Evidence map›Paper›PMID 35188856›Full record

ArticlePharmaceutical biology2022

M2b macrophages stimulate lymphangiogenesis to reduce myocardial fibrosis after myocardial ischaemia/reperfusion injury.

Cuiping Wang, Yuan Yue, Suiqing Huang, Keke Wang, Xiao Yang, Jiantao Chen, Jiaxing Huang, Zhongkai Wu

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutical biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  11. Angiogenesis-An Emerging Role in Organ Fibrosis.International journal of molecular sciences · 2023
    Review
  12. hESC-Derived Epicardial Cells Promote Repair of Infarcted Hearts in Mouse and Swine.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  13. Modeling lymphangiogenesis: Pairing in vitro and in vivo metrics.Microcirculation (New York, N.Y. : 1994) · 2023
    Review
  14. Review
  15. Review
  16. 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

8 authors at 3 institutions in 1 country.

Cuiping WangDepartment of Cardiothoracic ICU, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, PR China.
Yuan YueKey Laboratory on Assisted Circulation, Ministry of Health, Guangzhou, PR China.
Suiqing HuangKey Laboratory on Assisted Circulation, Ministry of Health, Guangzhou, PR China.
Keke WangKey Laboratory on Assisted Circulation, Ministry of Health, Guangzhou, PR China.
Xiao YangDepartment of Laboratory Medicine, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, PR China.
Jiantao ChenKey Laboratory on Assisted Circulation, Ministry of Health, Guangzhou, PR China.
Jiaxing HuangKey Laboratory on Assisted Circulation, Ministry of Health, Guangzhou, PR China.
Zhongkai WuKey Laboratory on Assisted Circulation, Ministry of Health, Guangzhou, PR China.
The First Affiliated Hospital, Sun Yat-sen University · CNSun Yat-sen University · CNGuangzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextTherapeutic lymphangiogenesis is a new treatment for cardiovascular diseases. Our previous study showed M2b macrophages can alleviate myocardial ischaemia/reperfusion injury (MI/RI). However, the relation between M2b macrophages and lymphangiogenesis is not clear.

objectiveTo investigate the effects of M2b macrophages on lymphangiogenesis after MI/RI. MATERIALS AND

methodsForty male Sprague-Dawley (SD) rats were randomized into Sham operation group (control,

resultsDISCUSSION AND

conclusionsOur study shows that M2b macrophages can promote lymphangiogenesis to reduce myocardial fibrosis and improve heart function, suggesting the possible use of M2b macrophage for myocardial protection therapy.

Indexed as

AnimalsCell MovementCell ProliferationDisease Models, AnimalEchocardiographyEndothelial CellsFibrosisLymphangiogenesisMacrophagesMaleMyocardial Reperfusion InjuryRandom AllocationRatsRats, Sprague-DawleyStroke VolumeVentricular Function, LeftCardiac fibrosisVEGFCVEGF receptor 3

Identifiers

PMID35188856
PMCPMC8865132
OpenAlexW4212795278

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.