Probing Single Synapses via the Photolytic Release of Neurotransmitters

The development of two-photon microscopy has revolutionized our understanding of how synapses are formed and how they transform synaptic inputs in dendritic spines—tiny protrusions that cover the dendrites of pyramidal neurons that receive most excitatory synaptic information in the brain. These dis...

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الحاوية / القاعدة:Frontiers in Synaptic Neuroscience
المؤلفون الرئيسيون: Diana E. Mitchell, Éric Martineau, Sabrina Tazerart, Roberto Araya
التنسيق: مقال
اللغة:الإنجليزية
منشور في: Frontiers Media S.A. 2019-07-01
الموضوعات:
الوصول للمادة أونلاين:https://www.frontiersin.org/article/10.3389/fnsyn.2019.00019/full
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author Diana E. Mitchell
Diana E. Mitchell
Éric Martineau
Éric Martineau
Sabrina Tazerart
Sabrina Tazerart
Roberto Araya
Roberto Araya
author_facet Diana E. Mitchell
Diana E. Mitchell
Éric Martineau
Éric Martineau
Sabrina Tazerart
Sabrina Tazerart
Roberto Araya
Roberto Araya
author_sort Diana E. Mitchell
collection DOAJ
container_title Frontiers in Synaptic Neuroscience
description The development of two-photon microscopy has revolutionized our understanding of how synapses are formed and how they transform synaptic inputs in dendritic spines—tiny protrusions that cover the dendrites of pyramidal neurons that receive most excitatory synaptic information in the brain. These discoveries have led us to better comprehend the neuronal computations that take place at the level of dendritic spines as well as within neuronal circuits with unprecedented resolution. Here, we describe a method that uses a two-photon (2P) microscope and 2P uncaging of caged neurotransmitters for the activation of single and multiple spines in the dendrites of cortical pyramidal neurons. In addition, we propose a cost-effective description of the components necessary for the construction of a one laser source-2P microscope capable of nearly simultaneous 2P uncaging of neurotransmitters and 2P calcium imaging of the activated spines and nearby dendrites. We provide a brief overview on how the use of these techniques have helped researchers in the last 15 years unravel the function of spines in: (a) information processing; (b) storage; and (c) integration of excitatory synaptic inputs.
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spelling doaj-art-5af59d2dfd1548e49fcdf60dce2207832025-08-19T22:07:18ZengFrontiers Media S.A.Frontiers in Synaptic Neuroscience1663-35632019-07-011110.3389/fnsyn.2019.00019469301Probing Single Synapses via the Photolytic Release of NeurotransmittersDiana E. Mitchell0Diana E. Mitchell1Éric Martineau2Éric Martineau3Sabrina Tazerart4Sabrina Tazerart5Roberto Araya6Roberto Araya7Department of Neurosciences, Faculty of Medicine, University of Montreal, Montreal, QC, CanadaThe CHU Sainte-Justine Research Center, Montreal, QC, CanadaDepartment of Neurosciences, Faculty of Medicine, University of Montreal, Montreal, QC, CanadaThe CHU Sainte-Justine Research Center, Montreal, QC, CanadaDepartment of Neurosciences, Faculty of Medicine, University of Montreal, Montreal, QC, CanadaThe CHU Sainte-Justine Research Center, Montreal, QC, CanadaDepartment of Neurosciences, Faculty of Medicine, University of Montreal, Montreal, QC, CanadaThe CHU Sainte-Justine Research Center, Montreal, QC, CanadaThe development of two-photon microscopy has revolutionized our understanding of how synapses are formed and how they transform synaptic inputs in dendritic spines—tiny protrusions that cover the dendrites of pyramidal neurons that receive most excitatory synaptic information in the brain. These discoveries have led us to better comprehend the neuronal computations that take place at the level of dendritic spines as well as within neuronal circuits with unprecedented resolution. Here, we describe a method that uses a two-photon (2P) microscope and 2P uncaging of caged neurotransmitters for the activation of single and multiple spines in the dendrites of cortical pyramidal neurons. In addition, we propose a cost-effective description of the components necessary for the construction of a one laser source-2P microscope capable of nearly simultaneous 2P uncaging of neurotransmitters and 2P calcium imaging of the activated spines and nearby dendrites. We provide a brief overview on how the use of these techniques have helped researchers in the last 15 years unravel the function of spines in: (a) information processing; (b) storage; and (c) integration of excitatory synaptic inputs.https://www.frontiersin.org/article/10.3389/fnsyn.2019.00019/fulldendritic spinespyramidal neuronnon-linear microscopysynaptic transmissionneocortextwo-photon (2P) uncaging
spellingShingle Diana E. Mitchell
Diana E. Mitchell
Éric Martineau
Éric Martineau
Sabrina Tazerart
Sabrina Tazerart
Roberto Araya
Roberto Araya
Probing Single Synapses via the Photolytic Release of Neurotransmitters
dendritic spines
pyramidal neuron
non-linear microscopy
synaptic transmission
neocortex
two-photon (2P) uncaging
title Probing Single Synapses via the Photolytic Release of Neurotransmitters
title_full Probing Single Synapses via the Photolytic Release of Neurotransmitters
title_fullStr Probing Single Synapses via the Photolytic Release of Neurotransmitters
title_full_unstemmed Probing Single Synapses via the Photolytic Release of Neurotransmitters
title_short Probing Single Synapses via the Photolytic Release of Neurotransmitters
title_sort probing single synapses via the photolytic release of neurotransmitters
topic dendritic spines
pyramidal neuron
non-linear microscopy
synaptic transmission
neocortex
two-photon (2P) uncaging
url https://www.frontiersin.org/article/10.3389/fnsyn.2019.00019/full
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