Sphingosine 1-phosphate (S1P) signalling: role in bone biology and potential therapeutic target for bone repair

dc.check.date2018-08-30
dc.check.infoAccess to this article is restricted until 12 months after publication by request of the publisher.en
dc.contributor.authorSartawi, Ziad
dc.contributor.authorSchipani, Ernestina
dc.contributor.authorRyan, Katie B.
dc.contributor.authorWaeber, Christian
dc.date.accessioned2017-10-20T11:06:49Z
dc.date.available2017-10-20T11:06:49Z
dc.date.issued2017-08-30
dc.date.updated2017-09-22T12:18:53Z
dc.description.abstractThe lipid mediator sphingosine 1-phosphate (S1P) affects cellular functions in most systems. Interest in its therapeutic potential has increased following the discovery of its G protein-coupled receptors and the recent availability of agents that can be safely administered in humans. Although the role of S1P in bone biology has been the focus of much less research than its role in the nervous, cardiovascular and immune systems, it is becoming clear that this lipid influences many of the functions, pathways and cell types that play a key role in bone maintenance and repair. Indeed, S1P is implicated in many osteogenesis-related processes including stem cell recruitment and subsequent differentiation, differentiation and survival of osteoblasts, and coupling of the latter cell type with osteoclasts. In addition, S1P’s role in promoting angiogenesis is well-established. The pleiotropic effects of S1P on bone and blood vessels have significant potential therapeutic implications, as current therapeutic approaches for critical bone defects show significant limitations. Because of the complex effects of S1P on bone, the pharmacology of S1P-like agents and their physico-chemical properties, it is likely that therapeutic delivery of S1P agents will offer significant advantages compared to larger molecular weight factors. Hence, it is important to explore novel methods of utilizing S1P agents therapeutically, and improve our understanding of how S1P and its receptors modulate bone physiology and repair.en
dc.description.statusPeer revieweden
dc.description.versionAccepted Versionen
dc.format.mimetypeapplication/pdfen
dc.identifier.citationSartawi, Z., Schipani, E., Ryan, K. B. and Waeber, C. (2017) 'Sphingosine 1-phosphate (S1P) signalling: role in bone biology and potential therapeutic target for bone repair', Pharmacological Research, 125, pp. 232-245. doi:10.1016/j.phrs.2017.08.013en
dc.identifier.doi10.1016/j.phrs.2017.08.013
dc.identifier.endpage245en
dc.identifier.issn1043-6618
dc.identifier.journaltitlePharmacological Researchen
dc.identifier.startpage232en
dc.identifier.urihttps://hdl.handle.net/10468/4922
dc.identifier.volume125en
dc.language.isoenen
dc.publisherElsevier Ltden
dc.rights© 2017, Elsevier Ltd. All rights reserved. This manuscript version is made available under the CC-BY-NC-ND 4.0 license.en
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en
dc.subjectBone regenerationen
dc.subjectBone defecten
dc.subjectOsteoblastsen
dc.subjectOsteoclastsen
dc.subjectSphingosine 1-phosphateen
dc.titleSphingosine 1-phosphate (S1P) signalling: role in bone biology and potential therapeutic target for bone repairen
dc.typeArticle (peer-reviewed)en
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