ArticleThe Journal of physiology1995
The non-specific ion channel in Torpedo ocellata fused synaptic vesicles.
Article in The Journal of physiology, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed, 17 citations in OpenAlex.
- Exocytotic catecholamine release is not associated with cation flux through channels in the vesicle membrane but Na+ influx through the fusion pore.Nature cell biology · 2007Article
- Hydrogen ions control synaptic vesicle ion channel activity in Torpedo electromotor neurones.The Journal of physiology · 2004Article
- Control of neurotransmitter release by an internal gel matrix in synaptic vesicles.Proceedings of the National Academy of Sciences of the United States of America · 2003Article
- Multitude of ion channels in the regulation of transmitter release.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 1999Review
- Ion channels from synaptic vesicle membrane fragments reconstituted into lipid bilayers.Biophysical journal · 1996Article
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
1. Synaptic vesicles were isolated and fused into large structures with a diameter of more than 20 microns to characterize their ionic channels. The 'cell'-attached and inside-out configurations of the patch clamp technique were used. 2. Two types of ion channels were most frequently observed: a low conductance chloride channel and a high conductance non-specific channel. 3. The non-specific channel has a main conducting state and a substate. The main conducting state has a slope conductance of 246 +/- 15 pS (+/- S.E.M., n = 15), in the presence of different combinations of KCl and potassium glutamate. 4. From the reversal potentials of the current-voltage (I-V) relation, it was concluded that this channel conducts both Cl- and K+. 5. The non-specific channel is highly voltage dependent: under steady-state voltages it has a high open probability near 0 mV and does not inactivate; when the membrane is hyperpolarized (pipette side more positive), the open probability decreases dramatically. 6. Voltage pulses showed that upon hyperpolarization (from holding potentials between -20 and + 20 mV), the channels deactivated; when the membrane was stepped back to the holding potential, the channels reactivated rapidly. 7. In a number of experiments, when the pipette side was made more negative than the bath, the open probability also decreased. 8. Frequently, a substate with a conductance of about 44 +/- 4% (+/- S.E.M., n = 3) of the main state was detected. 9. We speculate that this non-specific ion channel may have different roles at the various stages of the life cycle of the synaptic vesicle. When the synaptic vesicle is an intracellular structure, it might help its transmitter-concentrating capacity by dissipating the polarization. After fusion with the surface membrane, it might constitute an additional conductance pathway, taking part in frequency modulation of synaptic transmission.
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