Evidence map›Paper›PMID 37344492›Full record

ArticleCell death & disease2023

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, Yu-Guang Chen, Shih-Yun Wang, Rui-Nong Sun and 3 more

Abstract read
In one paragraph

Article in Cell death & disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed.

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  5. Scutellarein fromPharmaceuticals (Basel, Switzerland) · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Pei-Yao Liu *Department of Physiology & Biophysics, National Defense Medical Center, Taipei 114, Taiwan, Republic of China.
Chih-Yuan Chen *Department of Physiology & Biophysics, National Defense Medical Center, Taipei 114, Taiwan, Republic of China.
Yu-Lung Lin *The Ph.D. Program for Translational Medicine, College for Medical Science and Technology, Taipei Medical University, Taipei, 110, Taiwan.
Chien-Ming LinDepartment of Pediatrics, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan, Republic of China.
Wen-Chiuan TsaiDepartment of Pathology, Tri-Service General Hospital, National Defense Medical Center, Taipei 114, Taiwan, Republic of China.ORCID 0000-0003-1085-9014
Yu-Ling TsaiDepartment of Pathology, Tri-Service General Hospital, National Defense Medical Center, Taipei 114, Taiwan, Republic of China.
Gu-Jiun LinDepartment of Biology and Anatomy, National Defense Medical Center, Taipei 114, Taiwan, Republic of China.
Yu-Guang ChenDivision of Hematology/Oncology, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei 114, Taiwan, Republic of China.
Shih-Yun WangDepartment of Physiology & Biophysics, National Defense Medical Center, Taipei 114, Taiwan, Republic of China.
Rui-Nong SunDepartment of Physiology & Biophysics, National Defense Medical Center, Taipei 114, Taiwan, Republic of China.
Yu-Chuan HuangSchool of Pharmacy & Institute Pharmacy, National Defense Medical Center, Taipei, Republic of China.
Hung ChangDepartment of Physiology & Biophysics, National Defense Medical Center, Taipei 114, Taiwan, Republic of China. hung@ndmctsgh.edu.tw.
Ying-Chuan ChenDepartment of Physiology & Biophysics, National Defense Medical Center, Taipei 114, Taiwan, Republic of China. addy0918@gmail.com.ORCID 0000-0001-8031-1893

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Acute Lung InjuryNF-kappa BUbiquitin-Protein LigasesAnimalsLipopolysaccharidesLungMiceNeutrophil InfiltrationPeroxidaseToll-Like Receptor 4LipopolysaccharidesNF-kappa BPeroxidaseRNF128 protein, mouseToll-Like Receptor 4Ubiquitin-Protein Ligases

Identifiers

PMID37344492
PMCPMC10284794

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.