4.7 Article

Generation of heart-forming organoids from human pluripotent stem cells

Journal

NATURE PROTOCOLS
Volume 16, Issue 12, Pages 5652-5672

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41596-021-00629-8

Keywords

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Funding

  1. German Research Foundation (DFG) [REBIRTH EXC 62/2, ZW64/4-1, ZW64/4-2, KFO311/ZW64/7-1]
  2. German Ministry for Education and Science (BMBF) [13N14086, 01EK1601A, 01EK1602A, 13XP5092B, 031L0249]
  3. Forderung aus Mitteln des Niedersachsischen Vorab [ZN3340]
  4. European Union H2020 project TECHNOBEAT [66724]
  5. Cortiss Stiftung

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The research demonstrates a feasible protocol for directing human pluripotent stem cell aggregates to differentiate into heart-forming organoids using chemical modulators of the WNT pathway. This protocol, involving preculture and chemical induction steps, efficiently generates HFOs, offering a new tool for cell studies and drug development.
Human pluripotent stem cell aggregates are formed, embedded in Matrigel and directed to differentiate to heart-forming organoids by the chemical WNT pathway modulators CHIR99021 and IWP2. Heart-forming organoids (HFOs) derived from human pluripotent stem cells (hPSCs) are a complex, highly structured in vitro model of early heart, foregut and vasculature development. The model represents a potent tool for various applications, including teratogenicity studies, gene function analysis and drug discovery. Here, we provide a detailed protocol describing how to form HFOs within 14 d. In an initial 4 d preculture period, hPSC aggregates are individually formed in a 96-well format and then Matrigel-embedded. Subsequently, the chemical WNT pathway modulators CHIR99021 and IWP2 are applied, inducing directed differentiation. This highly robust protocol can be used on many different hPSC lines and be combined with manipulation technologies such as gene targeting and drug testing. HFO formation can be assessed by numerous complementary methods, ranging from various imaging approaches to gene expression studies. Here, we highlight the flow cytometry-based analysis of individual HFOs, enabling the quantitative monitoring of lineage formation.

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