Serum amyloid A induces mitogenic signals in regulatory T cells via monocyte activation

被引:23
作者
Nguyen, Khoa D. [1 ]
Macaubas, Claudia [1 ]
Phi Truong [1 ]
Wang, Nan [1 ]
Hou, Tieying [1 ]
Yoon, Taejin [1 ]
Mellins, Elizabeth D. [1 ]
机构
[1] Stanford Univ, Dept Pediat, Sch Med, Stanford, CA 94305 USA
关键词
Serum amyloid A; Regulatory T cells; Monocytes; IL-1; beta; IL-6; SUPPRESSIVE ACTIVITY; SYNOVIAL-FLUID; KAPPA-B; RECEPTOR; ARTHRITIS; EXPRESSION; EXPANSION; CYTOKINES; TOLERANCE; BINDING;
D O I
10.1016/j.molimm.2014.02.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Serum amyloid A (SAA) has recently been identified by our group as a mitogen for regulatory T cells (Treg). However, the molecular mechanism by which SAA induces Treg proliferation is unknown. Here we provide evidence that IL-1 beta and IL-6 are directly involved in the SAA-mediated proliferation of Treg. By engaging its several cognate receptors, SAA induces IL-113 and IL-6 secretion by monocytes and drives them toward an HLA-DRhi HVEMlo phenotype resembling immature dendritic cells, which have been implicated in tolerance generation. This monocyte-derived cytokine milieu is required for Treg expansion, as inhibition of IL-113 and IL-6 abrogate the ability of SAA to induce Treg proliferation. Furthermore, both IL-1 beta and IL-6 are required for ERK1/2 and ART signaling in proliferating Treg. Collectively, these results point to a novel mechanism, by which SAA initiates a monocyte-dependent process that drives mitogenic signals in Treg. (c) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:172 / 179
页数:8
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