RNF128 regulates neutrophil infiltration and myeloperoxidase functions to prevent acute lung injury
Pei‐Yao Liu, Chih‐Yuan Chen, Yu‐Lung Lin, Chien‐Ming Lin, Wen‐Chiuan Tsai, Yu‐Ling Tsai, Gu‐Jiun Lin, Yuguang Chen, Shih-Yun Wang, Rui-Nong Sun, Yuchuan Huang, Hung Chang, Ying‐Chuan Chen, Ying‐Chuan Chen, Ying‐Chuan Chen
Abstract
Acute lung injury (ALI) is characterised by severe pulmonary inflammation, alveolar-capillary barrier disruption, and pulmonary oedema. Therefore, establishing effective therapeutic targets for ALI prevention is crucial. The present study reports a novel function of RNF128 in regulating LPS-induced ALI. Severe lung damage and increased immune cell infiltration were detected in RNF128-deficient mice. In vitro experiments revealed that RNF128 inhibits neutrophil activation by binding to myeloperoxidase (MPO) and reducing its levels and activity. Moreover, RNF128 regulates alveolar macrophage activation and neutrophil infiltration by interacting with TLR4, targeting it for degradation, and inhibiting NF-κB activation, hence decreasing pro-inflammatory cytokines. Our results demonstrate for the first time that RNF128 is a negative regulator of MPO and TLR4 in neutrophils and alveolar macrophages, respectively. However, AAV9-mediated RNF128 overexpression alleviated lung tissue damage and reduced inflammatory cell infiltration. Thus, RNF128 is a promising therapeutic candidate for pharmacological interventions in ALI.