Identification of ceramide targets in interleukin-1 and tumor necrosis factor-α signaling in mesangial cells

被引:14
作者
Pfeilschifter, J
Huwiler, A
机构
[1] Univ Frankfurt Klinikum, Zentrum Pharmakol, D-60590 Frankfurt, Germany
[2] Univ Utrecht, Ctr Biomembranes & Lipid Enzymol, Utrecht, Netherlands
关键词
extracellular signal-regulated kinase; protein kinase C; sphingomyelin; mitogen-activated protein kinase; I-125]iodine-specific radioactivity;
D O I
10.1046/j.1523-1755.1998.06707.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
An increasing number of cell-surface receptors have been shown to trigger sphingomyelin turnover and generation of the lipid signaling molecule ceramide. Ceramide plays a role in mediating cellular responses as diverse as inflammation, differentiation, gene expression, growth suppression, and apoptosis. A radioiodinated, photoaffinity-labeling analog of ceramide ([I-125]TID-ceramide) was used to identify downstream signaling targets of ceramide. Ceramide was found to bind specifically to and activate protein kinase c-Raf, leading to subsequent activation of the extracellular signal-regulated kinase (ERK) module in mesangial cells. We found also that ceramide binds to and differentially modulates the activity of distinct protein kinase C isoenzymes. These data are discussed in the context of interleukin 1 beta-induced inflammatory gene expression in mesangial cells.
引用
收藏
页码:S34 / S39
页数:6
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