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IL-1β 激活中性鞘磷脂酶需要 1 型白细胞介素 1 受体。

Activation of neutral sphingomyelinase by IL-1beta requires the type 1 interleukin 1 receptor.

作者信息

Nalivaeva N N, Rybakina E G, Kozinets I A, Shanin S N, Bartfai T

机构信息

Department of Comparative Neurochemistry, Institute of Evolutionary Biochemistry and Physiology, St. Petersburg, Russia.

出版信息

Cytokine. 2000 Mar;12(3):229-32. doi: 10.1006/cyto.1999.0547.

Abstract

The cytokine interleukin 1beta (IL-1beta) plays an important role in host defence reactions and neuro-immune interactions but it is still not clear which of the two interleukin 1 receptor subtypes is coupled to activation of neutral sphingomyelinase (nSMase) by IL-1beta. To investigate involvement of neutral sphingomyelinase (nSMase) in central IL-1beta effects we used P(2)fractions of brain cerebral cortex from wild-type mice and mice deficient in the type 1 IL-1 receptor. IL-1beta (human, recombinant) was shown to activate, in a dose-dependent manner, nSMase in the P(2)brain fraction of the wild-type mice while in the knock-out mice the stimulatory effect of IL-1beta on nSMase was absent. In the presence of an IL-1 receptor antagonist (IL-1ra), IL-1beta did not activate nSMase either in the cortex of wild-type or knock-out mice. These data suggest that nSMase, a key enzyme of the sphingomyelin signal transduction pathway, might be involved in IL-1beta signalling in the brain and that activation of the enzyme requires the IL-1 receptor type 1.

摘要

细胞因子白细胞介素1β(IL-1β)在宿主防御反应和神经免疫相互作用中发挥着重要作用,但目前仍不清楚两种白细胞介素1受体亚型中的哪一种与IL-1β介导的中性鞘磷脂酶(nSMase)激活有关。为了研究中性鞘磷脂酶(nSMase)在中枢IL-1β效应中的作用,我们使用了野生型小鼠和缺乏1型IL-1受体的小鼠大脑皮质的P(2)组分。结果显示,IL-1β(重组人源)能以剂量依赖的方式激活野生型小鼠大脑P(2)组分中的nSMase,而在基因敲除小鼠中,IL-1β对nSMase的刺激作用则不存在。在存在IL-1受体拮抗剂(IL-1ra)的情况下,IL-1β在野生型或基因敲除小鼠的皮质中均未激活nSMase。这些数据表明,作为鞘磷脂信号转导途径关键酶的nSMase可能参与大脑中的IL-1β信号传导,且该酶的激活需要1型IL-1受体。

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