Sphingosine 1-Phosphate Receptor Signaling

被引:338
作者
Rosen, Hugh [1 ]
Gonzalez-Cabrera, Pedro J.
Sanna, M. Germana
Brown, Steven
机构
[1] Scripps Res Inst, Dept Physiol Chem, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
[3] Scripps Res Inst, Mol Screening Ctr, La Jolla, CA 92037 USA
关键词
chemical discovery; genetic modulation; GPCR; lysophospholipid; PROTEIN-COUPLED-RECEPTOR; CIRCULATING MATURE LYMPHOCYTES; ENDOTHELIAL-CELL CHEMOTAXIS; IMMUNE MODULATOR FTY720; N-ARYLAMIDE OXADIAZOLES; SKIN ALLOGRAFT SURVIVAL; OFF-THE-SHELF; LYMPHOID ORGANS; SPHINGOSINE-1-PHOSPHATE RECEPTORS; IN-VIVO;
D O I
10.1146/annurev.biochem.78.072407.103733
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
The sphingosine 1-phosphate (S1P) receptor signaling system is a productive model system. A hydrophobic zwitterionic lysophospholipid ligand with difficult physical properties interacts,with five high-affinity G protein-coupled receptors to generate multiple downstream signals. These signals Modulate homeostasis and pathology on a steep agonist concentration-response curve. Ligand presence is essential for vascular development and endothelial integrity, while acute increases in ligand concentrations result in cardiac death. Understanding this integrated biochemical system has exemplified the impact of both genetics and chemistry. Developing specific tools with defined biochemical properties for the reversible modulation of signals in real time has been essential to complement insights gained from genetic approaches that may be it-reversible and compensated. Despite its knife-edge between life and death, this system, based in part on receptor subtype-selectivity and in part on differential attenuation of deleterious signals, now appears to be on the cusp of meaningful therapy for multiple sclerosis.
引用
收藏
页码:743 / 768
页数:26
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