| Literature DB >> 31827102 |
Giovanni Giuseppe Giobbe1, Claire Crowley1, Camilla Luni2, Nicola Elvassore3,4,5, Paolo De Coppi6,7, Sara Campinoti1,8, Moustafa Khedr1, Kai Kretzschmar9, Martina Maria De Santis1, Elisa Zambaiti1, Federica Michielin1, Laween Meran1,10, Qianjiang Hu2, Gijs van Son9, Luca Urbani1, Anna Manfredi11, Monica Giomo12, Simon Eaton1, Davide Cacchiarelli11, Vivian S W Li10, Hans Clevers9,13, Paola Bonfanti1,8.
Abstract
Organoids have extensive therapeutic potential and are increasingly opening up new avenues within regenerative medicine. However, their clinical application is greatly limited by the lack of effective GMP-compliant systems for organoid expansion in culture. Here, we envisage that the use of extracellular matrix (ECM) hydrogels derived from decellularized tissues (DT) can provide an environment capable of directing cell growth. These gels possess the biochemical signature of tissue-specific ECM and have the potential for clinical translation. Gels from decellularized porcine small intestine (SI) mucosa/submucosa enable formation and growth of endoderm-derived human organoids, such as gastric, hepatic, pancreatic, and SI. ECM gels can be used as a tool for direct human organoid derivation, for cell growth with a stable transcriptomic signature, and for in vivo organoid delivery. The development of these ECM-derived hydrogels opens up the potential for human organoids to be used clinically.Entities:
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Year: 2019 PMID: 31827102 PMCID: PMC6906306 DOI: 10.1038/s41467-019-13605-4
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 17.694