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PMID: 21483802 Published · epublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

From molecular signal activation to locomotion: an integrated, multiscale analysis of cell motility on defined matrices.

PloS one ·Vol. 6 ·No. 3 ·2011-03-31 ·Pages e18423

Pathak A, Kumar S

Abstract

The adhesion, mechanics, and motility of eukaryotic cells are highly sensitive to the ligand density and stiffness of the extracellular matrix (ECM). This relationship bears profound implications for stem cell engineering, tumor invasion and metastasis. Yet, our quantitative understanding of how ECM biophysical properties, mechanotransductive signals, and assembly of contractile and adhesive structures collude to control these cell behaviors remains extremely limited. Here we present a novel multiscale model of cell migration on ECMs of defined biophysical properties that integrates local activation of biochemical signals with adhesion and force generation at the cell-ECM interface. We capture the mechanosensitivity of individual cellular components by dynamically coupling ECM properties to the activation of Rho and Rac GTPases in specific portions of the cell with actomyosin contractility, cell-ECM adhesion bond formation and rupture, and process extension and retraction. We show that our framework is capable of recreating key experimentally-observed features of the relationship between cell migration and ECM biophysical properties. In particular, our model predicts for the first time recently reported transitions from filopodial to "stick-slip" to gliding motility on ECMs of increasing stiffness, previously observed dependences of migration speed on ECM stiffness and ligand density, and high-resolution measurements of mechanosensitive protrusion dynamics during cell motility we newly obtained for this study. It also relates the biphasic dependence of cell migration speed on ECM stiffness to the tendency of the cell to polarize. By enabling the investigation of experimentally-inaccessible microscale relationships between mechanotransductive signaling, adhesion, and motility, our model offers new insight into how these factors interact with one another to produce complex migration patterns across a variety of ECM conditions.

MeSH Terms
Actomyosin/metabolism Cell Movement/genetics,physiology Extracellular Matrix/metabolism Mechanotransduction, Cellular Models, Theoretical rac GTP-Binding Proteins/metabolism
Chemicals
Actomyosin rac GTP-Binding Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Pathak Amit
Department of Bioengineering, University of California, Berkeley, California, United States of America.
Kumar Sanjay
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Article Info
Journal
PloS one
Abbr.
PLoS One
ISSN
1932-6203
Published
2011-03-31
Epub
2011-00-31
Pages
e18423
Language
English
Region
United States
NLM ID
101285081
PMCID
PMC3069105
Subset
IM
Grants
NIH HHS · DP2 OD004213 · United States
NCI NIH HHS · U54 CA143836 · United States
NCI NIH HHS · 1U54CA143836 · United States
NIH HHS · 1DP2OD004213 · United States
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