Source:http://linkedlifedata.com/resource/pubmed/id/10479687
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
18
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pubmed:dateCreated |
1999-10-4
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pubmed:abstractText |
Spatially localized Ca(2+) domains are thought to play a key role in action potential (AP)-evoked neurotransmitter release at fast synapses. We used a stage-scan confocal spot-detection method and the low-affinity Ca(2+) indicator Oregon Green 488 BAPTA-5N to study the spatiotemporal profile of presynaptic AP-induced Ca(2+) domains. Families of scanned AP-induced fluorescence transients were detected from spot locations separated by 200-300 nm, within the vicinity of Ca(2+) entry sites. Typically, the largest transient in a particular scan peaked within approximately 1 msec and decayed with rapid (tau(1) of 1.7 msec) and slow components (tau(2) of 16 msec, tau(3) of 78 msec). As the spot was incrementally displaced, transients progressively exhibited a slowing in their time-to-peak and a loss of the fast decay component. Three-dimensional graphs of fluorescence versus time and spot displacement revealed the presence of AP-induced fluorescence domains that dissipated within approximately 7 msec. The size of fluorescence domains were estimated from the full-width at half-maximum of gaussian fits to isochronal DeltaF/F plots and ranged from 0.6 to 3.0 micrometer, with a mean +/- SD of 1.6 +/- 0.6 micrometer. Model simulations of a localized Ca(2+) entry site predicted the major features of the fluorescence transients and suggested that, within approximately 1 msec of the initiation of the Ca(2+) current, both the fluorescence domain and the underlying Ca(2+) domain do not extend significantly beyond the site of entry. Consistent with this prediction, the intracellular addition of EGTA (up to 2 mM) accelerated the decay of the measured transients but did not affect the domain size.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1529-2401
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
15
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
7846-59
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:10479687-Action Potentials,
pubmed-meshheading:10479687-Analysis of Variance,
pubmed-meshheading:10479687-Animals,
pubmed-meshheading:10479687-Calcium,
pubmed-meshheading:10479687-Cells, Cultured,
pubmed-meshheading:10479687-Coculture Techniques,
pubmed-meshheading:10479687-Egtazic Acid,
pubmed-meshheading:10479687-Embryo, Nonmammalian,
pubmed-meshheading:10479687-Fluorescent Dyes,
pubmed-meshheading:10479687-Microscopy, Confocal,
pubmed-meshheading:10479687-Models, Neurological,
pubmed-meshheading:10479687-Models, Theoretical,
pubmed-meshheading:10479687-Neuromuscular Junction,
pubmed-meshheading:10479687-Neurons,
pubmed-meshheading:10479687-Patch-Clamp Techniques,
pubmed-meshheading:10479687-Presynaptic Terminals,
pubmed-meshheading:10479687-Xenopus
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pubmed:year |
1999
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pubmed:articleTitle |
Measurement of action potential-induced presynaptic calcium domains at a cultured neuromuscular junction.
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pubmed:affiliation |
Department of Physiology, University of California at Los Angeles School of Medicine, Los Angeles, California 90095, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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