Induced Pluripotent Stem Cells in Disease Biology and the Evidence for Their In Vitro Utility.

gene regulation genetics human disease induced pluripotent stem cells organoids

Journal

Annual review of genetics
ISSN: 1545-2948
Titre abrégé: Annu Rev Genet
Pays: United States
ID NLM: 0117605

Informations de publication

Date de publication:
27 Nov 2023
Historique:
medline: 29 11 2023
pubmed: 14 9 2023
entrez: 14 9 2023
Statut: ppublish

Résumé

Many human phenotypes are impossible to recapitulate in model organisms or immortalized human cell lines. Induced pluripotent stem cells (iPSCs) offer a way to study disease mechanisms in a variety of differentiated cell types while circumventing ethical and practical issues associated with finite tissue sources and postmortem states. Here, we discuss the broad utility of iPSCs in genetic medicine and describe how they are being used to study musculoskeletal, pulmonary, neurologic, and cardiac phenotypes. We summarize the particular challenges presented by each organ system and describe how iPSC models are being used to address them. Finally, we discuss emerging iPSC-derived organoid models and the potential value that they can bring to studies of human disease.

Identifiants

pubmed: 37708421
doi: 10.1146/annurev-genet-022123-090319
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

341-360

Auteurs

Ayodeji Adegunsoye (A)

Genetics, Genomics, and Systems Biology, Section of Pulmonary and Critical Care, and the Department of Medicine, University of Chicago, Chicago, Illinois, USA; email: deji@uchicago.edu.

Natalia M Gonzales (NM)

Section of Genetic Medicine, Department of Medicine, University of Chicago, Chicago, Illinois, USA; email: ngon@uchicago.edu, gilad@uchicago.edu.

Yoav Gilad (Y)

Section of Genetic Medicine, Department of Medicine, University of Chicago, Chicago, Illinois, USA; email: ngon@uchicago.edu, gilad@uchicago.edu.
Department of Human Genetics, University of Chicago, Chicago, Illinois, USA.

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Classifications MeSH