Mammalian cells measure the extracellular matrix area and respond through switching the adhesion state


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Date

2025

Publication Type

Journal Article

ETH Bibliography

yes

Citations

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Data

Abstract

Mammalian cells adjust integrin-mediated adhesion based on the composition and structure of the extracellular matrix (ECM). However, how spatially confined ECM ligands regulate cell adhesion initiation remains unclear. Here, we investigate how cells adapt early adhesion to different ECM protein areas. Through combining microcontact printing with single-cell force spectroscopy we measure cell adhesion initiation and strengthening to defined areas of ECM proteins. HeLa cells and mouse embryonic fibroblasts gradually increase adhesion with collagen I or fibronectin area, while reaching maximum adhesion force to ECM patterns having areas above certain thresholds. On much smaller patterns, both cell types switch to a different state and considerably increase the adhesion force per ECM protein area, which they strengthen much faster. This spatially enhanced adhesion state does not require talin or kindlin, indicating a fundamentally different adhesion mechanism. Mechanotransduction seems to play integrin and cell type-specific roles in the spatially enhanced adhesion state.

Publication status

published

Editor

Book title

Volume

16 (1)

Pages / Article No.

6870

Publisher

Nature

Event

Edition / version

Methods

Software

Geographic location

Date collected

Date created

Subject

Atomic force microscopy; Integrins; Mechanotransduction; Nanoscale biophysics

Organisational unit

03870 - Müller, Daniel J. / Müller, Daniel J. check_circle

Notes

Funding

182587 - Characterizing the cell cycle dependent regulation of adhesion to extracellular matrix proteins (SNF)
215690 - Characterizing molecular mechanisms by which cells sense extracellular matrices differentially to regulate adhesion and growth (SNF)

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