Critical centrifugal forces induce adhesion rupture or structural reorganization in cultured cells.

Cultured epithelial cells were exposed to accelerations ranging from 9,000 to 70,000g for time periods of 5, 15, or 60 min, by centrifugation in a direction tangential to their plastic substrate. Three regimes describe the cellular response: (1) Cell morphology and density remain unaltered at forces below a threshold of about 10(-7) N; (2) Between this critical force and a second threshold of about 1.5 10(-7)N, the number of adherent cells decreases exponentially with time and acceleration, with no alteration of cell morphology. This behavior can be modeled by a constant probability of detaching and by an exponential distribution of cell-to-substrate adhesive forces; (3) Past the second threshold, cells that are still adherent exhibit elongated morphologies, the degree of elongation increasing linearly with the force. The fact that cells lose their vinculin-rich focal contacts past the first threshold and that cells cultured on gelatin-coated plastic show an increased resistance to detachment suggests a rupture of cell-to-substrate adhesions upon centrifugation. Immunofluorescent labeling of cells for actin and tubulin shows a reorganization of the cytoskeleton upon centrifugation, and treatment of cells with the drugs cytochalasin D and nocodazole demonstrates that cytoskeletal elements are actively involved in the structural deformation of cells past the second acceleration threshold, microtubules and microfilaments paying antagonistic roles.

[1]  N O Petersen,et al.  Dependence of locally measured cellular deformability on position on the cell, temperature, and cytochalasin B. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[2]  T. Pollard,et al.  Interaction of actin filaments with microtubules , 1984, The Journal of cell biology.

[3]  R. Adler,et al.  Opposing microtubule- and actin-dependent forces in the development and maintenance of structural polarity in retinal photoreceptors. , 1989, Developmental biology.

[4]  D W James,et al.  The stress developed by sheets of chick fibroblasts in vitro. , 1969, Experimental cell research.

[5]  H. Horikawa,et al.  The role of gravity in chick embryogenesis , 1994, FEBS letters.

[6]  R M Nerem,et al.  An application of the micropipette technique to the measurement of the mechanical properties of cultured bovine aortic endothelial cells. , 1987, Journal of biomechanical engineering.

[7]  V. Quaranta,et al.  The internal affairs of an integrin. , 1991, Trends in cell biology.

[8]  D. Ingber,et al.  Altering the cellular mechanical force balance results in integrated changes in cell, cytoskeletal and nuclear shape. , 1992, Journal of cell science.

[9]  F. Sack,et al.  Plant gravity sensing. , 1991, International review of cytology.

[10]  O H Gauer,et al.  Venous pressure in man during weightlessness. , 1984, Science.

[11]  G. Truskey,et al.  The effect of fluid shear stress upon cell adhesion to fibronectin-treated surfaces. , 1990, Journal of biomedical materials research.

[12]  S. Penman,et al.  Rethinking cell structure. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[13]  R. Buxbaum,et al.  Tensile regulation of axonal elongation and initiation , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[14]  G. I. Bell Models for the specific adhesion of cells to cells. , 1978, Science.

[15]  E J Luna,et al.  Cytoskeleton--plasma membrane interactions. , 1992, Science.

[16]  A Cogoli,et al.  Cell sensitivity to gravity. , 1984, Science.

[17]  C. Le Chalony,et al.  Constitutive overexpression of a 89 kDa heat shock protein gene in the HBL100 human mammary cell line converted to a tumorigenic phenotype by the EJ/T24 Harvey-ras oncogene. , 1991, Oncogene.

[18]  R. Nerem,et al.  Elongation of confluent endothelial cells in culture: the importance of fields of force in the associated alterations of their cytoskeletal structure. , 1995, Experimental cell research.

[19]  A. Bushnell,et al.  Reversible compression of cytoplasm. , 1982, Experimental cell research.

[20]  T. Soussi,et al.  Epithelial HBL-100 cell line derived from milk of an apparently healthy woman harbours SV40 genetic information. , 1985, Experimental cell research.

[21]  B A Danowski,et al.  Fibroblast contractility and actin organization are stimulated by microtubule inhibitors. , 1989, Journal of cell science.

[22]  C. Turner,et al.  The role of phosphorylation and limited proteolytic cleavage of talin and vinculin in the disruption of focal adhesion integrity. , 1989, The Journal of biological chemistry.

[23]  A. Leopold,et al.  The contribution of the extracellular matrix to gravisensing in characean cells. , 1992, Journal of cell science.

[24]  P. Hollenbeck,et al.  Intermediate filament collapse is an ATP-dependent and actin-dependent process. , 1989, Journal of cell science.

[25]  A. Harris,et al.  Silicone rubber substrata: a new wrinkle in the study of cell locomotion. , 1980, Science.

[26]  R. Buxbaum,et al.  Investigation of microtubule assembly and organization accompanying tension-induced neurite initiation. , 1993, Journal of cell science.

[27]  C. Turner,et al.  Focal adhesions: transmembrane junctions between the extracellular matrix and the cytoskeleton. , 1988, Annual review of cell biology.

[28]  D. McClay,et al.  Cell adhesion to fibronectin and tenascin: quantitative measurements of initial binding and subsequent strengthening response , 1989, The Journal of cell biology.

[29]  R. Buxbaum,et al.  Tension and compression in the cytoskeleton of PC-12 neurites. II: Quantitative measurements. , 1988, The Journal of cell biology.

[30]  Libchaber,et al.  Phase diagram of microtubules. , 1994, Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics.

[31]  D. Ingber,et al.  Cellular tensegrity : defining new rules of biological design that govern the cytoskeleton , 2022 .

[32]  J. Vasiliev Actin Cortex and Microtubular System in Morphogenesis: Cooperation and Competition , 1987, Journal of Cell Science.

[33]  D. Ingber,et al.  Mechanotransduction across the cell surface and through the cytoskeleton , 1993 .