RAGE Expression in Human T Cells: A Link between Environmental Factors and Adaptive Immune Responses

被引:82
作者
Akirav, Eitan M. [1 ,2 ]
Preston-Hurlburt, Paula [1 ,2 ]
Garyu, Justin [1 ,2 ]
Henegariu, Octavian [1 ,2 ]
Clynes, Raphael [3 ]
Schmidt, Marie [4 ]
Herold, Kevan C. [1 ,2 ]
机构
[1] Yale Univ, Dept Immunobiol, New Haven, CT 06520 USA
[2] Yale Univ, Dept Internal Med, New Haven, CT USA
[3] Columbia Univ, Dept Med, New York, NY USA
[4] NYU, Dept Med, New York, NY 10016 USA
关键词
GLYCATION END-PRODUCTS; MOBILITY GROUP BOX-1; DIABETIC VASCULOPATHY; ALZHEIMERS-DISEASE; SIGNALING PATHWAYS; ENDOTHELIAL-CELLS; SOLUBLE RECEPTOR; DENDRITIC CELLS; ACTIVATION; ATHEROSCLEROSIS;
D O I
10.1371/journal.pone.0034698
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
The Receptor for Advanced Glycation Endproducts (RAGE) is a scavenger ligand that binds glycated endproducts as well as molecules released during cell death such as S100b and HMGB1. RAGE is expressed on antigen presenting cells where it may participate in activation of innate immune responses but its role in adaptive human immune responses has not been described. We have found that RAGE is expressed intracellularly in human T cells following TCR activation but constitutively on T cells from patients with diabetes. The levels of RAGE on T cells from patients with diabetes are not related to the level of glucose control. It co-localizes to the endosomes. Its expression increases in activated T cells from healthy control subjects but bystander cells also express RAGE after stimulation of the antigen specific T cells. RAGE ligands enhance RAGE expression. In patients with T1D, the level of RAGE expression decreases with T cell activation. RAGE+ T cells express higher levels of IL-17A, CD107a, and IL-5 than RAGE- cells from the same individual with T1D. Our studies have identified the expression of RAGE on adaptive immune cells and a role for this receptor and its ligands in modulating human immune responses.
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页数:10
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