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Journal of Biochemistry Advance Access published online on July 23, 2007

Journal of Biochemistry, doi:10.1093/jb/mvm141
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© 2007 The Japanese Biochemical Society

Involvement of sphingosine 1-phosphate, a platelet-derived bioactive lipid, in contraction of mesangium cells

Makoto Osada1, Yutaka Yatomi2,*, Tsukasa Ohmori1, Shinya Aoki2, Shigemi Hosogaya1 and Yukio Ozaki1

1Department of Clinical and Laboratory Medicine, Faculty of Medicine, University of Yamanashi, Yamanashi, Japan
2Department of Clinical Laboratory Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.

*Correspondence to: Yutaka Yatomi, MD, PhD, Department of Clinical Laboratory Medicine, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan. Tel: +81-3-5800-8721; Fax: +81-3-5689-0495; E-mail: yatoyuta-tky{at}umin.ac.jp

Received March 30, 2007; Accepted June 19, 2007


   Abstract

Platelet-derived mediators may play an important role in the development of renal diseases through interaction with glomerular mesangial cells (MCs), and we, in this study, examined the effect of sphingosine 1-phosphate (Sph-1-P), a bioactive lipid released from activated platelets, on the contraction of MCs. Sph-1-P was found to induce MC contraction through mediation of Rho kinase both in cell shape change and collagen gel contraction assays. The specific antagonist of the Sph-1-P receptor S1P2 inhibited the response. Similar results were obtained when the supernatant from activated platelet suspensions were used instead of Sph-1-P. Our findings suggest that platelet-derived Sph-1-P may be involved in MC contraction via S1P2 and that regulation of this receptor might be useful therapeutically.

Key Words: Contraction, Mesangial cell, Platelet, Rho kinase, S1P2, Sphingosine 1-phosphate


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