Ceftazidime reduces cellular Skp2 to promote type‐I interferon activity

Author:

Qiao Caixia1,Huang Fan12,He Jiuyi1,Wu Qiuyu1,Zheng Zhijin1,Zhang Tingting1,Miao Ying1,Yuan Yukang1ORCID,Chen Xiangjie1,Du Qian1,Xu Yang3,Wu Depei3,Yu Zhengyuan4,Zheng Hui1ORCID

Affiliation:

1. Institutes of Biology and Medical Sciences, Jiangsu Key Laboratory of Infection and Immunity Soochow University Suzhou Jiangsu China

2. The Fifth People's Hospital of Suzhou The Affiliated Infectious Diseases Hospital of Soochow University Suzhou Jiangsu China

3. National Clinical Research Center for Hematologic Diseases, Jiangsu Institute of Hematology The First Affiliated Hospital of Soochow University, Institute of Blood and Marrow Transplantation, Collaborative Innovation Center of Hematology, Soochow University Suzhou Jiangsu China

4. Department of Oncology The First Affiliated Hospital of Soochow University Suzhou Jiangsu China

Abstract

AbstractSkp2 plays multiple roles in malignant tumours. Here, we revealed that Skp2 negatively regulates type‐I interferon (IFN‐I)‐mediated antiviral activity. We first noticed that Skp2 can promote virus infection in cells. Further studies demonstrated that Skp2 interacts with IFN‐I receptor 2 (IFNAR2) and promotes K48‐linked polyubiquitination of IFNAR2, which accelerates the degradation of IFNAR2 proteins. Skp2‐mediated downregulation of IFNAR2 levels inhibits IFN‐I signalling and IFN‐I‐induced antiviral activity. In addition, we uncovered for the first time that the antibiotic ceftazidime can act as a repressor of Skp2. Ceftazidime reduces cellular Skp2 levels, thus enhancing IFNAR2 stability and IFN‐I antiviral activity. This study reveals a new role of Skp2 in regulating IFN‐I signalling and IFN‐I antiviral activity and reports the antibiotic ceftazidime as a potential repressor of Skp2.

Funder

National Natural Science Foundation of China

Priority Academic Program Development of Jiangsu Higher Education Institutions

Publisher

Wiley

Subject

Immunology,Immunology and Allergy

Reference56 articles.

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