Hypomethylation of IL10 and IL13 Promoters in CD4+ T Cells of Patients with Systemic Lupus Erythematosus

Interleukin- (IL-)10 and IL-13 play important roles in Th2 cell differentiation and production of autoantibodies in patients with (SLE). However, the mechanisms leading to IL10 and IL13 overexpression in SLE patients are not well understood. In this study, we confirm that the levels of both IL10 and...

Full description

Bibliographic Details
Main Authors: Ming Zhao, Jinling Tang, Fei Gao, Xiaoyan Wu, Yunsheng Liang, Heng Yin, Qianjin Lu
Format: Article
Language:English
Published: Hindawi Limited 2010-01-01
Series:Journal of Biomedicine and Biotechnology
Online Access:http://dx.doi.org/10.1155/2010/931018
id doaj-34e768dcb630410bb6cdd3e8e2a92be7
record_format Article
spelling doaj-34e768dcb630410bb6cdd3e8e2a92be72020-11-24T21:56:16ZengHindawi LimitedJournal of Biomedicine and Biotechnology1110-72431110-72512010-01-01201010.1155/2010/931018931018Hypomethylation of IL10 and IL13 Promoters in CD4+ T Cells of Patients with Systemic Lupus ErythematosusMing Zhao0Jinling Tang1Fei Gao2Xiaoyan Wu3Yunsheng Liang4Heng Yin5Qianjin Lu6Department of Dermatology, Epigenetic Research Center, Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, ChinaDepartment of Dermatology, Epigenetic Research Center, Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, ChinaDepartment of Dermatology, Epigenetic Research Center, Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, ChinaDepartment of Dermatology, Epigenetic Research Center, Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, ChinaDepartment of Dermatology, Epigenetic Research Center, Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, ChinaDepartment of Dermatology, Epigenetic Research Center, Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, ChinaDepartment of Dermatology, Epigenetic Research Center, Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, ChinaInterleukin- (IL-)10 and IL-13 play important roles in Th2 cell differentiation and production of autoantibodies in patients with (SLE). However, the mechanisms leading to IL10 and IL13 overexpression in SLE patients are not well understood. In this study, we confirm that the levels of both IL10 and IL13 mRNA in CD4+ T cells and of serum IL10 and IL13 proteins are increased in SLE patients. We show that the DNA methylation levels within IL10 and IL13 gene regulatory domains are reduced in SLE CD4+ T cells relative to healthy controls and negatively correlate with IL10 and IL13 mRNA expression. Moreover, treating healthy CD4+ T cells with the demethylating agent 5-azacytidine (5-azaC) increased IL10 and IL13 mRNA transcription. Together, our results show that promoter methylation is a determinant of IL10 and IL13 expression in CD4+ T cells, and we propose that DNA hypomethylation leads to IL10 and IL13 overexpression in SLE patients.http://dx.doi.org/10.1155/2010/931018
collection DOAJ
language English
format Article
sources DOAJ
author Ming Zhao
Jinling Tang
Fei Gao
Xiaoyan Wu
Yunsheng Liang
Heng Yin
Qianjin Lu
spellingShingle Ming Zhao
Jinling Tang
Fei Gao
Xiaoyan Wu
Yunsheng Liang
Heng Yin
Qianjin Lu
Hypomethylation of IL10 and IL13 Promoters in CD4+ T Cells of Patients with Systemic Lupus Erythematosus
Journal of Biomedicine and Biotechnology
author_facet Ming Zhao
Jinling Tang
Fei Gao
Xiaoyan Wu
Yunsheng Liang
Heng Yin
Qianjin Lu
author_sort Ming Zhao
title Hypomethylation of IL10 and IL13 Promoters in CD4+ T Cells of Patients with Systemic Lupus Erythematosus
title_short Hypomethylation of IL10 and IL13 Promoters in CD4+ T Cells of Patients with Systemic Lupus Erythematosus
title_full Hypomethylation of IL10 and IL13 Promoters in CD4+ T Cells of Patients with Systemic Lupus Erythematosus
title_fullStr Hypomethylation of IL10 and IL13 Promoters in CD4+ T Cells of Patients with Systemic Lupus Erythematosus
title_full_unstemmed Hypomethylation of IL10 and IL13 Promoters in CD4+ T Cells of Patients with Systemic Lupus Erythematosus
title_sort hypomethylation of il10 and il13 promoters in cd4+ t cells of patients with systemic lupus erythematosus
publisher Hindawi Limited
series Journal of Biomedicine and Biotechnology
issn 1110-7243
1110-7251
publishDate 2010-01-01
description Interleukin- (IL-)10 and IL-13 play important roles in Th2 cell differentiation and production of autoantibodies in patients with (SLE). However, the mechanisms leading to IL10 and IL13 overexpression in SLE patients are not well understood. In this study, we confirm that the levels of both IL10 and IL13 mRNA in CD4+ T cells and of serum IL10 and IL13 proteins are increased in SLE patients. We show that the DNA methylation levels within IL10 and IL13 gene regulatory domains are reduced in SLE CD4+ T cells relative to healthy controls and negatively correlate with IL10 and IL13 mRNA expression. Moreover, treating healthy CD4+ T cells with the demethylating agent 5-azacytidine (5-azaC) increased IL10 and IL13 mRNA transcription. Together, our results show that promoter methylation is a determinant of IL10 and IL13 expression in CD4+ T cells, and we propose that DNA hypomethylation leads to IL10 and IL13 overexpression in SLE patients.
url http://dx.doi.org/10.1155/2010/931018
work_keys_str_mv AT mingzhao hypomethylationofil10andil13promotersincd4tcellsofpatientswithsystemiclupuserythematosus
AT jinlingtang hypomethylationofil10andil13promotersincd4tcellsofpatientswithsystemiclupuserythematosus
AT feigao hypomethylationofil10andil13promotersincd4tcellsofpatientswithsystemiclupuserythematosus
AT xiaoyanwu hypomethylationofil10andil13promotersincd4tcellsofpatientswithsystemiclupuserythematosus
AT yunshengliang hypomethylationofil10andil13promotersincd4tcellsofpatientswithsystemiclupuserythematosus
AT hengyin hypomethylationofil10andil13promotersincd4tcellsofpatientswithsystemiclupuserythematosus
AT qianjinlu hypomethylationofil10andil13promotersincd4tcellsofpatientswithsystemiclupuserythematosus
_version_ 1725858855436419072