4.6 Article

OTUD1 Regulates Antifungal Innate Immunity through Deubiquitination of CARD9

Journal

JOURNAL OF IMMUNOLOGY
Volume 206, Issue 8, Pages 1832-1843

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.2001253

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Funding

  1. National Natural Science Foundation of China [81930039, 31730026, 81525012]
  2. Key Research and Development Projects of Shandong Province [2019GSF108133]

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This study identifies ovarian tumor deubiquitinase 1 (OTUD1) as an essential regulator of CARD9, which can activate the canonical NF-kappa B and MAPK pathway by deubiquitinating CARD9, impacting immune response following fungal stimulation.
CARD9 is an essential adaptor protein in antifungal innate immunity mediated by C-type lectin receptors. The activity of CARD9 is critically regulated by ubiquitination; however, the deubiquitinases involved in CARD9 regulation remain incompletely understood. In this study, we identified ovarian tumor deubiquitinase 1 (OTUD1) as an essential regulator of CARD9. OTUD1 directly interacted with CARD9 and cleaved polyubiquitin chains from CARD9, leading to the activation of the canonical NF-kappa B and MAPK pathway. OTUD1 deficiency impaired CARD9-mediated signaling and inhibited the proinflammatory cytokine production following fungal stimulation. Importantly, Otud1(-/-) mice were more susceptible to fungal infection than wild-type mice in vivo. Collectively, our results identify OTUD1 as an essential regulatory component for the CARD9 signaling pathway and antifungal innate immunity through deubiquitinating CARD9.

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