Automated production of cardiac organoids
Keywords
organoid,cardiac organoid,mini organ
Challenge
In vitro produced organoids are 3D-cellular aggregates, which are obtained from human pluripotent stem cells (PSC) and are often referred to as “mini organs”. According to their exceptional ability to resemble organ development, organoids have been used in various pharmacological studies. Unfortunately, all recent approaches to mimic the human embryonic heart failed and genuine cardiac organoids still do not exist. Thus, there is a strong need for (automated) production of cardiac organoids as an efficient tool in pharmacological research as well as in organ-specific lab-on-a-chip approaches.
Technology
The herewith presented technology comprises an approach for automated production of genuine cardiac organoids from human PSC to overcome the aforementioned limitations. The novel approach leads to the highly reproducible, screening platform-compatible generation of cardiac organoids in tissue culture, which contain all heart layers in an organized 3D pattern. Of particular importance, in depth analysis revealed that all cell types expected for the generation of the human heart are present in the novel cardiac organoids, including the formation of foregut endoderm and endothelial networks. As a consequence, cardiac organoids can be perfectly used as an in vitro model for drug screening on both differentiated organoids and during their development, e.g. in teratogenicity assays and safety pharmacology. Furthermore, the novel cardiac organoids have a significant value for organ-specific lab-on-a-chip approaches, e.g. in combination with genetic disease modeling e.g. by using patient-specific hiPSC lines and directed gene targeting.
Commercial Opportunity
In-licensing or collaboration for further development is possible.
Development Status
Well-established protocol for in vitro production of cardiac organoids. First teratogenicity test assays performed.
Patent Situation
Patent has been granted in Europe (EP 3765599B1, national validation in DE, CH, FR and GB) with priority of 2018.
Patent applications in US, CA and CN (based on PCT/EP2019/054225) with priority of 2018 are pending. Further EP patent application with priority of 2022 is pending.
Further Reading
Drakhlis L, Zweigerdt R et al. 2021. Human heart-forming organoids recapitulate early heart and foregut development. Nat Biotechnol. 2021 Jun;39(6):737-746. doi: 10.1038/s41587-021-00815-9. Epub 2021 Feb 8. Erratum in: Nat Biotechnol. 2021 May 20;: PMID: 33558697; PMCID: PMC8192303.
Drakhlis L, Devadas SB, Zweigerdt R. 2021. Generation of heart-forming organoids from human pluripotent stem cells. Nat Protoc. doi:10.1038/s41596-021-00629-8.
Kempf, H; Olmer, R; Haase, A; Franke, A; Bolesani, E; Schwanke, K; Robles-Diaz, D; Coffee, M; Göhring, G; Dräger, G; Pötz, O; Joos, T; Martinez-Hackert, E; Haverich, A; Buettner, F; Martin, U; Zweigerdt, R. Bulk cell density and Wnt/TGFbeta signalling regulate mesendodermal patterning of human pluripotent stem cells. Nat Commun7, 13602, (2016).
Halloin, C; Schwanke, K; Löbel, W; Franke, A; Szepes, M; Biswanath, S; Wunderlich, S; Merkert, S; Weber, N; Osten, F; de la Roche, J; Polten, F; Wollert, K; Kraft, T; Fischer, M; Martin, U; Gruh, I; Kempf, H; Zweigerdt, R. Continuous WNT Control Enables Advanced hPSC Cardiac Processing and Prognostic Surface Marker Identification in Chemically Defined Suspension Culture. Stem Cell Reports13 (2), (2019).