High CO2 Levels Cause Skeletal Muscle Atrophy via AMP-activated Kinase (AMPK), FoxO3a Protein, and Muscle-specific Ring Finger Protein 1 (MuRF1)

作者：Jaitovich Ariel; Angulo Martin; Lecuona Emilia; Dada Laura A; Welch Lynn C; Cheng Yuan; Gusarova Galina; Ceco Ermelinda; Liu Chang; Shigemura Masahiko; Barreiro Esther; Patterson Cam; Nader Gustavo A; Sznajder Jacob I^*

来源：JOURNAL OF BIOLOGICAL CHEMISTRY, 2015, 290(14): 9183-9194.

DOI：10.1074/jbc.M114.625715

Patients with chronic obstructive pulmonary disease, acute lung injury, and critical care illness may develop hypercapnia. Many of these patients often have muscle dysfunction which increases morbidity and impairs their quality of life. Here, we investigated whether hypercapnia leads to skeletal muscle atrophy. Mice exposed to high CO2 had decreased skeletal muscle wet weight, fiber diameter, and strength. Cultured myotubes exposed to high CO2 had reduced fiber diameter, protein/DNA ratios, and anabolic capacity. High CO2 induced the expression of MuRF1 in vivo and in vitro, whereas MuRF1(-/-) mice exposed to high CO2 did not develop muscle atrophy. AMP-activated kinase AMPK), a metabolic sensor, was activated in myotubes exposed to high CO2, and loss-of-function studies showed that the AMPK alpha 2 isoform is necessary for muscle-specific ring finger protein 1 MuRF1) up-regulation and myofiber size reduction. High CO2 induced AMPK alpha 2 activation, triggering the phosphorylation and nuclear translocation of FoxO3a, and leading to an increase in MuRF1 expression and myotube atrophy. Accordingly, we provide evidence that high CO2 activates skeletal muscle atrophy via AMPK alpha 2-FoxO3a-MuRF1, which is of biological and potentially clinical significance in patients with lung diseases and hypercapnia.

• 出版日期2015-4-3
• 单位西北大学