Act1 modulates autoimmunity through its dual functions in CD40L/BAFF and IL-17 signaling

Cytokine. 2008 Feb;41(2):105-13. doi: 10.1016/j.cyto.2007.09.015. Epub 2007 Dec 3.

Abstract

Coordinated regulation of T and B cell-mediated immune responses plays a critical role in the control and modulation of autoimmune diseases. This review is focused on the adapter molecule Act1 and its regulation of autoimmunity through its impact on both T and B cell-mediated immune responses. Whereas Act1 molecule is an important negative regulator for B cell-mediated humoral immune responses through its function in CD40L and BAFF signaling, recent studies have shown that Act1 is also a key positive signaling component for IL-17 signaling pathway, critical for T(H)17-mediated autoimmune and inflammatory responses. The dual functions of Act1 are evident in Act1-deficient mice that displayed B cell-mediated autoimmune phenotypes (including dramatic increase in peripheral B cells, lymphadenopathy and splenomegaly, hypergammaglobulinemia and Sjogren's disease in association with Lupus Nephritis), but showed resistance to T(H)17-dependent EAE and colitis. Such seemingly opposite functions of Act1 in CD40-BAFFR and IL-17R signaling are orchestrated by different domains in Act1. Whereas Act1 interacts with the IL-17R through the C-terminal SEFIR domain, Act1 is recruited to CD40 and BAFFR indirectly, which is mediated by TRAF3 through the TRAF binding site in Act1. Such delicate regulatory mechanisms may provide a common vehicle to promote balance between host defense to pathogens and tolerance to self.

Publication types

  • Review

MeSH terms

  • Adaptor Proteins, Signal Transducing / physiology
  • Antibody Formation / physiology
  • Autoimmunity / physiology*
  • B-Cell Activating Factor / physiology*
  • B-Cell Activation Factor Receptor / metabolism
  • CD4-Positive T-Lymphocytes / physiology
  • CD40 Antigens
  • CD40 Ligand / physiology*
  • Enzyme Activation
  • Humans
  • I-kappa B Kinase / metabolism
  • Inflammation / physiopathology
  • Interleukin-17 / physiology
  • Models, Biological
  • NF-kappa B / physiology
  • Receptors, Interleukin-1 / physiology
  • Receptors, Interleukin-17 / physiology
  • Signal Transduction / physiology
  • Toll-Like Receptors / physiology
  • Tumor Necrosis Factor Receptor-Associated Peptides and Proteins / physiology*

Substances

  • Adaptor Proteins, Signal Transducing
  • B-Cell Activating Factor
  • B-Cell Activation Factor Receptor
  • CD40 Antigens
  • Interleukin-17
  • NF-kappa B
  • Receptors, Interleukin-1
  • Receptors, Interleukin-17
  • TRAF3IP2 protein, human
  • Toll-Like Receptors
  • Traf3ip2 protein, mouse
  • Tumor Necrosis Factor Receptor-Associated Peptides and Proteins
  • CD40 Ligand
  • I-kappa B Kinase