Fibroblast cytoskeletal remodeling contributes to connective tissue tension.

The visco-elastic behavior of connective tissue is generally attributed to the material properties of the extracellular matrix rather than cellular activity. We have previously shown that fibroblasts within areolar connective tissue exhibit dynamic cytoskeletal remodeling within minutes in response to tissue stretch ex vivo and in vivo. Here, we tested the hypothesis that fibroblasts, through this cytoskeletal remodeling, actively contribute to the visco-elastic behavior of the whole tissue. We measured significantly increased tissue tension when cellular function was broadly inhibited by sodium azide and when cytoskeletal dynamics were compromised by disrupting microtubules (with colchicine) or actomyosin contractility (via Rho kinase inhibition). These treatments led to a decrease in cell body cross-sectional area and cell field perimeter (obtained by joining the end of all of a fibroblast's processes). Suppressing lamellipodia formation by inhibiting Rac-1 decreased cell body cross-sectional area but did not affect cell field perimeter or tissue tension. Thus, by changing shape, fibroblasts can dynamically modulate the visco-elastic behavior of areolar connective tissue through Rho-dependent cytoskeletal mechanisms. These results have broad implications for our understanding of the dynamic interplay of forces between fibroblasts and their surrounding matrix, as well as for the neural, vascular, and immune cell populations residing within connective tissue.

Two-state model of acto-myosin attachment-detachment predicts C-process of sinusoidal analysis.

The force response of activated striated muscle to length perturbations includes the so-called C-process, which has been considered the frequency domain representation of the fast single-exponential force decay after a length step (phases 1 and 2). The underlying molecular mechanisms of this phenomenon, however, are still the subject of various hypotheses. In this study, we derived analytical expressions and created a corresponding computer model to describe the consequences of independent acto-myosin cross-bridges characterized solely by 1), intermittent periods of attachment (t(att)) and detachment (t(det)), whose values are stochastically governed by independent probability density functions; and 2), a finite Hookian stiffness (k(stiff)) effective only during periods of attachment. The computer-simulated force response of 20,000 (N) cross-bridges making up a half-sarcomere (F(hs)(t)) to sinusoidal length perturbations (L(hs)(t)) was predicted by the analytical expression in the frequency domain, (F(hs)(omega)/L(hs)(omega))=(t(att)/t(cycle))Nk(stiff)(iomega/(t(att)(-1)+iomega)), where t(att) = mean value of t(att), t(cycle) = mean value of t(att) + t(det), k(stiff) = mean stiffness, and omega = 2pi x frequency of perturbation. The simulated force response due to a length step (L(hs)) was furthermore predicted by the analytical expression in the time domain, F(hs)(t)=(t(att)/t(cycle))Nk(stiff)L(hs)e(-t/t(att)). The forms of these analytically derived expressions are consistent with expressions historically used to describe these specific characteristics of a force response and suggest that the cycling of acto-myosin cross-bridges and their associated stiffnesses are responsible for the C-process and for phases 1 and 2. The rate constant 2pic, i.e., the frequency parameter of the historically defined C-process, is shown here to be equal to t(att)(-1). Experimental results from activated cardiac muscle examined at different temperatures and containing predominately alpha- or beta-myosin heavy chain isoforms were found to be consistent with the above interpretation.

Acto-myosin crossbridge kinetics in humans with coronary artery disease: influence of sex and diabetes mellitus.

Risk of heart failure (HF) is influenced by sex and diabetes mellitus (DM). To better understand these interactions, sub-epicardial myocardium from 26 patients with coronary artery disease (CAD) undergoing coronary bypass surgery was examined in vitro using sinusoidal length perturbation analysis at varying [Ca(2+)] to determine the viscoelastic properties of myofilaments related to acto-myosin crossbridge kinetics. Half of the patients had CAD only (four female, F-CAD; nine male, M-CAD), while the other half had both CAD and Type 2 DM (six F-DM; seven M-DM). At maximal and sub-maximal myofilament Ca(2+) activation there was a significant effect of sex and disease on frequency of maximum oscillatory work output during sinusoidal perturbation (P<0.05). Myofilaments from F-CAD produced oscillatory work at significantly higher frequencies compared with M-CAD, while myofilaments from F-DM and M-DM produced work at similar frequencies. Correspondingly, minimum viscoelastic stiffness at maximum Ca(2+) activation occurred at significantly higher frequencies in F-CAD (5.0+/-0.3 Hz) than M-CAD (3.3+/-0.3 Hz), but at similar frequencies in F-DM (3.7+/-0.3 Hz) and M-DM (4.3+/-0.2 Hz). Thus, sex influences acto-myosin crossbridge kinetics in myofilaments isolated from CAD patients. These sex-related differences were absent in DM, suggesting that differences in the properties of cardiac muscle contribute to reported sex differences in the incidence and mortality of HF in DM.