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The microRNA signature in response to insulin reveals their implication in the transcriptional action of insulin in human skeletal muscle and the role of a SREBP-1c/MEF2C pathway

  1. Aurélie Granjon1,
  2. Marie-Paule Gustin2,
  3. Jennifer Rieusset1,
  4. Etienne Lefai1,
  5. Emmanuelle Meugnier1,
  6. Isabelle Güller1,
  7. Catherine Cerutti2,
  8. Christian Paultre2,
  9. Emmanuel Disse3,4,
  10. Rémi Rabasa-Lhoret5,
  11. Martine Laville1,3,4,
  12. Hubert Vidal1,3,4 and
  13. Sophie Rome (srome{at}univ-lyon1.fr)1
  1. 1 INRA 1235 ; INSERM 870 ; INSA-Lyon ; Régulations Métaboliques Nutrition et Diabète ; Université Lyon; Oullins 69600-FRANCE
  2. 2INSERM ERI22/EA 4173, Biostatistiques ; Université Lyon; Lyon, 69008- FRANCE
  3. 3Hospices Civils de Lyon ; Service de Diabétologie et Nutrition, Hôpital Edouard-Herriot, Lyon, 69008- FRANCE
  4. 4Centre de Recherche en Nutrition Humaine Rhône-Alpes, Oullins 69600-FRANCE
  5. 5Chaire de recherche J-A DeSève, Institut de recherches cliniques de Montréal (IRCM), Montréal (Québec) H2W 1R7

    Abstract

    Objective Factors governing microRNA expressions in response to changes of cellular environment are still largely unknown. Our aim was to determine whether insulin, the major hormone controlling whole-body energy homeostasis, is involved in the regulation of microRNA expressions in human skeletal muscle.

    Research Design and Methods We carried out comparative miRNA expression profiles in human skeletal muscle biopsies before and after a 3-h euglycemic-hyperinsulinemic clamp, with TaqMan low density arrays. Then, using DNA microarrays we determined the response to insulin of the miRNA putative target genes in order to determine their role in the transcriptional action of insulin. We further characterized the mechanism of action of insulin on two representative miRNAs, miR-1 and miR-133a in human muscle cells.

    Results Insulin down-regulated the expressions of 39 distinct miRNAs in human skeletal muscle. Their potential target mRNAs coded for proteins that were mainly involved in insulin signaling and ubiquitination-mediated proteolysis. Bioinformatic analysis suggested that combinations of different down-regulated miRNAs worked in concert to regulate gene expressions in response to insulin. We further demonstrated that SREBP-1c and MEF2C were involved in the effect of insulin on miR-1 and miR-133a expression. Interestingly, we found an impaired-regulation of miRNAs by insulin in the skeletal muscle of type 2 diabetic patients, likely as consequences of altered SREBP-1c activation.

    Conclusions This work demonstrates a new role of insulin in the regulation of miRNAs in human skeletal muscleand suggests a possible implication of these new modulators in insulin-resistance.

    Footnotes

      • Received February 5, 2009.
      • Accepted August 5, 2009.
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