TY - JOUR
T1 - Quantitative analysis of G-actin transport in motile cells
AU - Novak, Igor L.
AU - Slepchenko, Boris M.
AU - Mogilner, Alex
N1 - Funding Information:
This work was supported by the National Institutes of Health Glue Grant “Cell Migration Consortium” (National Institute of General Medical Sciences U54 GM64346) and by National Science Foundation grant DMS-0315782 to A.M. and National Institutes of Health grant P41 RR13186 to I.N. and B.M.S.
PY - 2008/8/15
Y1 - 2008/8/15
N2 - Cell migration is based on an actin treadmill, which in turn depends on recycling of G-actin across the cell, from the rear where F-actin disassembles, to the front, where F-actin polymerizes. To analyze the rates of the actin transport, we used the Virtual Cell software to solve the diffusion-drift- reaction equations for the G-actin concentration in a realistic three-dimensional geometry of the motile cell. Numerical solutions demonstrate that F-actin disassembly at the cell rear and assembly at the front, along with diffusion, establish a G-actin gradient that transports G-actin forward "globally" across the lamellipod. Alternatively, if the F-actin assembly and disassembly are distributed throughout the lamellipod, F-/G-actin turnover is local, and diffusion plays little role. Chemical reactions and/or convective flow of cytoplasm of plausible magnitude affect the transport very little. Spatial distribution of G-actin is smooth and not sensitive to F-actin density fluctuations. Finally, we conclude that the cell body volume slows characteristic diffusion-related relaxation time in motile cell from ∼10 to ∼100 s. We discuss biological implications of the local and global regimes of the G-actin transport.
AB - Cell migration is based on an actin treadmill, which in turn depends on recycling of G-actin across the cell, from the rear where F-actin disassembles, to the front, where F-actin polymerizes. To analyze the rates of the actin transport, we used the Virtual Cell software to solve the diffusion-drift- reaction equations for the G-actin concentration in a realistic three-dimensional geometry of the motile cell. Numerical solutions demonstrate that F-actin disassembly at the cell rear and assembly at the front, along with diffusion, establish a G-actin gradient that transports G-actin forward "globally" across the lamellipod. Alternatively, if the F-actin assembly and disassembly are distributed throughout the lamellipod, F-/G-actin turnover is local, and diffusion plays little role. Chemical reactions and/or convective flow of cytoplasm of plausible magnitude affect the transport very little. Spatial distribution of G-actin is smooth and not sensitive to F-actin density fluctuations. Finally, we conclude that the cell body volume slows characteristic diffusion-related relaxation time in motile cell from ∼10 to ∼100 s. We discuss biological implications of the local and global regimes of the G-actin transport.
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U2 - 10.1529/biophysj.108.130096
DO - 10.1529/biophysj.108.130096
M3 - Article
C2 - 18502800
AN - SCOPUS:50349095873
SN - 0006-3495
VL - 95
SP - 1627
EP - 1638
JO - Biophysical journal
JF - Biophysical journal
IS - 4
ER -