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佩利诺2激活丝裂原活化蛋白激酶途径。

Pellino2 activates the mitogen activated protein kinase pathway.

作者信息

Jensen Liselotte E, Whitehead Alexander S

机构信息

Department of Pharmacology and Center for Pharmacogenetics, University of Pennsylvania School of Medicine, 153 Johnson Pavilion, 3620 Hamilton Walk, Philadelphia, PA 19104-6084, USA.

出版信息

FEBS Lett. 2003 Jun 19;545(2-3):199-202. doi: 10.1016/s0014-5793(03)00533-7.

Abstract

Engagement of the interleukin-1 (IL1) and Toll receptors, which are part of the innate immune system, facilitates activation of the transcription factors NF-kappaB, Elk-1 and AP-1. Pellino1 and Pellino2 have recently been shown to be intermediates in the pathway leading to activation of NF-kappaB. Here we demonstrate for the first time that human Pellino2 interacts with TRAF6 (tumor necrosis factor receptor associated factor 6) and that both Pellino1 and Pellino2 also interact with TAK1 (transforming growth factor-beta activated kinase 1). We also show that Pellino2, but not Pellino1, can activate the mitogen activated protein kinase pathway leading to activation of AP-1 and Elk-1. These observations suggest a role for the Pellino proteins in the IL1/Toll signaling cascades as scaffold proteins that may regulate signaling branch-points.

摘要

作为天然免疫系统一部分的白细胞介素-1(IL1)和Toll受体的激活,促进了转录因子NF-κB、Elk-1和AP-1的活化。最近研究表明,Pellino1和Pellino2是导致NF-κB活化途径中的中间介质。在此,我们首次证明人Pellino2与TRAF6(肿瘤坏死因子受体相关因子6)相互作用,并且Pellino1和Pellino2都与TAK1(转化生长因子-β激活激酶1)相互作用。我们还表明,Pellino2而非Pellino1能够激活丝裂原活化蛋白激酶途径,从而导致AP-1和Elk-1的活化。这些观察结果提示,Pellino蛋白在IL1/Toll信号级联反应中作为支架蛋白发挥作用,可能调节信号分支点。

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