Cargando…
Plasma-derived exosome characterization reveals a distinct microRNA signature in long duration Type 1 diabetes
Type 1 diabetes mellitus (T1DM) results from an autoimmune attack against the insulin-producing ß cells which leads to chronic hyperglycemia. Exosomes are lipid vesicles derived from cellular multivesicular bodies that are enriched in specific miRNAs, potentially providing a disease-specific diagnos...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5519761/ https://www.ncbi.nlm.nih.gov/pubmed/28729721 http://dx.doi.org/10.1038/s41598-017-05787-y |
_version_ | 1783251689013248000 |
---|---|
author | Garcia-Contreras, Marta Shah, Sanket H. Tamayo, Alejandro Robbins, Paul D. Golberg, Ronald B. Mendez, Armando J. Ricordi, Camillo |
author_facet | Garcia-Contreras, Marta Shah, Sanket H. Tamayo, Alejandro Robbins, Paul D. Golberg, Ronald B. Mendez, Armando J. Ricordi, Camillo |
author_sort | Garcia-Contreras, Marta |
collection | PubMed |
description | Type 1 diabetes mellitus (T1DM) results from an autoimmune attack against the insulin-producing ß cells which leads to chronic hyperglycemia. Exosomes are lipid vesicles derived from cellular multivesicular bodies that are enriched in specific miRNAs, potentially providing a disease-specific diagnostic signature. To assess the value of exosome miRNAs as biomarkers for T1DM, miRNA expression in plasma-derived exosomes was measured. Nanoparticle tracking analysis and transmission electron microscopy confirmed the presence of plasma-derived exosomes (EXOs) isolated by differential centrifugation. Total RNA extracted from plasma-derived EXOs of 12 T1DM and 12 control subjects was hybridized onto Nanostring human v2 miRNA microarray array and expression data were analyzed on nSolver analysis software. We found 7 different miRNAs (1 up-regulated and 6 down-regulated), that were differentially expressed in T1DM. The selected candidate miRNAs were validated by qRT-PCR analysis of cohorts of 24 T1DM and 24 control subjects. Most of the deregulated miRNAs are involved in progression of T1DM. These findings highlight the potential of EXOs miRNA profiling in the diagnosis as well as new insights into the molecular mechanisms involved in T1DM. |
format | Online Article Text |
id | pubmed-5519761 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55197612017-07-26 Plasma-derived exosome characterization reveals a distinct microRNA signature in long duration Type 1 diabetes Garcia-Contreras, Marta Shah, Sanket H. Tamayo, Alejandro Robbins, Paul D. Golberg, Ronald B. Mendez, Armando J. Ricordi, Camillo Sci Rep Article Type 1 diabetes mellitus (T1DM) results from an autoimmune attack against the insulin-producing ß cells which leads to chronic hyperglycemia. Exosomes are lipid vesicles derived from cellular multivesicular bodies that are enriched in specific miRNAs, potentially providing a disease-specific diagnostic signature. To assess the value of exosome miRNAs as biomarkers for T1DM, miRNA expression in plasma-derived exosomes was measured. Nanoparticle tracking analysis and transmission electron microscopy confirmed the presence of plasma-derived exosomes (EXOs) isolated by differential centrifugation. Total RNA extracted from plasma-derived EXOs of 12 T1DM and 12 control subjects was hybridized onto Nanostring human v2 miRNA microarray array and expression data were analyzed on nSolver analysis software. We found 7 different miRNAs (1 up-regulated and 6 down-regulated), that were differentially expressed in T1DM. The selected candidate miRNAs were validated by qRT-PCR analysis of cohorts of 24 T1DM and 24 control subjects. Most of the deregulated miRNAs are involved in progression of T1DM. These findings highlight the potential of EXOs miRNA profiling in the diagnosis as well as new insights into the molecular mechanisms involved in T1DM. Nature Publishing Group UK 2017-07-20 /pmc/articles/PMC5519761/ /pubmed/28729721 http://dx.doi.org/10.1038/s41598-017-05787-y Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Garcia-Contreras, Marta Shah, Sanket H. Tamayo, Alejandro Robbins, Paul D. Golberg, Ronald B. Mendez, Armando J. Ricordi, Camillo Plasma-derived exosome characterization reveals a distinct microRNA signature in long duration Type 1 diabetes |
title | Plasma-derived exosome characterization reveals a distinct microRNA signature in long duration Type 1 diabetes |
title_full | Plasma-derived exosome characterization reveals a distinct microRNA signature in long duration Type 1 diabetes |
title_fullStr | Plasma-derived exosome characterization reveals a distinct microRNA signature in long duration Type 1 diabetes |
title_full_unstemmed | Plasma-derived exosome characterization reveals a distinct microRNA signature in long duration Type 1 diabetes |
title_short | Plasma-derived exosome characterization reveals a distinct microRNA signature in long duration Type 1 diabetes |
title_sort | plasma-derived exosome characterization reveals a distinct microrna signature in long duration type 1 diabetes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5519761/ https://www.ncbi.nlm.nih.gov/pubmed/28729721 http://dx.doi.org/10.1038/s41598-017-05787-y |
work_keys_str_mv | AT garciacontrerasmarta plasmaderivedexosomecharacterizationrevealsadistinctmicrornasignatureinlongdurationtype1diabetes AT shahsanketh plasmaderivedexosomecharacterizationrevealsadistinctmicrornasignatureinlongdurationtype1diabetes AT tamayoalejandro plasmaderivedexosomecharacterizationrevealsadistinctmicrornasignatureinlongdurationtype1diabetes AT robbinspauld plasmaderivedexosomecharacterizationrevealsadistinctmicrornasignatureinlongdurationtype1diabetes AT golbergronaldb plasmaderivedexosomecharacterizationrevealsadistinctmicrornasignatureinlongdurationtype1diabetes AT mendezarmandoj plasmaderivedexosomecharacterizationrevealsadistinctmicrornasignatureinlongdurationtype1diabetes AT ricordicamillo plasmaderivedexosomecharacterizationrevealsadistinctmicrornasignatureinlongdurationtype1diabetes |