| First Author | O'Connell GC | Year | 2015 |
| Journal | Biochem Biophys Res Commun | Volume | 458 |
| Issue | 3 | Pages | 614-9 |
| PubMed ID | 25681766 | Mgi Jnum | J:220486 |
| Mgi Id | MGI:5634863 | Doi | 10.1016/j.bbrc.2015.02.015 |
| Citation | O'Connell GC, et al. (2015) Interleukin-15 directly stimulates pro-oxidative gene expression in skeletal muscle in-vitro via a mechanism that requires interleukin-15 receptor alpha. Biochem Biophys Res Commun 458(3):614-9 |
| abstractText | Interleukin-15 (IL-15) signaling is heavily regulated by a high specificity IL-15 binding protein known as interleukin-15 receptor alpha (IL-15Ralpha). In-vivo disruption of IL-15Ralpha in the constitutive IL-15Ralpha knock-out (IL-15RalphaKO) mouse results in a shift towards an oxidative muscle phenotype characterized by dramatic increases in mitochondrial density. The IL-15RalphaKO mouse displays elevated levels of IL-15 transcript in muscle tissue, along with increased circulating levels of IL-15. As a result, it has been suggested that loss of IL-15Ralpha from skeletal muscle enhances muscle IL-15 secretion, and that muscle-derived IL-15 acts in an autocrine fashion to elicit pro-oxidative effects. However, this proposed mechanism of IL-15/IL-15Ralpha action in skeletal muscle is based primarily on in-vivo associative observations, and has yet to be explored in a direct manner. Thus, our purpose was to assess the immediate influence of IL-15Ralpha on the capacity of skeletal muscle to secrete and respond to IL-15, and also to determine whether IL-15 has the ability to act directly on skeletal muscle to induce pro-oxidative changes. These aims were addressed in-vitro using primary myogenic cultures derived from IL-15RalphaKO mice and B6129 controls, as well as cultures of the C2C12 immortalized myogenic cell line. Cultures obtained from IL-15RalphaKO mice displayed a diminished capacity to secrete IL-15 in relation to B6129 controls. Acute treatment of B6129-derived cultures with recombinant IL-15 increased transcriptional expression of the pro-oxidative genes PGC1alpha and PPARdelta. IL-15 treatment failed to elicit a similar response in cultures generated from IL-15RalphaKO mice. Chronic treatment of C2C12 cultures with IL-15 during myogenic differentiation resulted in mature myocytes with greater mitochondrial density in relation to vehicle treated controls. Collectively, these results provide evidence that IL-15 has the capacity to act directly on skeletal muscle in a pro-oxidative manner, and that disruption of IL-15Ralpha ablates the ability of skeletal muscle to secrete and respond to IL-15. |
