• Title of article

    Peptidylarginine deiminase 4 and citrullination in health and disease

  • Author/Authors

    Consuelo Anzilotti، نويسنده , , Federico Pratesi، نويسنده , , Cristina Tommasi، نويسنده , , Paola Migliorini، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2010
  • Pages
    3
  • From page
    158
  • To page
    160
  • Abstract
    Deimination is catalyzed by a family of calcium binding enzymes, called peptidylarginine deiminases (PADs). Among these, the PAD4 isoform has been more extensively studied for its role in some autoimmune diseases. PAD4 is localized in the cytoplasm of monocytes, T and B cells, neutrophils, eosinophils and NK cells and can move to the nucleus upon cell activation. PAD4 plays a physiological role in gene regulation via citrullination of histones. In rheumatoid arthritis (RA), PAD4 contributes to the generation of ACPA specific substrates and is itself a target of autoantibodies; alleles of the PADI4 gene confer susceptibility to RA in Asians but not in Caucasians. In multiple sclerosis, extensive deimination of brain proteins is observed in active lesions, but no role for the PADI4 gene in susceptibility to MS has been so far described.
  • Keywords
    Peptidylarginine deiminase 4CitrullinationAnti-citrulllinated proteins/peptidesantibodiesRheumatoid arthritisMultiple sclerosis
  • Journal title
    Autoimmunity Reviews
  • Serial Year
    2010
  • Journal title
    Autoimmunity Reviews
  • Record number

    475101