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Supervised morphogenesis in gastruloidsbroad

SUMO · Horizon Europe grant · 2022-11-01–2027-10-31

EC contribution

€3,337,725

Total cost

€3,438,218

Beneficiaries

8
About the data

Source: CORDIS (official EU open data), Horizon Europe. Framework HORIZON · call HORIZON-EIC-2021-PATHFINDERCHALLENGES-01 · scheme HORIZON-EIC · topic HORIZON-EIC-2021-PATHFINDERCHALLENGES-01-05. CORDIS record →

Objective

The lack of realistic in vitro organ models that can faithfully represent in vivo physiological processes is a major obstacle affecting the biological and medical sciences. The current gold standard is animal experiments, but it is increasingly clear that these models mostly fail to recapitulate the human physiology. Moreover, animal experiments are controversial, and it is a common goal in the scientific community to minimize the use of animals to a strictly necessary minimum. The emergence of stem cell engineered organ models called organoids represents the only viable alternative to animal research. However, current organoid technology is yet to produce the larger physiologically relevant organmodels that the medical sciences really need. Specifically, current organoids are too small, not vascularized and lack the 3-dimensional organization found in vivo. In this interdisciplinary project we aim to challenge all these limitations by using the recently developed gastruloid technology guided by cutting edge bioengineering and artificial intelligence. Gastruloids are formed by initiating the very early developmental processes and develops along a highly coordinated three axial process that closely resembles mammalian embryogenesis. Moreover, gastruloids can develop several organ precursors simultaneously and thus constitutes important improvements over conventional single-tissue organoids. To harvest the potential of gastruloid technology we will first implement large sequencing and imaging experiments to optimize the developmental trajectory of gastruloids for organ inductions. We will then build these datasets into a multimodal data matrix to identify gastruloid candidates for cardiovascular and foregut development. Specifically, we will identify candidates that show strong vasculogenesis as candidates for later vascularisation by anastomose with endothelial cells.

Beneficiaries (8)

OrganisationCountryRoleEC contributionSME
OSLO UNIVERSITETSSYKEHUS HF NO coordinator €1,633,547
MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV DE participant €1,001,455
TEL AVIV UNIVERSITY IL participant €611,532
FORSCHUNGSVERBUND BERLIN EV DE participant €91,191
UNIVERSITETET I OSLO NO thirdParty €0
THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD UK associatedPartner
UNIVERSITY OF GLASGOW UK associatedPartner
IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE UK associatedPartner

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