The role of the nucleus for cell mechanics: an elastic phase field approach

The nucleus of eukaryotic cells typically makes up around 30% of the cell volume and has significantly different mechanics, which can make it effectively up to ten times stiffer than the surrounding cytoplasm. Therefore it is an important element for cell mechanics, but a quantitative understanding...

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Hauptverfasser: Chojowski, Robert (VerfasserIn) , Schwarz, Ulrich S. (VerfasserIn) , Ziebert, Falko (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 17 May 2024
In: Soft matter
Year: 2024, Jahrgang: 20, Heft: 22, Pages: 4488-4503
ISSN:1744-6848
DOI:10.1039/D4SM00345D
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1039/D4SM00345D
Verlag, lizenzpflichtig, Volltext: https://pubs.rsc.org/en/content/articlelanding/2024/sm/d4sm00345d
Volltext
Verfasserangaben:Robert Chojowski, Ulrich S. Schwarz and Falko Ziebert

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520 |a The nucleus of eukaryotic cells typically makes up around 30% of the cell volume and has significantly different mechanics, which can make it effectively up to ten times stiffer than the surrounding cytoplasm. Therefore it is an important element for cell mechanics, but a quantitative understanding of its mechanical role during whole cell dynamics is largely missing. Here we demonstrate that elastic phase fields can be used to describe dynamical cell processes in adhesive or confining environments in which the nucleus acts as a stiff inclusion in an elastic cytoplasm. We first introduce and verify our computational method and then study several prevalent cell-mechanical measurement methods. For cells on adhesive patterns, we find that nuclear stress is shielded by the adhesive pattern. For cell compression between two parallel plates, we obtain force-compression curves that allow us to extract an effective modulus for the cell–nucleus composite. For micropipette aspiration, the effect of the nucleus on the effective modulus is found to be much weaker, highlighting the complicated interplay between extracellular geometry and cell mechanics that is captured by our approach. We also show that our phase field approach can be used to investigate the effects of Kelvin–Voigt-type viscoelasticity and cortical tension. 
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