The ability of vascular endothelial cells to adjust their cytoplasmic properties under the stimulus of fluid shear stress is a key factor in the physiological control of the blood-vessel wall interface. Adjustments to fluid stress control exchange and cell traffic across the endothelium, influence humoral regulation, and are one of the main determinants of lesion formation in large arteries. Cytoplasmic actin plays a key role in these processes because it serves to define the cell's shape, mechanical properties, and motility. Actin polymer (F-actin) stability, arrangement, and extent of crosslinking and attachment to the substrate and the lumenal membrane determine the local stiffness of the cytoplasm. There exists today no measurements of the dynamics of actin in endothelial cells or the consequence of these dynamics for the mechanics and biology of endothelial cells under flow conditions commensurate with those experienced in vivo.
Aim 1 will determine actin dynamics in individual human umbilical vein endothelial cells (HUVEC) before and after the application of steady fluid shear to their surfaces. Cells are microinjected with caged resorufin-actin monomer (G-actin). After incorporation of the caged-actin into the cytoskeleton, spatial uncaging of its fluorophore will yield the F-/G-actin ratio, F-actin turnover time, and the G-actin diffusion coefficient.
In Aim 2, F-actin turnover data will be combined with a detailed 3D picture of F-actin structure in endothelial cells determined using high-resolution electron microscopy with the goal of developing a model to explain the mechanical properties of the cell and how these properties are altered by fluid flow.
In Aim 3, the measurements of actin dynamics and internal structure will be extended to disturbed and unsteady flow to create a complete biomechanical picture of normal in vivo conditions. These studies will provide new insight into the basic physiology of endothelial structure and function under flow conditions characteristic of those experienced in vivo. They will provide new data on cell stasis and motility as well as the coupling between arterial flow and the cell, and thereby contribute to our understanding of the pathologies associated with atherosclerosis and intimal hyperplasia in vascular grafts.
| Osborn, Eric A; Rabodzey, Aleksandr; Dewey Jr, C Forbes et al. (2006) Endothelial actin cytoskeleton remodeling during mechanostimulation with fluid shear stress. Am J Physiol Cell Physiol 290:C444-52 |
| Dewey Jr, C Forbes (2002) Haemodynamic flow: symmetry and synthesis. Biorheology 39:541-9 |
| Nakamura, Fumihiko; Osborn, Eric; Janmey, Paul A et al. (2002) Comparison of filamin A-induced cross-linking and Arp2/3 complex-mediated branching on the mechanics of actin filaments. J Biol Chem 277:9148-54 |
| McGrath, J L; Osborn, E A; Tardy, Y S et al. (2000) Regulation of the actin cycle in vivo by actin filament severing. Proc Natl Acad Sci U S A 97:6532-7 |
| Cheng, Y; Hartemink, C A; Hartwig, J H et al. (2000) Three-dimensional reconstruction of the actin cytoskeleton from stereo images. J Biomech 33:105-13 |
| Hartwig, J H; Barkalow, K; Azim, A et al. (1999) The elegant platelet: signals controlling actin assembly. Thromb Haemost 82:392-8 |
| Ohta, Y; Suzuki, N; Nakamura, S et al. (1999) The small GTPase RalA targets filamin to induce filopodia. Proc Natl Acad Sci U S A 96:2122-8 |
| McGrath, J L; Tardy, Y; Dewey Jr, C F et al. (1998) Simultaneous measurements of actin filament turnover, filament fraction, and monomer diffusion in endothelial cells. Biophys J 75:2070-8 |
| McGrath, J L; Hartwig, J H; Tardy, Y et al. (1998) Measuring actin dynamics in endothelial cells. Microsc Res Tech 43:385-94 |
| Satcher, R; Dewey Jr, C F; Hartwig, J H (1997) Mechanical remodeling of the endothelial surface and actin cytoskeleton induced by fluid flow. Microcirculation 4:439-53 |
