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Overcoming the Limitations of Stem Cell-Derived Beta Cells
Great advances in type 1 diabetes (T1D) and type 2 diabetes (T2D) treatment have been made to this day. However, modern diabetes therapy based on insulin injections and cadaveric islets transplantation has many disadvantages. That is why researchers are developing new methods to regenerate the pancr...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9221417/ https://www.ncbi.nlm.nih.gov/pubmed/35740935 http://dx.doi.org/10.3390/biom12060810 |
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author | Karimova, Mariana V. Gvazava, Inessa G. Vorotelyak, Ekaterina A. |
author_facet | Karimova, Mariana V. Gvazava, Inessa G. Vorotelyak, Ekaterina A. |
author_sort | Karimova, Mariana V. |
collection | PubMed |
description | Great advances in type 1 diabetes (T1D) and type 2 diabetes (T2D) treatment have been made to this day. However, modern diabetes therapy based on insulin injections and cadaveric islets transplantation has many disadvantages. That is why researchers are developing new methods to regenerate the pancreatic hormone-producing cells in vitro. The most promising approach is the generation of stem cell-derived beta cells that could provide an unlimited source of insulin-secreting cells. Recent studies provide methods to produce beta-like cell clusters that display glucose-stimulated insulin secretion—one of the key characteristics of the beta cell. However, in comparison with native beta cells, stem cell-derived beta cells do not undergo full functional maturation. In this paper we review the development and current state of various protocols, consider advantages, and propose ways to improve them. We examine molecular pathways, epigenetic modifications, intracellular components, and the microenvironment as a possible leverage to promote beta cell functional maturation. A possibility to create islet organoids from stem cell-derived components, as well as their encapsulation and further transplantation, is also examined. We try to combine modern research on beta cells and their crosstalk to create a holistic overview of developing insulin-secreting systems. |
format | Online Article Text |
id | pubmed-9221417 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-92214172022-06-24 Overcoming the Limitations of Stem Cell-Derived Beta Cells Karimova, Mariana V. Gvazava, Inessa G. Vorotelyak, Ekaterina A. Biomolecules Review Great advances in type 1 diabetes (T1D) and type 2 diabetes (T2D) treatment have been made to this day. However, modern diabetes therapy based on insulin injections and cadaveric islets transplantation has many disadvantages. That is why researchers are developing new methods to regenerate the pancreatic hormone-producing cells in vitro. The most promising approach is the generation of stem cell-derived beta cells that could provide an unlimited source of insulin-secreting cells. Recent studies provide methods to produce beta-like cell clusters that display glucose-stimulated insulin secretion—one of the key characteristics of the beta cell. However, in comparison with native beta cells, stem cell-derived beta cells do not undergo full functional maturation. In this paper we review the development and current state of various protocols, consider advantages, and propose ways to improve them. We examine molecular pathways, epigenetic modifications, intracellular components, and the microenvironment as a possible leverage to promote beta cell functional maturation. A possibility to create islet organoids from stem cell-derived components, as well as their encapsulation and further transplantation, is also examined. We try to combine modern research on beta cells and their crosstalk to create a holistic overview of developing insulin-secreting systems. MDPI 2022-06-09 /pmc/articles/PMC9221417/ /pubmed/35740935 http://dx.doi.org/10.3390/biom12060810 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Karimova, Mariana V. Gvazava, Inessa G. Vorotelyak, Ekaterina A. Overcoming the Limitations of Stem Cell-Derived Beta Cells |
title | Overcoming the Limitations of Stem Cell-Derived Beta Cells |
title_full | Overcoming the Limitations of Stem Cell-Derived Beta Cells |
title_fullStr | Overcoming the Limitations of Stem Cell-Derived Beta Cells |
title_full_unstemmed | Overcoming the Limitations of Stem Cell-Derived Beta Cells |
title_short | Overcoming the Limitations of Stem Cell-Derived Beta Cells |
title_sort | overcoming the limitations of stem cell-derived beta cells |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9221417/ https://www.ncbi.nlm.nih.gov/pubmed/35740935 http://dx.doi.org/10.3390/biom12060810 |
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