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Human induced pluripotent stem cells (hiPSC), enveloped in elastin-like recombinamers for cell therapy of type 1 diabetes mellitus (T1D): preliminary data
Introduction: Therapeutic application and study of type 1 diabetes disease could benefit from the use of functional β islet-like cells derived from human induced pluripotent stem cells (hiPSCs). Considerable efforts have been made to develop increasingly effective hiPSC differentiation protocols, al...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166868/ https://www.ncbi.nlm.nih.gov/pubmed/37180045 http://dx.doi.org/10.3389/fbioe.2023.1046206 |
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author | Montanucci, Pia Pescara, Teresa Greco, Alessia Basta, Giuseppe Calafiore, Riccardo |
author_facet | Montanucci, Pia Pescara, Teresa Greco, Alessia Basta, Giuseppe Calafiore, Riccardo |
author_sort | Montanucci, Pia |
collection | PubMed |
description | Introduction: Therapeutic application and study of type 1 diabetes disease could benefit from the use of functional β islet-like cells derived from human induced pluripotent stem cells (hiPSCs). Considerable efforts have been made to develop increasingly effective hiPSC differentiation protocols, although critical issues related to cost, the percentage of differentiated cells that are obtained, and reproducibility remain open. In addition, transplantation of hiPSC would require immunoprotection within encapsulation devices, to make the construct invisible to the host’s immune system and consequently avoid the recipient’s general pharmacologic immunosuppression. Methods: For this work, a microencapsulation system based on the use of “human elastin-like recombinamers” (ELRs) was tested to envelop hiPSC. Special attention was devoted to in vitro and in vivo characterization of the hiPSCs upon coating with ERLs. Results and Discussion: We observed that ELRs coating did not interfere with viability and function and other biological properties of differentiated hiPSCs, while in vivo, ELRs seemed to afford immunoprotection to the cell grafts in preliminary in vivo study. The construct ability to correct hyperglycemia in vivo is in actual progress. |
format | Online Article Text |
id | pubmed-10166868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101668682023-05-10 Human induced pluripotent stem cells (hiPSC), enveloped in elastin-like recombinamers for cell therapy of type 1 diabetes mellitus (T1D): preliminary data Montanucci, Pia Pescara, Teresa Greco, Alessia Basta, Giuseppe Calafiore, Riccardo Front Bioeng Biotechnol Bioengineering and Biotechnology Introduction: Therapeutic application and study of type 1 diabetes disease could benefit from the use of functional β islet-like cells derived from human induced pluripotent stem cells (hiPSCs). Considerable efforts have been made to develop increasingly effective hiPSC differentiation protocols, although critical issues related to cost, the percentage of differentiated cells that are obtained, and reproducibility remain open. In addition, transplantation of hiPSC would require immunoprotection within encapsulation devices, to make the construct invisible to the host’s immune system and consequently avoid the recipient’s general pharmacologic immunosuppression. Methods: For this work, a microencapsulation system based on the use of “human elastin-like recombinamers” (ELRs) was tested to envelop hiPSC. Special attention was devoted to in vitro and in vivo characterization of the hiPSCs upon coating with ERLs. Results and Discussion: We observed that ELRs coating did not interfere with viability and function and other biological properties of differentiated hiPSCs, while in vivo, ELRs seemed to afford immunoprotection to the cell grafts in preliminary in vivo study. The construct ability to correct hyperglycemia in vivo is in actual progress. Frontiers Media S.A. 2023-04-25 /pmc/articles/PMC10166868/ /pubmed/37180045 http://dx.doi.org/10.3389/fbioe.2023.1046206 Text en Copyright © 2023 Montanucci, Pescara, Greco, Basta and Calafiore. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Montanucci, Pia Pescara, Teresa Greco, Alessia Basta, Giuseppe Calafiore, Riccardo Human induced pluripotent stem cells (hiPSC), enveloped in elastin-like recombinamers for cell therapy of type 1 diabetes mellitus (T1D): preliminary data |
title | Human induced pluripotent stem cells (hiPSC), enveloped in elastin-like recombinamers for cell therapy of type 1 diabetes mellitus (T1D): preliminary data |
title_full | Human induced pluripotent stem cells (hiPSC), enveloped in elastin-like recombinamers for cell therapy of type 1 diabetes mellitus (T1D): preliminary data |
title_fullStr | Human induced pluripotent stem cells (hiPSC), enveloped in elastin-like recombinamers for cell therapy of type 1 diabetes mellitus (T1D): preliminary data |
title_full_unstemmed | Human induced pluripotent stem cells (hiPSC), enveloped in elastin-like recombinamers for cell therapy of type 1 diabetes mellitus (T1D): preliminary data |
title_short | Human induced pluripotent stem cells (hiPSC), enveloped in elastin-like recombinamers for cell therapy of type 1 diabetes mellitus (T1D): preliminary data |
title_sort | human induced pluripotent stem cells (hipsc), enveloped in elastin-like recombinamers for cell therapy of type 1 diabetes mellitus (t1d): preliminary data |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166868/ https://www.ncbi.nlm.nih.gov/pubmed/37180045 http://dx.doi.org/10.3389/fbioe.2023.1046206 |
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