Inhibition of receptor internalization attenuates the TNFα-induced ROS generation in non-phagocytic cells

被引:33
作者
Woo, Chang-Hoon
Kim, Tae-Hee
Choi, Jung-A
Ryu, Ho-Cheol
Lee, Jung Eun
You, Hye-Jin
Bae, Yun-Soo
Kim, Jae-Hong
机构
[1] Korea Univ, Sch Life Sci & Biotechnol, Seoul 136701, South Korea
[2] Univ Rochester, Inst Cardiovasc Res, Rochester, NY 14642 USA
[3] Duke Univ, Dept Med, Durham, NC 27710 USA
[4] Ewha Womans Univ, Div Mol & Life Sci, Ctr Cell Signaling Res, Seoul 120750, South Korea
关键词
TNF alpha; ROS; receptor internalization; signal transduction; nox; non-phagocytes; TUMOR-NECROSIS-FACTOR; REACTIVE OXYGEN; NADPH OXIDASE; ENDOCYTIC PATHWAY; ACTIVATION; DEATH; H2O2; NEUTROPHILS; COMPLEXES; KINASE;
D O I
10.1016/j.bbrc.2006.10.154
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Reactive oxygen species (ROS) are important regulatory molecules implicated in the signaling cascade triggered by tumor necrosis factor (TNF)alpha, although the events through which TNF alpha induces ROS generation are not well characterized. Here, we report that TNF alpha-induced ROS production was blocked by pretreatment with internalization inhibitor monodansyl cadaverine (MDC). Similarly, a transient expression of a GTP-binding and hydrolysis-defective dynamin mutant (dynamin(K44A)) that had been shown to be defective in internalization significantly attenuated the TNF alpha-induced intracellular ROS production. Importantly, the inhibition of receptor internalization suppressed TNF alpha signaling to mitogen-activated protein kinases (MAPKs) stimulation. Together, our results suggest that receptor internalization is somehow necessary for the TNF alpha-induced ROS generation and subsequent intracellular downstream signaling in non-phagocytes. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:972 / 978
页数:7
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