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Possibility of adiponectin use to improve islet transplantation outcomes
Although islet transplantation (ITx) is a promising therapy for severe diabetes mellitus, further advancements are necessary. Adiponectin, an adipokine that regulates lipid and glucose metabolism, exerts favorable effects on islets, such as reinforcement of the insulin-releasing function. This study...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748684/ https://www.ncbi.nlm.nih.gov/pubmed/35013505 http://dx.doi.org/10.1038/s41598-021-04245-0 |
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author | Sakata, Naoaki Yoshimatsu, Gumpei Chinen, Kiyoshi Kawakami, Ryo Kodama, Shohta |
author_facet | Sakata, Naoaki Yoshimatsu, Gumpei Chinen, Kiyoshi Kawakami, Ryo Kodama, Shohta |
author_sort | Sakata, Naoaki |
collection | PubMed |
description | Although islet transplantation (ITx) is a promising therapy for severe diabetes mellitus, further advancements are necessary. Adiponectin, an adipokine that regulates lipid and glucose metabolism, exerts favorable effects on islets, such as reinforcement of the insulin-releasing function. This study evaluated the possibility of adiponectin use to improve ITx outcomes. We treated mouse islets with 10 µg/mL recombinant mouse adiponectin by overnight culture and then assessed the insulin-releasing, angiogenic, and adhesion functions of the islets. Furthermore, 80 syngeneic islet equivalents with or without adiponectin treatment were transplanted into the renal subcapsular space of diabetic mice. In in vitro assessment, released insulin at high glucose stimulation, insulin content, and expressions of vascular endothelial growth factor and integrin β1 were improved in adiponectin-treated islets. Furthermore, adiponectin treatment improved the therapeutic effect of ITx on blood glucose levels and promoted angiogenesis of the transplanted islets. However, the therapeutic effect was not pronounced in glucose tolerance test results. In conclusion, adiponectin treatment had preferable effects in the insulin-releasing, angiogenic, and adhesion functions of islets and contributed to the improvement of ITx. The future use of adiponectin treatment in clinical settings to improve ITx outcomes should be investigated. |
format | Online Article Text |
id | pubmed-8748684 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87486842022-01-11 Possibility of adiponectin use to improve islet transplantation outcomes Sakata, Naoaki Yoshimatsu, Gumpei Chinen, Kiyoshi Kawakami, Ryo Kodama, Shohta Sci Rep Article Although islet transplantation (ITx) is a promising therapy for severe diabetes mellitus, further advancements are necessary. Adiponectin, an adipokine that regulates lipid and glucose metabolism, exerts favorable effects on islets, such as reinforcement of the insulin-releasing function. This study evaluated the possibility of adiponectin use to improve ITx outcomes. We treated mouse islets with 10 µg/mL recombinant mouse adiponectin by overnight culture and then assessed the insulin-releasing, angiogenic, and adhesion functions of the islets. Furthermore, 80 syngeneic islet equivalents with or without adiponectin treatment were transplanted into the renal subcapsular space of diabetic mice. In in vitro assessment, released insulin at high glucose stimulation, insulin content, and expressions of vascular endothelial growth factor and integrin β1 were improved in adiponectin-treated islets. Furthermore, adiponectin treatment improved the therapeutic effect of ITx on blood glucose levels and promoted angiogenesis of the transplanted islets. However, the therapeutic effect was not pronounced in glucose tolerance test results. In conclusion, adiponectin treatment had preferable effects in the insulin-releasing, angiogenic, and adhesion functions of islets and contributed to the improvement of ITx. The future use of adiponectin treatment in clinical settings to improve ITx outcomes should be investigated. Nature Publishing Group UK 2022-01-10 /pmc/articles/PMC8748684/ /pubmed/35013505 http://dx.doi.org/10.1038/s41598-021-04245-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Sakata, Naoaki Yoshimatsu, Gumpei Chinen, Kiyoshi Kawakami, Ryo Kodama, Shohta Possibility of adiponectin use to improve islet transplantation outcomes |
title | Possibility of adiponectin use to improve islet transplantation outcomes |
title_full | Possibility of adiponectin use to improve islet transplantation outcomes |
title_fullStr | Possibility of adiponectin use to improve islet transplantation outcomes |
title_full_unstemmed | Possibility of adiponectin use to improve islet transplantation outcomes |
title_short | Possibility of adiponectin use to improve islet transplantation outcomes |
title_sort | possibility of adiponectin use to improve islet transplantation outcomes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748684/ https://www.ncbi.nlm.nih.gov/pubmed/35013505 http://dx.doi.org/10.1038/s41598-021-04245-0 |
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