S-Nitrosylation of Drp1 Mediates β-Amyloid-Related Mitochondrial Fission and Neuronal Injury
Sanford Burnham Prebys Medical Discovery Institute
Abstract
Mitochondria continuously undergo two opposing processes, fission and fusion. The disruption of this dynamic equilibrium may herald cell injury or death and may contribute to developmental and neurodegenerative disorders. Nitric oxide functions as a signaling molecule, but in excess it mediates neuronal injury, in part via mitochondrial fission or fragmentation. However, the underlying mechanism for nitric oxide-induced pathological fission remains unclear. We found that nitric oxide produced in response to beta-amyloid protein, thought to be a key mediator of Alzheimer's disease, triggered mitochondrial fission, synaptic loss, and neuronal damage, in part via S-nitrosylation of dynamin-related protein 1…
Citation impact
- FWCI
- 36.54
- Percentile
- 100%
- References
- 23
Authors
7- DCDong‐Hyung ChoCorresponding
Sanford Burnham Prebys Medical Discovery Institute
- TNTomohiro Nakamura
Sanford Burnham Prebys Medical Discovery Institute
- JFJianguo Fang
Sanford Burnham Prebys Medical Discovery Institute
- PCPiotr Cieplak
Sanford Burnham Prebys Medical Discovery Institute
- AGAdam Godzik
Sanford Burnham Prebys Medical Discovery Institute
Topics & keywords
- Mitochondrial fission
- Neurodegeneration
- Nitric oxide
- S-Nitrosylation
- Cell biology
- Mitochondrion
- DNM1L
- Neuroscience
- Good health and well-being