1. CARD14/CARMA2sh and TANK differentially regulate poly(I:C)-induced inflammatory reaction in keratinocytes.
- Author
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Voccola S, Polvere I, Madera JR, Paolucci M, Varricchio E, Telesio G, Porcaro P, Vito P, Stilo R, and Zotti T
- Subjects
- CARD Signaling Adaptor Proteins genetics, Cell Line, Guanylate Cyclase genetics, HEK293 Cells, Humans, Interferon Regulatory Factor-3 metabolism, Membrane Proteins genetics, Mutation genetics, NF-kappa B metabolism, Protein Binding physiology, Protein Serine-Threonine Kinases metabolism, Psoriasis genetics, Psoriasis metabolism, Signal Transduction physiology, Adaptor Proteins, Signal Transducing metabolism, CARD Signaling Adaptor Proteins metabolism, Guanylate Cyclase metabolism, Inflammation metabolism, Keratinocytes metabolism, Membrane Proteins metabolism, Poly I-C metabolism
- Abstract
CARD14/CARMA2sh (CARMA2sh) is a scaffold protein whose mutations are associated with the onset of human genetic psoriasis and other inflammatory skin disorders. Here we show that the immunomodulatory adapter protein TRAF family member-associated NF-κB activator (TANK) forms a complex with CARMA2sh and MALT1 in a human keratinocytic cell line. We also show that CARMA2 and TANK are individually required to activate the nuclear factor κB (NF-κB) response following exposure to polyinosinic-polycytidylic (poly [I:C]), an agonist of toll-like receptor 3. Finally, we present data indicating that TANK is essential for activation of the TBK1/IRF3 pathway following poly (I:C) stimulation, whereas CARMA2sh functions as a repressor of it. More important, we report that two CARMA2sh mutants associated with psoriasis bind less efficiently to TANK and are therefore less effective in suppressing the TBK1/IRF3 pathway. Overall, our data indicate that TANK and CARMA2sh regulate TLR3 signaling in human keratinocytes, which could play a role in the pathophysiology of psoriasis., (© 2019 Wiley Periodicals, Inc.)
- Published
- 2020
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