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Time-scale and other invariants of integrative mechanical behavior in living cells.

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dc.creator Fabry, Ben
dc.creator Maksym, Geoffrey N.
dc.creator Butler, James P.
dc.creator Glogauer, Michael
dc.creator Navajas Navarro, Daniel
dc.creator Taback, Nathan A.
dc.creator Millet, Emil J.
dc.creator Fredberg, Jeffrey J.
dc.date 2011-07-07T12:50:32Z
dc.date 2011-07-07T12:50:32Z
dc.date 2003
dc.date.accessioned 2024-12-16T10:27:17Z
dc.date.available 2024-12-16T10:27:17Z
dc.identifier 1063-651X
dc.identifier http://hdl.handle.net/2445/18687
dc.identifier 510211
dc.identifier.uri http://fima-docencia.ub.edu:8080/xmlui/handle/123456789/22198
dc.description In dealing with systems as complex as the cytoskeleton, we need organizing principles or, short of that, an empirical framework into which these systems fit. We report here unexpected invariants of cytoskeletal behavior that comprise such an empirical framework. We measured elastic and frictional moduli of a variety of cell types over a wide range of time scales and using a variety of biological interventions. In all instances elastic stresses dominated at frequencies below 300 Hz, increased only weakly with frequency, and followed a power law; no characteristic time scale was evident. Frictional stresses paralleled the elastic behavior at frequencies below 10 Hz but approached a Newtonian viscous behavior at higher frequencies. Surprisingly, all data could be collapsed onto master curves, the existence of which implies that elastic and frictional stresses share a common underlying mechanism. Taken together, these findings define an unanticipated integrative framework for studying protein interactions within the complex microenvironment of the cell body, and appear to set limits on what can be predicted about integrated mechanical behavior of the matrix based solely on cytoskeletal constituents considered in isolation. Moreover, these observations are consistent with the hypothesis that the cytoskeleton of the living cell behaves as a soft glassy material, wherein cytoskeletal proteins modulate cell mechanical properties mainly by changing an effective temperature of the cytoskeletal matrix. If so, then the effective temperature becomes an easily quantified determinant of the ability of the cytoskeleton to deform, flow, and reorganize.
dc.format 18 p.
dc.format application/pdf
dc.language eng
dc.publisher The American Physical Society
dc.relation Reproducció digital del document publicat a: http://dx.doi.org/10.1103/PhysRevE.68.041914
dc.relation Physical Review E, 2003, vol. 68, núm. 4, p. 041914-1 - 041914-18 pages
dc.relation http://dx.doi.org/10.1103/PhysRevE.68.041914
dc.rights (c) The American Physical Society, 2003
dc.rights info:eu-repo/semantics/openAccess
dc.source Articles publicats en revistes (Ciències Fisiològiques)
dc.subject Reologia
dc.subject Física mèdica
dc.subject Biofísica
dc.subject Equacions d'estat
dc.subject Transformacions de fase (Física estadística)
dc.subject Rheology
dc.subject Medical physics
dc.subject Biophysics
dc.subject Equations of state
dc.subject Phase transformations (Statistical physics)
dc.title Time-scale and other invariants of integrative mechanical behavior in living cells.
dc.type info:eu-repo/semantics/article
dc.type info:eu-repo/semantics/publishedVersion


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