|Title||Nitration and Glycation Turn Mature NGF into a Toxic Factor for Motor Neurons: A Role for p75 and RAGE Signaling in ALS.|
|Publication Type||Journal Article|
|Year of Publication||2018|
|Authors||Kim MJin, Vargas MR, Harlan BA, Killoy KM, Ball LE, Comte-Walters S, Gooz M, Yamamoto Y, Beckman JS, Barbeito L, Pehar M|
|Journal||Antioxid Redox Signal|
|Date Published||2018 06 20|
|Keywords||Amyotrophic Lateral Sclerosis, Animals, Cells, Cultured, Humans, Mice, Mice, Inbred C57BL, Mice, Transgenic, Motor Neurons, Nerve Growth Factor, Receptor for Advanced Glycation End Products, Receptor, Nerve Growth Factor, Signal Transduction|
INTRODUCTION: Glycating stress can occur together with oxidative stress during neurodegeneration and contribute to the pathogenic mechanism. Nerve growth factor (NGF) accumulates in several neurodegenerative diseases. Besides promoting survival, NGF can paradoxically induce cell death by signaling through the p75 neurotrophin receptor (p75). The ability of NGF to induce cell death is increased by nitration of its tyrosine residues under conditions associated with increased peroxynitrite formation.
AIMS: Here we investigated whether glycation also changes the ability of NGF to induce cell death and assessed the ability of post-translational modified NGF to signal through the receptor for advanced glycation end products (RAGEs). We also explored the potential role of RAGE-p75 interaction in the motor neuron death occurring in amyotrophic lateral sclerosis (ALS) models.
RESULTS: Glycation promoted NGF oligomerization and ultimately allowed the modified neurotrophin to signal through RAGE and p75 to induce motor neuron death at low physiological concentrations. A similar mechanism was observed for nitrated NGF. We provide evidence for the interaction of RAGE with p75 at the cell surface. Moreover, we observed that post-translational modified NGF was present in the spinal cord of an ALS mouse model. In addition, NGF signaling through RAGE and p75 was involved in astrocyte-mediated motor neuron toxicity, a pathogenic feature of ALS.
INNOVATION: Oxidative modifications occurring under stress conditions can enhance the ability of mature NGF to induce neuronal death at physiologically relevant concentrations, and RAGE is a new p75 coreceptor contributing to this pathway.
CONCLUSION: Our results indicate that NGF-RAGE/p75 signaling may be a therapeutic target in ALS. Antioxid. Redox Signal. 28, 1587-1602.
|Alternate Journal||Antioxid. Redox Signal.|
|PubMed Central ID||PMC5962334|
|Grant List||P20 GM103542 / GM / NIGMS NIH HHS / United States |
R01 NS100835 / NS / NINDS NIH HHS / United States
S10 OD010731 / OD / NIH HHS / United States