Use of organoids to study regenerative responses to intestinal damage.


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 12 2019
Historique:
pubmed: 8 10 2019
medline: 9 4 2020
entrez: 8 10 2019
Statut: ppublish

Résumé

Intestinal organoid cultures provide an in vitro model system for studying pathways and mechanisms involved in epithelial damage and repair. Derived from either embryonic or induced pluripotent stem cells or adult intestinal stem cells or tissues, these self-organizing, multicellular structures contain polarized mature cells that recapitulate both the physiology and heterogeneity of the intestinal epithelium. These cultures provide a cutting-edge technology for defining regenerative pathways that are induced following radiation or chemical damage, which directly target the cycling intestinal stem cell, or damage resulting from viral, bacterial, or parasitic infection of the epithelium. Novel signaling pathways or biological mechanisms identified from organoid studies that mediate regeneration of the epithelium following damage are likely to be important targets of preventive or therapeutic modalities to mitigate intestinal injury. The evolution of these cultures to include more components of the intestinal wall and the ability to genetically modify them are key components for defining the mechanisms that modulate epithelial regeneration.

Identifiants

pubmed: 31589468
doi: 10.1152/ajpgi.00346.2018
pmc: PMC7132322
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

G845-G852

Subventions

Organisme : NIDDK NIH HHS
ID : R24 DK099803
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK103117
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK089502
Pays : United States
Organisme : NIDDK NIH HHS
ID : U24 DK085532
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK118904
Pays : United States
Organisme : NIAID NIH HHS
ID : U19 AI116497
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK085532
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK103168
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK056338
Pays : United States

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Auteurs

Sarah E Blutt (SE)

Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas.

Ophir D Klein (OD)

Department of Orofacial Sciences and Program in Craniofacial Biology, University of California, San Francisco, California.
Department of Pediatrics and Institute for Human Genetics, University of California, San Francisco, California.

Mark Donowitz (M)

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

Noah Shroyer (N)

Department of Medicine, Divisions of Gastroenterology and Hepatology and Infectious Diseases, Baylor College of Medicine, Houston, Texas.

Chandan Guha (C)

Department of Radiation Oncology, Albert Einstein, Bronx, New York.

Mary K Estes (MK)

Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas.
Department of Medicine, Divisions of Gastroenterology and Hepatology and Infectious Diseases, Baylor College of Medicine, Houston, Texas.

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Classifications MeSH