The induction of the lupus phenotype by estrogen is via an estrogen receptor-α-dependent pathway

被引:35
作者
Feng Feng [1 ]
Nyland, Jennifer [2 ]
Banyai, Michelle [3 ]
Tatum, Arthur [4 ]
Silverstone, Allen E. [2 ]
Gavalchin, Jerrie [1 ,2 ]
机构
[1] Cornell Univ, Dept Microbiol & Immunol, Ithaca, NY 14853 USA
[2] SUNY Upstate Med Univ, Dept Microbiol & Immunol, Syracuse, NY 13210 USA
[3] Cornell Univ, Dept Anim Sci, Ithaca, NY 14853 USA
[4] SUNY Upstate Med Univ, Dept Clin Pathol, Syracuse, NY 13210 USA
关键词
Lupus; Estrogen receptor; Estradiol; ER alpha-deficient mouse; Idiotypic-reactive T cells; CANCER CELL-LINES; F1 MOUSE MODEL; T-CELLS; MURINE MODEL; BODY-WEIGHT; NEPHRITOGENIC IDIOTYPE; AUTOIMMUNE-DISEASE; (NZBXSWR)F-1 MODEL; STEROID-HORMONES; DENDRITIC CELLS;
D O I
10.1016/j.clim.2009.10.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In order to investigate the roles of ER subtypes in the estrogen-induced lupus phenotype, ER alpha-deficient (ER alpha(-/-)) and wild-type mice (WT) were injected monthly with estradiol (E-2) starting at 8 weeks. In WT mice, E-2 treatment induced a lupus phenotype, with accelerated death and increased kidney damage, as well as Th2-type serum cytokine and autoantibody production. In contrast, only minimal changes were observed in ER alpha(-/-) mice after E-2 treatment. In a separate study, we found that in immune cells of autoimmune-prone SNF1 and non-autoimmune DBF1 mice, both ER alpha and ER beta were differentially expressed and modulated by E-2. In SNF1 mice, there were more CD4(+) and CD8(+) T cells constitutively expressing ER alpha, and the percentages of ER alpha+ dendritic cells and macrophages were increased after E-2 exposure compared to DBF1 mice. Taken together, these observations strongly suggest a role for ER alpha in E-2-induced development of the lupus phenotype. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:226 / 236
页数:11
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