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Nat Commun. 2015 Sep 29;6:8496. doi: 10.1038/ncomms9496.

A resilient formin-derived cortical actin meshwork in the rear drives actomyosin-based motility in 2D confinement.

Author information

1
Anatomy III/Cell Biology, BioMedCenter, Ludwig-Maximilians-University, Grosshaderner Str. 9, Planegg-Martinsried, Germany.
2
Institute for Biophysical Chemistry, Hannover Medical School, Carl-Neuberg-Strasse 1, Hannover 30625, Germany.
3
Institute of Complex Systems, ICS-7: Biomechanics, Forschungszentrum Jülich GmbH, Jülich 52425 Germany.
4
Institute of Biotechnology, University of Helsinki, PO Box 56, Helsinki 00014, Finland.
5
Center for Biochemistry, Medical Faculty, University of Cologne, Köln 50931, Germany.
6
Division of Molecular Biology, Ruder Bošković Institute, Bijenička 54, Zagreb 10000, Croatia.

Abstract

Cell migration is driven by the establishment of disparity between the cortical properties of the softer front and the more rigid rear allowing front extension and actomyosin-based rear contraction. However, how the cortical actin meshwork in the rear is generated remains elusive. Here we identify the mDia1-like formin A (ForA) from Dictyostelium discoideum that generates a subset of filaments as the basis of a resilient cortical actin sheath in the rear. Mechanical resistance of this actin compartment is accomplished by actin crosslinkers and IQGAP-related proteins, and is mandatory to withstand the increased contractile forces in response to mechanical stress by impeding unproductive blebbing in the rear, allowing efficient cell migration in two-dimensional-confined environments. Consistently, ForA supresses the formation of lateral protrusions, rapidly relocalizes to new prospective ends in repolarizing cells and is required for cortical integrity. Finally, we show that ForA utilizes the phosphoinositide gradients in polarized cells for subcellular targeting.

PMID:
26415699
PMCID:
PMC4598863
DOI:
10.1038/ncomms9496
[Indexed for MEDLINE]
Free PMC Article

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