Evidence map›Paper›PMID 40342203›Full record

ArticleJournal of diabetes investigation2025

Adipocyte exosome miR-4472 inhibits glucose uptake in skeletal muscle through downregulation of MEF2D.

Chaoyue Sun, Xin Wen, Xiaolong Chu, Fangyuan Yuan, Yao Chen, Chaoling Peng, Meiyu Qian, Jin Mei, Juan Wang, Yidan Jiang and 4 more

Abstract read
In one paragraph

Article in Journal of diabetes investigation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
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  3. Review
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.

Chaoyue Sun *Ministry of Education Key Laboratory of Xinjiang Endemic and Ethnic Disease, Shihezi, Xinjiang, China.
Xin Wen *Medical College of Shihezi University, Shihezi, Xinjiang, China.
Xiaolong ChuMedical College of Shihezi University, Shihezi, Xinjiang, China.
Fangyuan YuanMedical College of Shihezi University, Shihezi, Xinjiang, China.
Yao ChenMedical College of Shihezi University, Shihezi, Xinjiang, China.
Chaoling PengMedical College of Shihezi University, Shihezi, Xinjiang, China.
Meiyu QianMedical College of Shihezi University, Shihezi, Xinjiang, China.
Jin MeiMedical College of Shihezi University, Shihezi, Xinjiang, China.
Juan WangMedical College of Shihezi University, Shihezi, Xinjiang, China.
Yidan JiangMedical College of Shihezi University, Shihezi, Xinjiang, China.
Shibo XuMedical College of Shihezi University, Shihezi, Xinjiang, China.
Cuizhe WangMedical College of Shihezi University, Shihezi, Xinjiang, China.
Wei LiMedical College of Shihezi University, Shihezi, Xinjiang, China.
Jun ZhangMinistry of Education Key Laboratory of Xinjiang Endemic and Ethnic Disease, Shihezi, Xinjiang, China.ORCID https://orcid.org/0000-0001-9796-994X

Funding

National Natural Science Foundation of China 82160156National Natural Science Foundation of China 82260162Scientific and Technological Research Project of Xinjiang Production and Construction Corps 2022AB022Scientific and Technological Research Project of Xinjiang Production and Construction Corps 2022ZD001Scientific and Technological Research Project of Xinjiang Production and Construction Corps 2022ZD083Scientific and Technological Research Project of Xinjiang Production and Construction Corps 2023AB057Scientific and Technological Research Project of Xinjiang Production and Construction Corps 2023ZD037Tianshan Talent Project in Xinjiang Autonomous Region 2023TSYCCX0116
6 · The paper itself

Abstract

AIMS/

introductionPrevious studies have found that miR-4472 is overexpressed in the serum of individuals with obesity and type 2 diabetes mellitus (T2DM), which may participate in the process of obesity-induced T2DM. However, a role for miR-4472 in the process has not been demonstrated. Here, we aim to investigate whether the increased content of miR-4472 in adipose tissue derived from exosomes inhibits glucose uptake in skeletal muscle by downregulating the expression of its target gene. MATERIALS AND

methodsIn vitro C2C12 and 3T3-L1 cells, and in vivo diet-induced obesity mouse models and AT-Dicer KO mice were used to assess the impact of miR-4472 on glucose uptake and insulin sensitivity. We also evaluated the effects of serum exosomes from normal and obese individuals on insulin sensitivity in mice and the expression of miR-4472 and target genes in skeletal muscle.

resultsmiR-4472 exhibits a strong positive correlation with BMI, waist circumference, hip circumference, and FPG. The content of miR-4472 derived from adipose tissue exosomes increases in the circulation in a state of obesity, which can induce insulin resistance by targeting the expression of MEF2D/GLUT4, inhibiting the glucose consumption and uptake ability of skeletal muscle cells. Both exosome inhibitors and miR-4472 inhibitors can reverse the inhibitory effect of miR-4472 on MEF2D/GLUT4 expression and glucose intake and uptake ability. Additionally, they can improve insulin resistance caused by increased miR-4472 levels in mice with obesity.

conclusionsAdipocyte exosome miR-4472 inhibits glucose uptake in skeletal muscle through downregulating the expression of MEF2D/GLUT4.

Indexed as

AdipocytesExosomesGlucoseMEF2 Transcription FactorsMicroRNAsMuscle, Skeletal3T3-L1 CellsAnimalsDiabetes Mellitus, Type 2Down-RegulationGlucose Transporter Type 4HumansInsulin ResistanceMaleMiceMice, Inbred C57BLGlucoseGlucose Transporter Type 4MEF2D protein, humanMef2d protein, mouseMEF2 Transcription FactorsMicroRNAsMEF2DmiR‐4472Skeletal muscle

Identifiers

PMID40342203
PMCPMC12315254

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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.