Evidence map›Paper›PMID 41046976›Full record

ArticleJournal of sport and health science2025

Exercise training-induced extracellular miR-136-3p modulates glucose uptake and myogenesis through targeting of NRDC in human skeletal muscle.

Mutsumi Katayama, Elena Caria, Dimitri Van Simaeys, Anna Yagüe Sanz, Romain Barrès, Kenneth Caidahl, Oscar P B Wiklander, Samir El Andaloussi, Per-Olof Berggren, Juleen R Zierath and 1 more

Abstract read
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Article in Journal of sport and health science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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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

11 authors.

Mutsumi KatayamaDepartment of Physiology and Pharmacology, Integrative Physiology, Karolinska Institutet, Stockholm 17177, Sweden.
Elena CariaDepartment of Physiology and Pharmacology, Integrative Physiology, Karolinska Institutet, Stockholm 17177, Sweden.
Dimitri Van SimaeysRolf Luft Research Center for Diabetes and Endocrinology, Karolinska Institutet, Stockholm 17176, Sweden.
Anna Yagüe SanzDepartment of Physiology and Pharmacology, Integrative Physiology, Karolinska Institutet, Stockholm 17177, Sweden.
Romain BarrèsNovo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen, Copenhagen 2200, Denmark; Institute of Molecular and Cellular Pharmacology, Centre National de la Recherche Scientifique (CNRS) and Université Côte d'Azur, Valbonne 06560, France.
Kenneth CaidahlDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm 17176, Sweden.
Oscar P B WiklanderBiomolecular and Cellular Medicine, Department of Laboratory Medicine, Karolinska Institutet, Stockholm 17177, Sweden; Karolinska ATMP Center, ANA Futura, Huddinge 14157, Sweden; Breast Center, Karolinska Comprehensive Cancer Center, Karolinska University Hospital, Stockholm 17176, Sweden.
Samir El AndaloussiBiomolecular and Cellular Medicine, Department of Laboratory Medicine, Karolinska Institutet, Stockholm 17177, Sweden; Department of Cellular Therapy and Allogeneic Stem Cell Transplantation, Karolinska University Hospital, Huddinge 14157, Sweden.
Per-Olof BerggrenRolf Luft Research Center for Diabetes and Endocrinology, Karolinska Institutet, Stockholm 17176, Sweden; Research Center for Islet Transplantation, West China Hospital, Sichuan University, Chengdu 610041, China.
Juleen R ZierathDepartment of Physiology and Pharmacology, Integrative Physiology, Karolinska Institutet, Stockholm 17177, Sweden; Department of Molecular Medicine and Surgery, Integrative Physiology, Karolinska Institutet, Stockholm 17177, Sweden.
Anna KrookDepartment of Physiology and Pharmacology, Integrative Physiology, Karolinska Institutet, Stockholm 17177, Sweden. Electronic address: anna.krook@ki.se.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRegular physical training induces adaptive effects across multiple organ systems, highlighting the existence of inter-organ communication networks. However, the molecular mechanisms underlying both exercise-induced adaptations and organ-to-organ signaling are not fully characterized. Circulating extracellular vesicles (EVs), including exosomes, carry molecules like microRNAs (miRNAs) that may mediate tissue crosstalk. This study aimed to identify specific exercise training-responsive miRNAs that affect skeletal muscle function.

methodsmiRNA expression profiles of serum-derived EVs were analyzed in healthy young individuals before and after 3 weeks endurance exercise training. Exercise training-responsive miRNAs were then validated for a functional role in cellular metabolic processes in human myotubes.

resultsWe identified several exercise training-responsive miRNAs within exosome-rich EVs in serum, including miR-136-3p. In human myotubes, miR-136-3p enhanced glucose uptake and targeted the nardilysin convertase (NRDC) gene. Transfection of miR-136-3p or silencing of NRDC induced a shift towards glycolytic metabolism in mitochondria and modulated gene expressions related to myogenesis. Pancreatic islets were identified as a potential source of miR-136-3p based on in silico analysis of gene expression and a molecular analysis of conditioned media from isolated pancreatic islets.

conclusionMiR-136-3p is an endurance training-responsive molecular transducer that modulates glucose metabolism and cellular proliferation in myocytes. Associated with EVs, extracellular miR-136-3p may serve as a molecular messenger to communicate islet-skeletal muscle crosstalk after exercise. Extracellular miR-136-3p may serve as a molecular messenger to communicate islet-skeletal muscle crosstalk. Our results highlight a miRNA-mediated mechanism that participates in inter-organ communication to fine tune the metabolic adaptations to exercise.

Indexed as

Endurance trainingExtracellular miRNAHuman skeletal musclemiR-136-3pNardilycin convertase (NRDC)

Identifiers

PMID41046976
PMCPMC12811471

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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.