Peroxiredoxin I is a ROS/p38 MAPK-dependent inducible antioxidant that regulates NF-κB-mediated iNOS induction and microglial activation

J Neuroimmunol. 2013 Jun 15;259(1-2):26-36. doi: 10.1016/j.jneuroim.2013.03.006. Epub 2013 Apr 17.

Abstract

Reactive oxygen species (ROS) function as modulators of pro-inflammatory processes in microglia-associated neurodegenerative diseases. However, little is known about the involvement of specific antioxidants in regulating the microglial redox status. Here, we demonstrated that peroxiredoxin (Prx) I activity was induced by lipopolysaccharide (LPS), but not paraquat and hydrogen peroxide, through activation of the ROS/p38 MAPK signal pathway, and participated in alleviating the microglial activation and generation of nitric oxide (NO). Interestingly, a null mutation of Prx I accelerated NF-κB-mediated iNOS induction and subsequent NO secretion in LPS-stimulated microglia. Furthermore, F4/80 expression as microglial activation marker was notably up-regulated in primary cultures of microglia, hippocampal sections, and cerebral cortex of 15-month-old Prx I(-/-) mouse. Taken together, the results of our study indicated that Prx I is an antioxidant that is up-regulated in a ROS/p38 MAPK-dependent manner and governs the progression of neuroinflammation by suppressing microglial activation. In addition, Prx I deficiency increased the nuclear translocation of NF-κB mediated-iNOS induction as pro-inflammatory mediators. The findings of our work suggest possible strategies for developing novel therapies to treat inflammation-associated degenerative neurological diseases by targeting the induction of Prx I in microglial cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / metabolism*
  • Cell Line, Transformed
  • Cell Nucleus / metabolism
  • Hippocampus / immunology
  • Hippocampus / metabolism
  • Lipopolysaccharides / pharmacology
  • Mice
  • Mice, Knockout
  • Microglia / cytology
  • Microglia / immunology
  • Microglia / metabolism*
  • NF-kappa B / metabolism
  • Neuroimmunomodulation / immunology
  • Nitric Oxide Synthase Type II / genetics*
  • Nitric Oxide Synthase Type II / metabolism
  • Organ Culture Techniques
  • Peroxiredoxins / metabolism*
  • Primary Cell Culture
  • Reactive Oxygen Species / metabolism*
  • Transcriptional Activation / drug effects
  • Transcriptional Activation / immunology
  • p38 Mitogen-Activated Protein Kinases / metabolism*

Substances

  • Antioxidants
  • Lipopolysaccharides
  • NF-kappa B
  • Reactive Oxygen Species
  • Peroxiredoxins
  • Prdx1 protein, mouse
  • Nitric Oxide Synthase Type II
  • Nos2 protein, mouse
  • p38 Mitogen-Activated Protein Kinases