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1.
PLoS One ; 3(11): e3735, 2008.
Article in English | MEDLINE | ID: mdl-19011687

ABSTRACT

Actin-based cell motility and force generation are central to immune response, tissue development, and cancer metastasis, and understanding actin cytoskeleton regulation is a major goal of cell biologists. Cell spreading is a commonly used model system for motility experiments -- spreading fibroblasts exhibit stereotypic, spatially-isotropic edge dynamics during a reproducible sequence of functional phases: 1) During early spreading, cells form initial contacts with the surface. 2) The middle spreading phase exhibits rapidly increasing attachment area. 3) Late spreading is characterized by periodic contractions and stable adhesions formation. While differences in cytoskeletal regulation between phases are known, a global analysis of the spatial and temporal coordination of motility and force generation is missing. Implementing improved algorithms for analyzing edge dynamics over the entire cell periphery, we observed that a single domain of homogeneous cytoskeletal dynamics dominated each of the three phases of spreading. These domains exhibited a unique combination of biophysical and biochemical parameters -- a motility module. Biophysical characterization of the motility modules revealed that the early phase was dominated by periodic, rapid membrane blebbing; the middle phase exhibited continuous protrusion with very low traction force generation; and the late phase was characterized by global periodic contractions and high force generation. Biochemically, each motility module exhibited a different distribution of the actin-related protein VASP, while inhibition of actin polymerization revealed different dependencies on barbed-end polymerization. In addition, our whole-cell analysis revealed that many cells exhibited heterogeneous combinations of motility modules in neighboring regions of the cell edge. Together, these observations support a model of motility in which regions of the cell edge exhibit one of a limited number of motility modules that, together, determine the overall motility function. Our data and algorithms are publicly available to encourage further exploration.


Subject(s)
Cell Membrane/metabolism , Cell Movement , Fibroblasts/cytology , Animals , Apoptosis/drug effects , Biomechanical Phenomena , Cell Adhesion Molecules/metabolism , Cell Membrane/drug effects , Cell Movement/drug effects , Cytochalasin D/pharmacology , Fibroblasts/drug effects , Fibroblasts/metabolism , Mice , Microfilament Proteins/metabolism , Phosphoproteins/metabolism , Protein Transport/drug effects , Pseudopodia/drug effects , Pseudopodia/metabolism
2.
Cell ; 128(3): 561-75, 2007 Feb 09.
Article in English | MEDLINE | ID: mdl-17289574

ABSTRACT

Cell motility proceeds by cycles of edge protrusion, adhesion, and retraction. Whether these functions are coordinated by biochemical or biomechanical processes is unknown. We find that myosin II pulls the rear of the lamellipodial actin network, causing upward bending, edge retraction, and initiation of new adhesion sites. The network then separates from the edge and condenses over the myosin. Protrusion resumes as lamellipodial actin regenerates from the front and extends rearward until it reaches newly assembled myosin, initiating the next cycle. Upward bending, observed by evanescence and electron microscopy, results in ruffle formation when adhesion strength is low. Correlative fluorescence and electron microscopy shows that the regenerating lamellipodium forms a cohesive, separable layer of actin above the lamellum. Thus, actin polymerization periodically builds a mechanical link, the lamellipodium, connecting myosin motors with the initiation of adhesion sites, suggesting that the major functions driving motility are coordinated by a biomechanical process.


Subject(s)
Actins/metabolism , Cell Adhesion , Myosins/metabolism , Pseudopodia/chemistry , Animals , Cell Movement , Fibroblasts/cytology , Mice , Microscopy, Electron , Microscopy, Fluorescence , Myosin Type II/genetics , Myosin Type II/metabolism , Periodicity , Polymers/metabolism , Pseudopodia/ultrastructure
3.
Cell ; 127(5): 1015-26, 2006 Dec 01.
Article in English | MEDLINE | ID: mdl-17129785

ABSTRACT

How physical force is sensed by cells and transduced into cellular signaling pathways is poorly understood. Previously, we showed that tyrosine phosphorylation of p130Cas (Cas) in a cytoskeletal complex is involved in force-dependent activation of the small GTPase Rap1. Here, we mechanically extended bacterially expressed Cas substrate domain protein (CasSD) in vitro and found a remarkable enhancement of phosphorylation by Src family kinases with no apparent change in kinase activity. Using an antibody that recognized extended CasSD in vitro, we observed Cas extension in intact cells in the peripheral regions of spreading cells, where higher traction forces are expected and where phosphorylated Cas was detected, suggesting that the in vitro extension and phosphorylation of CasSD are relevant to physiological force transduction. Thus, we propose that Cas acts as a primary force sensor, transducing force into mechanical extension and thereby priming phosphorylation and activation of downstream signaling.


Subject(s)
Crk-Associated Substrate Protein/metabolism , Mechanotransduction, Cellular , src-Family Kinases/metabolism , Antibodies/immunology , Biomechanical Phenomena , Biotinylation , Crk-Associated Substrate Protein/chemistry , Cytoskeleton/metabolism , Humans , Models, Biological , Phosphorylation , Phosphotyrosine/metabolism , Polyethylene Glycols/metabolism , Protein Structure, Tertiary , Recombinant Proteins/metabolism , rap1 GTP-Binding Proteins/metabolism
4.
Phys Rev Lett ; 97(3): 038102, 2006 Jul 21.
Article in English | MEDLINE | ID: mdl-16907546

ABSTRACT

We have monitored active movements of the cell circumference on specifically coated substrates for a variety of cells including mouse embryonic fibroblasts and T cells, as well as wing disk cells from fruit flies. Despite having different functions and being from multiple phyla, these cell types share a common spatiotemporal pattern in their normal membrane velocity; we show that protrusion and retraction events are organized in lateral waves along the cell membrane. These wave patterns indicate both spatial and temporal long-range periodic correlations of the actomyosin gel.


Subject(s)
Cell Membrane/physiology , Cell Movement/physiology , Fibroblasts/physiology , T-Lymphocytes/physiology , Actomyosin/chemistry , Actomyosin/metabolism , Animals , Drosophila melanogaster/cytology , Drosophila melanogaster/physiology , Fibroblasts/cytology , Gels/chemistry , Mice , Models, Biological , T-Lymphocytes/cytology , Time Factors
5.
J Appl Physiol (1985) ; 98(4): 1542-6, 2005 Apr.
Article in English | MEDLINE | ID: mdl-15772064

ABSTRACT

Cellular morphology is determined by motility, force sensing, and force generation that must be finely controlled in a dynamic fashion. Contractile and extensile functions are integrated with the overall cytoskeleton, including linkages from the cytoplasmic cytoskeleton to the extracellular matrix and other cells by force sensing. During development, as cells differentiate, variations in protein expression levels result in morphological changes. There are two major explanations for motile behavior: either cellular motility depends in a continuous fashion on cell composition or it exhibits phases wherein only a few protein modules are activated locally for a given time. Indeed, in support of the latter model, the quantification of cell spreading and other motile activities shows multiple distinct modes of behavior, which we term "phases" because there exist abrupt transitions between them. Cells in suspension have a basal level of motility that enables them to probe their immediate environment. After contacting a matrix-coated surface, they rapidly transition to an activated spreading phase. After the development of a significant contact area, the cells contract repeatedly to determine the rigidity of the substrate and then develop force on matrix contacts. When cells are fully spread, extension activity is significantly decreased and focal complexes start to assemble near the cell periphery. For each of these phases, there are significant differences in protein activities, which correspond to differences in function. Thus overall morphological change of a tissue is driven by chemical signals and force-dependent activation of one or more motile phases in limited cell regions for defined periods.


Subject(s)
Cell Adhesion/physiology , Cell Movement/physiology , Cell Physiological Phenomena , Cell Proliferation , Extracellular Matrix/physiology , Mechanotransduction, Cellular/physiology , Animals , Humans , Stress, Mechanical
6.
Cell ; 116(3): 431-43, 2004 Feb 06.
Article in English | MEDLINE | ID: mdl-15016377

ABSTRACT

Cellular lamellipodia bind to the matrix and probe its rigidity through forces generated by rearward F-actin transport. Cells respond to matrix rigidity by moving toward more rigid matrices using an unknown mechanism. In spreading and migrating cells we find local periodic contractions of lamellipodia that depend on matrix rigidity, fibronectin binding and myosin light chain kinase (MLCK). These contractions leave periodic rows of matrix bound beta3-integrin and paxillin while generating waves of rearward moving actin bound alpha-actinin and MLCK. The period between contractions corresponds to the time for F-actin to move across the lamellipodia. Shortening lamellipodial width by activating cofilin decreased this period proportionally. Increasing lamellipodial width by Rac signaling activation increased this period. We propose that an actin bound, contraction-activated signaling complex is transported locally from the tip to the base of the lamellipodium, activating the next contraction/extension cycle.


Subject(s)
Actins/metabolism , Cell Movement/physiology , Periodicity , Pseudopodia/metabolism , Actin Depolymerizing Factors , Actinin/metabolism , Animals , Cell Line , Cytoskeletal Proteins/metabolism , Extracellular Matrix/metabolism , Fibroblasts , Fibronectins/metabolism , Integrin beta3/metabolism , Macromolecular Substances , Mice , Microfilament Proteins/metabolism , Models, Biological , Myosin-Light-Chain Kinase/metabolism , Paxillin , Phosphoproteins/metabolism , Protein Binding/physiology , Protein Transport/physiology , Pseudopodia/ultrastructure , rac GTP-Binding Proteins/metabolism
7.
Biophys J ; 86(3): 1794-806, 2004 Mar.
Article in English | MEDLINE | ID: mdl-14990505

ABSTRACT

When mouse embryonic fibroblasts in suspension contact a matrix-coated surface, they rapidly adhere and spread. Using total internal reflection fluorescence microscopy of dye-loaded fibroblasts to quantify cell-substrate contact, we found that increasing the surface matrix density resulted in faster spreading initiation whereas lamellipodial dynamics during spreading were unaltered. After spreading initiation, most cells spread in an anisotropic manner through stochastic, transient extension periods (STEPs) with approximately 30 STEPs over 10 min to reach an area of 1300 micro m(2) +/- 300 micro m(2). A second mode of spreading, increased in serum-deprived cells, lacked STEPs and spread in a rapid, isotropic manner for 1-4 min. This isotropic mode was characterized by a high rate of area increase, 340 micro m(2)/min with 78% of the cell edge extending. Anisotropic cells spread slower via STEPs, 126 micro m(2)/min with 34% of the edge extending. During the initial 2-4 min of fast, isotropic spreading, centripetal flow of actin was low (0.8 micro m/min) whereas in anisotropic cells it was high from early times (4.7 micro m/min). After initial isotropic spreading, rearward actin movement increased and isotropic cells displayed STEPs similar to anisotropic cells. Thus, the two cell states display dramatically different spreading whereas long-term motility is based on STEPs.


Subject(s)
Cell Adhesion/physiology , Cell Movement/physiology , Fibroblasts/cytology , Fibroblasts/physiology , Image Interpretation, Computer-Assisted/methods , Microscopy, Fluorescence/methods , Actinin/physiology , Actinin/ultrastructure , Animals , Anisotropy , Cells, Cultured , Extracellular Matrix/physiology , Mice , Molecular Motor Proteins/physiology , Molecular Motor Proteins/ultrastructure
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