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Insulin-producing organoids engineered from islet and amniotic epithelial cells to treat diabetes
Open accessAbstract
Maintaining long-term euglycemia after intraportal islet transplantation is hampered by the considerable islet loss in the peri-transplant period attributed to inflammation, ischemia and poor angiogenesis. Here, we show that viable and functional islet organoids can be successfully generated from dissociated islet cells (ICs) and human amniotic epithelial cells (hAECs). Incorporation of hAECs into islet organoids markedly enhances engraftment, viability and graft function in a mouse type 1 diabetes model. Our results demonstrate that the integration of hAECs into islet cell organoids has great potential in the development of cell-based therapies for type 1 diabetes. Engineering of functional mini-organs using this strategy will allow the exploration of more favorable implantation sites, and can be expanded to unlimited (stem-cell-derived or xenogeneic) sources of insulin-producing cells.
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“Transplanting islets with either human umbilical cord perivascular cells156 or amniotic epithelial cells157 also improved islet engraftment and vascularization.”
From Developments in stem cell-derived islet replacement therapy for treating type 1 diabetes (2023) · cites this paper as [157]
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Metadata
- Authors
- Lebreton, F., Lavallard, V., Bellofatto, K., Bonnet, R., Wassmer, C. H., Perez, L., Kalandadze, V., Follenzi, A., Boulvain, M., Kerr-Conte, J., Goodman, D. J., Bosco, D., Berney, T., & Berishvili, E.
- Affiliations
- University of Geneva (CH)
- Università degli Studi del Piemonte Orientale “Amedeo Avogadro” (IT)
- Inserm (FR)
- St Vincent's Hospital Melbourne (AU)
- Corresponding author
- Berishvili, Ekaterine
- ORCID
- Venue
- Nature Communications
- Published
- 2019-10-03
- Volume
- 10
- Issue
- 1
- Pages
- 4491-4491
- ISSN
- 2041-1723 (ISSN-L)
- PMC
- PMC6776618
- OpenAlex
- W2979290450
- Cited by
- 157
- References
- 49
- Citations by year
- 2026: 10 · 2025: 22 · 2024: 19 · 2023: 17 · 2022: 39 · 2021: 21 · 2020: 29
- FWCI
- 21.24
- Type
- journal article
- Language
- en
- Update notices
- correction (2020-10-09)
- Open access
- gold
- doi.org
- Locations
- Nature Communications (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Archive ouverte UNIGE (University of Geneva) (publishedVersion, other-oa)
- Minerva Access (University of Melbourne) (submittedVersion, cc-by)
- HAL (submittedVersion, cc-by)
- RePEc: Research Papers in Economics (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- LillOA (Université de Lille (University Of Lille)) (submittedVersion)
- Archive ouverte UNIGE (University of Geneva) (submittedVersion, cc-by)
- VUBIR (Vrije Universiteit Brussel) (submittedVersion)
- Funders
- National Science Foundation
- European Foundation for the Study of Diabetes
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (173138, 310030)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Pancreatic function and diabetes
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Diabetes and associated disorders
- Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
- Keywords
- islet organoids, amniotic epithelial cells, type 1 diabetes, islet transplantation, cell therapy, insulin-producing cells, stem cell-derived islets
- MeSH terms
- Amnion, Animals, Cell Survival, Diabetes Mellitus, Experimental, Diabetes Mellitus, Type 1, Epithelial Cells, Graft Survival, Humans, Insulin, Islets of Langerhans, Organoids, Streptozocin, Transplantation, Heterologous, Islets of Langerhans Transplantation, Mice, SCID, Rats, Sprague-Dawley, Spheroids, Cellular, Tissue Engineering, Regenerative Medicine, Tissue Culture Techniques, Mice, Rats, Heterografts
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