Abstract
Understanding cellular response to mechanical forces is immensely important for a plethora of biological processes. Focal adhesions are multimolecular protein assemblies that connect the cell to the extracellular matrix and play a pivotal role in cell mechanosensing. Under timevarying stretches, focal adhesions dynamically reorganize and reorient and as a result, regulate the response of cells in tissues. Here I present a simple theoretical model based on, to my knowledge, a novel approach in the understanding of stretchsensitive bond association and dissociation processes together with the elasticity of the cellsubstrate system to predict the growth, stability, and the orientation of focal adhesions in the presence of static as well as cyclically varying stretches. The model agrees well with several experimental observations; most importantly, it explains the puzzling observations of parallel orientation of focal adhesions under static stretch and nearly perpendicular orientation in response to fast varying cyclic stretch.
Introduction
Mechanical forces have long been known to play an important role in determining cellular functions and behaviors^{1}. Living cells actively respond to the mechanical properties of the extracellular matrix, its rigidity, also to the presence of external forces by regulating various processes such as cell adhesion, orientation, migration, differentiation, alteration in morphology, and even apoptosis^{1,2,3,4}. Moreover, the effect of timevarying cyclic stretch is particularly striking where each cycle of contraction and relaxation leads to dynamic changes that affect a wide range of activities involving cardiovascular cells, muscle cells, stem cells, and connective tissue cells to name a few^{1, 5,6,7}. It is not yet well understood how the stretch induces reorganization of the cellular cytoskeleton, assembly and disassembly of focal adhesions (FAs), or how it alters the gene expression, and affects the whole tissue adaptation in general. A deeper insight into the mechanical stretchinduced responses is thus envisaged to have wide impact in many cellular processes, wound healing, tissue engineering, and also regenerative medicine^{1}.
Recent researches have established that FAs play a crucial role in cell mechanotransduction^{1,2,3,4}. FAs are micronsized complex multimolecular protein assemblies linked on one side to the extracellular matrix via membranebound receptors and on other side to the actin stress fibers in the cell cytoskeleton. Experiments show that in response to substrate stretch, FAs reorganize and reorient and as a result, regulate the response of the cell^{2, 7,8,9,10,11,12}. It is also found that external force strongly affects the growth and the stability of FA contacts^{1,2,3,4}. FAs grow in the direction of tensile stretch^{13} and the stability increases with the increase in applied stretch magnitude upto an optimal value, however, eventually become unstable at higher stretches^{14, 15}. Moreover, another puzzling experimental observation is that FAs respond differently to static stretch compared to rapidly varying cyclic stretch. Subjected to static or quasistatic stretch, FAs tend to orient along the stretch direction^{7, 16,17,18}, whereas under fast varying stretch, FAs opt to orient away from the stretch direction; for highfrequency cyclic stretch, FAs align nearly perpendicular to the applied stretch direction^{8,9,10,11,12, 19,20,21}.
There are many theoretical studies that have contributed significantly to the understanding of how cells actively respond to the mechanical forces and regulate force transmission^{3, 4}. Quite a few studies have also been carried out to understand the stability and growth of FAs in response to forces. In a seminal work by Bell, the stability of adhesion cluster, modeled as a collection of molecular bonds, was first addressed using kinetic theory of chemical reactions. In Bell’s model the rupture rate of ligandreceptor bonds was proposed to increase exponentially with the mechanical force^{22}. Later, the bond dissociation pathways have been studied in the framework of Kramers theory as thermally assisted escape over an energy barrier under applied forces^{23, 24}. Also, the stochasticity in bond breaking and binding processes has been incorporated through the onestep master equation to investigate the stability of FAs under constant loading^{25}. However, relatively few studies have been performed on the orientational response of FAs to substrate stretching. Moreover, existing theories, which have provided many insights into the cellular orientation problem, including our earlier works, mostly dealt with the orientation of the whole cell modeled as a contractile force dipole in a coarsegrained picture^{26,27,28}; or studied the reorientation of twodimensional cells emphasizing on passively stored elastic energy^{29}; else described the formation and realignment of stress fibers in response to cyclic stretch^{21, 30}. Recently, Qian et al.^{31} constructed rate equations of the density of stress fibers and adhesive receptorligand bonds to describe the dynamics of cell realignment in response to cyclic stretch. It has been hypothesized that cells tend to orient in the direction where the formation of stress fibers is energetically most favorable. Moreover, the frequencydependent force generated within the stress fibers solely obtained from the structural considerations of the filament and does not depend on the description of assembly or disassembly of FA bonds. However, recent experiments have shown that orientationspecific activation of stretchsensitive proteins in FAs controls the orientationspecific responses of FA growth and disassembly^{7}. Also, other studies on FAs attempted till now have ignored the parallel orientation of FAs and focused only on the perpendicular orientation under cyclic stretching^{32,33,34}. Moreover, these studies predict that the orientational response of FAs remains unaffected under low frequency or quasistatic stretch^{32,33,34}. Therefore, though the previous studies have provided many insights into the orientationspecific response, however, so far the focus mainly remained on the dynamics of the cell, or the stress fibers, or the perpendicular orientation of FAs. Thus, a single theory, which explains the parallel orientation of FAs toward the static stretch direction as well as the perpendicular orientation under fast varying cyclic stretch, remains elusive.
In this paper, a theoretical model is presented to study the orientationspecific response of FAs in the presence of static as well as timevarying stretches within an unified framework. The crux of this model lies on a novel approach in the understanding of stretchsensitive bond association and dissociation processes of FA assembly, which play a crucial role in determining the orientational response of FAs. It also takes into account the elasticity of the cellmatrix system and the stochastic behavior of ligandreceptor bond breaking and binding processes of FA assembly. In particular, the forcesensitive catchbond behavior and also the timedependent binding rates under substrate stretching have been incorporated, which allow to capture the experimentally observed puzzle of the parallel alignment of FAs in response to static and quasistatic applied stretch, whereas nearly perpendicular alignment under fast varying cyclic stretch^{7,8,9,10,11,12, 16,17,18,19,20,21}. In addition, this theory predicts several other experimental observations such as the growth and the stability of FAs in the direction of tensile stretch^{13,14,15} and also the existence of threshold frequency and magnitude of the applied stretch that triggers reorganization of FAs^{19, 21, 35}. Moreover, it also elucidates the experimental observations where orientational responses have been found to vary across cell types as a function of frequency of the substrate stretch^{19,20,21}.
Results
Theoretical model of focal adhesions
The model takes the cue from the fact that FAs are clusters of ligandreceptor molecular bonds that provide the physical connection between the cell and the extracellular matrix. Figure 1a shows a schematic representation of a cell adhering to a substrate through two FAs. In a minimal model, it could be thought of an actin stress fiber (SF) adhered via two FAs. Figure 1b illustrates the instantaneous position of the cell, and hence of the FA, oriented at an angle θ relative to the applied stretch direction. Each FA site consists of uniformly distributed ligandreceptor bonds connected in parallel to the substrate. These bonds are considered as Hookian elastic springs of stiffness, k_{b}. Moreover, in this model, for simplicity, the elasticity of the cell or the SF is represented by a spring of rigidity k_{c} (is referred as cellular spring). The ligandreceptor bonds are considered to be either in closed or in open state. Due to substrate stretching, the closed bonds, attached at one side to the substrate, get elongated and thus, experience an additional tension (as illustrated in Fig. 1a); since the other side of the bonds is connected to the SF, the cellular spring also gets stretched. Thus, if the bond displacement along the stretch direction is denoted by u_{b} and the cell spring displacement as u_{c}, then the geometric constraint relation of elastic displacements is given by u_{b} + u_{c} = Lε. Here ε is the strain magnitude and L is the distance of the FA site from the cell center as shown in Fig. 1a (also, see Supplementary Fig. 1). Moreover, considering the force balance condition, \(k_{\mathrm{c}}u_{\mathrm{c}} = \mathop {\sum}\nolimits_n {\kern 1pt} k_{\mathrm{b}}u_{\mathrm{b}}\), the total force summing over all closed bonds must be balanced by the tension in the stretched cellular spring. The above elasticity modeling enables us to determine the single bond force f_{b} calculated as f_{b} = k_{b}u_{b} = Lεk_{b}k_{c}/(k_{c} + nk_{b}); n denotes the number of closed bonds at any instant.
Moreover, the dynamics of FAs is subjected to fluctuations in the surrounding microenvironment, thus, bonds can also undergo stochastic breaking or rebinding. To study the time evolution of the FA cluster, a master equation has been written by coupling the elasticity of the cellmatrix system with the statistical behavior of bond association and dissociation processes^{3, 25, 36},
where P_{ n }(t) is the probability that n bonds are formed at time t. The first two terms in the righthand side represent the gain term, i.e., the tendency for the number of bonds in state n to increase due to the formation of new bond in state (n − 1) and the dissociation of bond in state (n + 1), respectively. The last term represents the loss of bonds in state n, whereas K_{on} and K_{off} denote the total association and total dissociation rate of bonds at the respective state, n, at any instant of time t. This is further to note here that for mathematical simplicity, it has been considered that all bonds in the adhesion cluster experience the same elastic force or deformation. However, since the rates are subjected to fluctuations during stochastic simulation of the model, thus, it also takes care of the nonuniformity that may arise in bond forces across the adhesion cluster.
Moreover, during the time evolution, the bond reaction rate strongly depends on the instantaneous bond configuration. Recent singlemolecule experiments have revealed that the external force increases the lifetime of many FA molecules^{37, 38}. Tensile force, upto an optimal value, is found to strengthen and reinforce the molecular bonds; and bonds’ lifetime decreases with further increase in force^{14}. These type of forcestrengthening bonds are called catch bonds and are believed to play a crucial role in stabilizing the FA cluster^{15}. Motivated by the experimental findings, in this model, it is assumed that the FA cluster consists of catch bonds and thus the dissociation rate k_{off} of the closed bond is proposed to demonstrate the catch behavior as^{15, 39},
where k_{slip} and k_{catch} denote the rate constants for dissociation of the ligandreceptor pair via a slip pathway promoted by the force and a catch pathway opposed by the force, respectively^{39}; these rate constants depend on the type of the adhesion molecules. The total dissociation rate K_{off} is thus \(K_{{\mathrm{off}}} = \mathop {\sum}\nolimits_n {\kern 1pt} k_{{\mathrm{off}}}\), where n is the number of closed bonds at any given instant and f_{0} denotes a molecular force scale, typically of the order of piconewton.
On the other hand, it has generally been considered that the association or rebinding rate, k_{on}, increases with the number of available unbound bonds at any instant; thus, k_{on} = γ(N − n), where N is the total number of binding sites, n is the number of closed bond, and γ is the binding rate constant^{25}. However, in this model, motivated by the experiments^{40, 41}, it is considered that during the rebinding process, to facilitate the ligandreceptor bond formation, the pair needs to be in close proximity within a reaction radius l_{R}, and for a characteristic contact time t_{R}. Thus, the ligandreceptor bond has an intrinsic reaction rate v_{0} = l_{R}/t_{R} for binding to occur. Therefore, in the presence of a cyclically varying substrate stretch, as the substrate moves back and forth, the ligand attached to the substrate also moves back and forth from the cell receptor and hence the association or rebinding rate strongly depends on the time variation of the applied stretch. Thus, under a cyclic strain ε(t) = ε_{0}(1 − cosωt), where ε_{0} is the average magnitude and ω is the frequency of the applied stretch; the ligand, which was initially at a distance l_{R} from the cell receptor would now undergo a cyclically varying displacement u(t) = l_{R}ε(t); and hence, continuously moves away back and forth from the cell receptor. Therefore, the displacement rate \(\left {\dot u(t)} \right = l_{\mathrm{R}}\left {\dot \varepsilon (t)} \right\) has to be much smaller compared to the intrinsic binding rate v_{0}, so that the ligandreceptor pair gets sufficient time to rebind. If the absolute magnitude of the displacement rate \(v_\omega = l_{\mathrm{R}}\varepsilon _{\mathrm{0}}\omega \ll v_{\mathrm{0}}\), the ligandreceptor pair is in contact for long enough time so that the reaction can take place and binding can easily occur. However, as the displacement rate increases with increase in stretching magnitude or frequency of the external stretch, the ligandreceptor pair gets to spend less and less contact time as the ligand moves away rapidly from the cell receptor and therefore the probability of bond formation decreases. To incorporate these effects, in this model, the association rate is proposed to be ratedependent and described by
Also, this is to note here that even though l_{R} does not explicitly appeared in the expression of k_{on}, however, the effect of the reaction radius could be seen through its dependence on the strain magnitude ε_{0}. This dependence solely appears due to the consideration of the reaction radius. Therefore, in this model, the effective timescale turns out to be t_{ ω } = 1/(ε_{0}ω). Thus, the competition between the two timescales, the time variation of the substrate displacement t_{ ω } and the intrinsic binding timescale t_{R}, determines the probability of bond formation.
Now, in the presence of a static stretch, the association rate turns out to be k_{on} = γ(N − n), as ω = 0. Under a static stretch, the distance between the ligandreceptor pair increases with the external stretch; however, since the pair spends sufficiently long time in close contact, thus, there is always chances of ligandreceptor rebinding to occur and hence the adhesion bonds could be formed. In case of a static stretch, the dissociation rate k_{off} plays a major role in determining the stability of the adhesion cluster. Due to the catchbond behavior of the dissociation rate, FAs get strengthen with tensile stretch, however, above a threshold stretch value, the dissociation rate start increasing and eventually wins over the association rate and hence the cluster becomes unstable and thus, disassemble.
Numerical simulation method
All parameters of the model have been rewritten in dimensionless units. The scaled time is defined as τ = k_{0}t, where k_{0} is the spontaneous dissociation rate in the absence of any external force. Similarly, all other rates have been scaled, such as, K_{s} = k_{slip}/k_{0}, K_{c} = k_{catch}/k_{0}, Γ = γ/k_{0}, T_{R} = k_{0}t_{R}, and the scaled frequency ω = ω_{0}/k_{0}. The normalized bond force is defined as F_{b} = f_{b}/f_{0}. Moreover, all displacements have been scaled by the characteristic length l_{R}, such that U_{b} = u_{b}/l_{R}, U_{c} = u_{c}/l_{R}, and L^{s} = L/l_{R}.
The master equation has been numerically solved to investigate the time evolution, growth, stability, and the orientation of adhesion clusters in response to static as well as timevarying cyclic stretch. MonteCarlo method has been used based on Gillespie’s algorithm^{42}. In simulations, the FA cluster consisting of N binding sites, starts from an initial state with all bonds at closed state and proceeds until all bonds become open. Thus, the stochastic trajectories are simulated, which share many similarities with experimental realizations. Averaging has been done over many such trajectories to extract useful statistical information. In case of stable clusters, each simulation has run for at least one million events. The overall statistics have been accumulated from 500 such simulation results. In this model, following the existing literature, stability and growth of the adhesion cluster are represented by the mean number of closed bonds, n, under different conditions such as varying stretch, frequency, etc. Dynamics have been studied for a wide range of parameter values. Here the results presented for a cluster of size N = 200. The length L is taken as 20 μm and l_{R} ~ 1 nm. The ratio of single bond stiffness to cellular spring is taken as k_{b}/k_{c} = 5. The other scaled parameter values are kept at Γ = 2, K_{s} = 0.10, and K_{c} = 120 (following ref. ^{39}). The magnitude and frequency of the applied stretch and T_{R} remain variable parameters in the model.
Orientational response in the presence of static stretch
Figure 2a shows the typical simulation trajectories of instantaneous number of closed bonds for three different magnitudes of static strain. It is observed that the number of closed bonds stochastically varies around a mean value depending on the applied stretch magnitude and the cluster eventually becomes unstable above a threshold stretch. The effective strain magnitude along the FA cluster oriented at an angle θ is \(\varepsilon _{\mathrm{a}} = \varepsilon _{\mathrm{0}}{\kern 1pt} {\mathrm{cos}}^2\theta\) (as in Fig. 1b). The stability and the growth of the adhesion cluster (represented by the mean number of closed bonds, n) along the direction of the applied static stretch (i.e., θ = 0) have been studied as a function of strain magnitude as shown in Fig. 2b. It is found, as observed in experiments, the adhesion cluster grows with increasing strain, reaches a maximum under an optimal strain value, however, a further increase in stretch eventually results in disassembly of the cluster. This could be attributed to the catch behavior of FA molecules. Since the catch bonds in FAs get strengthen with tensile stretch, the dissociation rate decreases and that, in turn, promotes the growth and stability of FAs. The cluster becomes most stable for an optimal stretch at which the bond dissociation rate is minimum. Thus, in the presence of a static stretch, below the threshold magnitude, parallel to the stretch direction becomes the most stable direction for FA growth; whereas, perpendicular direction is the least stable (as ε_{a} = 0) associated with high dissociation rate of bonds. Therefore, FAs tend to align along the parallel direction of the applied stretch. The findings, thus, explain the recent experimental observation where FAs initially oriented at perpendicular direction, disassemble under a static stretch, and reorient toward the parallel direction of higher stability; whereas, FAs initially oriented parallel to the applied stretch direction remain stable^{7}.
Orientational response in the presence of dynamic stretch
However, in the presence of a highfrequency cyclic stretch, orientational response of FAs is found to be quite different^{8,9,10,11,12, 19,20,21}. Under a cyclically varying stretch ε(τ) = ε_{0}(1 − cosωτ), the competition between the two timescales, T_{ ω } = 1/ε_{0}ω, the time variation of the substrate displacement compared to T_{R}, the intrinsic binding timescale of the ligandreceptor pair determines the formation and stability of FA cluster. For highfrequency stretch, if \(T_\omega \ll T_{\mathrm{R}}\), the ligandreceptor pairs do not get sufficient contact time to rebind as the ligand on the substrate moves away rapidly from the cell receptor. Therefore, the chances of new bond formation decreases with increasing frequency and the FA cluster becomes unstable along the stretch direction. However, if FA orients, away from the stretch direction, at an angle θ, then the effective strain magnitude \(\varepsilon _{\mathrm{a}} = \varepsilon _{\mathrm{0}}{\kern 1pt} {\mathrm{cos}}^2\theta\) acting along the FA decreases and hence the contact time between the ligandreceptor pairs T_{ ω } increases with T_{ ω } ∝ 1/ε_{a}. Therefore, as the cluster orients away from the stretch direction, it becomes more and more stable with increase in probability of bond formation. At perpendicular direction, which is the zero strain direction, the binding of ligandreceptor pair is no longer affected by the fast varying stretch and thus, FAs become stable. Figure 3a shows the stability of the adhesion cluster as a function of orientation angle θ under highfrequency (for \(T_\omega \ll T_{\mathrm{R}}\)) cyclic stretch. As seen from the figure, cluster grows in size as it orients near perpendicular direction. There exists a distribution of orientation angles toward the perpendicular direction as found in experiments. However, as the stretching frequency decreases, ligandreceptor pairs get longer contact time and the ratio of the two timescales, T_{ ω } and T_{R}, determines the most stable orientation angle. When \(T_\omega \gg T_{\mathrm{R}}\), as the substrate moves slowly, ligandreceptor pairs get sufficient time to form new bonds and therefore, FAs, due to strengthening of the catch bonds, tend to align along the maximal stretch direction (ε_{a} = ε_{0} for θ = 0), i.e., parallel to the applied stretch, as shown in Fig. 3b.
Effect of intrinsic binding timescale on FA orientation
Moreover, this theory also elucidates the experimental observations where orientational responses have been found to vary from cell type to cell type under timedependent cyclic stretches. It is observed that some cell types prefer near perpendicular alignment, whereas some orient at different angles, or some do not exhibit considerable reorientation below a certain frequency^{19,20,21}. In this model, it could be attributed to different intrinsic timescales, T_{R}, characteristic to different cell types. Figure 4 shows the orientational stability of the adhesion cluster for different T_{R} values while keeping the magnitude and the frequency of the cyclic stretch constant. As seen from the figure, with decrease in the characteristic rebinding time T_{R}, the cluster becomes stable at a wide range of orientation angles. As T_{R} decreases, since the binding occurs at a faster rate, ligandreceptor pairs could increasingly cope up with the varying substrate stretch; and thus, the cluster becomes stable. Therefore, FAs and thus cells with fast binding rates do not show significant reorientation.
Existence of threshold stretch magnitude
Moreover, as found in experiments, this theory also captures the existence of a threshold stretch magnitude above which the orientational response becomes prominent^{19, 21, 35}. Figure 5 shows the stability of the adhesion cluster, oriented parallel to the applied stretch direction (θ = 0), as a function of strain magnitude and for different stretching frequencies. While keeping the frequency constant, if the magnitude of the applied stretch decreases, since T_{ ω } ∝ 1/ε_{a}, this leads to increase in the contact time between the ligandreceptor pair. As a result, for smaller stretch magnitudes, below a threshold value, when T_{ ω } > T_{R}, since the probability of bond formation increases with increasing contact time, hence, the adhesion cluster becomes stable. However, above the threshold stretch, as T_{ ω } < T_{R}, ligandreceptor pairs do not get sufficient contact time to rebind with the fast varying substrate; thus, the cluster becomes unstable and so orients away from the stretch direction. Therefore, orientational response of FAs becomes prominent above a threshold stretch value. Moreover, with increase in stretching frequency, as shown in Fig. 5, since T_{ ω } decreases with increasing ω (as T_{ ω } ∝ 1/ω), the magnitude of the threshold stretch shifts to a lower value.
Discussion
In summary, the theoretical model presented, by incorporating the catchbond behavior of FA assembly and the timedependent binding rates under substrate stretching, agrees well with several experimental observations. Apart from capturing the forcesensitive stability of FA clusters under tensile stretch, this model in an unified framework also unravels the puzzling observation of orientation of FAs along the parallel direction in response to static and quasistatic stretch, as well as the perpendicular orientation under fast varying cyclic stretch. Moreover, it explains the variation in alignment angles in different cell types and also predicts the existence of threshold stretch as observed in experiments. As discussed, the competition between the timescales involved in the process, namely, the time variation of the substrate displacement and the intrinsic binding time of the ligandreceptor pairs determines the stability of FAs under timevarying stretches. Importantly, it is shown that the sole consideration of the stretchdependent association and dissociation processes of adhesion clusters could successfully predict the orientational response of FAs. Indeed, it has been shown in recent experiments that the orientationspecific activation of stretchsensitive proteins in FAs play a crucial role in determining the orientationspecific FA growth and disassembly^{7}. This is also to note that the complex mechanisms of viscoelasticity of stress fibers and actinmyosin contraction may affect the overall cellular mechanosensing processes^{43, 44}. Thus, adding these effects one would get an inclusive picture, however, it is outside the present theory. While this model correctly predicts the major experimental features on the orientation of FAs reported so far, the finer predictions could be further tested by suitable experiments.
Data availability
The data supporting the findings of this study are available within the paper and its supplementary information file.
References
Iskratsch, T., Wolfenson, H. & Sheetz, M. P. Appreciating force and shape—the rise of mechanotransduction in cell biology. Nat. Rev. Mol. Cell Biol. 12, 825–833 (2014).
Geiger, B., Spatz, J. P. & Bershadsky, A. D. Environmental sensing through focal adhesions. Nat. Rev. Mol. Cell Biol. 10, 21–33 (2009).
Schwarz, U. S. & Safran, S. A. Physics of adherent cells. Rev. Mod. Phys. 85, 1327–1381 (2013).
Ladoux, B. & Nicolas, A. Physically based principles of cell adhesion mechanosensitivity in tissues. Rep. Prog. Phys. 72, 116601–116625 (2012).
De, R., Zemel, A. & Safran, S. A. Theoretical concepts and models of cellular mechanosensing. Methods Cell Biol. 98, 143–175 (2010).
Tamada, M., Sheetz, M. P. & Sawada, Y. Activation of a signalling cascade by cytoskeleton stretch. Dev. Cell 7, 709–718 (2004).
Chen, Y., Pasapera, A. M., Koretsky, A. P. & Waterman, C. M. Orientationspecific responses to sustained uniaxial stretching in focal adhesion growth and turnover. Proc. Natl Acad. Sci. USA 110, E2352–E2361 (2013).
Goldyn, A. M., Rioja, B. A., Spatz, J. P., Ballestrem, C. & Kemkemer, R. Forceinduced cell polarization is linked to RhoAdriven microtubuleindependent focaladhesion sliding. J. Cell Sci. 122, 3644–3651 (2009).
Carisey, A. et al. Vinculin regulates the recruitment and release of core focal adhesion proteins in a forcedependent manner. Curr. Biol. 23, 271–281 (2013).
Greiner, A. M., Chen, H., Spatz, J. P. & Kemkemer, R. Cyclic tensile strain controls cell shape and directs actin stress fiber formation and focal adhesion alignment in spreading cells. PLoS ONE 8, e77328–e77336 (2013).
Huang, W., Sakamoto, N., Miyazawa, R. & Sato, M. Role of paxillin in the early phase of orientation of the vascular endothelial cells exposed to cyclic stretching. Biochem. Biophys. Res. Commun. 418, 708–713 (2012).
Yoshigi., M., Hoffman, L. M., Jensen, C., Yost, H. J. & Beckerle, M. C. Mechanical force mobilizes zyxin from focal adhesions to actin filaments and regulates cytoskeletal reinforcement. J. Cell Biol. 171, 209–215 (2005).
Balaban, N. Q. et al. Force and focal adhesion assembly: a close relationship studied using elastic micropatterned substrates. Nat. Cell Biol. 3, 466–472 (2001).
Marshall, B. T. et al. Direct observation of catch bonds involving celladhesion molecules. Nature 423, 190–193 (2003).
Thomas, W. E., Vogel, V. & Sokurenko, E. Biophysics of catch bonds. Annu. Rev. Biophys. 37, 399–416 (2008).
Liu, C. et al. Effect of static prestretch induced surface anisotropy on orientation of mesenchymal stem cells. Cell Mol. Bioeng. 7, 106–121 (2014).
Eastwood, M., Mudera, V. C., McGrouther, D. A. & Brown, R. A. Effect of precise mechanical loading on fibroblast populated collagen lattices: morphological changes. Cell Motil. Cytoskelet. 40, 13–21 (1998).
Collinsworth, A. M. et al. Orientation and length of mammalian skeletal myocytes in response to a unidirectional stretch. Cell Tissue Res. 302, 243–251 (2000).
Jungbauer, S., Gao, H. J., Spatz, J. P. & Kemkemer, R. Two characteristic regimes in frequencydependent dynamic reorientation of fibroblasts on cyclically stretched substrates. Biophys. J. 95, 3470–3478 (2008).
Wang, J. H.C., GoldschmidtClermont, P., Wille, J. & Yin, F. C. P. Specificity of endothelial cell reorientation in response to cyclic mechanical stretching. J. Biomech. 34, 1563–1572 (2001).
Hsu, H.J., Lee, C.F. & Kaunas, R. A dynamic stochastic model of frequencydependent stress fiber alignment induced by cyclic stretch. PLoS ONE 4, e4853–e4860 (2009).
Bell, G. I. Models for the specific adhesion of cells to cells. Science 200, 618–627 (1978).
Evans, E. & Ritchie, K. Dynamic strength of molecular adhesion bonds. Biophys. J. 72, 1541–1555 (1997).
Evans, E. A. & Calderwood, D. A. Forces and bond dynamics in cell adhesion. Science 316, 1148–1153 (2007).
Erdmann, T. & Schwarz, U. S. Stability of adhesion clusters under constant force. Phys. Rev. Lett. 92, 108102–108105 (2004).
De, R., Zemel, A. & Safran, S. A. Dynamics of cell orientation. Nat. Phys. 3, 655–659 (2007).
De, R. & Safran, S. A. Dynamical theory of active cellular response to external stress. Phys. Rev. E 78, 031923–031940 (2008).
De, R., Zemel, A. & Safran, S. A. Do cells sense stress or strain? Measurement of cellular orientation can provide a clue. Biophys. J. 94, L29–L31 (2008).
Livne, A., Bouchbinder, E. & Geiger, B. Cell orientation under cyclic stretching. Nat. Commun. 5, 3938–3945 (2014).
Wei, Z., Deshpande, V. S., McMeeking, R. M. & Evans, A. G. Analysis and interpretation of stress fiber organization in cells subject to cyclic stretch. J. Biomech. Eng. 130, 031009–031017 (2008).
Qian, J., Liu, H., Lin, Y., Chen, W. & Gao, H. A mechanochemical model of cell reorientation on substrates under cyclic stretch. PLoS ONE 8, e65864–e65876 (2013).
Chen, B., Kemkemer, R., Deibler, M., Spatz, J. & Gao, H. Cyclic stretch induces cell reorientation on substrates by destabilizing catch bonds in focal adhesions. PLoS ONE 7, e48346–e48356 (2012).
Zhong, Y., Kong, D., Dai, L. & Ji, B. Frequencydependent focal adhesion instability and cell reorientation under cyclic substrate stretching. Cell Mol. Bioeng. 4, 442–456 (2011).
Kong, D., Ji, B. & Dai, L. Stability of adhesion clusters and cell reorientation under lateral cyclic tension. Biophys. J. 95, 4034–4044 (2008).
Dartsch, P. C. & Hammerle, H. Orientation response of arterial smoothmuscle cells to mechanical stimulation. Eur. J. Cell Biol. 41, 339–346 (1986).
Van Kampen, N. G. Stochastic Processes in Physics and Chemistry (Elsevier, North Holland, Amsterdam, 2011).
Kong, F., García, A. J., Paul Mould, A., Humphries, M. J. & Zhu, C. Demonstration of catch bonds between an integrin and its ligand. J. Cell Biol. 185, 1275–1284 (2009).
RocaCusachs, P., Gauthier, N. C., Rio, A. & Sheetz, M. P. Clustering of α5β1 integrins determines adhesion strength whereas αvβ3 and talin enable mechanotransduction. Proc. Natl Acad. Sci. USA 106, 16245–16250 (2009).
Pereverzev, Y. V., Prezhdo, O. V., Forero, M., Sokurenko, E. V. & Thomas, W. E. The twopathway model for the catchslip transition in biological adhesion. Biophys. J. 89, 1446–1454 (2005).
Robert, P., Limozin, L., Pierres, A. & Bongrand, P. Biomolecule association rates do not provide a complete description of bond formation. Biophys. J. 96, 4642–4650 (2009).
Robert, P., Nicolas, A., ArandaEspinoza, S., Bongrand, P. & Limozin, L. Minimal encounter time and separation determine ligandreceptor binding in cell adhesion. Biophys. J. 100, 2642–2651 (2011).
Gillespie, D. T. Exact stochastic simulation of coupled chemical reactions. J. Phys. Chem. 81, 2340–2361 (1977).
Deguchi, S., Ohashi, T. & Sato, M. Tensile properties of single stress fibers isolated from cultured vascular smooth muscle cells. J. Biomech. 39, 2603–2610 (2006).
Kumar, S. et al. Viscoelastic retraction of single living stress fibers and its impact on cell shape, cytoskeletal organization, and extracellular matrix mechanics. Biophys. J. 90, 3762–3773 (2006).
Acknowledgements
The author thanks Dr. Rangeet Bhattacharyya for insightful discussions and also acknowledges the financial support from Science and Engineering Research Board (SERB), Grant No. SR/FTP/PS105/2013, Department of Science & Technology (DST), India.
Author information
Authors and Affiliations
Contributions
R.D. developed the model, carried out the entire work, and wrote the manuscript.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Electronic supplementary material
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
De, R. A general model of focal adhesion orientation dynamics in response to static and cyclic stretch. Commun Biol 1, 81 (2018). https://doi.org/10.1038/s4200301800849
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s4200301800849
This article is cited by

A brief overview on mechanosensing and stickslip motion at the leading edge of migrating cells
Indian Journal of Physics (2022)

Cell Mechanosensing
Resonance (2019)
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.