Evidence map›Paper›PMID 33313154›Full record

ArticleAnnals of translational medicine2020

M2b macrophages protect against myocardial remodeling after ischemia/reperfusion injury by regulating kinase activation of platelet-derived growth factor receptor of cardiac fibroblast.

Yuan Yue, Suiqing Huang, Huayang Li, Wei Li, Jian Hou, Li Luo, Quan Liu, Cuiping Wang, Song Yang, Linhua Lv and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Annals of translational medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
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  7. Macrophage fate: to kill or not to kill?Infection and immunity · 2024
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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

12 authors at 3 institutions in 1 country.

Yuan YueDepartment of Cardiac Surgery, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Suiqing HuangDepartment of Cardiac Surgery, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Huayang LiDepartment of Cardiac Surgery, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Wei LiDepartment of Medical Ultrasound, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Jian HouDepartment of Cardiac Surgery, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Li LuoDepartment of Cardiac Surgery, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Quan LiuDepartment of Cardiac Surgery, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Cuiping WangDepartment of Cardiothoracic Surgery ICU, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Song YangDepartment of Cardiothoracic Surgery ICU, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Linhua LvDepartment of Cardiac Surgery, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Jinghua ShaoOut-Patient Department, Shenxian Second People's Hospital, Shenxian, China.
Zhongkai WuDepartment of Cardiac Surgery, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
The First Affiliated Hospital, Sun Yat-sen University · CNSun Yat-sen University · CNXian Yang Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMyocardial injury is a major cause of myocardial remodeling. Macrophages are important in cardiac repair as a result of their interactions with fibroblasts. As regulatory macrophages, M2b macrophages modulate inflammatory immune responses without participating in wound healing and could have enhanced protective effects on myocardial remodeling. Therefore, we tested the hypothesis that M2b macrophages could improve cardiac function and ameliorate myocardial fibrosis after the myocardial ischemia/reperfusion injury (MI/RI).

methods

resultsA significantly higher rat survival rate, improved left ventricular (LV) systolic function, decreased diameter of the LV and alleviated myocardial fibrosis were observed in the MT group than in the CK group.

conclusionsOur study demonstrated that the administration of M2b macrophages could attenuate myocardial remodeling after MI/RI. The regulation of the activation of PDGFRs in CFs is an important part of the protective mechanism.

Indexed as

cardiac fibroblast (CF)M2b macrophagemyocardial ischemia/reperfusion injury (MI/RI)myocardial remodeling

Identifiers

PMID33313154
PMCPMC7723613
OpenAlexW3093237889

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.