Mechanosensing in actin stress fibers revealed by a close correlation between force and protein localization

Skip to Next Section, The mechanics of the actin cytoskeleton have a central role in the regulation of cells and tissues, but the details of how molecular sensors recognize deformations and forces are elusive. By performing cytoskeleton laser nanosurgery in cultured epithelial cells and fibroblasts,...

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Hauptverfasser: Colombelli, Julien (VerfasserIn) , Besser, Achim (VerfasserIn) , Schwarz, Ulrich S. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2009
In: Journal of cell science
Year: 2009, Jahrgang: 122, Heft: 10, Pages: 1665-1679
ISSN:1477-9137
DOI:10.1242/jcs.042986
Online-Zugang:Verlag, kostenfrei, Volltext: http://dx.doi.org/10.1242/jcs.042986
Verlag, kostenfrei, Volltext: http://jcs.biologists.org/content/122/10/1665
Volltext
Verfasserangaben:Julien Colombelli, Achim Besser, Holger Kress, Emmanuel G. Reynaud, Philippe Girard, Emmanuel Caussinus, Uta Haselmann, John V. Small, Ulrich S. Schwarz, and Ernst H.K. Stelzer
Beschreibung
Zusammenfassung:Skip to Next Section, The mechanics of the actin cytoskeleton have a central role in the regulation of cells and tissues, but the details of how molecular sensors recognize deformations and forces are elusive. By performing cytoskeleton laser nanosurgery in cultured epithelial cells and fibroblasts, we show that the retraction of stress fibers (SFs) is restricted to the proximity of the cut and that new adhesions form at the retracting end. This suggests that SFs are attached to the substrate. A new computational model for SFs confirms this hypothesis and predicts the distribution and propagation of contractile forces along the SF. We then analyzed the dynamics of zyxin, a focal adhesion protein present in SFs. Fluorescent redistribution after laser nanosurgery and drug treatment shows a high correlation between the experimentally measured localization of zyxin and the computed localization of forces along SFs. Correlative electron microscopy reveals that zyxin is recruited very fast to intermediate substrate anchor points that are highly tensed upon SF release. A similar acute localization response is found if SFs are mechanically perturbed with the cantilever of an atomic force microscope. If actin bundles are cut by nanosurgery in living Drosophila egg chambers, we also find that zyxin redistribution dynamics correlate to force propagation and that zyxin relocates at tensed SF anchor points, demonstrating that these processes also occur in living organisms. In summary, our quantitative analysis shows that force and protein localization are closely correlated in stress fibers, suggesting a very direct force-sensing mechanism along actin bundles.
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Beschreibung:Online Resource
ISSN:1477-9137
DOI:10.1242/jcs.042986