Unknown

Dataset Information

0

The receptor for advanced glycation endproducts (RAGE) modulates T cell signaling.


ABSTRACT: The receptor for advanced glycation endproducts (RAGE) is expressed in T cells after activation with antigen and is constitutively expressed in T cells from patients at-risk for and with type 1 diabetes mellitus (T1D). RAGE expression was associated with an activated T cell phenotype, leading us to examine whether RAGE is involved in T cell signaling. In primary CD4+ and CD8+ T cells from patients with T1D or healthy control subjects, RAGE- cells showed reduced phosphorylation of Erk. To study T cell receptor signaling in RAGE+ or-T cells, we compared signaling in RAGE+/+ Jurkat cells, Jurkat cells with RAGE eliminated by CRISPR/Cas9, or silenced with siRNA. In RAGE KO Jurkat cells, there was reduced phosphorylation of Zap70, Erk and MEK, but not Lck or CD3?. RAGE KO cells produced less IL-2 when activated with anti-CD3 +/- anti-CD28. Stimulation with PMA restored signaling and (with ionomycin) IL-2 production. Silencing RAGE with siRNA also decreased signaling. Our studies show that RAGE expression in human T cells is associated with an activated signaling cascade. These findings suggest a link between inflammatory products that are found in patients with diabetes, other autoimmune diseases, and inflammation that may enhance T cell reactivity.

SUBMITTER: Reed JC 

PROVIDER: S-EPMC7521722 | biostudies-literature | 2020

REPOSITORIES: biostudies-literature

altmetric image

Publications

The receptor for advanced glycation endproducts (RAGE) modulates T cell signaling.

Reed James C JC   Preston-Hurlburt Paula P   Philbrick William W   Betancur Gabriel G   Korah Maria M   Lucas Carrie C   Herold Kevan C KC  

PloS one 20200928 9


The receptor for advanced glycation endproducts (RAGE) is expressed in T cells after activation with antigen and is constitutively expressed in T cells from patients at-risk for and with type 1 diabetes mellitus (T1D). RAGE expression was associated with an activated T cell phenotype, leading us to examine whether RAGE is involved in T cell signaling. In primary CD4+ and CD8+ T cells from patients with T1D or healthy control subjects, RAGE- cells showed reduced phosphorylation of Erk. To study T  ...[more]

Similar Datasets

| S-EPMC5601361 | biostudies-literature
| S-EPMC7591811 | biostudies-literature
| S-EPMC7326105 | biostudies-literature
| S-EPMC3345001 | biostudies-literature
| S-EPMC5509466 | biostudies-literature
| S-EPMC4392170 | biostudies-literature
| S-EPMC3003376 | biostudies-literature
| S-EPMC4847335 | biostudies-literature
| S-EPMC6862609 | biostudies-literature
| S-EPMC5053332 | biostudies-literature