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Optical Mapping of Release Properties in Synapses

Synapses are important functional units that determine how information flows through the brain. Understanding their biophysical properties and the molecules that underpin them is an important goal of cellular neuroscience. Thus, it is of interest to develop protocols that allow easy measurement of s...

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Detalles Bibliográficos
Autores principales: Ariel, Pablo, Ryan, Timothy A.
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2928663/
https://www.ncbi.nlm.nih.gov/pubmed/20802854
http://dx.doi.org/10.3389/fncir.2010.00018
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author Ariel, Pablo
Ryan, Timothy A.
author_facet Ariel, Pablo
Ryan, Timothy A.
author_sort Ariel, Pablo
collection PubMed
description Synapses are important functional units that determine how information flows through the brain. Understanding their biophysical properties and the molecules that underpin them is an important goal of cellular neuroscience. Thus, it is of interest to develop protocols that allow easy measurement of synaptic parameters in model systems that permit molecular manipulations. Here, we used a sensitive and high-time resolution optical approach that allowed us to characterize two functional parameters critical to presynaptic efficacy: vesicle fusion probability (Pv) and readily-releasable pool size (RRP). We implemented two different approaches to determine the RRP size that were in broad agreement: depletion of the RRP by high-frequency stimulation and saturation of the calcium sensor during single action potential stimuli. Our methods are based on reporters that provide a robust, quantitative, purely presynaptic readout and present a new avenue to study molecules that affect synaptic vesicle exocytosis.
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spelling pubmed-29286632010-08-27 Optical Mapping of Release Properties in Synapses Ariel, Pablo Ryan, Timothy A. Front Neural Circuits Neural Circuits Synapses are important functional units that determine how information flows through the brain. Understanding their biophysical properties and the molecules that underpin them is an important goal of cellular neuroscience. Thus, it is of interest to develop protocols that allow easy measurement of synaptic parameters in model systems that permit molecular manipulations. Here, we used a sensitive and high-time resolution optical approach that allowed us to characterize two functional parameters critical to presynaptic efficacy: vesicle fusion probability (Pv) and readily-releasable pool size (RRP). We implemented two different approaches to determine the RRP size that were in broad agreement: depletion of the RRP by high-frequency stimulation and saturation of the calcium sensor during single action potential stimuli. Our methods are based on reporters that provide a robust, quantitative, purely presynaptic readout and present a new avenue to study molecules that affect synaptic vesicle exocytosis. Frontiers Research Foundation 2010-08-12 /pmc/articles/PMC2928663/ /pubmed/20802854 http://dx.doi.org/10.3389/fncir.2010.00018 Text en Copyright © 2010 Ariel and Ryan. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Neural Circuits
Ariel, Pablo
Ryan, Timothy A.
Optical Mapping of Release Properties in Synapses
title Optical Mapping of Release Properties in Synapses
title_full Optical Mapping of Release Properties in Synapses
title_fullStr Optical Mapping of Release Properties in Synapses
title_full_unstemmed Optical Mapping of Release Properties in Synapses
title_short Optical Mapping of Release Properties in Synapses
title_sort optical mapping of release properties in synapses
topic Neural Circuits
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2928663/
https://www.ncbi.nlm.nih.gov/pubmed/20802854
http://dx.doi.org/10.3389/fncir.2010.00018
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