TRAF6 is required for the GM-CSF-induced JNK, p38 and Akt activation
Yiwu Wang1, Chenchen Zhou2, Jiang Huo3
1Department of Biomedical Engineering, Chinese PLA 307 Hospital, Beijing 100071, China; Department of Infectious Diseases, Chinese PLA 532 Hospital, Anhui 242700, China.
Abstract:
JNK, p38 and Akt signalings have been shown to be activated by granulocyte-macrophage colony-stimulating factor (GM-CSF) and are pivotal for GM-CSF-mediated survival, proliferation and differentiation of macrophages and their progenitors. However, the detailed mechanism of how these signalings is activated by GM-CSF is not fully elucidated. We report here that E3 ligase TRAF6 is required for the GM-CSF-induced activation of JNK, p38 and Akt. GM-CSF triggers autoubiquitination of TRAF6 and TRAF6 knocked down results in impaired activation of JNK and p38 signaling. TRAF6 is also required for GM-CSF-induced ubiquitination and activation of Akt. These findings reveal novel roles of TRAF6 in GM-CSF signaling.
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