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Beyond Immune Cell Migration: The Emerging Role of the Sphingosine-1-phosphate Receptor S1PR4 as a Modulator of Innate Immune Cell Activation
被引:54
|作者:
Olesch, Catherine
[1
]
Ringel, Christian
[1
]
Bruene, Bernhard
[1
]
Weigert, Andreas
[1
]
机构:
[1] Goethe Univ Frankfurt, Inst Biochem 1, Fac Med, D-60590 Frankfurt, Germany
关键词:
PLASMACYTOID DENDRITIC CELLS;
IFN-ALPHA PRODUCTION;
SPHINGOSINE KINASE 2;
CERAMIDE SYNTHASE 2;
LYMPH-NODES;
ACTIN DYNAMICS;
T(H)17 CELLS;
SAR ANALYSIS;
1-PHOSPHATE;
TRAFFICKING;
D O I:
10.1155/2017/6059203
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
The sphingolipid sphingosine-1-phosphate (S1P) emerges as an important regulator of immunity, mainly by signaling through a family of five specific G protein-coupled receptors (S1PR1-5). While S1P signaling generally has the potential to affect not only trafficking but also differentiation, activation, and survival of a diverse range of immune cells, the specific outcome depends on the S1P receptor repertoire expressed on a given cell. Among the S1PRs, S1PR4 is specifically abundant in immune cells, suggesting a major role of the S1P/S1PR4 axis in immunity. Recent studies indeed highlight its role in activation of immune cells, differentiation, and, potentially, trafficking. In this review, we summarize the emerging data that support a major role of S1PR4 in modulating immunity in humans and mice and discuss therapeutic implications.
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页数:12
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