Lysophospholipid receptor nomenclature review: IUPHAR Review 8

被引:303
作者
Kihara, Yasuyuki [1 ]
Maceyka, Michael [2 ,3 ]
Spiegel, Sarah [2 ,3 ]
Chun, Jerold [1 ]
机构
[1] Scripps Res Inst, Dorris Neurosci Ctr, Mol & Cellular Neurosci Dept, La Jolla, CA 92037 USA
[2] Virginia Commonwealth Univ, Dept Biochem & Mol Biol, Sch Med, Richmond, VA 23298 USA
[3] Virginia Commonwealth Univ, Massey Canc Ctr, Sch Med, Richmond, VA 23298 USA
基金
美国国家卫生研究院;
关键词
PROTEIN-COUPLED RECEPTOR; LYSOPHOSPHATIDIC ACID RECEPTOR; SPHINGOSINE 1-PHOSPHATE RECEPTOR; PANCREATIC-CANCER CELLS; HEPATIC STELLATE CELLS; LYMPHOCYTE EGRESS; CONCISE GUIDE; EDG-FAMILY; INTERNATIONAL UNION; LPA RECEPTORS;
D O I
10.1111/bph.12678
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Lysophospholipids encompass a diverse range of small, membrane-derived phospholipids that act as extracellular signals. The signalling properties are mediated by 7-transmembrane GPCRs, constituent members of which have continued to be identified after their initial discovery in the mid-1990s. Here we briefly review this class of receptors, with a particular emphasis on their protein and gene nomenclatures that reflect their cognate ligands. There are six lysophospholipid receptors that interact with lysophosphatidic acid (LPA): protein names LPA(1) - LPA(6) and italicized gene names LPAR1-LPAR6 (human) and Lpar1-Lpar6 (non-human). There are five sphingosine 1-phosphate (S1P) receptors: protein names S1P(1)-S1P(5) and italicized gene names S1PR1-S1PR5 (human) and S1pr1-S1pr5 (non-human). Recent additions to the lysophospholipid receptor family have resulted in the proposed names for a lysophosphatidyl inositol (LPI) receptor - protein name LPI1 and gene name LPIR1 (human) and Lpir1 (non-human) - and three lysophosphatidyl serine receptors - protein names LyPS(1), LyPS(2), LyPS(3) and gene names LYPSR1-LYPSR3 (human) and Lypsr1-Lypsr3 (non-human) along with a variant form that does not appear to exist in humans that is provisionally named LyPS(2L). This nomenclature incorporates previous recommendations from the International Union of Basic and Clinical Pharmacology, the Human Genome Organization, the Gene Nomenclature Committee, and the Mouse Genome Informatix.
引用
收藏
页码:3575 / 3594
页数:20
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