Normal acute and chronic inflammatory responses in sphingosine kinase 1 knockout mice

被引:69
作者
Michaud, Jason
Kohno, Masataka
Proia, Richard L.
Hla, Timothy
机构
[1] Univ Connecticut, Ctr Hlth, Ctr Vasc Biol, Dept Cell Biol, Farmington, CT 06030 USA
[2] Kyoto Prefectural Univ Med, Grad Sch Med Sci, Kyoto 6028566, Japan
[3] NIDDK, Genet Dev & Dis Branch, NIH, Bethesda, MD 20892 USA
来源
FEBS LETTERS | 2006年 / 580卷 / 19期
关键词
sphingosine kinase; sphingolipids; inflammation; arthritis;
D O I
10.1016/j.febslet.2006.07.035
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sphingosine-1-phosophate, generated from the phosphorylation of sphingosine by sphingosine kinase enzymes, is suggested to function as an intracellular second messenger for inflammatory mediators, including formyl peptide, C5a, and Fc. More recently, a role for sphingosine kinases during inflammation has also been proposed. Here we show that sphingosine kinase 1 knockout mice exhibit normal inflammatory cell recruitment during thioglycollate-induced peritonitis and that sphingosine kinase 1-null neutrophils respond normally to formyl peptide. In the collagen-induced arthritis model of rheumatoid arthritis, sphingosine kinase 1 knockout mice developed arthritis with normal incidence and severity. Our findings show that sphingosine kinase 1 is dispensable for inflammatory responses and support the need for more extensive studies of sphingosine kinases in inflammation. (c) 2006 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:4607 / 4612
页数:6
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