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Causes of retrograde flow in fish keratocytes.

Cytoskeleton (Hoboken, N.J.) (2013-10-16)
Thomas Fuhs, Michael Goegler, Claudia A Brunner, Charles W Wolgemuth, Josef A Kaes
ABSTRACT

Confronting motile cells with obstacles doubling as force sensors we tested the limits of the driving actin and myosin machinery. We could directly measure the force necessary to stop actin polymerization as well as the force present in the retrograde actin flow. Combined with detailed measurements of the retrograde flow velocity and specific manipulation of actin and myosin we found that actin polymerization and myosin contractility are not enough to explain the cells behavior. We show that ever-present depolymerization forces, a direct entropic consequence of actin filament recycling, are sufficient to fill this gap, even under heavy loads.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
HEPES, BioPerformance Certified, ≥99.5% (titration), suitable for cell culture
Sigma-Aldrich
(−)-Blebbistatin, solid, synthetic
Sigma-Aldrich
Jasplakinolide, ≥97% (HPLC)
Sigma-Aldrich
Cytochalasin D, Ready Made Solution, from Zygosporium mansonii, 5 mg/mL in DMSO
Sigma-Aldrich
ML-7, powder