Emergence of Large-Scale Cell Morphology and Movement from Local Actin Filament Growth Dynamics

@article{citeulike:1640533, abstract = {Variations in cell migration and morphology are consequences of changes in underlying cytoskeletal organization and dynamics. We investigated how these large-scale cellular events emerge as direct consequences of small-scale cytoskeletal molecular activities. Because the properties of the actin cytoskeleton can be modulated by actin-remodeling proteins, we quantitatively examined how one such family of proteins, enabled/vasodilator-stimulated phosphoprotein (Ena/VASP), affects the migration and morphology of epithelial fish keratocytes. Keratocytes generally migrate persistently while exhibiting a characteristic smooth-edged \&\#8220;canoe\&\#8221; shape, but may also exhibit less regular morphologies and less persistent movement. When we observed that the smooth-edged canoe keratocyte morphology correlated with enrichment of Ena/VASP at the leading edge, we mislocalized and overexpressed Ena/VASP proteins and found that this led to changes in the morphology and movement persistence of cells within a population. Thus, local changes in actin filament dynamics due to Ena/VASP activity directly caused changes in cell morphology, which is coupled to the motile behavior of keratocytes. We also characterized the range of natural cell-to-cell variation within a population by using measurable morphological and behavioral features\&\#8212;cell shape, leading-edge shape, filamentous actin (F-actin) distribution, cell speed, and directional persistence\&\#8212;that we have found to correlate with each other to describe a spectrum of coordinated phenotypes based on Ena/VASP enrichment at the leading edge. This spectrum stretched from smooth-edged, canoe-shaped keratocytes\&\#8212;which had VASP highly enriched at their leading edges and migrated fast with straight trajectories\&\#8212;to more irregular, rounder cells migrating slower with less directional persistence and low levels of VASP at their leading edges. We developed a mathematical model that accounts for these coordinated cell-shape and behavior phenotypes as large-scale consequences of kinetic contributions of VASP to actin filament growth and protection from capping at the leading edge. This work shows that the local effects of actin-remodeling proteins on cytoskeletal dynamics and organization can manifest as global modifications of the shape and behavior of migrating cells and that mathematical modeling can elucidate these large-scale cell behaviors from knowledge of detailed multiscale protein interactions.}, author = {Lacayo, Catherine I. and Pincus, Zachary and Vanduijn, Martijn M. and Wilson, Cyrus A. and Fletcher, Daniel A. and Gertler, Frank B. and Mogilner, Alex and Theriot, Julie A. }, citeulike-article-id = {1640533}, comment = {voir aussi article J. Microscopy M\'{e}thode de quantification de la forme des cellules par d\'{e}composition en composantes principales Les logiciels ne sont pas disponible (scripts compliqu\'{e}s)}, doi = {10.1371/journal.pbio.0050233}, journal = {PLoS Biology}, keywords = {actin, cell\_culture, image\_processing, model}, month = {September}, number = {9}, pages = {e233+}, posted-at = {2008-02-25 15:49:05}, priority = {0}, title = {Emergence of Large-Scale Cell Morphology and Movement from Local Actin Filament Growth Dynamics}, url = {http://dx.doi.org/10.1371/journal.pbio.0050233}, volume = {5}, year = {2007} }

TY - JOUR ID - citeulike:1640533 L3 - citeulike-article-id:1640533 TI - Emergence of Large-Scale Cell Morphology and Movement from Local Actin Filament Growth Dynamics JF - PLoS Biology VL - 5 IS - 9 SP - e233 N2 - Variations in cell migration and morphology are consequences of changes in underlying cytoskeletal organization and dynamics. We investigated how these large-scale cellular events emerge as direct consequences of small-scale cytoskeletal molecular activities. Because the properties of the actin cytoskeleton can be modulated by actin-remodeling proteins, we quantitatively examined how one such family of proteins, enabled/vasodilator-stimulated phosphoprotein (Ena/VASP), affects the migration and morphology of epithelial fish keratocytes. Keratocytes generally migrate persistently while exhibiting a characteristic smooth-edged “canoe” shape, but may also exhibit less regular morphologies and less persistent movement. When we observed that the smooth-edged canoe keratocyte morphology correlated with enrichment of Ena/VASP at the leading edge, we mislocalized and overexpressed Ena/VASP proteins and found that this led to changes in the morphology and movement persistence of cells within a population. Thus, local changes in actin filament dynamics due to Ena/VASP activity directly caused changes in cell morphology, which is coupled to the motile behavior of keratocytes. We also characterized the range of natural cell-to-cell variation within a population by using measurable morphological and behavioral features—cell shape, leading-edge shape, filamentous actin (F-actin) distribution, cell speed, and directional persistence—that we have found to correlate with each other to describe a spectrum of coordinated phenotypes based on Ena/VASP enrichment at the leading edge. This spectrum stretched from smooth-edged, canoe-shaped keratocytes—which had VASP highly enriched at their leading edges and migrated fast with straight trajectories—to more irregular, rounder cells migrating slower with less directional persistence and low levels of VASP at their leading edges. We developed a mathematical model that accounts for these coordinated cell-shape and behavior phenotypes as large-scale consequences of kinetic contributions of VASP to actin filament growth and protection from capping at the leading edge. This work shows that the local effects of actin-remodeling proteins on cytoskeletal dynamics and organization can manifest as global modifications of the shape and behavior of migrating cells and that mathematical modeling can elucidate these large-scale cell behaviors from knowledge of detailed multiscale protein interactions. KW - actin KW - cell_culture KW - image_processing KW - model N1 - voir aussi article J. Microscopy Méthode de quantification de la forme des cellules par décomposition en composantes principales Les logiciels ne sont pas disponible (scripts compliqués) AU - Lacayo, Catherine AU - Pincus, Zachary AU - Vanduijn, Martijn AU - Wilson, Cyrus AU - Fletcher, Daniel AU - Gertler, Frank AU - Mogilner, Alex AU - Theriot, Julie PY - 2007/09/01/ UR - http://dx.doi.org/10.1371/journal.pbio.0050233 ER -