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Status |
Public on Nov 03, 2016 |
Title |
Palmitate-induced inhibition of C2C12 insulin pathway modifies the release of exosomes and their biological actions on muscle cells |
Organism |
Mus musculus |
Experiment type |
Expression profiling by array
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Summary |
Exosomes are cell-released bioactive nanovesicles now considered as new partners in the inter-organ cross-talks. The possibility that skeletal muscle (SkM)-derived exosomes act as a mode of systemic communication has hitherto never been described. Thus, in this study we have tested the hypothesis that through the exosomal route, muscle cells might transmit specific signals during insulin-resistance.
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Overall design |
C2C12 myoblasts were differentiated into myotubes and then treated with 0.5mM palmitate in order to alter insulin signaling pathway or BSA as control. Exosomes released from palmitate-treated cells (EXO-palm) and from BSA-treated cells (EXO-BSA) were collected by ultracentrifugation. Then C2C12 were treated with either EXO-palm or EXO-BSA. RNA was extracted and global transcriptomic analysis was performed.
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Contributor(s) |
Rome S, Meugnier E |
Citation missing |
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Submission date |
Nov 04, 2013 |
Last update date |
Jan 19, 2018 |
Contact name |
emmanuelle meugnier |
E-mail(s) |
emmanuelle.meugnier@univ-lyon1.fr
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Organization name |
INSERMU1060/INRAE1397
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Lab |
CarMeN
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Street address |
Cens Eli Bat 2 D- Hopital Lyon Sud
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City |
Pierre BĂ©nite |
ZIP/Postal code |
69495 |
Country |
France |
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Platforms (1) |
GPL10333 |
Agilent-026655 Whole Mouse Genome Microarray 4x44K v2 (Feature Number version) |
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Samples (7)
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Relations |
BioProject |
PRJNA226583 |