Evidence map›Paper›PMID 41361470›Full record

ArticleCell communication and signaling : CCS2025

PD-L1 mediates M1 polarization of macrophages via the AIM2/IL-18/STAT1 signaling axis during sepsis.

Guomei Yang, Luoquan Ao, Qing Zhao, Chengyi Hu, Xiaofeng Wu, Mengwei Yao, Mu Yuan, Tong Jin, Weijun Wan, Quan Chen and 3 more

Abstract read
In one paragraph

Article in Cell communication and signaling : CCS, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Guomei Yang *Department of Stem Cell & Regenerative Medicine, State Key Laboratory of Trauma and Chemical Poisoning, Daping Hospital, Army Medical University, Yuzhong District, Chongqing, 400042, China.
Luoquan Ao *Department of Stem Cell & Regenerative Medicine, State Key Laboratory of Trauma and Chemical Poisoning, Daping Hospital, Army Medical University, Yuzhong District, Chongqing, 400042, China.
Qing Zhao *Department of Stem Cell & Regenerative Medicine, State Key Laboratory of Trauma and Chemical Poisoning, Daping Hospital, Army Medical University, Yuzhong District, Chongqing, 400042, China.
Chengyi HuDepartment of Stem Cell & Regenerative Medicine, State Key Laboratory of Trauma and Chemical Poisoning, Daping Hospital, Army Medical University, Yuzhong District, Chongqing, 400042, China.
Xiaofeng WuDepartment of Stem Cell & Regenerative Medicine, State Key Laboratory of Trauma and Chemical Poisoning, Daping Hospital, Army Medical University, Yuzhong District, Chongqing, 400042, China.
Mengwei YaoDepartment of Stem Cell & Regenerative Medicine, State Key Laboratory of Trauma and Chemical Poisoning, Daping Hospital, Army Medical University, Yuzhong District, Chongqing, 400042, China.
Mu YuanDepartment of Stem Cell & Regenerative Medicine, State Key Laboratory of Trauma and Chemical Poisoning, Daping Hospital, Army Medical University, Yuzhong District, Chongqing, 400042, China.
Tong JinDepartment of Stem Cell & Regenerative Medicine, State Key Laboratory of Trauma and Chemical Poisoning, Daping Hospital, Army Medical University, Yuzhong District, Chongqing, 400042, China.
Weijun WanDepartment of Stem Cell & Regenerative Medicine, State Key Laboratory of Trauma and Chemical Poisoning, Daping Hospital, Army Medical University, Yuzhong District, Chongqing, 400042, China.
Quan ChenDepartment of Stem Cell & Regenerative Medicine, State Key Laboratory of Trauma and Chemical Poisoning, Daping Hospital, Army Medical University, Yuzhong District, Chongqing, 400042, China.
Yuchuan YuanDepartment of Stem Cell & Regenerative Medicine, State Key Laboratory of Trauma and Chemical Poisoning, Daping Hospital, Army Medical University, Yuzhong District, Chongqing, 400042, China.
Xiang XuDepartment of Stem Cell & Regenerative Medicine, State Key Laboratory of Trauma and Chemical Poisoning, Daping Hospital, Army Medical University, Yuzhong District, Chongqing, 400042, China. xiangxu@tmmu.edu.cn.
Lixing TianDepartment of Stem Cell & Regenerative Medicine, State Key Laboratory of Trauma and Chemical Poisoning, Daping Hospital, Army Medical University, Yuzhong District, Chongqing, 400042, China. tianlixing@tmmu.edu.cn.

Funding

Chonqing Science and Technology Bureau CSTB2023NSCQ-BHX0199National Natural Science Foundation of China 82303757National Natural Science Foundation of China 82402548Special Project for Stem Cell Clinical Research of DAPING HOSPITAL NO.085121XXSpecial Project of Science and Technology Innovation Capacity Promotion of Army Medical University 2021XQN11
6 · The paper itself

Abstract

backgroundSepsis, a life-threatening organ dysfunction caused by dysregulated host responses to infection, has emerged as a leading cause of mortality in ICU patients. Macrophages, crucial effector cells in innate immunity, play pivotal regulatory roles in sepsis pathogenesis. While Programmed death-ligand 1 (PD-L1), a key immune checkpoint molecule, is traditionally believed to exert immunosuppressive effects through membrane anchoring, its involvement in macrophage polarization during sepsis remains unclear. This study investigated the spatial distribution of PD-L1 in macrophages and its regulatory effects on inflammatory responses during sepsis.

methodsThis study investigated PD-L1’s regulatory role in macrophage polarization through RNA sequencing, Immunoprecipitation-mass spectrometry, molecular docking, and site-directed mutagenesis, with preliminary validation in C57BL/6 mice.

resultsUsing GEO database analysis combined with qRT-PCR and Western blotting, we confirmed elevated PD-L1 expression in sepsis and M1-polarized macrophages. Laser scanning confocal microscopy demonstrated dual localization of PD-L1, appearing both on the plasma membrane and intracellularly within M1 macrophages. RNA sequencing revealed PD-L1’s promotion of M1 polarization through enhanced AIM2 expression in the NOD-like receptor pathway. Integrated analyses employing mass spectrometry, molecular docking, site-directed mutagenesis, and Western blotting demonstrated PD-L1 binding to AIM2, which augmented expression of downstream effector molecules (IL-18 and IFN-γ) and potentiated STAT1 activation. Silencing AIM2 by siRNA or IL-18 antagonism reversed PD-L1-induced M1 markers (IL-27, IL-6, iNOS/NO). PD-L1 was further shown to exacerbate pathological progression in septic mouse models.

conclusionsOur study demonstrated that sepsis-induced PD-L1 overexpression in macrophages exacerbates pathological progression by upregulating AIM2 expression, binding to AIM2 to enhance IL-18 production, which activates STAT1 to drive M1 polarization.

Indexed as

B7-H1 AntigenCell PolarityDNA-Binding ProteinsInterleukin-18MacrophagesSepsisSignal TransductionSTAT1 Transcription FactorAnimalsMaleMiceMice, Inbred C57BLMolecular Docking SimulationB7-H1 AntigenCd274 protein, mouseDNA-Binding ProteinsInterleukin-18Stat1 protein, mouseSTAT1 Transcription FactorMacrophagesPD-L1Sepsis

Identifiers

PMID41361470
PMCPMC12817491

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.