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Analysis of inflammatory cytokine and TLR expression levels in Type 2 Diabetes with complications

The pathogenesis and complications of type 2 diabetes (T2DM) are closely linked with defective glucose metabolism, obesity, cardiovascular disease and an inability to mount an effective immune response to certain pathogenic organisms. Perturbations in key innate immune receptors known as Toll-like r...

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Autores principales: Gupta, Saket, Maratha, Ashwini, Siednienko, Jakub, Natarajan, Anandan, Gajanayake, Thusitha, Hoashi, Shu, Miggin, Sinéad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5550417/
https://www.ncbi.nlm.nih.gov/pubmed/28794498
http://dx.doi.org/10.1038/s41598-017-07230-8
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author Gupta, Saket
Maratha, Ashwini
Siednienko, Jakub
Natarajan, Anandan
Gajanayake, Thusitha
Hoashi, Shu
Miggin, Sinéad
author_facet Gupta, Saket
Maratha, Ashwini
Siednienko, Jakub
Natarajan, Anandan
Gajanayake, Thusitha
Hoashi, Shu
Miggin, Sinéad
author_sort Gupta, Saket
collection PubMed
description The pathogenesis and complications of type 2 diabetes (T2DM) are closely linked with defective glucose metabolism, obesity, cardiovascular disease and an inability to mount an effective immune response to certain pathogenic organisms. Perturbations in key innate immune receptors known as Toll-like receptors (TLRs) and inflammatory mediators such as IL-6, TNFα and IL-1β have been linked with T2DM. Herein, we sought to establish whether patients with T2DM and underlying complications exhibit perturbations in cytokine and TLR expression. Serum cytokine and mRNA levels of cytokines/TLRs in monocytes (M) and neutrophils (N) were measured in a cohort of 112 diabetic patients: good glycaemic control without complications (GC), good glycaemic control with complications (GCC), poor glycaemic control without complications (PC) and poor glycaemic control with complications (PCC) and compared them with 34 non-diabetic volunteers (NGT). Serum cytokine levels were normal in all study participants. In the GC group, cytokine and TLR gene expression were enhanced compared to NGT. In contrast, suppressed cytokine and TLR gene expression were evident in PC, GCC & PCC groups when compared to the GC. In conclusion, whereas serum pro-inflammatory cytokine levels are unaltered in T2DM patients, differences in inflammatory gene profiles exist among the T2DM patient groups.
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spelling pubmed-55504172017-08-11 Analysis of inflammatory cytokine and TLR expression levels in Type 2 Diabetes with complications Gupta, Saket Maratha, Ashwini Siednienko, Jakub Natarajan, Anandan Gajanayake, Thusitha Hoashi, Shu Miggin, Sinéad Sci Rep Article The pathogenesis and complications of type 2 diabetes (T2DM) are closely linked with defective glucose metabolism, obesity, cardiovascular disease and an inability to mount an effective immune response to certain pathogenic organisms. Perturbations in key innate immune receptors known as Toll-like receptors (TLRs) and inflammatory mediators such as IL-6, TNFα and IL-1β have been linked with T2DM. Herein, we sought to establish whether patients with T2DM and underlying complications exhibit perturbations in cytokine and TLR expression. Serum cytokine and mRNA levels of cytokines/TLRs in monocytes (M) and neutrophils (N) were measured in a cohort of 112 diabetic patients: good glycaemic control without complications (GC), good glycaemic control with complications (GCC), poor glycaemic control without complications (PC) and poor glycaemic control with complications (PCC) and compared them with 34 non-diabetic volunteers (NGT). Serum cytokine levels were normal in all study participants. In the GC group, cytokine and TLR gene expression were enhanced compared to NGT. In contrast, suppressed cytokine and TLR gene expression were evident in PC, GCC & PCC groups when compared to the GC. In conclusion, whereas serum pro-inflammatory cytokine levels are unaltered in T2DM patients, differences in inflammatory gene profiles exist among the T2DM patient groups. Nature Publishing Group UK 2017-08-09 /pmc/articles/PMC5550417/ /pubmed/28794498 http://dx.doi.org/10.1038/s41598-017-07230-8 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
Gupta, Saket
Maratha, Ashwini
Siednienko, Jakub
Natarajan, Anandan
Gajanayake, Thusitha
Hoashi, Shu
Miggin, Sinéad
Analysis of inflammatory cytokine and TLR expression levels in Type 2 Diabetes with complications
title Analysis of inflammatory cytokine and TLR expression levels in Type 2 Diabetes with complications
title_full Analysis of inflammatory cytokine and TLR expression levels in Type 2 Diabetes with complications
title_fullStr Analysis of inflammatory cytokine and TLR expression levels in Type 2 Diabetes with complications
title_full_unstemmed Analysis of inflammatory cytokine and TLR expression levels in Type 2 Diabetes with complications
title_short Analysis of inflammatory cytokine and TLR expression levels in Type 2 Diabetes with complications
title_sort analysis of inflammatory cytokine and tlr expression levels in type 2 diabetes with complications
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5550417/
https://www.ncbi.nlm.nih.gov/pubmed/28794498
http://dx.doi.org/10.1038/s41598-017-07230-8
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