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A Presynaptic ENaC Channel Drives Homeostatic Plasticity

A Presynaptic ENaC Channel Drives Homeostatic Plasticity
An electrophysiology-based forward genetic screen has identified two genes, pickpocket11 (ppk11) and pickpocket16 (ppk16), as being necessary for the homeostatic modulation of presynaptic neurotransmitter release at the Drosophila neuromuscular junction (NMJ). Pickpocket genes encode Degenerin/Epithelial Sodium channel subunits (DEG/ENaC). We demonstrate that ppk11 and ppk16 are necessary in presynaptic motoneurons for both the acute induction and long-term maintenance of synaptic homeostasis. We show that ppk11 and ppk16 are cotranscribed as a single mRNA that is upregulated during homeostatic plasticity. Acute pharmacological inhibition of a PPK11- and PPK16-containing channel abolishes the expression of short- and long-term homeostatic plasticity without altering baseline presynaptic neurotransmitter release, indicating remarkable specificity for homeostatic plasticity rather than NMJ development. Finally, presynaptic calcium imaging experiments support a model in which a PPK11- and PPK16-containing DEG/ENaC channel modulates presynaptic membrane voltage and, thereby, controls calcium channel activity to homeostatically regulate neurotransmitter release.
- University of California System United States
- University of California, San Francisco United States
Central Nervous System, Patch-Clamp Techniques, 1.1 Normal biological development and functioning, Neuroscience(all), Medical Physiology, Presynaptic Terminals, Neuromuscular Junction, Genetically Modified, Nerve Tissue Proteins, Nicotinic Antagonists, Sodium Channels, Dose-Response Relationship, Amiloride, Animals, Genetically Modified, Underpinning research, Genetics, Polyamines, Psychology, Animals, Drosophila Proteins, Homeostasis, Epithelial Sodium Channels, Neurology & Neurosurgery, Neuronal Plasticity, Biomedical and Clinical Sciences, Dose-Response Relationship, Drug, Neurosciences, Excitatory Postsynaptic Potentials, Drosophila melanogaster, Neuroprotective Agents, Larva, Mutation, Biological psychology, Cognitive Sciences, Calcium, Drug
Central Nervous System, Patch-Clamp Techniques, 1.1 Normal biological development and functioning, Neuroscience(all), Medical Physiology, Presynaptic Terminals, Neuromuscular Junction, Genetically Modified, Nerve Tissue Proteins, Nicotinic Antagonists, Sodium Channels, Dose-Response Relationship, Amiloride, Animals, Genetically Modified, Underpinning research, Genetics, Polyamines, Psychology, Animals, Drosophila Proteins, Homeostasis, Epithelial Sodium Channels, Neurology & Neurosurgery, Neuronal Plasticity, Biomedical and Clinical Sciences, Dose-Response Relationship, Drug, Neurosciences, Excitatory Postsynaptic Potentials, Drosophila melanogaster, Neuroprotective Agents, Larva, Mutation, Biological psychology, Cognitive Sciences, Calcium, Drug
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