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


Journal

Lab on a chip
ISSN: 1473-0189
Titre abrégé: Lab Chip
Pays: England
ID NLM: 101128948

Informations de publication

Date de publication:
10 10 2023
Historique:
medline: 11 10 2023
pubmed: 23 9 2023
entrez: 23 9 2023
Statut: epublish

Résumé

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.

Identifiants

pubmed: 37740366
doi: 10.1039/d3lc00313b
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4445-4455

Auteurs

Zacchari Ben Meriem (Z)

LAAS-CNRS, Université de Toulouse, CNRS, Toulouse, France. morgan.delarue@laas.fr.

Tiphaine Mateo (T)

LAAS-CNRS, Université de Toulouse, CNRS, Toulouse, France. morgan.delarue@laas.fr.

Julien Faccini (J)

LAAS-CNRS, Université de Toulouse, CNRS, Toulouse, France. morgan.delarue@laas.fr.

Céline Denais (C)

LAAS-CNRS, Université de Toulouse, CNRS, Toulouse, France. morgan.delarue@laas.fr.

Romane Dusfour-Castan (R)

Laboratoire de Microbiologie et de Génétique Moléculaires, Centre de Biologie Intégrative (CBI), CNRS, Université de Toulouse, F-31000, Toulouse, France.

Catherine Guynet (C)

Laboratoire de Microbiologie et de Génétique Moléculaires, Centre de Biologie Intégrative (CBI), CNRS, Université de Toulouse, F-31000, Toulouse, France.

Tatiana Merle (T)

Molecular, Cellular and Developmental Biology unit (MCD), Centre de Biologie Intégrative (CBI), Université de Toulouse, CNRS, UPS, France.

Magali Suzanne (M)

Molecular, Cellular and Developmental Biology unit (MCD), Centre de Biologie Intégrative (CBI), Université de Toulouse, CNRS, UPS, France.

Mickaël Di-Luoffo (M)

INSERM U1037, CRCT, Université de Toulouse, F-31037 Toulouse, France.

Julie Guillermet-Guibert (J)

INSERM U1037, CRCT, Université de Toulouse, F-31037 Toulouse, France.
Laboratoire d'Excellence TouCAN, F-31037 Toulouse, France.

Baptiste Alric (B)

LAAS-CNRS, Université de Toulouse, CNRS, Toulouse, France. morgan.delarue@laas.fr.

Sylvain Landiech (S)

LAAS-CNRS, Université de Toulouse, CNRS, Toulouse, France. morgan.delarue@laas.fr.

Laurent Malaquin (L)

LAAS-CNRS, Université de Toulouse, CNRS, Toulouse, France. morgan.delarue@laas.fr.

Fabien Mesnilgrente (F)

LAAS-CNRS, Université de Toulouse, CNRS, Toulouse, France. morgan.delarue@laas.fr.

Adrian Laborde (A)

LAAS-CNRS, Université de Toulouse, CNRS, Toulouse, France. morgan.delarue@laas.fr.

Laurent Mazenq (L)

LAAS-CNRS, Université de Toulouse, CNRS, Toulouse, France. morgan.delarue@laas.fr.

Rémi Courson (R)

Ifremer, RDT, F-29280 Plouzané, France.

Morgan Delarue (M)

LAAS-CNRS, Université de Toulouse, CNRS, Toulouse, France. morgan.delarue@laas.fr.

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