Evidence map›Paper›PMID 39620220›Full record

ArticleFrontiers in immunology2024

Placental mesenchymal stem cells suppress inflammation and promote M2-like macrophage polarization through the IL-10/STAT3/NLRP3 axis in acute lung injury.

Zhihao Nie, Qinglu Fan, Wanli Jiang, Shujian Wei, Renwei Luo, Haifeng Hu, Gaoli Liu, Yufei Lei, Songping Xie

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. TMEM16F deficiency alleviates sepsis-induced acute lung injury through regulating macrophage polarization.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
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  4. [UltrafineNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2026
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  12. The Impact ofMicroorganisms · 2025
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  13. Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2025
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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

9 authors.

Zhihao Nie *Department of Thoracic Surgery, Renmin Hospital of Wuhan University, Wuhan, China.
Qinglu Fan *Department of Thoracic Surgery, Renmin Hospital of Wuhan University, Wuhan, China.
Wanli JiangDepartment of Thoracic Surgery, Renmin Hospital of Wuhan University, Wuhan, China.
Shujian WeiDepartment of Thoracic Surgery, Renmin Hospital of Wuhan University, Wuhan, China.
Renwei LuoDepartment of Thoracic Surgery, Renmin Hospital of Wuhan University, Wuhan, China.
Haifeng HuDepartment of Thoracic Surgery, Renmin Hospital of Wuhan University, Wuhan, China.
Gaoli LiuDepartment of Thoracic Surgery, Renmin Hospital of Wuhan University, Wuhan, China.
Yufei LeiInstitute of Life Sciences, Chongqing Medical University, Chongqing, China.
Songping XieDepartment of Thoracic Surgery, Renmin Hospital of Wuhan University, Wuhan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Acute lung injury (ALI) is a clinically severe respiratory disorder that currently lacks specific and effective pharmacotherapy. The imbalance of M1/M2 macrophage polarization is pivotal in the initiation and progression of ALI. Shifting macrophage polarization from the proinflammatory M1 phenotype to the anti-inflammatory M2 phenotype could be a potential therapeutic strategy. The intratracheal administration of placental mesenchymal stem cells (pMSCs) has emerged as a novel and effective treatment for ALI. This study aimed to investigate the role and downstream mechanisms of pMSCs in reprogramming macrophage polarization to exert anti-inflammatory effects in ALI. Methods: The study used lipopolysaccharide (LPS) to induce inflammation in both cell and rat models of ALI. Intratracheal administration of pMSCs was tested as a therapeutic intervention. An expression dataset for MSCs cultured with LPS-treated macrophages was collected from the Gene Expression Omnibus database to predict downstream regulatory mechanisms. Experimental validation was conducted through in vitro and in vivo assays to assess pMSCs effects on macrophage polarization and inflammation. Results: Both Conclusion: The study concluded that pMSCs alleviated lung injury in an LPS-induced ALI model by inhibiting M1 macrophage polarization and proinflammatory factor secretion, while promoting M2 macrophage polarization. This effect was mediated via the IL-10/STAT3/NLRP3 axis, presenting a novel therapeutic pathway for ALI treatment.

Indexed as

Acute Lung InjuryInterleukin-10MacrophagesMesenchymal Stem CellsNLR Family, Pyrin Domain-Containing 3 ProteinPlacentaSTAT3 Transcription FactorAnimalsDisease Models, AnimalFemaleHumansInflammationLipopolysaccharidesMacrophage ActivationMaleMesenchymal Stem Cell TransplantationInterleukin-10LipopolysaccharidesNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, ratSTAT3 Transcription Factoracute lung injuryIL-10/STAT3 signalingmacrophage polarizationNLRP3 inflammasomeplacenta-derived mesenchymal stem cells

Identifiers

PMID39620220
PMCPMC11604576

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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.