Evidence map›Paper›PMID 35548775›Full record

ArticleDisease markers2022

Role of Cardiomyocyte-Derived Exosomal MicroRNA-146a-5p in Macrophage Polarization and Activation.

Cong Chen, Sidong Cai, Min Wu, Run Wang, Mingya Liu, Gaozhen Cao, Min Dong, Kai-Hang Yiu

Open access · hybridAbstract read
In one paragraph

Article in Disease markers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

29 citing papers in PubMed, 28 citations in OpenAlex.

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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 2 institutions in 2 countries.

Cong ChenDivision of Cardiology, Department of Medicine, The University of Hong Kong Shenzhen Hospital, Shenzhen, China.ORCID https://orcid.org/0000-0001-7125-871X
Sidong CaiDivision of Cardiology, Department of Medicine, The University of Hong Kong Shenzhen Hospital, Shenzhen, China.ORCID https://orcid.org/0000-0002-3899-6013
Min WuDivision of Cardiology, Department of Medicine, The University of Hong Kong Shenzhen Hospital, Shenzhen, China.ORCID https://orcid.org/0000-0001-8447-5318
Run WangDivision of Cardiology, Department of Medicine, The University of Hong Kong Shenzhen Hospital, Shenzhen, China.ORCID https://orcid.org/0000-0002-1610-677X
Mingya LiuDivision of Cardiology, Department of Medicine, The University of Hong Kong Shenzhen Hospital, Shenzhen, China.ORCID https://orcid.org/0000-0002-3039-1060
Gaozhen CaoDivision of Cardiology, Department of Medicine, The University of Hong Kong Shenzhen Hospital, Shenzhen, China.ORCID https://orcid.org/0000-0002-1150-4146
Min DongBioland Laboratory (Guangzhou Regenerative Medicine and Health Guangdong Laboratory), China.ORCID https://orcid.org/0000-0003-0765-6208
Kai-Hang YiuDivision of Cardiology, Department of Medicine, The University of Hong Kong Shenzhen Hospital, Shenzhen, China.ORCID https://orcid.org/0000-0003-2145-3108
University of Hong Kong - Shenzhen Hospital · CNGuangzhou Regenerative Medicine and Health Guangdong Laboratory · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myocardial infarction arises from an excessive or prolonged inflammatory response, leading to ventricular remodeling or impaired cardiac function. Macrophages exhibit different polarization types associated with inflammation both at steady state and after myocardial infarction. Exosomal miR-146a-5p has been identified as an important molecule in the cardiovascular field in recent years. However, the effect of cardiomyocyte-derived exosomal miR-146a-5p on macrophages has not yet been elucidated. Initially, we found that exosomes with low expression of miR-146a-5p derived from myocardial infarction tissues modulated macrophage polarization. To determine whether cardiomyocyte-derived exosomal miR-146a-5p mediated macrophage polarization, we treated macrophages with exosomes rich in miR-146a-5p collected from neonatal mouse cardiomyocytes. The effects of exosomal miR-146a-5p on macrophage polarization were measured using RT-qPCR, transwell assays, and western blotting. The results showed that the increased expression of miR-146a-5p promoted M1 macrophage polarization, inhibited M2 macrophage polarization, and increased the expression of VEGFA. However, the decreased expression of exosomalmiR-146a-5p showed the opposite trends. Interestingly, in contrast to treatment with the solitary miR-146a-5p mimic, exosomal miR-146a-5p derived from neonatal mouse cardiomyocytes reduced TNF

Indexed as

ExosomesMicroRNAsMyocardial InfarctionAnimalsInflammationMacrophage ActivationMacrophagesMiceMyocytes, CardiacTNF Receptor-Associated Factor 6MicroRNAsTNF Receptor-Associated Factor 6

Identifiers

PMID35548775
PMCPMC9085364
OpenAlexW4225314138

What OpenQuestion holds

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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 OpenQuestion graph.