Confinement induces internal flows in adherent cell aggregates.

Autor: Yousafzai MS; Department of Biomedical Engineering, Yale University , , CT 06511, USA.; Systems Biology Institute, Yale University , CT 06516, USA., Amiri S; Systems Biology Institute, Yale University , CT 06516, USA.; Department of Mechanical Engineering and Materials Science, Yale University , , CT 06511, USA., Sun ZG; Systems Biology Institute, Yale University , CT 06516, USA.; Department of Physics, Yale University , , CT 06511, USA., Pahlavan AA; Department of Mechanical Engineering and Materials Science, Yale University , , CT 06511, USA., Murrell M; Department of Biomedical Engineering, Yale University , , CT 06511, USA.; Systems Biology Institute, Yale University , CT 06516, USA.; Department of Physics, Yale University , , CT 06511, USA.
Jazyk: angličtina
Zdroj: Journal of the Royal Society, Interface [J R Soc Interface] 2024 May; Vol. 21 (214), pp. 20240105. Date of Electronic Publication: 2024 May 22.
DOI: 10.1098/rsif.2024.0105
Abstrakt: During mesenchymal migration, F-actin protrusion at the leading edge and actomyosin contraction determine the retrograde flow of F-actin within the lamella. The coupling of this flow to integrin-based adhesions determines the force transmitted to the extracellular matrix and the net motion of the cell. In tissues, motion may also arise from convection, driven by gradients in tissue-scale surface tensions and pressures. However, how migration coordinates with convection to determine the net motion of cellular ensembles is unclear. To explore this, we study the spreading of cell aggregates on adhesive micropatterns on compliant substrates. During spreading, a cell monolayer expands from the aggregate towards the adhesive boundary. However, cells are unable to stabilize the protrusion beyond the adhesive boundary, resulting in retraction of the protrusion and detachment of cells from the matrix. Subsequently, the cells move upwards and rearwards, yielding a bulk convective flow towards the centre of the aggregate. The process is cyclic, yielding a steady-state balance between outward (protrusive) migration along the surface, and 'retrograde' (contractile) flows above the surface. Modelling the cell aggregates as confined active droplets, we demonstrate that the interplay between surface tension-driven flows within the aggregate, radially outward monolayer flow and conservation of mass leads to an internal circulation.
Databáze: MEDLINE