首页> 美国卫生研究院文献>The Journal of Experimental Medicine >A Role for Neutral Sphingomyelinase-mediated Ceramide Production in T Cell Receptor–induced Apoptosis and Mitogen-activated Protein Kinase–mediated Signal Transduction
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A Role for Neutral Sphingomyelinase-mediated Ceramide Production in T Cell Receptor–induced Apoptosis and Mitogen-activated Protein Kinase–mediated Signal Transduction

机译:中性鞘磷脂酶介导的神经酰胺产生在T细胞受体诱导的细胞凋亡和丝裂原激活的蛋白激酶介导的信号转导中的作用。

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摘要

Studying apoptosis induced by T cell receptor (TCR) cross-linking in the T cell hybridoma, 3DO, we found both neutral sphingomyelinase activation and production of ceramide upon receptor engagement. Pharmacological inhibition of ceramide production by the fungal toxin, fumonisin B1, impaired TCR-induced interleukin (IL)-2 production and programmed cell death. Addition of either exogenous ceramide or bacterial sphingomyelinase reconstituted both responses. Moreover, specific inactivation of neutral sphingomyelinase by antisense RNA inhibited IL-2 production and mitogen-activated protein kinase activation after TCR triggering. These results suggest that ceramide production by activation of neutral sphingomyelinase is an essential component of the TCR signaling machinery.
机译:研究T细胞杂交瘤3DO中T细胞受体(TCR)交联诱导的凋亡,我们发现中性鞘磷脂酶激活和受体参与后神经酰胺的产生。药理学上抑制真菌毒素,伏马毒素B1产生的神经酰胺的产生,损害TCR诱导的白介素(IL)-2的产生和程序性细胞死亡。外源神经酰胺或细菌鞘磷脂酶的添加重建了两种反应。此外,TCR触发后,反义RNA对中性鞘磷脂酶的特异性失活抑制了IL-2的产生和丝裂原活化的蛋白激酶的活化。这些结果表明,通过激活中性鞘磷脂酶产生的神经酰胺是TCR信号转导机制的重要组成部分。

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