Evidence map›Paper›PMID 33994863›Full record

ArticleInternational journal of biological sciences2021

MicroRNA-370 carried by M2 macrophage-derived exosomes alleviates asthma progression through inhibiting the FGF1/MAPK/STAT1 axis.

Chunlu Li, Chengsi Deng, Tingting Zhou, Jiapeng Hu, Bing Dai, Fei Yi, Na Tian, Lijun Jiang, Xiang Dong, Qingfeng Zhu and 4 more

Open access · goldAbstract read
In one paragraph

Article in International journal of biological sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

44 citing papers in PubMed, 57 citations in OpenAlex.

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  17. Harmonising cellular conversations: decoding the vital roles of extracellular vesicles in respiratory system intercellular communications.European respiratory review : an official journal of the European Respiratory Society · 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

14 authors at 1 institution in 1 country.

Chunlu LiDepartment of Pediatrics, Shengjing Hospital of China Medical University, Shenyang 110004, China.
Chengsi DengCollege of Basic Medicine Science, China Medical University, Shenyang 110122, China.
Tingting ZhouCollege of Basic Medicine Science, China Medical University, Shenyang 110122, China.
Jiapeng HuDepartment of Pediatrics, Shengjing Hospital of China Medical University, Shenyang 110004, China.
Bing DaiDepartment of Pediatrics, Shengjing Hospital of China Medical University, Shenyang 110004, China.
Fei YiCollege of Basic Medicine Science, China Medical University, Shenyang 110122, China.
Na TianJilin Tuohua Biotechnology Co., Ltd. Changchun, Jilin 13000, China.
Lijun JiangJilin Tuohua Biotechnology Co., Ltd. Changchun, Jilin 13000, China.
Xiang DongCollege of Basic Medicine Science, China Medical University, Shenyang 110122, China.
Qingfeng ZhuCollege of Basic Medicine Science, China Medical University, Shenyang 110122, China.
Siyi ZhangCollege of Basic Medicine Science, China Medical University, Shenyang 110122, China.
Hongyan CuiCollege of Basic Medicine Science, China Medical University, Shenyang 110122, China.
Liu CaoCollege of Basic Medicine Science, China Medical University, Shenyang 110122, China.
Yunxiao ShangDepartment of Pediatrics, Shengjing Hospital of China Medical University, Shenyang 110004, China.
China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Emerging evidence has suggested the functions of exosomes in allergic diseases including asthma. By using a mouse model with asthma induced by ovalbumin (OVA), we explored the roles of M2 macrophage-derived exosomes (M2Φ-Exos) in asthma progression. M2Φ-Exos significantly alleviated OVA-induced fibrosis and inflammatory responses in mouse lung tissues, as well as inhibited abnormal proliferation, invasion, and fibrosis-related protein production in platelet derived growth factor (PDGF-BB) treated primary mouse airway smooth muscle cells (ASMCs). The OVA administration in mice or the PDGF-BB treatment in ASMCs reduced the expression of miR-370, which was detected in M2Φ-Exos by miRNA sequencing. However, treating the mice or ASMCs with M2Φ-Exos reversed the inhibitory effect of OVA or PDGF-BB on miR-370 expression. We identified that the target of miR-370 was fibroblast growth factor 1 (

Indexed as

Gene Expression RegulationAnimalsAsthmaCell ProliferationCells, CulturedDisease Models, AnimalDown-RegulationExosomesFibroblast Growth Factor 1Macrophages, AlveolarMiceMice, Inbred C57BLMicroRNAsMitogen-Activated Protein Kinase KinasesMyocytes, Smooth MuscleSignal TransductionFibroblast Growth Factor 1MicroRNAsMIRN370 microRNA, mouseMitogen-Activated Protein Kinase KinasesStat1 protein, mouseSTAT1 Transcription FactorasthmaexosomesFGF1M2 macrophagesmiR-370

Identifiers

PMID33994863
PMCPMC8120458
OpenAlexW3157459040

What OpenQuestion holds

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LicenceCC BY
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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.