Experimental autoimmune encephalomyelitis induction in peptidylarginine deiminase 2 knockout mice

J Comp Neurol. 2006 Sep 10;498(2):217-26. doi: 10.1002/cne.21055.


During the development of multiple sclerosis the destruction of the myelin sheath surrounding the neurites is accompanied by citrullination of several central nervous system (CNS) proteins, including myelin basic protein and glial fibrillary acidic protein. In experimental autoimmune encephalomyelitis (EAE), a disease induced in animals by immunization with proteins or peptides from the CNS, the animals develop symptoms similar to multiple sclerosis (MS). The increased levels of citrullinated CNS proteins associated with MS are also observed during the development of EAE. To study the role of CNS protein citrullination in EAE development, we induced EAE with a peptide derived from myelin oligodendrocyte glycoprotein (MOG(35-55)) in mice lacking the peptidylarginine deiminase 2 (PAD2) protein, because this enzyme was the most likely candidate to be involved in catalyzing CNS protein citrullination in the diseased state. Even though the PAD2 knockout mice displayed a dramatic reduction in the amount of citrullination present in the CNS, indicating that PAD2 is indeed responsible for the majority of detectable citrullination observed in EAE, the development of EAE was not impaired by genetic deletion of PAD2, suggesting that PAD2 catalyzed citrullination is not essential to the development of EAE.

MeSH terms

  • Animals
  • Citrulline / metabolism
  • Encephalomyelitis, Autoimmune, Experimental / physiopathology*
  • Humans
  • Hydrolases / genetics
  • Hydrolases / metabolism*
  • Isoenzymes / genetics
  • Isoenzymes / metabolism
  • Mice
  • Mice, Knockout
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Protein-Arginine Deiminase Type 2
  • Protein-Arginine Deiminases
  • Spinal Cord / cytology
  • Spinal Cord / metabolism


  • Isoenzymes
  • Nerve Tissue Proteins
  • Citrulline
  • Hydrolases
  • PADI2 protein, human
  • Protein-Arginine Deiminase Type 2
  • Protein-Arginine Deiminases