Abstract

As cells move forward, they pull rearward against extracellular matrices (ECMs), exerting traction forces. However, no rearward forces have been seen in the fish keratocyte. To address this discrepancy, we have measured the propulsive forces generated by the keratocyte lamella on both the ventral and the dorsal surfaces. On the ventral surface, a micromachined device revealed that traction forces were small and rearward directed under the lamella, changed direction in front of the nucleus, and became larger under the cell body. On the dorsal surface of the lamella, an optical gradient trap measured rearward forces generated against fibronectin-coated beads. The retrograde force exerted by the cell on the bead increased in the thickened region of the lamella where myosin condensation has been observed (Svitkina, T.M., A.B. Verkhovsky, K.M. McQuade, and G. G. Borisy. 1997. J. Cell Biol. 139:397-415). Similar forces were generated on both the ventral (0.2 nN/microm(2)) and the dorsal (0.4 nN/microm(2)) surfaces of the lamella, suggesting that dorsal matrix contacts are as effectively linked to the force-generating cytoskeleton as ventral contacts. The correlation between the level of traction force and the density of myosin suggests a model for keratocyte movement in which myosin condensation in the perinuclear region generates rearward forces in the lamella and forward forces in the cell rear.

Highlights

  • As cells move forward, they pull rearward against extracellular matrices (ECMs), exerting traction forces

  • The total traction force exerted on the ventral surface of a migrating fish keratocyte is ‫ف‬45 nN (Oliver et al, 1995), an order of magnitude smaller than the migration force exerted by fibroblasts (Harris et al, 1980)

  • Propulsive forces are generated by the keratocyte lamella

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Summary

Introduction

As cells move forward, they pull rearward against extracellular matrices (ECMs), exerting traction forces. No propulsive forces acting against the substratum have been found in the direction of migration (Oliver et al, 1999), and no significant traction forces have been found in the lamella region where myosin actively reorganizes and condenses the actin network (Svitkina et al, 1997). One might expect that the lamella could exert proportional propulsive traction forces and, be part of a cell body contraction This scenario would suggest that keratocytes migrate by a mechanism similar to that used by fibroblasts (Harris et al, 1980; Galbraith and Sheetz, 1997; Dembo and Wang, 1999). To distinguish between possible mechanisms, we need to measure these potential forces in relation to the dynamics of the force generating cytoskeleton to understand the mechanism of migration in keratocytes

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