IKKβ/NF-κB Activation Causes Severe Muscle Wasting in Mice

• Published in: Cell 2004-10, Vol.119 (2), p.285-298
• Main Authors: Cai, Dongsheng, Frantz, J.Daniel, Tawa, Nicholas E., Melendez, Peter A., Oh, Byung-Chul, Lidov, Hart G.W., Hasselgren, Per-Olof, Frontera, Walter R., Lee, Jongsoon, Glass, David J., Shoelson, Steven E.
• Format: Article
• Language: English
• ISSN: 0092-8674; 1097-4172
• DOI: 10.1016/j.cell.2004.09.027

Muscle wasting accompanies aging and pathological conditions ranging from cancer, cachexia, and diabetes to denervation and immobilization. We show that activation of NF-κB, through muscle-specific transgenic expression of activated IκB kinase β (MIKK), causes profound muscle wasting that resembles clinical cachexia. In contrast, no overt phenotype was seen upon muscle-specific inhibition of NF-κB through expression of IκBα superrepressor (MISR). Muscle loss was due to accelerated protein breakdown through ubiquitin-dependent proteolysis. Expression of the E3 ligase MuRF1, a mediator of muscle atrophy, was increased in MIKK mice. Pharmacological or genetic inhibition of the IKKβ/NF-κB/MuRF1 pathway reversed muscle atrophy. Denervation- and tumor-induced muscle loss were substantially reduced and survival rates improved by NF-κB inhibition in MISR mice, consistent with a critical role for NF-κB in the pathology of muscle wasting and establishing it as an important clinical target for the treatment of muscle atrophy.