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Altered microRNAs expression in T cells of patients with SLE involved in the lack of vitamin D

Vitamin D has been recognized as a potent immunomodulator and its deficiency is common in different population groups including patients with SLE. As miRNAs regulation plays a significant role in SLE, the present study aimed to evaluate the association between vitamin D status and miRNAs levels in p...

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Autores principales: Chen, Dao-Jun, Li, Lan-Ju, Yang, Xiao-Ke, Yu, Tao, Leng, Rui-Xue, Pan, Hai-Feng, Ye, Dong-Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617489/
https://www.ncbi.nlm.nih.gov/pubmed/28977929
http://dx.doi.org/10.18632/oncotarget.19062
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author Chen, Dao-Jun
Li, Lan-Ju
Yang, Xiao-Ke
Yu, Tao
Leng, Rui-Xue
Pan, Hai-Feng
Ye, Dong-Qing
author_facet Chen, Dao-Jun
Li, Lan-Ju
Yang, Xiao-Ke
Yu, Tao
Leng, Rui-Xue
Pan, Hai-Feng
Ye, Dong-Qing
author_sort Chen, Dao-Jun
collection PubMed
description Vitamin D has been recognized as a potent immunomodulator and its deficiency is common in different population groups including patients with SLE. As miRNAs regulation plays a significant role in SLE, the present study aimed to evaluate the association between vitamin D status and miRNAs levels in patients with SLE. The serum concentrations of vitamin D (25-hydroxyvitamin D) and the levels of six miRNAs in T cells from patients with SLE were measured in 42 SLE cases and 48 healthy controls. Vitamin D treatment was also performed in isolated and cultured T cells from SLE patients in different times and doses. Vitamin D insufficiency (25-hydroxyvitamin D concentration <20 ng/ml) was more common in cases than in controls. Although age and BMI were similar, cases had significantly lower concentrations of miRNA-377, miRNA-342, miRNA-10a, miRNA-374b, miRNA-125a, and miRNA-410 than controls. Furthermore, a significant positive correlation was also observed between 25-hydroxyvitamin D concentrations and measured miRNAs levels. A significant difference in observed miRNAs levels was also observed in patients with 25-hydroxyvitamin D insufficiency compared with patients with 25-hydroxyvitamin D concentration ≥20 ng/ml. And 1α,25(OH)(2)D(3) differentially regulated miRNAs expression in dose- and time- manner in vitro. Lower expressions of miRNA-377, miRNA-342, miRNA-10a, miRNA-374b, miRNA-125a, and miRNA-410 were found in SLE patients. And severe vitamin D deficiency is associated with decreased observed miRNAs levels in SLE patients. A 25-hydroxyvitamin D concentration value <20 ng/ml is suggested as the “cut-off” for such immunological alterations in patients with SLE.
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spelling pubmed-56174892017-10-03 Altered microRNAs expression in T cells of patients with SLE involved in the lack of vitamin D Chen, Dao-Jun Li, Lan-Ju Yang, Xiao-Ke Yu, Tao Leng, Rui-Xue Pan, Hai-Feng Ye, Dong-Qing Oncotarget Research Paper Vitamin D has been recognized as a potent immunomodulator and its deficiency is common in different population groups including patients with SLE. As miRNAs regulation plays a significant role in SLE, the present study aimed to evaluate the association between vitamin D status and miRNAs levels in patients with SLE. The serum concentrations of vitamin D (25-hydroxyvitamin D) and the levels of six miRNAs in T cells from patients with SLE were measured in 42 SLE cases and 48 healthy controls. Vitamin D treatment was also performed in isolated and cultured T cells from SLE patients in different times and doses. Vitamin D insufficiency (25-hydroxyvitamin D concentration <20 ng/ml) was more common in cases than in controls. Although age and BMI were similar, cases had significantly lower concentrations of miRNA-377, miRNA-342, miRNA-10a, miRNA-374b, miRNA-125a, and miRNA-410 than controls. Furthermore, a significant positive correlation was also observed between 25-hydroxyvitamin D concentrations and measured miRNAs levels. A significant difference in observed miRNAs levels was also observed in patients with 25-hydroxyvitamin D insufficiency compared with patients with 25-hydroxyvitamin D concentration ≥20 ng/ml. And 1α,25(OH)(2)D(3) differentially regulated miRNAs expression in dose- and time- manner in vitro. Lower expressions of miRNA-377, miRNA-342, miRNA-10a, miRNA-374b, miRNA-125a, and miRNA-410 were found in SLE patients. And severe vitamin D deficiency is associated with decreased observed miRNAs levels in SLE patients. A 25-hydroxyvitamin D concentration value <20 ng/ml is suggested as the “cut-off” for such immunological alterations in patients with SLE. Impact Journals LLC 2017-07-07 /pmc/articles/PMC5617489/ /pubmed/28977929 http://dx.doi.org/10.18632/oncotarget.19062 Text en Copyright: © 2017 Chen et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Chen, Dao-Jun
Li, Lan-Ju
Yang, Xiao-Ke
Yu, Tao
Leng, Rui-Xue
Pan, Hai-Feng
Ye, Dong-Qing
Altered microRNAs expression in T cells of patients with SLE involved in the lack of vitamin D
title Altered microRNAs expression in T cells of patients with SLE involved in the lack of vitamin D
title_full Altered microRNAs expression in T cells of patients with SLE involved in the lack of vitamin D
title_fullStr Altered microRNAs expression in T cells of patients with SLE involved in the lack of vitamin D
title_full_unstemmed Altered microRNAs expression in T cells of patients with SLE involved in the lack of vitamin D
title_short Altered microRNAs expression in T cells of patients with SLE involved in the lack of vitamin D
title_sort altered micrornas expression in t cells of patients with sle involved in the lack of vitamin d
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617489/
https://www.ncbi.nlm.nih.gov/pubmed/28977929
http://dx.doi.org/10.18632/oncotarget.19062
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