Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.
Sci. Signal., 1 November 2011
Vol. 4, Issue 197, p. ra73
[DOI: 10.1126/scisignal.2001653]
RESEARCH ARTICLES
Persistent Stimulation with Interleukin-17 Desensitizes Cells Through SCFβ-TrCP-Mediated Degradation of Act1
Peiqing Shi1,
Shu Zhu1,
Yingying Lin1,
Yongfeng Liu1,
Yan Liu1,
Zhijian Chen2,
Yufang Shi1, and
Youcun Qian1*
1 The Key Laboratory of Stem Cell Biology, Institute of Health Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences and Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China. 2 Department of Molecular Biology and Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Abstract:
The proinflammatory cytokine interleukin-17 (IL-17) is important for the immune response to pathogens and also contributes to the pathogenesis of various inflammatory diseases. To avoid persistent inflammation, signaling by the IL-17 receptor (IL-17R), which involves the adaptor protein Act1, must be tightly controlled. Here, we report that persistent stimulation of HeLa cells with IL-17 resulted in degradation of Act1 and desensitization of IL-17R signaling. IL-17 stimulated the Lys48-linked polyubiquitination and degradation of Act1, which was phosphorylation-dependent, similar to the IL-17–dependent degradation of inhibitor of nuclear factor B α. Act1 was recruited to SCF (Skp1–cullin-1–F-box)–type E3 ubiquitin ligase complexes containing β-transducin repeat–containing protein 1 (β-TrCP1) or β-TrCP2 in a phosphorylation-dependent manner upon stimulation of cells with IL-17. Dominant-negative β-TrCP or knockdown of β-TrCP1 and β-TrCP2 markedly reduced IL-17–induced, phosphorylation-dependent ubiquitination and degradation of Act1. Thus, our studies identify a previously uncharacterized desensitization mechanism, involving the SCFβ-TrCP-mediated degradation of Act1, that occurs during persistent stimulation with IL-17.
* To whom correspondence should be addressed. E-mail: ycqian{at}sibs.ac.cn
Citation: P. Shi, S. Zhu, Y. Lin, Y. Liu, Y. Liu, Z. Chen, Y. Shi, Y. Qian, Persistent Stimulation with Interleukin-17 Desensitizes Cells Through SCFβ-TrCP-Mediated Degradation of Act1. Sci. Signal.4, ra73 (2011).
Luca Busino, Scott E. Millman, and Michele Pagano (4 December 2012) Sci. Signal.5 (253), pt14.
[DOI: 10.1126/scisignal.2003408] |Abstract »|Full Text »|PDF »|Slideshow »
RESEARCH ARTICLES
Caini Liu, Shadi Swaidani, Wen Qian, Zizhen Kang, Paige Sun, Yue Han, Chenhui Wang, Muhammet Fatih Gulen, Weiguo Yin, Chunjiang Zhang, Paul L. Fox, Mark Aronica, Thomas A. Hamilton, Saurav Misra, Junpeng Deng, and Xiaoxia Li (1 November 2011) Sci. Signal.4 (197), ra72.
[DOI: 10.1126/scisignal.2001843] |Editor's Summary »|Abstract »|Full Text »|PDF »|Supplementary Materials »
RESEARCH ARTICLES
Caini Liu, Wen Qian, Youcun Qian, Natalia V. Giltiay, Yi Lu, Shadi Swaidani, Saurav Misra, Li Deng, Zhijian J. Chen, and Xiaoxia Li (13 October 2009) Sci. Signal.2 (92), ra63.
[DOI: 10.1126/scisignal.2000382] |Editor's Summary »|Abstract »|Full Text »|PDF »|Supplementary Materials »
RESEARCH ARTICLES
Fang Shen, Nan Li, Padmaja Gade, Dhananjaya V. Kalvakolanu, Timothy Weibley, Brad Doble, James R. Woodgett, Troy D. Wood, and Sarah L. Gaffen (24 February 2009) Sci. Signal.2 (59), ra8.
[DOI: 10.1126/scisignal.2000066] |Editor's Summary »|Abstract »|Full Text »|PDF »|Supplementary Materials »
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
The Deubiquitinase A20 Mediates Feedback Inhibition of Interleukin-17 Receptor Signaling.
A. V. Garg, M. Ahmed, A. N. Vallejo, A. Ma, and S. L. Gaffen (2013)
Science Signaling
6, ra44
|Abstract »|Full Text »|PDF »
TRAF6-Dependent Act1 Phosphorylation by the I{kappa}B Kinase-Related Kinases Suppresses Interleukin-17-Induced NF-{kappa}B Activation.
F. Qu, H. Gao, S. Zhu, P. Shi, Y. Zhang, Y. Liu, B. Jallal, Y. Yao, Y. Shi, and Y. Qian (2012)
Mol. Cell. Biol.
32, 3925-3937
|Abstract »|Full Text »|PDF »