Endurance exercise training-responsive miR-19b-3p improves skeletal muscle glucose metabolism.
Julie MassartRasmus J O SjögrenBrendan EganChristian GardeMagnus LindgrenWeifeng GuDuarte M S FerreiraMutsumi KatayamaJorge L RuasRomain BarresDonal J O'GormanJuleen R ZierathAnna KrookPublished in: Nature communications (2021)
Skeletal muscle is a highly adaptable tissue and remodels in response to exercise training. Using short RNA sequencing, we determine the miRNA profile of skeletal muscle from healthy male volunteers before and after a 14-day aerobic exercise training regime. Among the exercise training-responsive miRNAs identified, miR-19b-3p was selected for further validation. Overexpression of miR-19b-3p in human skeletal muscle cells increases insulin signaling, glucose uptake, and maximal oxygen consumption, recapitulating the adaptive response to aerobic exercise training. Overexpression of miR-19b-3p in mouse flexor digitorum brevis muscle enhances contraction-induced glucose uptake, indicating that miR-19b-3p exerts control on exercise training-induced adaptations in skeletal muscle. Potential targets of miR-19b-3p that are reduced after aerobic exercise training include KIF13A, MAPK6, RNF11, and VPS37A. Amongst these, RNF11 silencing potentiates glucose uptake in human skeletal muscle cells. Collectively, we identify miR-19b-3p as an aerobic exercise training-induced miRNA that regulates skeletal muscle glucose metabolism.
Keyphrases
- skeletal muscle
- insulin resistance
- endothelial cells
- high glucose
- high intensity
- induced apoptosis
- diabetic rats
- type diabetes
- cell proliferation
- oxidative stress
- transcription factor
- cell cycle arrest
- signaling pathway
- induced pluripotent stem cells
- endoplasmic reticulum stress
- blood pressure
- resistance training
- single cell
- dna damage
- pluripotent stem cells
- glycemic control