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鞭毛蛋白和脂多糖通过小GTP酶Ras和Rap1的差异激活来刺激鸡异嗜性粒细胞中的MEK-ERK信号通路。

Flagellin and lipopolysaccharide stimulate the MEK-ERK signaling pathway in chicken heterophils through differential activation of the small GTPases, Ras and Rap1.

作者信息

Kogut M H, Genovese K J, He H

机构信息

Laboratory of Avian Innate Immunity, USDA-ARS, Southern Plains Agricultural Research Center, 2881 F&B Road, College Station, TX 77845, USA.

出版信息

Mol Immunol. 2007 Mar;44(7):1729-36. doi: 10.1016/j.molimm.2006.07.292. Epub 2006 Oct 12.

Abstract

The TLR agonists, flagellin (FLG) and lipopolysaccharide (LPS) stimulate functional activation and cytokine gene expression via the extracellular signal regulated kinase 1/2 (ERK1/2) MAP kinase cascade. However, the upstream mechanisms of these signaling events remain unknown. In mammals, the small GTP-binding protein Ras mediates ERK1/2 activation through activation of downstream effectors Raf-1-MEK1/2-ERK1/2 in response to a variety of stimuli. It is not clear whether this classic Ras cascade plays a role in TLR signaling in avian cells. In the present study, we investigated the role of Ras in FLG- and LPS-mediated signaling in ERK activation in chicken heterophils. Treatment of heterophils with LPS caused a rapid (within 5min) activation of Ras-GTP. The role of Ras activation in LPS-induced stimulation of ERK1/2 was corroborated when the specific Ras inhibitor, FTI-277, inhibited ERK1/2 activation. The classic Ras-mediated pathway of ERK1/2 activation by LPS was confirmed when the specific Raf-1 inhibitor, GW 5074, and the MEK1/2 inhibitor, U0126, both reduced ERK activation by 51-60%. Of more interest was that treatment of the heterophils with FLG did not activate Ras-GTP. Likewise, neither FTI-277 nor GW 5074 had any effect on FLG-mediated activation of ERK1/2. Another small GTPase, Rap1, has been shown to play a role in mammalian neutrophil function. Using a Rap1-GTP pull-down assay, we found that FLG stimulation, but not LPS, of avian heterophils induced a rapid and transient Rap1 activation. Rap1 has been shown to activate the ERK1/2 via a different Raf family member B-Raf whose downstream effector is MEK1/2. We show here that FLG stimulation of heterophils induces the phosphorylation of Rap1. The FLG induction of the Rap1-->B-Raf-->MEK1/2-->ERK1/2 cascade was confirmed by the reduction of ERK1/2 activation by the specific Rap1 inhibitor (GGTI-298) and U0126. The results demonstrate that for the first time that the small GTPase Ras family is involved in TLR signaling of avian heterophils with the TLR agonists LPS (Ras) and FLG (Rap1) inducing differential signaling cascades to activate the downstream ERK MAP kinase.

摘要

Toll样受体(TLR)激动剂鞭毛蛋白(FLG)和脂多糖(LPS)通过细胞外信号调节激酶1/2(ERK1/2)丝裂原活化蛋白激酶级联反应刺激功能激活和细胞因子基因表达。然而,这些信号事件的上游机制仍不清楚。在哺乳动物中,小GTP结合蛋白Ras通过激活下游效应物Raf-1-MEK1/2-ERK1/2来介导ERK1/2的激活,以响应多种刺激。目前尚不清楚这种经典的Ras级联反应是否在禽类细胞的TLR信号传导中发挥作用。在本研究中,我们研究了Ras在鸡异嗜性粒细胞中FLG和LPS介导的ERK激活信号传导中的作用。用LPS处理异嗜性粒细胞可导致Ras-GTP迅速(5分钟内)激活。当特异性Ras抑制剂FTI-277抑制ERK1/2激活时,证实了Ras激活在LPS诱导的ERK1/2刺激中的作用。当特异性Raf-1抑制剂GW 5074和MEK1/2抑制剂U0126均使ERK激活降低51%-60%时,证实了LPS激活ERK1/2的经典Ras介导途径。更有趣的是,用FLG处理异嗜性粒细胞不会激活Ras-GTP。同样,FTI-277和GW 5074对FLG介导的ERK1/2激活均无任何影响。另一种小GTP酶Rap1已被证明在哺乳动物中性粒细胞功能中发挥作用。使用Rap1-GTP下拉试验,我们发现FLG刺激而非LPS刺激禽类异嗜性粒细胞会诱导Rap1迅速短暂激活。Rap1已被证明可通过不同的Raf家族成员B-Raf激活ERK1/2,其下游效应物是MEK1/2。我们在此表明,FLG刺激异嗜性粒细胞会诱导Rap1磷酸化。特异性Rap1抑制剂(GGTI-298)和U0126降低ERK1/2激活,证实了FLG诱导的Rap1→B-Raf→MEK1/2→ERK1/2级联反应。结果首次证明小GTP酶Ras家族参与禽类异嗜性粒细胞的TLR信号传导,其中TLR激动剂LPS(Ras)和FLG(Rap1)诱导不同的信号级联反应以激活下游ERK丝裂原活化蛋白激酶。

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