Intracellular crowding links dimensionality to cell fate through a mechano-metabolic signalling axis

Abstract Three-dimensional (3D) cell culture systems exhibit more native-like cell behaviour compared to conventional two-dimensional (2D) cell culture systems. However, it remains largely unknown how dimensionality alters cell behaviour. Here, we identify intracellular crowding as a key biophysical parameter altered by cell culture dimensionality, which directs cell fate over a mechano-metabolic axis. Specifically, culture dimensionality controlled intracellular crowding by altering cell volume, which was confirmed across multiple cell types and cell culture platforms. Using chondrogenesis as a model system, we demonstrated that dimensionality-induced intracellular changes lead to improved chondrogenic stem cell differentiation in microtissue culture via a FOXO1 signalling axis. Our findings highlight intracellular crowding as an important parameter of cell culture systems, and present a novel strategy for engineering biomimetic cell culture systems, which has implications for a multitude of applications including disease modelling, in vitro drug screening models, developmental biology, and cell-based therapies.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-01-22
DOI
https://doi.org/10.64898/2026.01.20.700361
Primary Topic
3D Printing in Biomedical Research
Type
article
Field-Weighted Citation Impact
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article

Intracellular crowding links dimensionality to cell fate through a mechano-metabolic signalling axis

Marieke Meteling, I. Meulenbelt, Bas van Loo, Y.F. Ramos et al.
bioRxiv (Cold Spring Harbor Laboratory)
3D Printing in Biomedical Research
article

Intracellular crowding links dimensionality to cell fate through a mechano-metabolic signalling axis

Marieke Meteling, I. Meulenbelt, Bas van Loo, Y.F. Ramos, Jeroen Leijten, Rick Mulders, Liesbet Geris, Liliana Moreira Teixeira, Roos Wijngaarden, Ceri-Anne Suurmond, Kannan Govindaraj
article en

Abstract

Abstract Three-dimensional (3D) cell culture systems exhibit more native-like cell behaviour compared to conventional two-dimensional (2D) cell culture systems. However, it remains largely unknown how dimensionality alters cell behaviour. Here, we identify intracellular crowding as a key biophysical parameter altered by cell culture dimensionality, which directs cell fate over a mechano-metabolic axis. Specifically, culture dimensionality controlled intracellular crowding by altering cell volume, which was confirmed across multiple cell types and cell culture platforms. Using chondrogenesis as a model system, we demonstrated that dimensionality-induced intracellular changes lead to improved chondrogenic stem cell differentiation in microtissue culture via a FOXO1 signalling axis. Our findings highlight intracellular crowding as an important parameter of cell culture systems, and present a novel strategy for engineering biomimetic cell culture systems, which has implications for a multitude of applications including disease modelling, in vitro drug screening models, developmental biology, and cell-based therapies.

bioRxiv (Cold Spring Harbor Laboratory)
Leiden University Medical Center (NL), University of Twente (NL), KU Leuven (BE)
Openalex Percentile: Top 80%
3D Printing in Biomedical Research
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