CCRL2 regulates M1/M2 polarization during EAE recovery phase

J Leukoc Biol. 2016 Jun;99(6):1027-33. doi: 10.1189/jlb.3MA0915-444RR. Epub 2016 Jan 7.

Abstract

Chemokine (CC motif) receptor-like 2 is a 7-transmembrane protein related to the family of the atypical chemokine receptors, which are proteins devoid of chemotactic activity and involved in the control of inflammation. Experimental autoimmune encephalitis is an autoimmune disorder that replicates the inflammatory aspects of multiple sclerosis. Chemokine (CC motif) receptor-like 2-deficient mice developed exacerbated, nonresolving disease with protracted inflammatory response and increased demyelination. The increased severity of the disease was associated with higher levels of microglia/macrophage activation markers and imbalanced M1/M2 polarization. Thus, chemokine (CC motif) receptor-like 2 is involved in the downregulation of central nervous system-associated experimental autoimmune encephalitis inflammation in the recovery phase of the disease. Therefore chemokine (CC motif) receptor-like 2 should be considered to be a molecule involved in the regulation of the inflammatory response associated with multiple sclerosis.

Keywords: atypical chemokine receptors; chemokines; inflammation; macrophages; microglia; multiple sclerosis.

MeSH terms

  • Animals
  • Antigens / immunology
  • Cell Polarity* / drug effects
  • Cell Proliferation / drug effects
  • Central Nervous System / drug effects
  • Central Nervous System / pathology
  • Cross-Priming / immunology
  • Disease Progression
  • Encephalomyelitis, Autoimmune, Experimental / immunology
  • Encephalomyelitis, Autoimmune, Experimental / pathology*
  • Female
  • Immunization
  • Inflammation / pathology
  • Interferon-gamma / pharmacology
  • Macrophages / drug effects
  • Macrophages / metabolism
  • Macrophages / pathology*
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Microglia / drug effects
  • Microglia / metabolism
  • Myelin Sheath / metabolism
  • Myelin-Oligodendrocyte Glycoprotein / immunology
  • Peptide Fragments / immunology
  • Receptors, CCR
  • Receptors, Chemokine / metabolism*
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / immunology

Substances

  • Antigens
  • Ccrl2 protein, mouse
  • Myelin-Oligodendrocyte Glycoprotein
  • Peptide Fragments
  • Receptors, CCR
  • Receptors, Chemokine
  • myelin oligodendrocyte glycoprotein (35-55)
  • Interferon-gamma