1. Academic Validation
  2. NOX2 deficiency promotes GSDME-related pyroptosis by reducing AMPK activation in neutrophils

NOX2 deficiency promotes GSDME-related pyroptosis by reducing AMPK activation in neutrophils

  • Int Immunopharmacol. 2024 Dec 25;143(Pt 2):113504. doi: 10.1016/j.intimp.2024.113504.
Ang Li 1 Baoyi Liu 2 Qingyue Xia 1 Yi Liu 3 Zhou Zhuang 4 Xinzhu Zhou 4 Yue Yang 5 Ke Xue 5 Yujun Sheng 5 Xianbo Zuo 5 Jingkai Xu 6 Yong Cui 7
Affiliations

Affiliations

  • 1 Department of Dermatology, China-Japan Friendship Hospital, Beijing, China; China-Japan Friendship Hospital (Institute of Clinical Medical Sciences), Chinese Academy of Medical Sciences & Peking Union Medical College, China.
  • 2 Changhai Hospital, The Second Military Medical University, Shanghai, China.
  • 3 Department of Dermatology, China-Japan Friendship Hospital, Beijing, China; Capital Medical University, Beijing, China.
  • 4 Department of Dermatology, China-Japan Friendship Hospital, Beijing, China; Peking University China-Japan Friendship School of Clinical Medicine, Beijing, China.
  • 5 Department of Dermatology, China-Japan Friendship Hospital, Beijing, China.
  • 6 Department of Dermatology, China-Japan Friendship Hospital, Beijing, China. Electronic address: jkaixu1992@163.com.
  • 7 Department of Dermatology, China-Japan Friendship Hospital, Beijing, China. Electronic address: wuhucuiyong@vip.163.com.
Abstract

Nicotinamide adenine dinucleotide phosphate oxidase complex 2 (NOX2) is an effector molecule expressed predominantly in neutrophils. Its deficiency is present in immune disorders, including systemic lupus erythematosus, chronic granulomatous disease, and rheumatoid arthritis. Recent reports indicated that NOX2 regulates autoimmunity and programmed cell death. However, the exact mechanism is unclear. In this study, we explored the effect of NOX2 on neutrophil Apoptosis. We demonstrated that NOX2 deficiency caused neutrophil Pyroptosis. Mechanistically, the NOX2 Inhibitor GSK2795039 application or knockdown of NOX2 components resulted in increased mitochondrial ROS, inhibition of AMP-activated protein kinase (AMPK), and activation of Gasdermin E. AMPK activators, metformin and epigallocatechin gallate, inhibited deficient NOX2-induced Pyroptosis. Together, these findings illustrate the involvement of NOX2 in regulating neutrophil death and emphasize its importance in autoimmunity.

Keywords

AMPK; Autoimmune; Gasdermin E; NOX2; Neutrophil.

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