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Sphingosine-1-phosphate receptors: Biology and therapeutic potential in kidney disease

Authors
Jo, S-KBajwa, A.Awad, A. S.Lynch, K. R.Okusa, M. D.
Issue Date
6월-2008
Publisher
ELSEVIER SCIENCE INC
Keywords
FTY720; SEW2871; ischemia-reperfusion injury; acute kidney injury; sphingolipid; S1P
Citation
KIDNEY INTERNATIONAL, v.73, no.11, pp.1220 - 1230
Indexed
SCIE
SCOPUS
Journal Title
KIDNEY INTERNATIONAL
Volume
73
Number
11
Start Page
1220
End Page
1230
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/123412
DOI
10.1038/ki.2008.34
ISSN
0085-2538
Abstract
The major sphingolipid metabolite, sphingosine-1-phosphate (S1P), has important biological functions. S1P is the ligand for a family of five G-protein-coupled receptors with distinct signaling pathways that regulate angiogenesis, vascular maturation, immunity, chemotaxis, and other important biological pathways. Recently, clinical trials have targeted S1P receptors (S1PRs) for autoimmune diseases and transplantation and have generated considerable interest in developing additional, more selective compounds. This review summarizes current knowledge on the biology of S1P and S1PRs that forms the basis for future drug development and the treatment of kidney disease.
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