TANK is a negative regulator of Toll-like receptor signaling and is critical for the prevention of autoimmune nephritis.

Journal:

Nat. Immunol. 2009 Sep

Authors:

Kawagoe T, Takeuchi O, Takabatake Y, Kato H, Isaka Y, Tsujimura T, Akira S

Abstract

The intensity and duration of immune responses are controlled by many proteins that modulate Toll-like receptor (TLR) signaling. TANK has been linked to positive regulation of the transcription factors IRF3 and NF-kappaB. Here we demonstrate that TANK is not involved in interferon responses and is a negative regulator of proinflammatory cytokine production induced by TLR signaling. TLR-induced polyubiquitination of the ubiquitin ligase TRAF6 was upregulated in Tank(-/-) macrophages. Notably, Tan
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k(-/-) mice spontaneously developed fatal glomerulonephritis owing to deposition of immune complexes. Autoantibody production in Tank(-/-) mice was abrogated by antibiotic treatment or the absence of interleukin 6 (IL-6) or the adaptor MyD88. Our results demonstrate that constitutive TLR signaling by intestinal commensal microflora is suppressed by TANK.[less]

Mesh Headings:

Adaptor Proteins, Signal Transducing, Animals, Antigens, CD40, Autoimmune Diseases, Autoimmunity, Female, Glomerulonephritis, Intestines, Mice, Mice, Inbred C57BL, Myeloid Differentiation Factor 88, Receptors, Antigen, B-Cell, Signal Transduction, TNF Receptor-Associated Factor 6, Toll-Like Receptors, Ubiquitin