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Status |
Public on Dec 07, 2021 |
Title |
TGF-β-induced miR143/145 influences differentiation, insulin signaling and exercise response in human skeletal muscle [RNA-seq] |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Physical training improves insulin sensitivity and can prevent type 2 diabetes. However, approximately 20% of individuals lack a beneficial outcome in glycemic control. TGF-β, identified as a possible upstream regulator involved in this low response is also a potent regulator of microRNAs (miRs). Aim of this study was to elucidate the potential impact of TGF-β-driven miRNAs on individual exercise response. Non-targeted long and sncRNA sequencing analyses of TGF-β1-treated human skeletal muscle cells corroborated the effects of TGF-β1 on muscle cell differentiation and the induction of extracellular matrix components, and identified several TGF-β1-regulated miRs. qPCR validated a potent upregulation of miR143/145 and miR181a2 by TGF-β1 in both human myoblasts and differentiating myotubes. Human skeletal muscle biopsy donors participating in a supervised 8-week endurance training intervention (n=40) were categorized as responder based on fold change ISIMats (≥ +1.1) or low responder. In skeletal muscle of low responders, TGF-β signaling and miR143/145 levels were stronger induced by training than in responders. Target-mining revealed HDACs, MYHs and insulin signaling components INSR and IRS1 as potential miR143/145 targets. All these targets were down-regulated in TGF-β1-treated myotubes. Transfection of miR mimics in differentiated myotubes validated MYH1, MYH4, and IRS1 as miR143/145 targets. Elevated TGF-β signaling and miR143/145 induction in skeletal muscle of low responders might obstruct improvements in insulin sensitivity by training in two ways: By negatively impacting cell fusion and myofiber functionality via miR143 suppressing its novel targets MYH1/4; by directly impairing insulin signaling via reduction of INSR by TGF-β and fine-tuned IRS1 suppression by miR143.
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Overall design |
Human skeletal muscle cells treated with TGF-β1, TGF-β1 + SB431542, or control cells. Data was analysed by RNAseq.
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Contributor(s) |
Dreher SI, Höckele S, Huypens P, Irmler M, Hoffmann C, Jeske T, Hastreiter M, Moller A, Birkenfeld AL, Häring HU, Peter A, Beckers J, Hrabě de Angelis M, Weigert C |
Citation(s) |
34943951 |
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Submission date |
Nov 04, 2021 |
Last update date |
Dec 29, 2021 |
Contact name |
Johannes Beckers |
E-mail(s) |
[email protected]
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Organization name |
Helmholtz Zentrum Muenchen
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Department |
Institute of Experimental Genetics
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Street address |
Ingolstaedter Landstr. 1
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City |
Neuherberg |
ZIP/Postal code |
85764 |
Country |
Germany |
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Platforms (1) |
GPL16791 |
Illumina HiSeq 2500 (Homo sapiens) |
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Samples (15)
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GSM5673193 |
Human_skeletal_muscle_cells_rep1 [RNA-seq] |
GSM5673194 |
Human_skeletal_muscle_cells_rep2 [RNA-seq] |
GSM5673195 |
Human_skeletal_muscle_cells_rep3 [RNA-seq] |
GSM5673196 |
Human_skeletal_muscle_cells_rep4 [RNA-seq] |
GSM5673197 |
Human_skeletal_muscle_cells_rep5 [RNA-seq] |
GSM5673198 |
Human_skeletal_muscle_cells_TGFB1_rep1 [RNA-seq] |
GSM5673199 |
Human_skeletal_muscle_cells_TGFB1_rep2 [RNA-seq] |
GSM5673200 |
Human_skeletal_muscle_cells_TGFB1_rep3 [RNA-seq] |
GSM5673201 |
Human_skeletal_muscle_cells_TGFB1_rep4 [RNA-seq] |
GSM5673202 |
Human_skeletal_muscle_cells_TGFB1_rep5 [RNA-seq] |
GSM5673203 |
Human_skeletal_muscle_cells_TGFB1_SB431542_rep1 [RNA-seq] |
GSM5673204 |
Human_skeletal_muscle_cells_TGFB1_SB431542_rep2 [RNA-seq] |
GSM5673205 |
Human_skeletal_muscle_cells_TGFB1_SB431542_rep3 [RNA-seq] |
GSM5673206 |
Human_skeletal_muscle_cells_TGFB1_SB431542_rep4 [RNA-seq] |
GSM5673207 |
Human_skeletal_muscle_cells_TGFB1_SB431542_rep5 [RNA-seq] |
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This SubSeries is part of SuperSeries: |
GSE188236 |
TGF-β Induction of miR-143/145 Is Associated to Exercise Response by Influencing Differentiation and Insulin Signaling Molecules in Human Skeletal Muscle |
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Relations |
BioProject |
PRJNA777956 |
SRA |
SRP344642 |