JNK regulates FoxO-dependent autophagy in neurons
Ping Xu(University of Massachusetts Chan Medical School), Madhumita Das(University of Massachusetts Chan Medical School), Judith Reilly(University of Massachusetts Chan Medical School), Roger J. Davis(Howard Hughes Medical Institute)
Cited by 216Open Access
Abstract
The cJun N-terminal kinase (JNK) signal transduction pathway is implicated in the regulation of neuronal function. JNK is encoded by three genes that play partially redundant roles. Here we report the creation of mice with targeted ablation of all three Jnk genes in neurons. Compound JNK-deficient neurons are dependent on autophagy for survival. This autophagic response is caused by FoxO-induced expression of Bnip3 that displaces the autophagic effector Beclin-1 from inactive Bcl-XL complexes. These data identify JNK as a potent negative regulator of FoxO-dependent autophagy in neurons.
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