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The p75 neurotrophin receptor (p75NTR), a member of the tumor necrosis factor receptor superfamily, facilitates apoptosis during development and after injury to the CNS. The signaling cascades activated by p75NTR that result in apoptosis remain poorly understood. In this study, we show that overexpression of p75NTR in primary cortical neurons, in pheochromocytoma cell line (PC12) cells, and in glioma cells results in activation of Jun kinase (JNK), accumulation of cytochrome c within the cytosol, and activation of caspases 9, 6, and 3. To link p75NTR-dependent JNK activation to mitochondrial cytochrome c release, regulation of BH3-domain-only family members was examined. Transcription of BH3-domain-only family members was not induced by p75NTR, but p75NTR-dependent JNK activation resulted in phosphorylation and oligomerization of the BH3-domain-only family member Bad. Loss of function experiments using Bad dominant negatives or RNA interference demonstrated a requirement for Bad in p75NTR-induced apoptosis. Together, these studies provide the first data linking apoptosis induced by p75NTR to the phosphorylation of BH3-domain-only family members.


Journal article


J Neurosci

Publication Date





11373 - 11381


Animals, Apoptosis, Carrier Proteins, Caspases, Cell Line, Tumor, Cell Survival, Cells, Cultured, Cytochromes c, Humans, JNK Mitogen-Activated Protein Kinases, MAP Kinase Signaling System, Mice, Mitogen-Activated Protein Kinases, Neurons, PC12 Cells, Phosphorylation, Rats, Receptor, Nerve Growth Factor, Receptors, Nerve Growth Factor, Transfection, bcl-Associated Death Protein