The compass to follow: Focal adhesion turnover
How cells move is a fundamental biological question. The directionality of adherent migrating cells depends on the assembly and disassembly (turnover) of focal adhesions (FAs). FAs are micron-sized actin-based structures that link cells to the extracellular matrix. Traditionally, microtubules have b...
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Veröffentlicht in: | Current opinion in cell biology 2023-02, Vol.80, p.102152-102152, Article 102152 |
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Sprache: | eng |
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Zusammenfassung: | How cells move is a fundamental biological question. The directionality of adherent migrating cells depends on the assembly and disassembly (turnover) of focal adhesions (FAs). FAs are micron-sized actin-based structures that link cells to the extracellular matrix. Traditionally, microtubules have been considered key to triggering FA turnover. Through the years, advancements in biochemistry, biophysics, and bioimaging tools have been invaluable for many research groups to unravel a variety of mechanisms and molecular players that contribute to FA turnover, beyond microtubules. Here, we discuss recent discoveries of key molecular players that affect the dynamics and organization of the actin cytoskeleton to enable timely FA turnover and consequently proper directed cell migration.
Schematic of a migrating cell showing some focal adhesions and key players involved in focal adhesion turnover (actin – including different types of stress fibers, microtubules and septins). The inset shows the different actin nucleator factors that nucleate actin at/near focal adhesions. [Display omitted] |
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ISSN: | 0955-0674 1879-0410 |
DOI: | 10.1016/j.ceb.2023.102152 |