Microtubules control cellular shape and coherence in amoeboid migrating cells

Author:

Kopf Aglaja1ORCID,Renkawitz Jörg12ORCID,Hauschild Robert1ORCID,Girkontaite Irute3ORCID,Tedford Kerry4ORCID,Merrin Jack1ORCID,Thorn-Seshold Oliver5ORCID,Trauner Dirk6,Häcker Hans7,Fischer Klaus-Dieter4,Kiermaier Eva18ORCID,Sixt Michael1ORCID

Affiliation:

1. Institute of Science and Technology Austria, Klosterneuburg, Austria

2. Biomedical Center, Walter Brendel Center of Experimental Medicine, Institute of Cardiovascular Physiology and Pathophysiology, University Hospital, Ludwig-Maximilians University of Munich, Munich, Germany

3. Department of Immunology, State Research Institute Centre for Innovative Medicine, Vilnius, Lithuania

4. Institute of Biochemistry and Cell Biology, Medical Faculty, Otto-von-Guericke University, Magdeburg, Germany

5. Department of Pharmacy, Ludwig-Maximilians University of Munich, Munich, Germany

6. Department of Chemistry, New York University, New York, NY

7. Division of Microbiology and Immunology, Department of Pathology, University of Utah, Salt Lake City, UT

8. Life and Medical Sciences Institute (LIMES), Immune and Tumor Biology, University of Bonn, Bonn, Germany

Abstract

Cells navigating through complex tissues face a fundamental challenge: while multiple protrusions explore different paths, the cell needs to avoid entanglement. How a cell surveys and then corrects its own shape is poorly understood. Here, we demonstrate that spatially distinct microtubule dynamics regulate amoeboid cell migration by locally promoting the retraction of protrusions. In migrating dendritic cells, local microtubule depolymerization within protrusions remote from the microtubule organizing center triggers actomyosin contractility controlled by RhoA and its exchange factor Lfc. Depletion of Lfc leads to aberrant myosin localization, thereby causing two effects that rate-limit locomotion: (1) impaired cell edge coordination during path finding and (2) defective adhesion resolution. Compromised shape control is particularly hindering in geometrically complex microenvironments, where it leads to entanglement and ultimately fragmentation of the cell body. We thus demonstrate that microtubules can act as a proprioceptive device: they sense cell shape and control actomyosin retraction to sustain cellular coherence.

Funder

European Research Council

German Research Foundation

Seventh Framework Programme

European Commission

DFG

American Lebanese Syrian Associated Charities

Ministry of Economics, Science, and Digitisation

Austrian Science Fund

European Molecular Biology Organization

Publisher

Rockefeller University Press

Subject

Cell Biology

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