TY - JOUR
T1 - Actin-myosin viscoelastic flow in the keratocyte lamellipod
AU - Rubinstein, Boris
AU - Fournier, Maxime F.
AU - Jacobson, Ken
AU - Verkhovsky, Alexander B.
AU - Mogilner, Alex
N1 - Funding Information:
This work was supported by National Institutes of Health GLUE grant “Cell Migration Consortium” (No. NIGMS U54 GM64346) to A.M. and K.J., and by National Science Foundation grant No. DMS-0315782 to A.M.; A.B.V. and M.F.F. were supported by Swiss National Science Foundation grant No. 3100A0-112413.
PY - 2009/10/7
Y1 - 2009/10/7
N2 - The lamellipod, the locomotory region of migratory cells, is shaped by the balance of protrusion and contraction. The latter is the result of myosin-generated centripetal flow of the viscoelastic actin network. Recently, quantitative flow data was obtained, yet there is no detailed theory explaining the flow in a realistic geometry. We introduce models of viscoelastic actin mechanics and myosin transport and solve the model equations numerically for the flat, fan-shaped lamellipodial domain of keratocytes. The solutions demonstrate that in the rapidly crawling cell, myosin concentrates at the rear boundary and pulls the actin network inward, so the centripetal actin flow is very slow at the front, and faster at the rear and at the sides. The computed flow and respective traction forces compare well with the experimental data. We also calculate the graded protrusion at the cell boundary necessary to maintain the cell shape and make a number of other testable predictions. We discuss model implications for the cell shape, speed, and bi-stability.
AB - The lamellipod, the locomotory region of migratory cells, is shaped by the balance of protrusion and contraction. The latter is the result of myosin-generated centripetal flow of the viscoelastic actin network. Recently, quantitative flow data was obtained, yet there is no detailed theory explaining the flow in a realistic geometry. We introduce models of viscoelastic actin mechanics and myosin transport and solve the model equations numerically for the flat, fan-shaped lamellipodial domain of keratocytes. The solutions demonstrate that in the rapidly crawling cell, myosin concentrates at the rear boundary and pulls the actin network inward, so the centripetal actin flow is very slow at the front, and faster at the rear and at the sides. The computed flow and respective traction forces compare well with the experimental data. We also calculate the graded protrusion at the cell boundary necessary to maintain the cell shape and make a number of other testable predictions. We discuss model implications for the cell shape, speed, and bi-stability.
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U2 - 10.1016/j.bpj.2009.07.020
DO - 10.1016/j.bpj.2009.07.020
M3 - Article
C2 - 19804715
AN - SCOPUS:70350001721
SN - 0006-3495
VL - 97
SP - 1853
EP - 1863
JO - Biophysical journal
JF - Biophysical journal
IS - 7
ER -