Evidence map›Paper›PMID 40601208›Full record

ArticleApplied biochemistry and biotechnology2025

KAT3B Protects Against Septic Lung Injury by Regulating TSLP Succinylation and Macrophage Polarization.

Chao Li, Jialiang Zhang, Fuhong Zheng, Haibo Liu

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Article in Applied biochemistry and biotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Chao Li *Department of Emergency, The First Hospital of Jilin University, No.3302, Jilin Broad Road, Changchun, 130021, China.
Jialiang Zhang *Department of Emergency, The First Hospital of Jilin University, No.3302, Jilin Broad Road, Changchun, 130021, China.
Fuhong ZhengDepartment of Emergency, The First Hospital of Jilin University, No.3302, Jilin Broad Road, Changchun, 130021, China. zhengfh2018@jlu.edu.cn.
Haibo LiuDepartment of Emergency, The First Hospital of Jilin University, No.3302, Jilin Broad Road, Changchun, 130021, China. hhbbliuliu@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As a serious complication of sepsis, septic lung injury has a high rate of morbidity and mortality. However, the mechanism of septic lung injury remain unclear. The present study aims to explore the role of succinylation and KAT3B in the polarization of macrophages and the progression of septic lung injury. The cecal ligation and puncture (CLP) was used to establish the septic lung injury model. HE staining was performed to evaluate the lung injury. Raw264.7 cells were treated with lipopolysaccharide (LPS) to establish the cell model of septic lung injury. Macrophage polarization was evaluated by detecting M1 and M2 markers using quantitative real-time polymerase chain reaction and immunofluorescence. CO-IP was used to investigate the interaction between proteins. The experimental results indicated that KAT3B and the total succinylation was down-regulated in septic lung injury. LPS promoted M1 polarization and inhibited M2 polarization of Raw264.7 cells. KAT3B suppressed M1 polarization and promoted M2 polarization. Mechanistically, KAT3B desuccinylates TSLP at K239 and K292 site and promotes its stability. TSLP silencing reversed the effects of KAT3B. In vivo, KAT3B significantly reduced the lung injury and inflammation response of mice after CLP treatment. The present research unveiled the KAT3B acts as a protector against sepsis induced injury by mediating the succinylation of TLSP.

Indexed as

Acute Lung InjuryCytokinesHistone AcetyltransferasesLung InjuryMacrophagesSepsisAnimalsCell PolarityDisease Models, AnimalLipopolysaccharidesMaleMiceMice, Inbred C57BLRAW 264.7 CellsThymic Stromal LymphopoietinCytokinesHistone AcetyltransferasesLipopolysaccharidesThymic Stromal LymphopoietinKAT3BSeptic lung injurySuccinylationTSLP

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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.