RNF128 regulates neutrophil infiltration and myeloperoxidase functions to prevent acute lung injury.
Pei-Yao LiuChih-Yuan ChenYu-Lung LinChien-Ming LinWen-Chiuan TsaiYu-Ling TsaiGu-Jiun LinYu-Guang ChenShih-Yun WangRui-Nong SunYu-Chuan HuangHung ChangYing-Chuan ChenPublished in: Cell death & disease (2023)
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.
Keyphrases
- lps induced
- inflammatory response
- oxidative stress
- dna damage response
- lipopolysaccharide induced
- toll like receptor
- pulmonary hypertension
- signaling pathway
- early onset
- single cell
- transcription factor
- anti inflammatory
- stem cells
- bone marrow
- emergency department
- physical activity
- cell therapy
- adverse drug
- nuclear factor