dSarm/Sarm1 Is Required for Activation of an Injury-Induced Axon Death Pathway
dSarm/Sarm1 Is Required for Activation of an Injury-Induced Axon Death Pathway
Sarm-Assisted Suicide Neurodegenerative disease or nerve lesions cause axons and synapses to disintegrate through a process known as Wallerian degeneration, which may involve an active “axon death program.” Osterloh et al. (p. 481 , published online 7 June; see the Perspective by Yu and Luo ) identify loss-of-function mutations in Drosophila dSarm that are capable of blocking the degeneration of severed axons for the fly life span. Deletion of mouse Sarm1 provides similar protection to severed axons for weeks after injury, which suggests that Sarm is part of an ancient axonal death signaling cascade.
- Queen's Medical Centre United Kingdom
- University of Massachusetts Medical School United States
- Miami University United States
- Cornell University United States
- Nottingham University Hospitals NHS Trust United Kingdom
570, Cell Survival, 610, Apoptosis, Superior Cervical Ganglion, Animals, Genetically Modified, Tissue Culture Techniques, Mice, Animals, Drosophila Proteins, Cells, Cultured, Armadillo Domain Proteins, Neurons, Axotomy, Denervation, Sciatic Nerve, Axons, Cytoskeletal Proteins, Mutation, Drosophila, Wallerian Degeneration, Signal Transduction
570, Cell Survival, 610, Apoptosis, Superior Cervical Ganglion, Animals, Genetically Modified, Tissue Culture Techniques, Mice, Animals, Drosophila Proteins, Cells, Cultured, Armadillo Domain Proteins, Neurons, Axotomy, Denervation, Sciatic Nerve, Axons, Cytoskeletal Proteins, Mutation, Drosophila, Wallerian Degeneration, Signal Transduction
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