Login / Signup

Fascin-induced bundling protects actin filaments from disassembly by cofilin.

Jahnavi ChikireddyLéana LengagneRémi Le BorgneCatherine Pioche-DurieuHugo WiolandGuillaume Romet-LemonneAntoine Jegou
Published in: The Journal of cell biology (2024)
Actin filament turnover plays a central role in shaping actin networks, yet the feedback mechanism between network architecture and filament assembly dynamics remains unclear. The activity of ADF/cofilin, the main protein family responsible for filament disassembly, has been mainly studied at the single filament level. This study unveils that fascin, by crosslinking filaments into bundles, strongly slows down filament disassembly by cofilin. We show that this is due to a markedly slower initiation of the first cofilin clusters, which occurs up to 100-fold slower on large bundles compared with single filaments. In contrast, severing at cofilin cluster boundaries is unaffected by fascin bundling. After the formation of an initial cofilin cluster on a filament within a bundle, we observed the local removal of fascin. Notably, the formation of cofilin clusters on adjacent filaments is highly enhanced, locally. We propose that this interfilament cooperativity arises from the local propagation of the cofilin-induced change in helicity from one filament to the other filaments of the bundle. Overall, taking into account all the above reactions, we reveal that fascin crosslinking slows down the disassembly of actin filaments by cofilin. These findings highlight the important role played by crosslinkers in tuning actin network turnover by modulating the activity of other regulatory proteins.
Keyphrases
  • cell migration
  • diabetic rats
  • gene expression
  • computed tomography
  • drug induced
  • oxidative stress
  • postmenopausal women
  • small molecule
  • protein protein