Role of CREM in systemic lupus erythematosus

被引：10

作者：

Xu, Wang-Dong ^{[1
]}

Zhang, Yu-Jing ^{[1
]}

Wang, Wei ^{[1
]}

Li, Rui ^{[1
]}

Pan, Hai-Feng ^{[1
]}

Ye, Dong-Qing ^{[1
]}

机构：

[1] Anhui Med Univ, Sch Publ Hlth, Dept Epidemiol & Biostat, Hefei 230032, Anhui, Peoples R China

来源：

CELLULAR IMMUNOLOGY | 2012年 / 276卷 / 1-2期

基金：

中国国家自然科学基金;

关键词：

cAMP response element modulator; Autoimmune; Systemic lupus erythematosus; RESPONSE ELEMENT MODULATOR; REGULATORY T-CELLS; SUPPRESSES IL-2 PRODUCTION; SPLEEN TYROSINE KINASE; TRANSCRIPTIONAL REGULATION; C-FOS; RHEUMATOID-ARTHRITIS; INTERLEUKIN-2; GENE; EXPRESSION; PROMOTER;

D O I：

10.1016/j.cellimm.2012.04.008

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 ; 090102 ;

摘要：

Systemic lupus erythematosus (SLE) is a complex autoimmune disease. Immune complex, autoantibodies and autoreactive lymphocytes are involved in manifestations of SLE. Recently, investigations have indicated that expression of the transcription factor cAMP responsive element modulator (CREM) is abnormal in T cells and might play an important role in the pathogenesis of SLE. CREM has much influence on the promoters, such as IL-2, c-fos, TCR zeta, and SYK. Moreover, activity of CREM itself has been demonstrated, particularly with an auto-regulatory feedback mechanism. Therefore, we will discuss the association of CREM and SLE based on current knowledge to unravel the mechanism of CREM performance. Crown Copyright (C) 2012 Published by Elsevier Inc. All rights reserved.

引用

页码：10 / 15

页数：6

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