Microtubule acetylation but not detyrosination promotes focal adhesion dynamics and astrocyte migration

Author:

Bance Bertille12,Seetharaman Shailaja13ORCID,Leduc Cécile1ORCID,Boëda Batiste1,Etienne-Manneville Sandrine1ORCID

Affiliation:

1. Cell Polarity, Migration and Cancer Unit, Institut Pasteur,UMR3691 CNRS, , Equipe Labellisée Ligue Contre le Cancer, F-75015, Paris, France

2. Sorbonne Université, Collège doctoral, F-75005 Paris, France

3. Université Paris Descartes, Sorbonne Paris Cité, F-75006 Paris, France

Abstract

Microtubules play a crucial role in mesenchymal migration by controlling cell polarity and the turnover of cell adhesive structures on the extracellular matrix. The polarized functions of microtubules imply that microtubules are locally regulated. Here, we investigated the regulation and role of two major tubulin post-translational modifications, acetylation and detyrosination, which have been associated with stable microtubules. Using primary astrocytes in a wound healing assay, we show that these tubulin modifications are independently regulated during cell polarization and differently affect cell migration. In contrast to microtubule detyrosination, αTAT1-mediated microtubule acetylation increases in the vicinity of focal adhesions and promotes cell migration. We further demonstrate that αTAT1 increases focal adhesion turnover by promoting Rab6-positive vesicle fusion at focal adhesions. Our results highlight the specificity of microtubule post-translational modifications and bring new insight into the regulatory functions of tubulin acetylation.

Funder

Ligue Contre le Cancer

Centre National de la Recherche Scientifique

Institut Pasteur

PolarNet

Publisher

The Company of Biologists

Subject

Cell Biology

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