Kozawa O, Tanabe K, Ito H, Matsuno H, Niwa M, Kato K, Uematsu T
Department of Pharmacology, Gifu University School of Medicine, Gifu, 500-8705, Japan.
Exp Cell Res. 1999 Aug 1;250(2):376-80. doi: 10.1006/excr.1999.4536.
In an aortic smooth muscle cell line, A10 cells, we investigated the effect of sphingosine 1-phosphate on the induction of heat shock protein 27 (HSP27), a low-molecular-weight heat shock protein. Sphingosine 1-phosphate significantly induced the accumulation of HSP27 in a pertussis toxin-sensitive manner. The effect was dose-dependent in the range between 0.1 and 30 microM. Sphingosine 1-phosphate stimulated an increase in the levels of mRNA for HSP27. Sphingosine 1-phosphate stimulated both p42/p44 mitogen-activated protein (MAP) kinase and p38 MAP kinase activation. PD98059, an inhibitor of the upstream kinase that activates p42/p44 MAP kinase, did not affect sphingosine 1-phosphate-stimulated HSP27 induction. In contrast, SB203580, an inhibitor of p38 MAP kinase, reduced sphingosine 1-phosphate-induced HSP27 induction. SB203580 reduced the levels of mRNA for HSP27 induced by sphingosine 1-phosphate. These results indicate that sphingosine 1-phosphate stimulates the induction of HSP27 via p38 MAP kinase activation in aortic smooth muscle cells.
在主动脉平滑肌细胞系A10细胞中,我们研究了1 -磷酸鞘氨醇对低分子量热休克蛋白热休克蛋白27(HSP27)诱导的影响。1 -磷酸鞘氨醇以百日咳毒素敏感的方式显著诱导HSP27的积累。在0.1至30微摩尔的范围内,该效应呈剂量依赖性。1 -磷酸鞘氨醇刺激HSP27的mRNA水平升高。1 -磷酸鞘氨醇刺激p42 / p44丝裂原活化蛋白(MAP)激酶和p38 MAP激酶的激活。PD98059,一种激活p42 / p44 MAP激酶的上游激酶抑制剂,不影响1 -磷酸鞘氨醇刺激的HSP27诱导。相反,p38 MAP激酶抑制剂SB203580降低了1 -磷酸鞘氨醇诱导的HSP27诱导。SB203580降低了1 -磷酸鞘氨醇诱导的HSP27的mRNA水平。这些结果表明,1 -磷酸鞘氨醇通过激活主动脉平滑肌细胞中的p38 MAP激酶刺激HSP27的诱导。