Formyl Peptide Receptor 1-Mediated Glial Cell Activation in a Mouse Model of Cuprizone-Induced Demyelination

J Mol Neurosci. 2017 Jun;62(2):232-243. doi: 10.1007/s12031-017-0924-y. Epub 2017 May 2.

Abstract

Multiple sclerosis (MS) is a chronic degenerative disease of the central nervous system that is characterized by myelin abnormalities, oligodendrocyte pathology, and concomitant glia activation. Unclear are the factors triggering gliosis and demyelination. New findings suggest an important role of the innate immune response in the initiation and progression of active demyelinating lesions. The innate immune response is induced by pathogen-associated or danger-associated molecular patterns, which are identified by pattern recognition receptors (PRRs), including the G-protein coupled with formyl peptide receptors (FPRs). Glial cells, the immune cells of the central nervous system, also express the PRRs. In this study, we used the cuprizone mice model to investigate the expression of the FPR1 in the course of cuprizone-induced demyelination In addition, we used FPR1-deficient mice to analyze glial cell activation through immunohistochemistry and real-time RT-PCR in cuprizone model. Our results revealed a significantly increased expression of FPR1 in the cortex of cuprizone-treated mice. FPR1-deficient mice showed a slight but significant decrease of demyelination in the corpus callosum compared to the wild-type mice. Furthermore, FPR1 deficiency resulted in reduced glial cell activation and mRNA expression of microglia/macrophages markers, as well as pro- and anti-inflammatory cytokines in the cortex, compared to wild-type mice after cuprizone-induced demyelination. Combined together, these results suggest that the FPR1 is an important part of the innate immune response in the course of cuprizone-induced demyelination.

Keywords: CNS; Cuprizone; Demyelination; Formyl peptide receptor; Multiple sclerosis; Pattern recognition receptor.

MeSH terms

  • Animals
  • Corpus Callosum / immunology
  • Corpus Callosum / pathology
  • Cuprizone / toxicity
  • Cytokines / genetics
  • Cytokines / metabolism
  • Demyelinating Diseases / etiology
  • Demyelinating Diseases / immunology*
  • Immunity, Innate
  • Macrophage Activation
  • Macrophages / immunology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Neuroglia / immunology*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptors, Formyl Peptide / genetics
  • Receptors, Formyl Peptide / metabolism*

Substances

  • Cytokines
  • Fpr1 protein, mouse
  • RNA, Messenger
  • Receptors, Formyl Peptide
  • Cuprizone