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Structure-activity relationships of lysophosphatidylserine analogs as agonists of G-protein-coupled receptors GPR34, P2Y10, and GPR174.溶血磷脂酰丝氨酸类似物作为 G 蛋白偶联受体 GPR34、P2Y10 和 GPR174 的激动剂的构效关系。
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本文引用的文献

1
Lysophospholipid receptor nomenclature review: IUPHAR Review 8.溶血磷脂受体命名综述:IUPHAR综述8。
Br J Pharmacol. 2014 Aug;171(15):3575-94. doi: 10.1111/bph.12678. Epub 2014 Jul 12.
2
Identification of a unique TGF-β-dependent molecular and functional signature in microglia.鉴定小胶质细胞中独特的 TGF-β 依赖性分子和功能特征。
Nat Neurosci. 2014 Jan;17(1):131-43. doi: 10.1038/nn.3599. Epub 2013 Dec 8.
3
rs3827440, a nonsynonymous single nucleotide polymorphism within GPR174 gene in X chromosome, is associated with Graves' disease in Polish Caucasian population.rs3827440,位于X染色体上GPR174基因内的一个非同义单核苷酸多态性,与波兰白种人群中的格雷夫斯病相关。
Tissue Antigens. 2014 Jan;83(1):41-4. doi: 10.1111/tan.12259. Epub 2013 Nov 30.
4
Genetic background can result in a marked or minimal effect of gene knockout (GPR55 and CB2 receptor) in experimental autoimmune encephalomyelitis models of multiple sclerosis.在多发性硬化症的实验性自身免疫性脑脊髓炎模型中,遗传背景可能导致基因敲除(GPR55和CB2受体)产生显著或微小的影响。
PLoS One. 2013 Oct 9;8(10):e76907. doi: 10.1371/journal.pone.0076907. eCollection 2013.
5
Lysophosphatidylethanolamine utilizes LPA(1) and CD97 in MDA-MB-231 breast cancer cells.溶血磷脂酰乙醇胺在 MDA-MB-231 乳腺癌细胞中利用 LPA(1)和 CD97。
Cell Signal. 2013 Nov;25(11):2147-54. doi: 10.1016/j.cellsig.2013.07.001. Epub 2013 Jul 6.
6
Upregulation of GPR34 expression affects the progression and prognosis of human gastric adenocarcinoma by PI3K/PDK1/AKT pathway.GPR34 表达上调通过 PI3K/PDK1/AKT 通路影响人胃腺癌的进展和预后。
Histol Histopathol. 2013 Dec;28(12):1629-38. doi: 10.14670/HH-28.1629. Epub 2013 Jul 9.
7
The actions and metabolism of lysophosphatidylinositol, an endogenous agonist for GPR55.溶血磷脂酰肌醇的作用和代谢,GPR55 的内源性激动剂。
Prostaglandins Other Lipid Mediat. 2013 Dec;107:103-16. doi: 10.1016/j.prostaglandins.2013.05.004. Epub 2013 May 25.
8
An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves' disease.全染色体 X 连锁关联分析发现 GPR174 中的变异是 Graves 病的风险因素。
J Med Genet. 2013 Jul;50(7):479-85. doi: 10.1136/jmedgenet-2013-101595. Epub 2013 May 10.
9
Neutrophils regulate tissue Neutrophilia in inflammation via the oxidant-modified lipid lysophosphatidylserine.中性粒细胞通过氧化修饰的脂质溶血磷脂酰丝氨酸调节炎症中的组织嗜中性粒细胞增多症。
J Biol Chem. 2013 Feb 15;288(7):4583-93. doi: 10.1074/jbc.M112.438507. Epub 2013 Jan 5.
10
Expression of orphan G-protein coupled receptor GPR174 in CHO cells induced morphological changes and proliferation delay via increasing intracellular cAMP.孤儿 G 蛋白偶联受体 GPR174 在 CHO 细胞中的表达通过增加细胞内 cAMP 引起形态变化和增殖延迟。
Biochem Biophys Res Commun. 2013 Jan 4;430(1):190-5. doi: 10.1016/j.bbrc.2012.11.046. Epub 2012 Nov 23.

新型溶血磷脂受体:其结构与功能

Novel lysophosphoplipid receptors: their structure and function.

作者信息

Makide Kumiko, Uwamizu Akiharu, Shinjo Yuji, Ishiguro Jun, Okutani Michiyo, Inoue Asuka, Aoki Junken

机构信息

Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai, Japan PRESTO Japan Science and Technology Corporation, Saitama, Japan.

Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai, Japan.

出版信息

J Lipid Res. 2014 Oct;55(10):1986-95. doi: 10.1194/jlr.R046920. Epub 2014 Jun 2.

DOI:10.1194/jlr.R046920
PMID:24891334
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4173991/
Abstract

It is now accepted that lysophospholipids (LysoGPs) have a wide variety of functions as lipid mediators that are exerted through G protein-coupled receptors (GPCRs) specific to each lysophospholipid. While the roles of some LysoGPs, such as lysophosphatidic acid and sphingosine 1-phosphate, have been thoroughly examined, little is known about the roles of several other LysoGPs, such as lysophosphatidylserine (LysoPS), lysophosphatidylthreonine, lysophosphatidylethanolamine, lysophosphatidylinositol (LPI), and lysophosphatidylglycerol. Recently, a GPCR was found for LPI (GPR55) and three GPCRs (GPR34/LPS1, P2Y10/LPS2, and GPR174/LPS3) were found for LysoPS. In this review, we focus on these newly identified GPCRs and summarize the actions of LysoPS and LPI as lipid mediators.

摘要

现在人们已经认识到,溶血磷脂(LysoGPs)作为脂质介质具有多种功能,这些功能是通过每种溶血磷脂特有的G蛋白偶联受体(GPCRs)发挥的。虽然一些溶血磷脂的作用,如溶血磷脂酸和1-磷酸鞘氨醇,已经得到了深入研究,但对于其他几种溶血磷脂的作用,如溶血磷脂酰丝氨酸(LysoPS)、溶血磷脂酰苏氨酸、溶血磷脂酰乙醇胺、溶血磷脂酰肌醇(LPI)和溶血磷脂酰甘油,人们却知之甚少。最近,发现了一种LPI的GPCR(GPR55),并发现了三种LysoPS的GPCR(GPR34/LPS1、P2Y10/LPS2和GPR174/LPS3)。在这篇综述中,我们重点关注这些新发现的GPCR,并总结LysoPS和LPI作为脂质介质的作用。