Fluid shear stress enhances differentiation of jejunal human enteroids in Intestine-Chip.


Journal

American journal of physiology. Gastrointestinal and liver physiology
ISSN: 1522-1547
Titre abrégé: Am J Physiol Gastrointest Liver Physiol
Pays: United States
ID NLM: 100901227

Informations de publication

Date de publication:
01 03 2021
Historique:
pubmed: 20 10 2020
medline: 25 12 2021
entrez: 19 10 2020
Statut: ppublish

Résumé

There is increasing evidence that the study of normal human enteroids duplicates many known aspects of human intestinal physiology. However, this epithelial cell-only model lacks the many nonepithelial intestinal cells present in the gastrointestinal tract and exposure to the mechanical forces to which the intestine is exposed. We tested the hypothesis that physical shear forces produced by luminal and blood flow would provide an intestinal model more closely resembling normal human jejunum. Jejunal enteroid monolayers were studied in the Emulate, Inc. Intestine-Chip under conditions of constant luminal and basolateral flow that was designed to mimic normal intestinal fluid flow, with human umbilical vein endothelial cells (HUVECs) on the basolateral surface and with Wnt3A, R-spondin, and Noggin only on the luminal surface. The jejunal enteroids formed monolayers that remained confluent for 6-8 days, began differentiating at least as early as

Identifiants

pubmed: 33074011
doi: 10.1152/ajpgi.00282.2020
pmc: PMC8202237
doi:

Substances chimiques

Carrier Proteins 0
Lithostathine 0
REG1A protein, human 0
SLC12A2 protein, human 0
Solute Carrier Family 12, Member 2 0
Thrombospondins 0
WNT3A protein, human 0
Wnt3A Protein 0
noggin protein 148294-77-3

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

G258-G271

Subventions

Organisme : NIDDK NIH HHS
ID : U24 DK085532
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK085532
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK116352
Pays : United States
Organisme : NCATS NIH HHS
ID : U18 TR000552
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK089502
Pays : United States

Auteurs

Jianyi Yin (J)

Department of Medicine, Division of Gastroenterology and Hepatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Laxmi Sunuwar (L)

Department of Medicine, Division of Gastroenterology and Hepatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Magdalena Kasendra (M)

Emulate, Inc., Boston, Massachusetts.

Huimin Yu (H)

Department of Medicine, Division of Gastroenterology and Hepatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Chung-Ming Tse (CM)

Department of Medicine, Division of Gastroenterology and Hepatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.

C Conover Talbot (CC)

Institute for Basic Biomedical Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Tatiana Boronina (T)

Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Robert Cole (R)

Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Katia Karalis (K)

Emulate, Inc., Boston, Massachusetts.
Biomedical Sciences Research Center (BSRC) Alexander Fleming, Vari, Greece.
Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Mark Donowitz (M)

Department of Medicine, Division of Gastroenterology and Hepatology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland.

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Classifications MeSH