Endogenous Nur77 Is a Specific Indicator of Antigen Receptor Signaling in Human T and B Cells

被引:142
作者
Ashouri, Judith F.
Weiss, Arthur
机构
[1] Univ Calif San Francisco, Rosalind Russell & Ephraim P Engleman Rheumatol R, Dept Med, Div Rheumatol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
GREEN FLUORESCENT PROTEIN; TYROSINE KINASE INHIBITOR; ORPHAN NUCLEAR RECEPTORS; RHEUMATOID-ARTHRITIS; STEROID-RECEPTOR; CYCLOSPORINE-A; DIFFERENTIAL REGULATION; NEGATIVE SELECTION; CENTRAL MEMORY; ACTIVATION;
D O I
10.4049/jimmunol.1601301
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Distinguishing true Ag-stimulated lymphocytes from bystanders activated by the inflammatory milieu has been difficult. Nur77 is an immediate early gene whose expression is rapidly upregulated by TCR signaling in murine T cells and human thymocytes. Nur77-GFP transgenes serve as specific TCR and BCR signaling reporters in murine transgenic models. In this study, we demonstrate that endogenous Nur77 protein expression can serve as a reporter of TCR and BCR specific signaling in human PBMCs. Nur77 protein amounts were assessed by immunofluorescence and flow cytometry in T and B cells isolated from human PBMCs obtained from healthy donors that had been stimulated by their respective Ag receptors. We demonstrate that endogenous Nur77 is a more specific reporter of Ag-specific signaling events than the commonly used CD69 activation marker in both human T and B cells. This is reflective of the disparity in signaling pathways that regulate the expression of Nur77 and CD69. Assessing endogenous Nur77 protein expression has great potential to identify Ag-activated lymphocytes in human disease.
引用
收藏
页码:657 / 668
页数:12
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