Mechanical Fingerprint of Senescence in Endothelial Cells.

Nano Lett

Laboratory of Thermodynamics in Emerging Technologies, Department of Mechanical and Process Engineering, ETH Zurich, Sonneggstrasse 3, 8092 Zürich, Switzerland.

Published: June 2021

AI Article Synopsis

  • - Endothelial senescence leads to changes in cell behavior over time, which can contribute to cardiovascular issues, and mechanical factors like adhesion and response to flow play a role in this process.
  • - Researchers used force microscopy to study how aging affects cell anchoring and force generation, finding that senescent cells show significantly increased adhesion and force due to strong focal adhesions.
  • - While the stronger interaction of senescent cells with their substrate helps prevent cell loss, it hampers their ability to adapt and reshape in response to blood flow changes, indicating a trade-off in their functionality.

Article Abstract

Endothelial senescence entails alterations of the healthy cell phenotype, which accumulate over time and contribute to cardiovascular disease. Mechanical aspects regulating cell adhesion, force generation, and the response to flow contribute to the senescence-associated drift; however, they remain largely unexplored. Here, we exploit force microscopy to resolve variations of the cell anchoring to the substrate and the tractions generated upon aging in the nanonewton (nN) range. Senescent endothelial cells display a multifold increase in the levels of basal adhesion and force generation supported by mature and strong focal adhesions. The enhanced mechanical interaction with the substrate yields static endothelial monolayers that polarize in response to flow but fail the process of coordinated cell shape remodeling and reorientation. The emerging picture indicates that senescence reinforces the local cell interaction with the substrate and may therefore prevent endothelial denudation; however, it compromises the ability to functionally adapt to the local hemodynamic conditions.

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Source
http://dx.doi.org/10.1021/acs.nanolett.1c00064DOI Listing

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