PPARα, δ and FOXO1 Gene Silencing Overturns Palmitate-Induced Inhibition of Pyruvate Oxidation Differentially in C2C12 Myotubes
The molecular mechanisms by which free fatty acids (FFA) inhibit muscle glucose oxidation is still elusive. We recently showed that C2C12 myotubes treated with palmitate (PAL) presented with greater protein expression levels of PDK4 and transcription factors <i>PPARα</i> and <i>PPA...
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| Autores principales: | , , , |
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| Formato: | article |
| Lenguaje: | EN |
| Publicado: |
MDPI AG
2021
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| Materias: | |
| Acceso en línea: | https://doaj.org/article/dd0e320f408a417c96cb06e994deeb33 |
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| Sumario: | The molecular mechanisms by which free fatty acids (FFA) inhibit muscle glucose oxidation is still elusive. We recently showed that C2C12 myotubes treated with palmitate (PAL) presented with greater protein expression levels of PDK4 and transcription factors <i>PPARα</i> and <i>PPARδ</i> and lower <i>p</i>-<i>FOXO</i>/<i>t</i>-<i>FOXO</i> protein ratios when compared to control. This was complemented with the hallmarks of metabolic inflexibility (MI), i.e., reduced rates of glucose uptake, PDC activity and maximal pyruvate-derived ATP production rates (MAPR). However, the relative contribution of these transcription factors to the increase in PDK4 and reduced glucose oxidation could not be established. Therefore, by using a similar myotube model, a series of individual siRNA gene silencing experiments, validated at transcriptional and translation levels, were performed in conjunction with measurements of glucose uptake, PDC activity, MAPR and concentrations of metabolites reflecting PDC flux (lactate and acetylcarnitine). Gene silencing of <i>PPARα</i>, <i>δ</i> and <i>FOXO1</i> individually reduced PAL-mediated inhibition of PDC activity and increased glucose uptake, albeit by different mechanisms as only <i>PPARδ</i> and <i>FOXO1</i> silencing markedly reduced PDK4 protein content. Additionally, <i>PPARα</i> and <i>FOXO1</i> silencing, but not <i>PPARδ</i>, increased MAPR with PAL. <i>PPARδ</i> silencing also decreased FOXO1 protein. Since <i>FOXO1</i> silencing did not alter PPARδ protein, this suggests that <i>FOXO1</i> might be a <i>PPARδ</i> downstream target. In summary, this study suggests that the molecular mechanisms by which PAL reduces PDC-mediated glucose-derived pyruvate oxidation in muscle occur primarily through increased <i>PPARδ</i> and <i>FOXO1</i> mediated increases in PDK4 protein expression and secondarily through PPARα mediated allosteric inhibition of PDC flux. Furthermore, since <i>PPARδ</i> seems to control FOXO1 expression, this may reflect an important role for <i>PPARδ</i> in preventing glucose oxidation under conditions of increased lipid availability. |
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