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Series GSE188234 Query DataSets for GSE188234
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
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.
 
Overall design Human skeletal muscle cells treated with TGF-β1, TGF-β1 + SB431542, or control cells. Data was analysed by RNAseq.
 
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
Submission date Nov 04, 2021
Last update date Dec 29, 2021
Contact name Johannes Beckers
E-mail(s) [email protected]
Organization name Helmholtz Zentrum Muenchen
Department Institute of Experimental Genetics
Street address Ingolstaedter Landstr. 1
City Neuherberg
ZIP/Postal code 85764
Country Germany
 
Platforms (1)
GPL16791 Illumina HiSeq 2500 (Homo sapiens)
Samples (15)
GSM5673193 Human_skeletal_muscle_cells_rep1 [RNA-seq]
GSM5673194 Human_skeletal_muscle_cells_rep2 [RNA-seq]
GSM5673195 Human_skeletal_muscle_cells_rep3 [RNA-seq]
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
Relations
BioProject PRJNA777956
SRA SRP344642

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Supplementary file Size Download File type/resource
GSE188234_RAW.tar 3.5 Mb (http)(custom) TAR (of TXT)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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