Evidence map›Paper›PMID 31157263›Full record

ArticleAnnals of translational medicine2019

M2 macrophages promote pulmonary endothelial cells regeneration in sepsis-induced acute lung injury.

Yaxing Shen, Jieqiong Song, Yingqin Wang, Zhenglong Chen, Lin Zhang, Jie Yu, Duming Zhu, Ming Zhong

Open access · diamondAbstract read
In one paragraph

Article in Annals of translational medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.5field-weighted citation impact, top 10% of its field
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

39 citing papers in PubMed, 50 citations in OpenAlex.

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  15. Demonstration of ameliorating effect of papaverine in sepsis-induced acute lung injury on rat model through radiology and histology.Ulusal travma ve acil cerrahi dergisi = Turkish journal of trauma & emergency surgery : TJTES · 2023
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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

8 authors at 6 institutions in 1 country.

Yaxing ShenDepartment of Thoracic Surgery, Zhongshan Hospital Fudan University, Shanghai 200032, China.
Jieqiong SongDepartment of Critical Care Medicine, Zhongshan Hospital Fudan University, Shanghai 200032, China.
Yingqin WangDepartment of Critical Care Medicine, Zhongshan Hospital Fudan University, Shanghai 200032, China.
Zhenglong ChenSchool of Medical Instrumentation, Shanghai University of Medicine & Health Sciences, Shanghai 201318, China.
Lin ZhangCenter of Emergency and Intensive Care Unit, Jinshan Hospital Fudan University, Shanghai 201508, China.
Jie YuDepartment of Critical Care Medicine, Zhongshan Hospital Fudan University, Shanghai 200032, China.
Duming ZhuDepartment of Critical Care Medicine, Zhongshan Hospital Fudan University, Shanghai 200032, China.
Ming ZhongDepartment of Critical Care Medicine, Zhongshan Hospital Fudan University, Shanghai 200032, China.
Sun Yat-sen University · CNFudan University · CNJinshan Hospital of Fudan University · CNShanghai University of Medicine and Health Sciences · CNThe First Affiliated Hospital, Sun Yat-sen University · CNZhongshan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMacrophages can polarize to M2 phenotype to decrease inflammation and encourage tissue repair. Nonetheless, its role in sepsis-induced acute lung injury and its effect on endothelial cells (ECs) regeneration remains unknown. The aim of the current study was to explore the impact of M2 macrophages on pulmonary ECs proliferation in sepsis-induced acute lung injury.

methodsWe co-cultured mouse lung microvascular endothelial cells (MLMVECs) with M2 macrophages following LPS challenge. M2 macrophages were intratracheally transplanted into mice subjected to cecal ligation and puncture (CLP). We further performed cytokine array for the supernatant from M2 macrophages and serum from mice subjected with CLP.

resultsWe found both co-culture with M2 macrophages and treating with supernatant from M2 macrophages increased ECs viability following LPS challenge. Intratracheal transplantation of M2 macrophages markedly promoted pulmonary ECs proliferation, manifesting as attenuation of lung microvascular permeability and lung tissue edema, as well as improvement of survival rate. We further found that CXCL12, IL-1ra, TIMP-1, IL-4, and CXCL1 were increased in the supernatant of M2 macrophages

conclusionsThe present study suggested M2 macrophages could promote ECs proliferation in sepsis-induced ALI through secretion of anti-inflammatory cytokines and growth factors.

Indexed as

endothelial cells (EC)M2 macrophagesproliferationsepsis

Identifiers

PMID31157263
PMCPMC6511576
OpenAlexW2921729329

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.