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哺乳动物细胞中的1-磷酸鞘氨醇受体1信号传导

Sphingosine 1-Phosphate Receptor 1 Signaling in Mammalian Cells.

作者信息

Pyne Nigel J, Pyne Susan

机构信息

Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow G4 0RE, UK.

出版信息

Molecules. 2017 Feb 23;22(3):344. doi: 10.3390/molecules22030344.

Abstract

The bioactive lipid, sphingosine 1-phosphate (S1P) binds to a family of G protein-coupled receptors, termed S1P₁-S1P₅. These receptors function in, for example, the cardiovascular system to regulate vascular barrier integrity and tone, the nervous system to regulate neuronal differentiation, myelination and oligodendrocyte/glial cell survival and the immune system to regulate T- and B-cell subsets and trafficking. S1P receptors also participate in the pathophysiology of autoimmunity, inflammatory disease, cancer, neurodegeneration and others. In this review, we describe how S1P₁ can form a complex with G-protein and β-arrestin, which function together to regulate effector pathways. We also discuss the role of the S1P₁-Platelet derived growth factor receptor β functional complex (which deploys G-protein/β-arrestin and receptor tyrosine kinase signaling) in regulating cell migration. Possible mechanisms by which different S1P-chaperones, such as Apolipoprotein M-High-Density Lipoprotein induce biological programmes in cells are also described. Finally, the role of S1P₁ in health and disease and as a target for clinical intervention is appraised.

摘要

生物活性脂质鞘氨醇-1-磷酸(S1P)与一类称为S1P₁ - S1P₅的G蛋白偶联受体结合。这些受体在例如心血管系统中发挥作用,调节血管屏障的完整性和张力;在神经系统中调节神经元分化、髓鞘形成以及少突胶质细胞/神经胶质细胞存活;在免疫系统中调节T细胞和B细胞亚群及运输。S1P受体还参与自身免疫、炎症性疾病、癌症、神经退行性变等的病理生理学过程。在本综述中,我们描述了S1P₁如何与G蛋白和β - 抑制蛋白形成复合物,它们共同发挥作用来调节效应器途径。我们还讨论了S1P₁ - 血小板衍生生长因子受体β功能复合物(其利用G蛋白/β - 抑制蛋白和受体酪氨酸激酶信号传导)在调节细胞迁移中的作用。还描述了不同的S1P伴侣分子,如载脂蛋白M - 高密度脂蛋白在细胞中诱导生物学程序的可能机制。最后,对S1P₁在健康和疾病中的作用以及作为临床干预靶点进行了评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0de9/6155263/a70cc605bf37/molecules-22-00344-g001.jpg

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