Sphingosine-1-Phosphate and Its Receptors: A Mutual Link between Blood Coagulation and Inflammation

Bibliographic Details
Title: Sphingosine-1-Phosphate and Its Receptors: A Mutual Link between Blood Coagulation and Inflammation
Authors: Shailaja Mahajan-Thakur, Andreas Böhm, Gabriele Jedlitschky, Karsten Schrör, Bernhard H. Rauch
Source: Mediators of Inflammation, Vol 2015 (2015)
Publisher Information: Hindawi Limited, 2015.
Publication Year: 2015
Collection: LCC:Pathology
Subject Terms: Pathology, RB1-214
More Details: Sphingosine-1-phosphate (S1P) is a versatile lipid signaling molecule and key regulator in vascular inflammation. S1P is secreted by platelets, monocytes, and vascular endothelial and smooth muscle cells. It binds specifically to a family of G-protein-coupled receptors, S1P receptors 1 to 5, resulting in downstream signaling and numerous cellular effects. S1P modulates cell proliferation and migration, and mediates proinflammatory responses and apoptosis. In the vascular barrier, S1P regulates permeability and endothelial reactions and recruitment of monocytes and may modulate atherosclerosis. Only recently has S1P emerged as a critical mediator which directly links the coagulation factor system to vascular inflammation. The multifunctional proteases thrombin and FXa regulate local S1P availability and interact with S1P signaling at multiple levels in various vascular cell types. Differential expression patterns and intracellular signaling pathways of each receptor enable S1P to exert its widespread functions. Although a vast amount of information is available about the functions of S1P and its receptors in the regulation of physiological and pathophysiological conditions, S1P-mediated mechanisms in the vasculature remain to be elucidated. This review summarizes recent findings regarding the role of S1P and its receptors in vascular wall and blood cells, which link the coagulation system to inflammatory responses in the vasculature.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 0962-9351
1466-1861
Relation: https://doaj.org/toc/0962-9351; https://doaj.org/toc/1466-1861
DOI: 10.1155/2015/831059
Access URL: https://doaj.org/article/4db6e6eae99c4bdeae06847c644d6125
Accession Number: edsdoj.4db6e6eae99c4bdeae06847c644d6125
Database: Directory of Open Access Journals
More Details
ISSN:09629351
14661861
DOI:10.1155/2015/831059
Published in:Mediators of Inflammation
Language:English