RESEARCH ARTICLE

LRRK2 enhances Nod1/2-mediated inflammatory cytokine production by promoting Rip2 phosphorylation

  • Ruiqing Yan 1,2 ,
  • Zhihua Liu , 1,3
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  • 1. Key Laboratory of Infection and Immunity of CAS, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China
  • 2. University of Chinese Academy of Sciences, Beijing 100049, China
  • 3. CAS Center for Excellence in Biomacromolecules, Chinese Academy of Sciences, Beijing 100101, China

Received date: 03 Jun 2016

Accepted date: 08 Sep 2016

Published date: 13 Feb 2017

Copyright

2016 The Author(s) 2016. This article is published with open access at Springerlink.com and journal.hep.com.cn

Abstract

The innate immune systemis critical for clearing infection, and is tightly regulated to avert excessive tissue damage. Nod1/2-Rip2 signaling, which is essential for initiating the innate immune response to bacterial infection and ER stress, is subject to many regulatory mechanisms. In this study, wefound that LRRK2, encoded by a gene implicated in Crohn’s disease, leprosy and familial Parkinson’s disease, modulates the strength of Nod1/2-Rip2 signaling by enhancing Rip2 phosphorylation. LRRK2 deficiency markedly reduces cytokine production in macrophages upon Nod2 activation by muramyl dipeptide (MDP), Nod1 activation by D-gamma-Glu-meso-diaminopimelic acid (iE-DAP) or ER stress. Our biochemical study shows that the presence of LRRK2 is necessary for optimal phosphorylation of Rip2 upon Nod2 activation. Therefore, this study reveals that LRRK2 is a new positive regulator of Rip2 and promotes inflammatory cytokine induction through the Nod1/2-Rip2 pathway.

Cite this article

Ruiqing Yan , Zhihua Liu . LRRK2 enhances Nod1/2-mediated inflammatory cytokine production by promoting Rip2 phosphorylation[J]. Protein & Cell, 2017 , 8(1) : 55 -66 . DOI: 10.1007/s13238-016-0326-x

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