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CRL4DCAF2 negatively regulates IL-23 production in dendritic cells and limits the development of psoriasis.


ABSTRACT: The E3 ligase CRL4DCAF2 is believed to be a pivotal regulator of the cell cycle and is required for mitotic and S phase progression. The NEDD8-targeting drug MLN4924, which inactivates cullin ring-finger ubiquitin ligases (CRLs), has been examined in clinical trials for various types of lymphoma and acute myeloid leukemia. However, the essential role of CRL4DCAF2 in primary myeloid cells remains poorly understood. MLN4924 treatment, which mimics DCAF2 depletion, also promotes the severity of mouse psoriasis models, consistent with the effects of reduced DCAF2 expression in various autoimmune diseases. Using transcriptomic and immunological approaches, we showed that CRL4DCAF2 in dendritic cells (DCs) regulates the proteolytic fate of NIK and negatively regulates IL-23 production. CRL4DCAF2 promoted the polyubiquitination and subsequent degradation of NIK independent of TRAF3 degradation. DCAF2 deficiency facilitated NIK accumulation and RelB nuclear translocation. DCAF2 DC-conditional knockout mice displayed increased sensitivity to autoimmune diseases. This study shows that CRL4DCAF2 is crucial for controlling NIK stability and highlights a unique mechanism that controls inflammatory diseases.

SUBMITTER: Huang T 

PROVIDER: S-EPMC6080916 | biostudies-literature | 2018 Aug

REPOSITORIES: biostudies-literature

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CRL4<sup>DCAF2</sup> negatively regulates IL-23 production in dendritic cells and limits the development of psoriasis.

Huang Tao T   Gao Zhengjun Z   Zhang Yu Y   Fan Keqi K   Wang Fei F   Li Yiyuan Y   Zhong Jiangyan J   Fan Heng Y HY   Cao Qian Q   Zhou Jiyong J   Xiao Yichuan Y   Hu Hongbo H   Hu Hongbo H   Jin Jin J  

The Journal of experimental medicine 20180717 8


The E3 ligase CRL4<sup>DCAF2</sup> is believed to be a pivotal regulator of the cell cycle and is required for mitotic and S phase progression. The NEDD8-targeting drug MLN4924, which inactivates cullin ring-finger ubiquitin ligases (CRLs), has been examined in clinical trials for various types of lymphoma and acute myeloid leukemia. However, the essential role of CRL4<sup>DCAF2</sup> in primary myeloid cells remains poorly understood. MLN4924 treatment, which mimics DCAF2 depletion, also promot  ...[more]

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