ArticleThe Journal of physiology2001
Presynaptic target of Ca2+ action on neuropeptide and acetylcholine release in Aplysia californica.
Article in The Journal of physiology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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Who cites it
12 citing papers in PubMed, 27 citations in OpenAlex.
- Neurotrophic factors and target-specific retrograde signaling interactions define the specificity of classical and neuropeptide cotransmitter release at identified Lymnaea synapses.Scientific reports · 2020Article
- Peptide Cotransmitters as Dynamic, Intrinsic Modulators of Network Activity.Frontiers in neural circuits · 2018Review
- Presynaptic inhibition selectively weakens peptidergic cotransmission in a small motor system.Journal of neurophysiology · 2009Article
- Neuropeptide signaling near and far: how localized and timed is the action of neuropeptides in brain circuits?Invertebrate neuroscience : IN · 2009Review
- Trafficking and fusion of neuropeptide Y-containing dense-core granules in astrocytes.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2008Article
- CAPS and syntaxin dock dense core vesicles to the plasma membrane in neurons.The Journal of cell biology · 2008Article
- Increased Ca2+ influx through Na+/Ca2+ exchanger during long-term facilitation at crayfish neuromuscular junctions.The Journal of physiology · 2007Article
- Calcium sensitivity of neurotransmitter release differs at phasic and tonic synapses.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2005Article
- Facilitation through buffer saturation: constraints on endogenous buffering properties.Biophysical journal · 2004Article
- Target-specific neuropeptide Y-ergic synaptic inhibition and its network consequences within the mammalian thalamus.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2003Article
- Nerve growth factor-induced differentiation changes the cellular organization of regulated Peptide release by PC12 cells.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2002Article
- Photolysis-induced suppression of inhibition in rat hippocampal CA1 pyramidal neurons.The Journal of physiology · 2001Article
Corrections and comments
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Authors and funding
5 authors at 3 institutions in 2 countries.
Funding
Abstract
1. When buccal neuron B2 of Aplysia californica is co-cultured with sensory neurons (SNs), slow peptidergic synapses are formed. When B2 is co-cultured with neurons B3 or B6, fast cholinergic synapses are formed. 2. Patch pipettes were used to voltage clamp pre- and postsynaptic neurons and to load the caged Ca2+ chelator o-nitrophenyl EGTA (NPE) and the Ca2+ indicator BTC into presynaptic neurons. The relationships between presynaptic [Ca2+]i and postsynaptic responses were compared between peptidergic and cholinergic synapses formed by cell B2. 3. Using variable intensity flashes, Ca2+ stoichiometries of peptide and acetylcholine (ACh) release were approximately 2 and 3, respectively. The difference did not reach statistical significance. 4. ACh quanta summate linearly postsynaptically. We also found a linear dose-response curve for peptide action, indicating a linear relationship between submaximal peptide concentration and response of the SN. 5. The minimum intracellular calcium concentrations ([Ca2+]i) for triggering peptidergic and cholinergic transmission were estimated to be about 5 and 10 microM, respectively. 6. By comparing normal postsynaptic responses to those evoked by photolysis of NPE, we estimate [Ca2+]i at the release trigger site elicited by a single action potential (AP) to be at least 10 microM for peptidergic synapses and probably higher for cholinergic synapses. 7. Cholinergic release is brief (half-width approximately 200 ms), even in response to a prolonged rise in [Ca2+]i, while some peptidergic release appears to persist for as long as [Ca2+]i remains elevated (for up to 10 s). This may reflect differences in sizes of reserve pools, or in replenishment rates of immediately releasable pools of vesicles. 8. Electron microscopy revealed that most synaptic contacts had at least one morphologically docked dense core vesicle that presumably contained peptide; these were often located within conventional active zones. 9. Both cholinergic and peptidergic vesicles are docked within active zones, but cholinergic vesicles may be located closer to Ca2+ channels than are peptidergic vesicles.
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