A Novel Human Epithelial Enteroid Model of Necrotizing Enterocolitis.


Journal

Journal of visualized experiments : JoVE
ISSN: 1940-087X
Titre abrégé: J Vis Exp
Pays: United States
ID NLM: 101313252

Informations de publication

Date de publication:
10 04 2019
Historique:
entrez: 30 4 2019
pubmed: 30 4 2019
medline: 20 3 2020
Statut: epublish

Résumé

Necrotizing enterocolitis (NEC) is a devastating disease of newborn infants. It is characterized by multiple pathophysiologic alterations in the human intestinal epithelium, leading to increased intestinal permeability, impaired restitution, and increased cell death. Although there are numerous animal models of NEC, response to injury and therapeutic interventions may be highly variable between species. Furthermore, it is ethically challenging to study disease pathophysiology or novel therapeutic agents directly in human subjects, especially children. Therefore, it is highly desirable to develop a novel model of NEC using human tissue. Enteroids are 3-dimensional organoids derived from intestinal epithelial cells. They are ideal for the study of complex physiologic interactions, cell signaling, and host-pathogen defense. In this manuscript we describe a protocol that cultures human enteroids after isolating intestinal stem cells from patients undergoing bowel resection. The crypt cells are cultured in media containing growth factors that encourage differentiation into the various cell types native of the human intestinal epithelium. These cells are grown in a synthetic, collagenous mix of proteins that serve as a scaffold, mimicking the extra-cellular basement membrane. As a result, enteroids develop apical-basolateral polarity. Co-administration of lipopolysaccharide (LPS) in media causes an inflammatory response in the enteroids, leading to histologic, genetic, and protein expression alterations similar to those seen in human NEC. An experimental model of NEC using human tissue may provide a more accurate platform for drug and treatment testing prior to human trials, as we strive to identify a cure for this disease.

Identifiants

pubmed: 31033943
doi: 10.3791/59194
pmc: PMC6814448
mid: NIHMS1055477
doi:

Substances chimiques

Lipopolysaccharides 0
Toll-Like Receptor 4 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIDDK NIH HHS
ID : K08 DK106450
Pays : United States
Organisme : NIDDK NIH HHS
ID : R03 DK117216
Pays : United States

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Auteurs

Guillermo J Ares (GJ)

Department of Pediatrics, Northwestern University.

Christie Buonpane (C)

Department of Pediatrics, Northwestern University.

Carrie Yuan (C)

Department of Pediatrics, Northwestern University.

Douglas Wood (D)

Department of Pediatrics, Northwestern University.

Catherine J Hunter (CJ)

Department of Pediatrics, Northwestern University; Division of Pediatric Surgery, Ann & Robert H. Lurie Children's Hospital of Chicago; CHunter@luriechildrens.org.

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Classifications MeSH