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Sci. Signal., 21 August 2012
Vol. 5, Issue 238, p. ra61
[DOI: 10.1126/scisignal.2002946]


The Protease Omi Cleaves the Mitogen-Activated Protein Kinase Kinase MEK1 to Inhibit Microglial Activation

Qingsong Hu1,2, Bin Li1, Ranjie Xu1, Dong Chen2, Chenchen Mu2, Erkang Fei1, and Guanghui Wang1,2*

1 Laboratory of Molecular Neuropathology, Key Laboratory of Brain Function and Diseases and School of Life Sciences, University of Science and Technology of China, Chinese Academy of Sciences, Hefei, Anhui 230027, China.
2 Laboratory of Molecular Neuropathology, Department of Pharmacology, Soochow University College of Pharmaceutical Sciences, Suzhou, Jiangsu 201203, China.

Abstract: Inflammation in Parkinson’s disease is closely associated with disease pathogenesis. Mutations in Omi, which encodes the protease Omi, are linked to neurodegeneration and Parkinson’s disease in humans and in mouse models. The severe neurodegeneration and neuroinflammation that occur in mnd2 (motor neuron degeneration 2) mice result from loss of the protease activity of Omi by the point mutation S276C; however, the substrates of Omi that induce neurodegeneration are unknown. We showed that Omi was required for the production of inflammatory molecules by microglia, which are the resident macrophages in the central nervous system. Omi suppressed the activation of the mitogen-activated protein kinases (MAPKs) extracellular signal–regulated kinase 1 and 2 (ERK1/2) by cleaving the upstream kinase MEK1 (mitogen-activated or extracellular signal–regulated protein kinase kinase 1). Knockdown of Omi in microglial cell lines led to activation of ERK1/2 and resulted in degradation of I{kappa}Bα [α inhibitor of nuclear factor {kappa}B (NF-{kappa}B)], resulting in NF-{kappa}B activation and the expression of genes encoding inflammatory molecules, such as tumor necrosis factor–α and inducible nitric oxide synthase. The production of inflammatory molecules induced by the knockdown of Omi was blocked by the MEK1-specific inhibitor U0126. Furthermore, expression of the protease-deficient S276C Omi mutant in a microglial cell line had no effect on MEK1 cleavage or ERK1/2 activation. In the brains of mnd2 mice, we observed increased transcription of several genes encoding inflammatory molecules, as well as activation of astrocytes and microglia. Therefore, our study demonstrates that Omi is an intrinsic cellular factor that inhibits neuroinflammation.

* To whom correspondence should be addressed. E-mail: wghui{at}

Citation: Q. Hu, B. Li, R. Xu, D. Chen, C. Mu, E. Fei, G. Wang, The Protease Omi Cleaves the Mitogen-Activated Protein Kinase Kinase MEK1 to Inhibit Microglial Activation. Sci. Signal. 5, ra61 (2012).

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Science Signaling Podcast: 28 August 2012.
G. Wang and A. M. VanHook (2012)
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