Vitamin D controls T cell antigen receptor signaling and activation of human T cells

被引:405
作者
von Essen, Marina Rode [1 ]
Kongsbak, Martin [1 ]
Schjerling, Peter [2 ,4 ]
Olgaard, Klaus [5 ]
Odum, Niels [1 ,3 ]
Geisler, Carsten [1 ]
机构
[1] Univ Copenhagen, Dept Int Hlth Immunol & Microbiol, Copenhagen, Denmark
[2] Univ Copenhagen, Ctr Healthy Aging, Fac Hlth Sci, Copenhagen, Denmark
[3] Univ Copenhagen, Dept Biol, Fac Sci, Copenhagen, Denmark
[4] Univ Copenhagen, Bispebjerg Hosp, Inst Sports Med, Copenhagen, Denmark
[5] Univ Copenhagen, Rigshosp, Dept Nephrol, Copenhagen, Denmark
关键词
PROTEIN-KINASE; MEDIATED ACTIVATION; IMMUNE-SYSTEM; IN-VITRO; DIFFERENTIAL ACTIVATION; PHOSPHOLIPASE C-GAMMA-1; DOWN-REGULATION; TCR; PHOSPHORYLATION; REQUIREMENTS;
D O I
10.1038/ni.1851
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Phospholipase C (PLC) isozymes are key signaling proteins downstream of many extracellular stimuli. Here we show that naive human T cells had very low expression of PLC-gamma 1 and that this correlated with low T cell antigen receptor (TCR) responsiveness in naive T cells. However, TCR triggering led to an upregulation of similar to 75-fold in PLC-gamma 1 expression, which correlated with greater TCR responsiveness. Induction of PLC-gamma 1 was dependent on vitamin D and expression of the vitamin D receptor (VDR). Naive T cells did not express VDR, but VDR expression was induced by TCR signaling via the alternative mitogen-activated protein kinase p38 pathway. Thus, initial TCR signaling via p38 leads to successive induction of VDR and PLC-gamma 1, which are required for subsequent classical TCR signaling and T cell activation.
引用
收藏
页码:344 / U56
页数:7
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