Source:http://linkedlifedata.com/resource/pubmed/id/10632586
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
2000-2-9
|
pubmed:abstractText |
The capacitance technique was used to investigate exocytosis at the ribbon synapse of depolarizing bipolar cells from the goldfish retina. When the Ca(2+) current was activated strongly, the rapidly releasable pool of vesicles (RRP) was released with a single rate-constant of approximately 300-500 sec(-1). However, when the Ca(2+) current was activated weakly by depolarization in the physiological range (-45 to -25 mV), exocytosis from the RRP occurred in two phases. After the release of 20% or more of the RRP, the rate-constant of exocytosis fell by a factor of 4-10. Thus, synaptic depression was caused by a reduced sensitivity to Ca(2+) influx, as well as simple depletion of the RRP. In the resting state, the rate of exocytosis varied with the amplitude of the Ca(2+) current raised to the power of 2. In the depressed state, the sensitivity to Ca(2+) influx was reduced approximately fourfold. The initial phase of exocytosis accelerated e-fold for every 2.1 mV depolarization over the physiological range and averaged 120 sec(-1) at -25 mV. The synapse of depolarizing bipolar cells therefore responds to a step depolarization in a manner similar to a high-pass filter. This transformation appears to be determined by the presence of rapidly releasable vesicles with differing sensitivities to Ca(2+) influx. This might occur if vesicles were docked to the plasma membrane at different distances from Ca(2+) channels. These results suggest that the ribbon synapse of depolarizing bipolar cells may be a site of adaptation in the retina.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jan
|
pubmed:issn |
1529-2401
|
pubmed:author | |
pubmed:issnType |
Electronic
|
pubmed:day |
15
|
pubmed:volume |
20
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
568-78
|
pubmed:dateRevised |
2003-11-14
|
pubmed:meshHeading |
pubmed-meshheading:10632586-Animals,
pubmed-meshheading:10632586-Calcium,
pubmed-meshheading:10632586-Calcium Channels,
pubmed-meshheading:10632586-Exocytosis,
pubmed-meshheading:10632586-Goldfish,
pubmed-meshheading:10632586-Kinetics,
pubmed-meshheading:10632586-Membrane Potentials,
pubmed-meshheading:10632586-Neurons,
pubmed-meshheading:10632586-Patch-Clamp Techniques,
pubmed-meshheading:10632586-Presynaptic Terminals,
pubmed-meshheading:10632586-Retina,
pubmed-meshheading:10632586-Synapses
|
pubmed:year |
2000
|
pubmed:articleTitle |
Synaptic depression and the kinetics of exocytosis in retinal bipolar cells.
|
pubmed:affiliation |
Medical Research Council Laboratory of Molecular Biology, Cambridge CB2 2QH, United Kingdom.
|
pubmed:publicationType |
Journal Article
|