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

被引:51
作者
Bance, Bertille [1 ,2 ]
Seetharaman, Shailaja [1 ,3 ]
Leduc, Cecile [1 ]
Boeda, Batiste [1 ]
Etienne-Manneville, Sandrine [1 ]
机构
[1] CNRS, Inst Pasteur, Cell Polar Migrat & Canc Unit, Equipe Labellisee Ligue Canc,UMR3691, F-75015 Paris, France
[2] Sorbonne Univ, Coll Doctoral, F-75005 Paris, France
[3] Univ Paris 05, Sorbonne Paris Cite, F-75006 Paris, France
关键词
Microtubules; Adhesion; Migration; Post-translational modifications; ALPHA-TUBULIN; SELECTIVE STABILIZATION; HDAC6; ACETYLTRANSFERASE; TRANSPORT; RAB6; PAXILLIN; ACTIN; CODE;
D O I
10.1242/jcs.225805
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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, alpha TAT1 (ATAT1)-mediated microtubule acetylation increases in the vicinity of focal adhesions and promotes cell migration. We further demonstrate that alpha TAT1 increases focal adhesion turnover by promoting Rabb-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. This article has an associated First Person interview with the first author of the paper.
引用
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页数:10
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