4.2 Editorial Material

What is the natural ligand of GPR55?

期刊

JOURNAL OF BIOCHEMISTRY
卷 149, 期 5, 页码 495-497

出版社

OXFORD UNIV PRESS
DOI: 10.1093/jb/mvr022

关键词

GPR55; LPI; natural ligand; lipid; mass spectrometry

资金

  1. Grants-in-Aid for Scientific Research [22116001, 22116002, 23659157, 21590256, 21390083, 22790296] Funding Source: KAKEN

向作者/读者索取更多资源

GPR55 is a seven transmembrane G protein-coupled receptor and was originally identified as a putative third cannabinoid receptor. Recently, lysophosphatidylinositol (LPI) was reported to be a GPR55 ligand. Stimulation of GPR55 by LPI activates G(12/13) and G(q/11) proteins, induces phosphorylation of the extracellular signal-regulated kinase and increases intracellular calcium concentration. Lysophospholipids are molecularly quite diverse across species and tissues. A recent report showed that the predominant fatty acyl moiety of LPI in rat brain is stearic acid followed by arachidonic acid. The biological activity of arachidonic acid-containing LPI species towards GPR55 was shown to be markedly higher than that of LPI species containing other fatty acyl groups, suggesting that 2-arachidonolyl LPI is the most likely natural ligand of GPR55.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.2
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据