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Microtubule detyrosination drives symmetry breaking to polarize cells for directed cell migration.

Abstract
To initiate directed movement, cells must become polarized, establishing a protrusive leading edge and a contractile trailing edge. This symmetry-breaking process involves reorganization of cytoskeleton and asymmetric distribution of regulatory molecules. However, what triggers and maintains this asymmetry during cell migration remains largely elusive. Here, we established a micropatterning-based 1D motility assay to investigate the molecular basis of symmetry breaking required for directed cell migration. We show that microtubule (MT) detyrosination drives cell polarization by directing kinesin-1-based transport of the adenomatous polyposis coli (APC) protein to cortical sites. This is essential for the formation of cell's leading edge during 1D and 3D cell migration. These data, combined with biophysical modeling, unveil a key role for MT detyrosination in the generation of a positive feedback loop linking MT dynamics and kinesin-1-based transport. Thus, symmetry breaking during cell polarization relies on a feedback loop driven by MT detyrosination that supports directed cell migration.
AuthorsKirstine Lavrsen, Girish Rajendraprasad, Marcin Leda, Susana Eibes, Elisa Vitiello, Vasileios Katopodis, Andrew B Goryachev, Marin Barisic
JournalProceedings of the National Academy of Sciences of the United States of America (Proc Natl Acad Sci U S A) Vol. 120 Issue 22 Pg. e2300322120 (05 30 2023) ISSN: 1091-6490 [Electronic] United States
PMID37216553 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Kinesins
Topics
  • Kinesins (metabolism)
  • Microtubules (metabolism)
  • Cell Movement
  • Cytoskeleton (metabolism)

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