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Heavy water induces bundling in entangled actin networks.
Mollenkopf, Paul; Prascevic, Dusan; Bayerl, Thomas M; Käs, Josef A; Schnauß, Jörg.
Afiliação
  • Mollenkopf P; Department of Physiology, University of Pennsylvania Philadelphia PA 19104 USA.
  • Prascevic D; Peter-Debye Institute for Soft Matter Physics, Leipzig University 04103 Leipzig Germany joerg.schnauss@uni-leipzig.de.
  • Bayerl TM; Inventages 16 Northfields Prospect Business Centre, Putney Bridge Rd London SW181PE UK.
  • Käs JA; Peter-Debye Institute for Soft Matter Physics, Leipzig University 04103 Leipzig Germany joerg.schnauss@uni-leipzig.de.
  • Schnauß J; Peter-Debye Institute for Soft Matter Physics, Leipzig University 04103 Leipzig Germany joerg.schnauss@uni-leipzig.de.
RSC Adv ; 13(35): 24795-24800, 2023 Aug 11.
Article em En | MEDLINE | ID: mdl-37601592
ABSTRACT
Heavy water is known to affect many different biological systems, with the most striking effects observed at the cellular level. Many dynamic processes, such as migration or invasion, but also central processes of cell proliferation are measurably inhibited by the presence of deuterium oxide (D2O). Furthermore, individual cell deformabilities are significantly decreased upon D2O treatment. In order to understand the origin of these effects, we studied entangled filamentous actin networks, a commonly used model system for the cytoskeleton, which is considered a central functional element for dynamic cellular processes. Using bulk shear rheology to extract rheological signatures of reconstituted actin networks at varying concentrations of D2O, we found a non-monotonic behavior, which is explainable by a drastic change in the actin network architecture. Applying light scattering and fluorescence microscopy, we were able to demonstrate that the presence of deuterium oxide induces bundling in reconstituted entangled networks of filamentous actin. This constitutes an entirely novel and previously undescribed actin bundling mechanism.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: RSC Adv Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: RSC Adv Ano de publicação: 2023 Tipo de documento: Article