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Circulating MiR-374a-5p is a potential modulator of the inflammatory process in obesity

Obese individuals without expected metabolic co-morbidities are referred to as metabolically healthy obese (MHO). The molecular mechanisms underlying this phenotype remain elusive. MicroRNAs may be involved in the MHO phenotype. To test this hypothesis, we screened 179 serum miRNAs in 20 African-Ame...

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Autores principales: Doumatey, Ayo P., He, William J., Gaye, Amadou, Lei, Lin, Zhou, Jie, Gibbons, Gary H., Adeyemo, Adebowale, Rotimi, Charles N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955981/
https://www.ncbi.nlm.nih.gov/pubmed/29769661
http://dx.doi.org/10.1038/s41598-018-26065-5
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author Doumatey, Ayo P.
He, William J.
Gaye, Amadou
Lei, Lin
Zhou, Jie
Gibbons, Gary H.
Adeyemo, Adebowale
Rotimi, Charles N.
author_facet Doumatey, Ayo P.
He, William J.
Gaye, Amadou
Lei, Lin
Zhou, Jie
Gibbons, Gary H.
Adeyemo, Adebowale
Rotimi, Charles N.
author_sort Doumatey, Ayo P.
collection PubMed
description Obese individuals without expected metabolic co-morbidities are referred to as metabolically healthy obese (MHO). The molecular mechanisms underlying this phenotype remain elusive. MicroRNAs may be involved in the MHO phenotype. To test this hypothesis, we screened 179 serum miRNAs in 20 African-American women (10 MHOs and 10 metabolically abnormal obese individuals -MAO). We identified 8 differentially expressed miRNAs (DEMs) with validation in an independent sample of 64 MHO and 34 MAO. Of the eight DEMs in the screening phase (p ≤ 0.05), miR-374a-5p remained significant (p = 0.04) with directional consistency in the validation sample. Ingenuity Pathway analysis revealed that miR-374a-5p putatively targeted 37 mRNAs (e.g. chemokines and transcription factors) which are members of canonical pathways involved in inflammation (IL-17A signaling) and lipid metabolism. Analysis restricted to adipocytes, the main source of circulating miRNAs in obesity, identified 3 mRNAs (CCL2, STEAP2, EN1) as the main target of miR-374a-5p. Evaluation of the 3 mRNAs in an independent sample showed that CCL2 was significantly downregulated (p = 0.0005). In summary, MiR-374a-5p is upregulated in MHO compared to MAO individuals and appears to show association with downregulation of pro-inflammatory markers that are linked to insulin resistance. Given the correlative nature of our findings, functional studies are needed.
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spelling pubmed-59559812018-05-21 Circulating MiR-374a-5p is a potential modulator of the inflammatory process in obesity Doumatey, Ayo P. He, William J. Gaye, Amadou Lei, Lin Zhou, Jie Gibbons, Gary H. Adeyemo, Adebowale Rotimi, Charles N. Sci Rep Article Obese individuals without expected metabolic co-morbidities are referred to as metabolically healthy obese (MHO). The molecular mechanisms underlying this phenotype remain elusive. MicroRNAs may be involved in the MHO phenotype. To test this hypothesis, we screened 179 serum miRNAs in 20 African-American women (10 MHOs and 10 metabolically abnormal obese individuals -MAO). We identified 8 differentially expressed miRNAs (DEMs) with validation in an independent sample of 64 MHO and 34 MAO. Of the eight DEMs in the screening phase (p ≤ 0.05), miR-374a-5p remained significant (p = 0.04) with directional consistency in the validation sample. Ingenuity Pathway analysis revealed that miR-374a-5p putatively targeted 37 mRNAs (e.g. chemokines and transcription factors) which are members of canonical pathways involved in inflammation (IL-17A signaling) and lipid metabolism. Analysis restricted to adipocytes, the main source of circulating miRNAs in obesity, identified 3 mRNAs (CCL2, STEAP2, EN1) as the main target of miR-374a-5p. Evaluation of the 3 mRNAs in an independent sample showed that CCL2 was significantly downregulated (p = 0.0005). In summary, MiR-374a-5p is upregulated in MHO compared to MAO individuals and appears to show association with downregulation of pro-inflammatory markers that are linked to insulin resistance. Given the correlative nature of our findings, functional studies are needed. Nature Publishing Group UK 2018-05-16 /pmc/articles/PMC5955981/ /pubmed/29769661 http://dx.doi.org/10.1038/s41598-018-26065-5 Text en © The Author(s) 2018 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
Doumatey, Ayo P.
He, William J.
Gaye, Amadou
Lei, Lin
Zhou, Jie
Gibbons, Gary H.
Adeyemo, Adebowale
Rotimi, Charles N.
Circulating MiR-374a-5p is a potential modulator of the inflammatory process in obesity
title Circulating MiR-374a-5p is a potential modulator of the inflammatory process in obesity
title_full Circulating MiR-374a-5p is a potential modulator of the inflammatory process in obesity
title_fullStr Circulating MiR-374a-5p is a potential modulator of the inflammatory process in obesity
title_full_unstemmed Circulating MiR-374a-5p is a potential modulator of the inflammatory process in obesity
title_short Circulating MiR-374a-5p is a potential modulator of the inflammatory process in obesity
title_sort circulating mir-374a-5p is a potential modulator of the inflammatory process in obesity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955981/
https://www.ncbi.nlm.nih.gov/pubmed/29769661
http://dx.doi.org/10.1038/s41598-018-26065-5
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