Extracellular Matrix Mechanical Properties and Regulation of the Intestinal Stem Cells: When Mechanics Control Fate.


Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
07 12 2020
Historique:
received: 31 10 2020
revised: 01 12 2020
accepted: 04 12 2020
entrez: 10 12 2020
pubmed: 11 12 2020
medline: 9 7 2021
Statut: epublish

Résumé

Intestinal stem cells (ISC) are crucial players in colon epithelium physiology. The accurate control of their auto-renewal, proliferation and differentiation capacities provides a constant flow of regeneration, maintaining the epithelial intestinal barrier integrity. Under stress conditions, colon epithelium homeostasis in disrupted, evolving towards pathologies such as inflammatory bowel diseases or colorectal cancer. A specific environment, namely the ISC niche constituted by the surrounding mesenchymal stem cells, the factors they secrete and the extracellular matrix (ECM), tightly controls ISC homeostasis. Colon ECM exerts physical constraint on the enclosed stem cells through peculiar topography, stiffness and deformability. However, little is known on the molecular and cellular events involved in ECM regulation of the ISC phenotype and fate. To address this question, combining accurately reproduced colon ECM mechanical parameters to primary ISC cultures such as organoids is an appropriated approach. Here, we review colon ECM physical properties at physiological and pathological states and their bioengineered in vitro reproduction applications to ISC studies.

Identifiants

pubmed: 33297478
pii: cells9122629
doi: 10.3390/cells9122629
pmc: PMC7762382
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Lauriane Onfroy-Roy (L)

IRSD, Université de Toulouse, INSERM, INRA, ENVT, UPS, 31024 Toulouse, France.

Dimitri Hamel (D)

IRSD, Université de Toulouse, INSERM, INRA, ENVT, UPS, 31024 Toulouse, France.
LAAS-CNRS, Université de Toulouse, CNRS, 31400 Toulouse, France.

Julie Foncy (J)

LAAS-CNRS, Université de Toulouse, CNRS, 31400 Toulouse, France.

Laurent Malaquin (L)

LAAS-CNRS, Université de Toulouse, CNRS, 31400 Toulouse, France.

Audrey Ferrand (A)

IRSD, Université de Toulouse, INSERM, INRA, ENVT, UPS, 31024 Toulouse, France.

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