Overexpression of Interleukin-15 exhibits improved glucose tolerance and promotes GLUT4 translocation via AMP-Activated protein kinase pathway in skeletal muscle

• Published in: Biochemical and biophysical research communications 2019-02, Vol.509 (4), p.994-1000
• Main Authors: Fujimoto, Taku, Sugimoto, Ken, Takahashi, Toshimasa, Yasunobe, Yukiko, Xie, Keyu, Tanaka, Minoru, Ohnishi, Yuri, Yoshida, Shino, Kurinami, Hitomi, Akasaka, Hiroshi, Takami, Yoichi, Takeya, Yasushi, Yamamoto, Koichi, Rakugi, Hiromi
• Format: Article
• Language: English
• Subjects: AMPK; Glucose metabolism; GLUT4; Interleukin-15; Myokine
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2019.01.024

Skeletal muscle performs 80% of the glucose metabolism in the body. Improvement of insulin resistance and prevention of diabetes by habitual exercise is considered beneficial due to the improved glucose uptake in skeletal muscles. Investigation of the mechanism by which skeletal muscles regulate glucose uptake can contribute to the prevention and treatment of diabetes. Myokines are a kind of cytokine secreted from skeletal muscle, which are expected to regulate muscle metabolism. Interleukin-15 (IL-15) is one such myokine that has been reported to improve glucose metabolism in vitro, although the mechanism remains unclear. In this study, we examined the glucose metabolism of skeletal muscle-specific IL-15 transgenic mice (IL-15TG), and investigated how IL-15 affects glucose metabolism in skeletal muscles. Although High Fat Diet-fed IL-15TG did not exhibit obvious difference in intraperitoneal insulin tolerance test, they had less impaired glucose tolerance compared to wild-type C57BL/6. Phosphorylation of AMP-activated protein kinase (AMPK), Akt substrate of 160 kDa (AS160), tre-2/USP6, BUB2, and cdc16 domain family member 1 (TBC1D1), and translocation of Glucose transporter type 4 (GLUT4) were accelerated in the skeletal muscle of IL-15TG. Our study demonstrated that overexpression of IL-15 in skeletal muscle improves glucose metabolism in skeletal muscle via AMPK pathway. We report the first in-vivo study that describes the signaling pathway of IL-15 in muscle glucose metabolism, and thereby contributes to the elucidation of the regulatory mechanism of muscle glucose metabolism by myokines. •Fatty diet-fed IL-15-transgenic mice had better glucose tolerance than wild-type.•GLUT4 translocation was accelerated in the skeletal muscle of IL-15-transgenic mice.•IL-15 overexpression in skeletal muscle improved glucose metabolism via AMPK pathway.•This is the first in-vivo report of IL-15 signaling in muscle glucose metabolism.