -- U01 GM067230/GM/NIGMS NIH HHS/ -- U01 GM067230-07/GM/NIGMS NIH HHS/ -- U01GM67230/GM/NIGMS NIH HHS/ -- U54GM64346/GM/NIGMS NIH HHS/ -- Howard Hughes Medical Institute/ -- England -- Nature. 2010 May 20;465(7296):373-7. doi: 10.1038/nature08994.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biochemistry and Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, California 94305, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/20485438" target="_blank"〉PubMed〈/a〉
Keywords:
Actins/*chemistry/*metabolism
;
Adenosine Triphosphate/pharmacology
;
Animals
;
Cell Movement/drug effects
;
Cichlids
;
Cytoskeleton/chemistry/drug effects/metabolism
;
Depsipeptides/pharmacology
;
Detergents
;
Epithelial Cells/*cytology/*metabolism
;
Heterocyclic Compounds with 4 or More Rings/pharmacology
;
Myosin Type II/antagonists & inhibitors/*metabolism
;
Protein Binding/drug effects
;
Protein Transport
Print ISSN:
0028-0836
Electronic ISSN:
1476-4687
Topics:
Biology
,
Chemistry and Pharmacology
,
Medicine
,
Natural Sciences in General
,
Physics
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