Quasi-3D cytoskeletal dynamics of osteocytes under fluid flow.

Osteocytes respond to dynamic fluid shear loading by activating various biochemical pathways, mediating a dynamic process of bone formation and resorption. Whole-cell deformation and regional deformation of the cytoskeleton may be able to directly regulate this process. Attempts to image cellular deformation by conventional microscopy techniques have been hindered by low temporal or spatial resolution. In this study, we developed a quasi-three-dimensional microscopy technique that enabled us to simultaneously visualize an osteocyte's traditional bottom-view profile and a side-view profile at high temporal resolution. Quantitative analysis of the plasma membrane and either the intracellular actin or microtubule (MT) cytoskeletal networks provided characterization of their deformations over time. Although no volumetric dilatation of the whole cell was observed under flow, both the actin and MT networks experienced primarily tensile strains in all measured strain components. Regional heterogeneity in the strain field of normal strains was observed in the actin networks, especially in the leading edge to flow, but not in the MT networks. In contrast, side-view shear strains exhibited similar subcellular distribution patterns in both networks. Disruption of MT networks caused actin normal strains to decrease, whereas actin disruption had little effect on the MT network strains, highlighting the networks' mechanical interactions in osteocytes.

[1]  X. Guo,et al.  Substrate modulation of osteoblast adhesion strength, focal adhesion kinase activation, and responsiveness to mechanical stimuli. , 2006, Molecular & cellular biomechanics : MCB.

[2]  G. Ateshian,et al.  An automated approach for direct measurement of two-dimensional strain distributions within articular cartilage under unconfined compression. , 2002, Journal of biomechanical engineering.

[3]  Ning Wang,et al.  Rapid signal transduction in living cells is a unique feature of mechanotransduction , 2008, Proceedings of the National Academy of Sciences.

[4]  Christopher R Jacobs,et al.  Time-dependent deformations in bone cells exposed to fluid flow in vitro: investigating the role of cellular deformation in fluid flow-induced signaling. , 2007, Journal of biomechanics.

[5]  Donald E. Ingber,et al.  Jcb: Article Introduction , 2002 .

[6]  Masaaki Sato,et al.  Direct measurement of shear strain in adherent vascular endothelial cells exposed to fluid shear stress. , 2010, Biochemical and biophysical research communications.

[7]  Daisuke Mizuno,et al.  Round versus flat: bone cell morphology, elasticity, and mechanosensing. , 2008, Journal of biomechanics.

[8]  H J Donahue,et al.  Differential effect of steady versus oscillating flow on bone cells. , 1998, Journal of biomechanics.

[9]  Cheng Dong,et al.  Design of a side-view particle imaging velocimetry flow system for cell-substrate adhesion studies. , 2006, Journal of biomechanical engineering.

[10]  Fred C. MacKintosh,et al.  Viscoelastic properties of microtubule networks , 2007 .

[11]  W. Bae,et al.  Indentation testing of human articular cartilage: effects of probe tip geometry and indentation depth on intra-tissue strain. , 2006, Journal of biomechanics.

[12]  T. Smit,et al.  Osteocyte morphology in fibula and calvaria --- is there a role for mechanosensing? , 2008, Bone.

[13]  Minqi Li,et al.  Targeted ablation of osteocytes induces osteoporosis with defective mechanotransduction. , 2007, Cell metabolism.

[14]  Jian Cao,et al.  Mechanics of Leukocyte Deformation and Adhesion to Endothelium in Shear Flow , 1999, Annals of Biomedical Engineering.

[15]  D. Stamenović,et al.  Cell prestress. I. Stiffness and prestress are closely associated in adherent contractile cells. , 2002, American journal of physiology. Cell physiology.

[16]  C. Dong,et al.  In vitro side-view imaging technique and analysis of human T-leukemic cell adhesion to ICAM-1 in shear flow. , 1998, Microvascular research.

[17]  Daniel A. Fletcher,et al.  Combined atomic force microscopy and side-view optical imaging for mechanical studies of cells , 2009, Nature Methods.

[18]  C. Brangwynne,et al.  Nonequilibrium microtubule fluctuations in a model cytoskeleton. , 2007, Physical review letters.

[19]  M M Saunders,et al.  Mechanically stimulated osteocytes regulate osteoblastic activity via gap junctions. , 2007, American journal of physiology. Cell physiology.

[20]  Christopher R. Jacobs,et al.  Osteocytes as mechanosensors in the inhibition of bone resorption due to mechanical loading , 2006 .

[21]  Cheng Dong,et al.  Development of a side-view chamber for studying cell-surface adhesion under flow conditions , 1997, Annals of Biomedical Engineering.

[22]  Ning Wang,et al.  Effect of the cytoskeletal prestress on the mechanical impedance of cultured airway smooth muscle cells. , 2002, Journal of applied physiology.

[23]  J. Fredberg,et al.  Mapping the cytoskeletal prestress. , 2010, American journal of physiology. Cell physiology.

[24]  Kevin D. Costa,et al.  Osteoblast Elastic Modulus Measured by Atomic Force Microscopy Is Substrate Dependent , 2005, Annals of Biomedical Engineering.

[25]  S. Weinbaum,et al.  A model for the role of integrins in flow induced mechanotransduction in osteocytes , 2007, Proceedings of the National Academy of Sciences.

[26]  F. Guilak,et al.  The role of the cytoskeleton in the viscoelastic properties of human articular chondrocytes. , 2004, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[27]  K. Athanasiou,et al.  Contribution of the cytoskeleton to the compressive properties and recovery behavior of single cells. , 2009, Biophysical journal.

[28]  B. Helmke,et al.  Mapping the dynamics of shear stress-induced structural changes in endothelial cells. , 2007, American journal of physiology. Cell physiology.

[29]  Masaki Hojo,et al.  Calcium response in single osteocytes to locally applied mechanical stimulus: differences in cell process and cell body. , 2009, Journal of biomechanics.

[30]  D. Ingber Tensegrity I. Cell structure and hierarchical systems biology , 2003, Journal of Cell Science.

[31]  Jason W. Triplett,et al.  Osteoblasts and osteocytes respond differently to oscillatory and unidirectional fluid flow profiles , 2007, Journal of cellular biochemistry.

[32]  E. Salmon,et al.  E-MAP-115 (ensconsin) associates dynamically with microtubules in vivo and is not a physiological modulator of microtubule dynamics. , 1999, Journal of cell science.

[33]  Daniel A. Fletcher,et al.  Cell mechanics and the cytoskeleton , 2010, Nature.

[34]  B. Helmke,et al.  Mapping mechanical strain of an endogenous cytoskeletal network in living endothelial cells. , 2003, Biophysical journal.

[35]  Dimitrije Stamenović,et al.  Cell prestress. II. Contribution of microtubules. , 2002, American journal of physiology. Cell physiology.

[36]  D. Ingber,et al.  Mechanical behavior in living cells consistent with the tensegrity model , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[37]  D. Smith,et al.  Active fluidization of polymer networks through molecular motors , 2002, Nature.

[38]  E H Burger,et al.  Pulsating fluid flow increases prostaglandin production by cultured chicken osteocytes--a cytoskeleton-dependent process. , 1996, Biochemical and biophysical research communications.

[39]  W. H. Peters,et al.  Application of an optimized digital correlation method to planar deformation analysis , 1986, Image Vis. Comput..

[40]  Microelastic mapping of living endothelial cells exposed to shear stress in relation to three-dimensional distribution of actin filaments. , 2007, Acta biomaterialia.

[41]  Huimin Xie,et al.  Full-field strain measurement using a two-dimensional Savitzky-Golay digital differentiator in digital image correlation , 2007 .

[42]  D L Bader,et al.  Chondrocyte Deformation Induces Mitochondrial Distortion and Heterogeneous Intracellular Strain Fields , 2006, Biomechanics and modeling in mechanobiology.