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Exosomes; a Potential Source of Biomarkers, Therapy, and Cure for Type-1 Diabetes

The scourge of type-1 diabetes (T1D) is the morbidity and mortality it and its complications cause at a younger age. This propels the constant search for better diagnostic, treatment, and management strategies, with the ultimate quest being a cure for T1D. Recently, the therapeutic potential of exos...

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Detalles Bibliográficos
Autores principales: Lakey, Jonathan R. T., Wang, Yanmin, Alexander, Michael, Chan, Mike K. S., Wong, Michelle B. F., Casazza, Krista, Jenkins, Ian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10647572/
https://www.ncbi.nlm.nih.gov/pubmed/37958696
http://dx.doi.org/10.3390/ijms242115713
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author Lakey, Jonathan R. T.
Wang, Yanmin
Alexander, Michael
Chan, Mike K. S.
Wong, Michelle B. F.
Casazza, Krista
Jenkins, Ian
author_facet Lakey, Jonathan R. T.
Wang, Yanmin
Alexander, Michael
Chan, Mike K. S.
Wong, Michelle B. F.
Casazza, Krista
Jenkins, Ian
author_sort Lakey, Jonathan R. T.
collection PubMed
description The scourge of type-1 diabetes (T1D) is the morbidity and mortality it and its complications cause at a younger age. This propels the constant search for better diagnostic, treatment, and management strategies, with the ultimate quest being a cure for T1D. Recently, the therapeutic potential of exosomes has generated a lot of interest. Among the characteristics of exosomes of particular interest are (a) their regenerative capacity, which depends on their “origin”, and (b) their “content”, which determines the cell communication and crosstalk they influence. Other functional capacities, including paracrine and endocrine homeostatic regulation, pathogenic response ability resulting in insulin secretory defects or β-cell death under normal metabolic conditions, immunomodulation, and promotion of regeneration, have also garnered significant interest. Exosome “specificity” makes them suitable as biomarkers or predictors, and their “mobility” and “content” lend credence to drug delivery and therapeutic suitability. This review aims to highlight the functional capacities of exosomes and their established as well as novel contributions at various pathways in the onset and progression of T1D. The pathogenesis of T1D involves a complex crosstalk between insulin-secreting pancreatic β-cells and immune cells, which is partially mediated by exosomes. We also examine the potential implications for type 2 diabetes (T2D), as the link in T2D has guided T1D exploration. The collective landscape presented is expected to help identify how a deeper understanding of exosomes (and their cargo) can provide a framework for actionable solutions to prevent, halt, or change the very course of T1D and its complications.
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spelling pubmed-106475722023-10-28 Exosomes; a Potential Source of Biomarkers, Therapy, and Cure for Type-1 Diabetes Lakey, Jonathan R. T. Wang, Yanmin Alexander, Michael Chan, Mike K. S. Wong, Michelle B. F. Casazza, Krista Jenkins, Ian Int J Mol Sci Review The scourge of type-1 diabetes (T1D) is the morbidity and mortality it and its complications cause at a younger age. This propels the constant search for better diagnostic, treatment, and management strategies, with the ultimate quest being a cure for T1D. Recently, the therapeutic potential of exosomes has generated a lot of interest. Among the characteristics of exosomes of particular interest are (a) their regenerative capacity, which depends on their “origin”, and (b) their “content”, which determines the cell communication and crosstalk they influence. Other functional capacities, including paracrine and endocrine homeostatic regulation, pathogenic response ability resulting in insulin secretory defects or β-cell death under normal metabolic conditions, immunomodulation, and promotion of regeneration, have also garnered significant interest. Exosome “specificity” makes them suitable as biomarkers or predictors, and their “mobility” and “content” lend credence to drug delivery and therapeutic suitability. This review aims to highlight the functional capacities of exosomes and their established as well as novel contributions at various pathways in the onset and progression of T1D. The pathogenesis of T1D involves a complex crosstalk between insulin-secreting pancreatic β-cells and immune cells, which is partially mediated by exosomes. We also examine the potential implications for type 2 diabetes (T2D), as the link in T2D has guided T1D exploration. The collective landscape presented is expected to help identify how a deeper understanding of exosomes (and their cargo) can provide a framework for actionable solutions to prevent, halt, or change the very course of T1D and its complications. MDPI 2023-10-28 /pmc/articles/PMC10647572/ /pubmed/37958696 http://dx.doi.org/10.3390/ijms242115713 Text en © 2023 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
Lakey, Jonathan R. T.
Wang, Yanmin
Alexander, Michael
Chan, Mike K. S.
Wong, Michelle B. F.
Casazza, Krista
Jenkins, Ian
Exosomes; a Potential Source of Biomarkers, Therapy, and Cure for Type-1 Diabetes
title Exosomes; a Potential Source of Biomarkers, Therapy, and Cure for Type-1 Diabetes
title_full Exosomes; a Potential Source of Biomarkers, Therapy, and Cure for Type-1 Diabetes
title_fullStr Exosomes; a Potential Source of Biomarkers, Therapy, and Cure for Type-1 Diabetes
title_full_unstemmed Exosomes; a Potential Source of Biomarkers, Therapy, and Cure for Type-1 Diabetes
title_short Exosomes; a Potential Source of Biomarkers, Therapy, and Cure for Type-1 Diabetes
title_sort exosomes; a potential source of biomarkers, therapy, and cure for type-1 diabetes
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10647572/
https://www.ncbi.nlm.nih.gov/pubmed/37958696
http://dx.doi.org/10.3390/ijms242115713
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