Pfeilschifter J, Huwiler A
Zentrum der Pharmakologie, Klinikum der Johann Wolfgang Goethe-Universität, Frankfurt am Main, Germany.
Kidney Int Suppl. 1998 Sep;67:S34-9. doi: 10.1046/j.1523-1755.1998.06707.x.
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 ([125I]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 1beta-induced inflammatory gene expression in mesangial cells.
越来越多的细胞表面受体已被证明可触发鞘磷脂周转并生成脂质信号分子神经酰胺。神经酰胺在介导多种细胞反应中发挥作用,如炎症、分化、基因表达、生长抑制和细胞凋亡。一种放射性碘化的神经酰胺光亲和标记类似物([125I]TID-神经酰胺)被用于鉴定神经酰胺的下游信号靶点。发现神经酰胺可特异性结合并激活蛋白激酶c-Raf,从而导致系膜细胞中细胞外信号调节激酶(ERK)模块的后续激活。我们还发现神经酰胺可结合并差异性调节不同蛋白激酶C同工酶的活性。这些数据在白细胞介素1β诱导的系膜细胞炎症基因表达的背景下进行了讨论。