Issue 20, 2023

A microfluidic mechano-chemostat for tissues and organisms reveals that confined growth is accompanied with increased macromolecular crowding

Abstract

Conventional culture conditions are oftentimes insufficient to study tissues, organisms, or 3D multicellular assemblies. They lack both dynamic chemical and mechanical control over the microenvironment. While specific microfluidic devices have been developed to address chemical control, they often do not allow the control of compressive forces emerging when cells proliferate in a confined environment. Here, we present a generic microfluidic device to control both chemical and mechanical compressive forces. This device relies on the use of sliding elements consisting of microfabricated rods that can be inserted inside a microfluidic device. Sliding elements enable the creation of reconfigurable closed culture chambers for the study of whole organisms or model micro-tissues. By confining the micro-tissues, we studied the biophysical impact of growth-induced pressure and showed that this mechanical stress is associated with an increase in macromolecular crowding, shedding light on this understudied type of mechanical stress. Our mechano-chemostat allows the long-term culture of biological samples and can be used to study both the impact of specific conditions as well as the consequences of mechanical compression.

Graphical abstract: A microfluidic mechano-chemostat for tissues and organisms reveals that confined growth is accompanied with increased macromolecular crowding

Supplementary files

Article information

Article type
Paper
Submitted
11 Apr 2023
Accepted
09 Sep 2023
First published
14 Sep 2023

Lab Chip, 2023,23, 4445-4455

A microfluidic mechano-chemostat for tissues and organisms reveals that confined growth is accompanied with increased macromolecular crowding

Z. Ben Meriem, T. Mateo, J. Faccini, C. Denais, R. Dusfour-Castan, C. Guynet, T. Merle, M. Suzanne, M. Di-Luoffo, J. Guillermet-Guibert, B. Alric, S. Landiech, L. Malaquin, F. Mesnilgrente, A. Laborde, L. Mazenq, R. Courson and M. Delarue, Lab Chip, 2023, 23, 4445 DOI: 10.1039/D3LC00313B

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