نتایج جستجو برای: s1p receptor

تعداد نتایج: 591328  

Journal: :Cardiovascular research 2009
Christopher K Means Joan Heller Brown

The five known members of the sphingosine-1-phosphate (S1P) receptor family exhibit diverse tissue expression profiles and couple to distinct G-protein-mediated signalling pathways. S1P1, S1P2, and S1P3 receptors are all present in the heart, but the ratio of these subtypes differs for various cardiac cells. The goal of this review is to summarize data concerning which S1P receptor subtypes reg...

2014
Johannes Keller Philip Catala-Lehnen Antje K. Huebner Anke Jeschke Timo Heckt Anja Lueth Matthias Krause Till Koehne Joachim Albers Jochen Schulze Sarah Schilling Michael Haberland Hannah Denninger Mona Neven Irm Hermans-Borgmeyer Thomas Streichert Stefan Breer Florian Barvencik Bodo Levkau Birgit Rathkolb Eckhard Wolf Julia Calzada-Wack Frauke Neff Valerie Gailus-Durner Helmut Fuchs Martin Hrabě de Angelis Susanne Klutmann Elena Tsourdi Lorenz C. Hofbauer Burkhard Kleuser Jerold Chun Thorsten Schinke Michael Amling

The hormone calcitonin (CT) is primarily known for its pharmacologic action as an inhibitor of bone resorption, yet CT-deficient mice display increased bone formation. These findings raised the question about the underlying cellular and molecular mechanism of CT action. Here we show that either ubiquitous or osteoclast-specific inactivation of the murine CT receptor (CTR) causes increased bone ...

2012
P Gergely B Nuesslein-Hildesheim D Guerini V Brinkmann M Traebert C Bruns S Pan NS Gray K Hinterding NG Cooke A Groenewegen A Vitaliti T Sing O Luttringer J Yang A Gardin N Wang WJ Crumb Jr M Saltzman M Rosenberg E Wallström

BACKGROUND AND PURPOSE BAF312 is a next-generation sphingosine 1-phosphate (S1P) receptor modulator, selective for S1P(1) and S1P(5 ) receptors. S1P(1) receptors are essential for lymphocyte egress from lymph nodes and a drug target in immune-mediated diseases. Here, we have characterized the immunomodulatory potential of BAF312 and the S1P receptor-mediated effects on heart rate using precli...

Journal: :American journal of physiology. Lung cellular and molecular physiology 2008
Li-Yuan Chen Grzegorz Woszczek Sahrudaya Nagineni Carolea Logun James H Shelhamer

Cytosolic phospholipase A(2)alpha (cPLA(2)alpha) activation is a regulatory step in the control of arachidonic acid (AA) liberation for eicosanoid formation. Sphingosine 1-phosphate (S1P) is a bioactive lipid mediator involved in the regulation of many important proinflammatory processes and has been found in the airways of asthmatic subjects. We investigated the mechanism of S1P-induced AA rel...

2011
Andrea Huwiler Florence Bourquin Nataliya Kotelevets Oleksandr Pastukhov Guido Capitani Markus G. Grütter Uwe Zangemeister-Wittke

Sphingosine-1-phosphate (S1P) regulates a broad spectrum of fundamental cellular processes like proliferation, death, migration and cytokine production. Therefore, elevated levels of S1P may be causal to various pathologic conditions including cancer, fibrosis, inflammation, autoimmune diseases and aberrant angiogenesis. Here we report that S1P lyase from the prokaryote Symbiobacterium thermoph...

2015
Daniela Weth Camilla Benetti Caroline Rauch Gerhard Gstraunthaler Helmut Schmidt Gerd Geisslinger Roger Sabbadini Richard L. Proia Michaela Kress

At the site of injury activated platelets release various mediators, one of which is sphingosine 1-phosphate (S1P). It was the aim of this study to explore whether activated human platelets had a pronociceptive effect in an in vivo mouse model and whether this effect was based on the release of S1P and subsequent activation of neuronal S1P receptors 1 or 3. Human platelets were prepared in diff...

Journal: :The Biochemical journal 2000
T Kimura T Watanabe K Sato J Kon H Tomura K Tamama A Kuwabara T Kanda I Kobayashi H Ohta M Ui F Okajima

Sphingosine 1-phosphate (S1P) stimulates thymidine incorporation (DNA synthesis), cell growth and cell migration in human aortic endothelial cells (HAECs). The extent of the S1P-induced responses are comparable to those stimulated by vascular endothelial growth factor, one of the most potent stimulators of angiogenesis. These responses to S1P were mimicked by dihydrosphingosine 1-phosphate, an ...

Journal: :The Journal of pharmacology and experimental therapeutics 2011
Perry C Kennedy Ran Zhu Tao Huang Jose L Tomsig Thomas P Mathews Marion David Olivier Peyruchaud Timothy L Macdonald Kevin R Lynch

Sphingosine 1-phosphate (S1P) is a phospholipid that binds to a set of G protein-coupled receptors (S1P(1)-S1P(5)) to initiate an array of signaling cascades that affect cell survival, differentiation, proliferation, and migration. On a larger physiological scale, the effects of S1P on immune cell trafficking, vascular barrier integrity, angiogenesis, and heart rate have also been observed. An ...

Journal: :Journal of immunology 2005
Niklas Czeloth Günter Bernhardt Fred Hofmann Harald Genth Reinhold Förster

Sphingosine-1-phosphate (S1P) represents a potent modulator of diverse cellular activities, including lymphocyte trafficking and maintenance of lymphocyte homeostasis. The five known receptors for S1P (S1P(1-5)) belong to the family of G protein-coupled receptors. Upon binding S1P, they act downstream via heterotrimeric G proteins on members of the small GTPase family (Cdc42/Rac/Rho), evoking a...

Journal: :Critical reviews in biochemistry and molecular biology 2011
Kyoko Noguchi Jerold Chun

Sphingosine 1-phosphate (S1P) signaling in the treatment of multiple sclerosis (MS) has been highlighted by the efficacy of FTY720 (fingolimod), which upon phosphorylation can modulate S1P receptor activities. FTY720 has become the first oral treatment for relapsing MS that was approved by the FDA in September 2010. Phosphorylated FTY720 modulates four of the five known S1P receptors (S1P(1), S...

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