Deaf1 isoforms control the expression of genes encoding peripheral tissue antigens in the pancreatic lymph nodes during type 1 diabetes

被引:112
作者
Yip, Linda [1 ]
Su, Leon [1 ]
Sheng, Deqiao [1 ]
Chang, Pearl [1 ]
Atkinson, Mark [2 ]
Czesak, Margaret [3 ,4 ]
Albert, Paul R. [3 ,4 ]
Collier, Ai-Ris [5 ]
Turley, Shannon J. [5 ]
Fathman, C. Garrison [1 ]
Creusot, Remi J. [1 ]
机构
[1] Stanford Univ, Sch Med, Div Rheumatol & Immunol, Dept Med, Stanford, CA 94305 USA
[2] Univ Florida, Dept Pathol, Gainesville, FL 32611 USA
[3] Univ Ottawa, Ottawa Hlth Res Inst Neurosci, Ottawa, ON, Canada
[4] Univ Ottawa, Dept Cellular & Mol Med, Ottawa, ON, Canada
[5] Dana Farber Canc Inst, Dept Canc Immunol & AIDS, Boston, MA 02115 USA
基金
加拿大健康研究院; 美国国家卫生研究院;
关键词
THYMIC EPITHELIAL-CELLS; MESSENGER-RNA; SELF; TOLERANCE; PROTEIN; MICE; AUTOIMMUNITY; TRANSCRIPTION; POLYMORPHISM; FIBRONECTIN;
D O I
10.1038/ni.1773
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Type 1 diabetes may result from a breakdown in peripheral tolerance that is partially controlled by the expression of peripheral tissue antigens (PTAs) in lymph nodes. Here we show that the transcriptional regulator Deaf1 controls the expression of genes encoding PTAs in the pancreatic lymph nodes (PLNs). The expression of canonical Deaf1 was lower, whereas that of an alternatively spliced variant was higher, during the onset of destructive insulitis in the PLNs of nonobese diabetic (NOD) mice. We identified an equivalent variant Deaf1 isoform in the PLNs of patients with type 1 diabetes. Both the NOD mouse and human Deaf1 variant isoforms suppressed PTA expression by inhibiting the transcriptional activity of canonical Deaf1. Lower PTA expression resulting from the alternative splicing of DEAF1 may contribute to the pathogenesis of type 1 diabetes.
引用
收藏
页码:1026 / U107
页数:9
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