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Standardized GMP-compliant scalable production of human pancreas organoids

BACKGROUND: Organoids are three-dimensional in vitro-grown cell clusters that recapitulate key features of native organs. In regenerative medicine, organoid technology represents a promising approach for the replacement of severely damaged organs, such as the pancreas in patients with type 1 diabete...

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Autores principales: Dossena, Marta, Piras, Roberta, Cherubini, Alessandro, Barilani, Mario, Dugnani, Erica, Salanitro, Francesca, Moreth, Till, Pampaloni, Francesco, Piemonti, Lorenzo, Lazzari, Lorenza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7055108/
https://www.ncbi.nlm.nih.gov/pubmed/32127043
http://dx.doi.org/10.1186/s13287-020-1585-2
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author Dossena, Marta
Piras, Roberta
Cherubini, Alessandro
Barilani, Mario
Dugnani, Erica
Salanitro, Francesca
Moreth, Till
Pampaloni, Francesco
Piemonti, Lorenzo
Lazzari, Lorenza
author_facet Dossena, Marta
Piras, Roberta
Cherubini, Alessandro
Barilani, Mario
Dugnani, Erica
Salanitro, Francesca
Moreth, Till
Pampaloni, Francesco
Piemonti, Lorenzo
Lazzari, Lorenza
author_sort Dossena, Marta
collection PubMed
description BACKGROUND: Organoids are three-dimensional in vitro-grown cell clusters that recapitulate key features of native organs. In regenerative medicine, organoid technology represents a promising approach for the replacement of severely damaged organs, such as the pancreas in patients with type 1 diabetes. Isolation human pancreas organoids (hPOs) in chemically defined serum-free culture media would be a major milestone for this approach. METHODS: Starting from discarded pancreatic tissues, we developed a large-scale process for obtaining clinically relevant quantities of undifferentiated organoids, obviating enzymatic digestion and operator-dependent pancreatic ducts picking steps. hPO identity was characterized by molecular and flow cytometry analysis. RESULTS: This work demonstrates that it is possible to obtain a large-scale production of organoids. We introduced some innovations in the isolation, expansion, and freezing of hPOs from five donors. First of all, the choice of the starting material (islet-depleted pancreas) that allows obtaining a high quantity of hPOs at low passages. On the other hand, we introduced mechanical dissociation and we eliminated the picking step to exclude the operator-depending steps, without affecting the success of the culture (100% success rate). Another important improvement was to replace R-spondin-1 (Rspo1) conditioned medium with Rspo1 recombinant molecule to obtain a well-defined composition of the expansion medium. Finally, we implemented a GMP-compliant freezing protocol. hPOs showed exponential growth with diameter and area that increased three- and eight-fold in 7 days, respectively. Immunophenotypic profile and gene expression analysis revealed that hPOs were composed of ductal (82.33 ± 8.37%), acinar (2.80 ± 1.25%) cells, and pancreatic progenitors (5.81 ± 2.65%). CONCLUSION: This work represents a milestone for a GMP-compliance hPO production and, ultimately, their clinical application as a type 1 diabetes therapy.
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spelling pubmed-70551082020-03-10 Standardized GMP-compliant scalable production of human pancreas organoids Dossena, Marta Piras, Roberta Cherubini, Alessandro Barilani, Mario Dugnani, Erica Salanitro, Francesca Moreth, Till Pampaloni, Francesco Piemonti, Lorenzo Lazzari, Lorenza Stem Cell Res Ther Research BACKGROUND: Organoids are three-dimensional in vitro-grown cell clusters that recapitulate key features of native organs. In regenerative medicine, organoid technology represents a promising approach for the replacement of severely damaged organs, such as the pancreas in patients with type 1 diabetes. Isolation human pancreas organoids (hPOs) in chemically defined serum-free culture media would be a major milestone for this approach. METHODS: Starting from discarded pancreatic tissues, we developed a large-scale process for obtaining clinically relevant quantities of undifferentiated organoids, obviating enzymatic digestion and operator-dependent pancreatic ducts picking steps. hPO identity was characterized by molecular and flow cytometry analysis. RESULTS: This work demonstrates that it is possible to obtain a large-scale production of organoids. We introduced some innovations in the isolation, expansion, and freezing of hPOs from five donors. First of all, the choice of the starting material (islet-depleted pancreas) that allows obtaining a high quantity of hPOs at low passages. On the other hand, we introduced mechanical dissociation and we eliminated the picking step to exclude the operator-depending steps, without affecting the success of the culture (100% success rate). Another important improvement was to replace R-spondin-1 (Rspo1) conditioned medium with Rspo1 recombinant molecule to obtain a well-defined composition of the expansion medium. Finally, we implemented a GMP-compliant freezing protocol. hPOs showed exponential growth with diameter and area that increased three- and eight-fold in 7 days, respectively. Immunophenotypic profile and gene expression analysis revealed that hPOs were composed of ductal (82.33 ± 8.37%), acinar (2.80 ± 1.25%) cells, and pancreatic progenitors (5.81 ± 2.65%). CONCLUSION: This work represents a milestone for a GMP-compliance hPO production and, ultimately, their clinical application as a type 1 diabetes therapy. BioMed Central 2020-03-04 /pmc/articles/PMC7055108/ /pubmed/32127043 http://dx.doi.org/10.1186/s13287-020-1585-2 Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Dossena, Marta
Piras, Roberta
Cherubini, Alessandro
Barilani, Mario
Dugnani, Erica
Salanitro, Francesca
Moreth, Till
Pampaloni, Francesco
Piemonti, Lorenzo
Lazzari, Lorenza
Standardized GMP-compliant scalable production of human pancreas organoids
title Standardized GMP-compliant scalable production of human pancreas organoids
title_full Standardized GMP-compliant scalable production of human pancreas organoids
title_fullStr Standardized GMP-compliant scalable production of human pancreas organoids
title_full_unstemmed Standardized GMP-compliant scalable production of human pancreas organoids
title_short Standardized GMP-compliant scalable production of human pancreas organoids
title_sort standardized gmp-compliant scalable production of human pancreas organoids
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7055108/
https://www.ncbi.nlm.nih.gov/pubmed/32127043
http://dx.doi.org/10.1186/s13287-020-1585-2
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