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Differentiating functional human islet-like aggregates from pluripotent stem cells.
Barsby, Tom; Ibrahim, Hazem; Lithovius, Väinö; Montaser, Hossam; Balboa, Diego; Vähäkangas, Eliisa; Chandra, Vikash; Saarimäki-Vire, Jonna; Otonkoski, Timo.
Afiliação
  • Barsby T; Stem Cells and Metabolism Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland. Electronic address: tom.barsby@helsinki.fi.
  • Ibrahim H; Stem Cells and Metabolism Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
  • Lithovius V; Stem Cells and Metabolism Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
  • Montaser H; Stem Cells and Metabolism Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
  • Balboa D; Stem Cells and Metabolism Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland; Bioinformatics and Genomics Program, Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.
  • Vähäkangas E; Stem Cells and Metabolism Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
  • Chandra V; Stem Cells and Metabolism Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
  • Saarimäki-Vire J; Stem Cells and Metabolism Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
  • Otonkoski T; Stem Cells and Metabolism Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland; Department of Pediatrics, Helsinki University Hospital and University of Helsinki, Helsinki, Finland. Electronic address: timo.otonkoski@helsinki.fi.
STAR Protoc ; 3(4): 101711, 2022 12 16.
Article em En | MEDLINE | ID: mdl-36136756
ABSTRACT
We present here a robust and reliable protocol by which to differentiate pancreatic islet-like aggregates (SC-islets) from human pluripotent stem cells. The 7-stage protocol mimics developmental patterning factors that induce endocrine lineage formation and spans monolayer, microwell, and aggregate suspension culture. The SC-islets demonstrate dynamic glucose-sensitive insulin secretion and an endocrine cell composition similar to those of primary human islets. SC-islets generated using this optimized protocol are suitable for in vitro modeling of islet cell pathophysiology and therapeutic applications. For complete details on the use and execution of this protocol, please refer to Balboa et al. (2022).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ilhotas Pancreáticas / Células-Tronco Pluripotentes Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ilhotas Pancreáticas / Células-Tronco Pluripotentes Idioma: En Ano de publicação: 2022 Tipo de documento: Article