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Synapse Development

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Cover of 'Synapse Development'

Table of Contents

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    Book Overview
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    Chapter 1 A Cell Culture System to Investigate the Presynaptic Control of Subsynaptic Membrane Differentiation at the Neuromuscular Junction.
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    Chapter 2 Co-culture Synaptogenic Assay: A New Look at Fluorescence Reporters and Technological Devices.
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    Chapter 3 Synaptogenic Assays Using Neurons Cultured on Micropatterned Substrates.
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    Chapter 4 Monitoring Synapses Via Trans-Synaptic GFP Complementation.
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    Chapter 5 Generation of Spinal Motor Neurons from Human Pluripotent Stem Cells.
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    Chapter 6 Biochemical Purification of Binding Partners of Synaptic Scaffold Proteins.
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    Chapter 7 In Situ Protein Binding Assay Using Fc-Fusion Proteins.
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    Chapter 8 Reconstitution of Synaptic SNAREs into Large Liposomes with Reduced Curvature Stress.
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    Chapter 9 Isolation of Synaptosomes, Synaptic Plasma Membranes, and Synaptic Junctional Complexes.
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    Chapter 10 Purification of Synaptosome Populations Using Fluorescence-Activated Synaptosome Sorting.
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    Chapter 11 Optimized Protocol for Imaging Cleared Neural Tissues Using Light Microscopy.
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    Chapter 12 Structured Illumination Microscopy for the Investigation of Synaptic Structure and Function.
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    Chapter 13 3D d STORM Imaging of Fixed Brain Tissue.
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    Chapter 14 Synapse Development
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    Chapter 15 3D Analysis of Synaptic Ultrastructure in Organotypic Hippocampal Slice Culture by High-Pressure Freezing and Electron Tomography.
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    Chapter 16 Analyzing Endosomal Docking, Fusion, Sorting, and Budding Mechanisms in Isolated Organelles.
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    Chapter 17 Concurrent Imaging of Receptor Trafficking and Calcium Dynamics by Spinning Disk Confocal Microscopy.
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    Chapter 18 Imaging Activity-Dependent Signaling Dynamics at the Neuronal Synapse Using FRET-Based Biosensors.
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    Chapter 19 Analyzing Structural Plasticity of Dendritic Spines in Organotypic Slice Culture.
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    Chapter 20 Using Fluorescent Markers to Estimate Synaptic Connectivity In Situ.
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    Chapter 21 Dual Anterograde and Retrograde Viral Tracing of Reciprocal Connectivity.
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    Chapter 22 Mapping Synaptic Inputs of Developing Neurons Using Calcium Imaging.
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    Chapter 23 Monosynaptic Tracing in Developing Circuits Using Modified Rabies Virus.
Attention for Chapter 21: Dual Anterograde and Retrograde Viral Tracing of Reciprocal Connectivity.
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Chapter title
Dual Anterograde and Retrograde Viral Tracing of Reciprocal Connectivity.
Chapter number 21
Book title
Synapse Development
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6688-2_21
Pubmed ID
Book ISBNs
978-1-4939-6686-8, 978-1-4939-6688-2
Authors

Matthias G. Haberl, Melanie Ginger, Andreas Frick Ph.D., Andreas Frick

Editors

Alexandros Poulopoulos

Abstract

Current large-scale approaches in neuroscience aim to unravel the complete connectivity map of specific neuronal circuits, or even the entire brain. This emerging research discipline has been termed connectomics. Recombinant glycoprotein-deleted rabies virus (RABV ∆G) has become an important tool for the investigation of neuronal connectivity in the brains of a variety of species. Neuronal infection with even a single RABV ∆G particle results in high-level transgene expression, revealing the fine-detailed morphology of all neuronal features-including dendritic spines, axonal processes, and boutons-on a brain-wide scale. This labeling is eminently suitable for subsequent post-hoc morphological analysis, such as semiautomated reconstruction in 3D. Here we describe the use of a recently developed anterograde RABV ∆G variant together with a retrograde RABV ∆G for the investigation of projections both to, and from, a particular brain region. In addition to the automated reconstruction of a dendritic tree, we also give as an example the volume measurements of axonal boutons following RABV ∆G-mediated fluorescent marker expression. In conclusion RABV ∆G variants expressing a combination of markers and/or tools for stimulating/monitoring neuronal activity, used together with genetic or behavioral animal models, promise important insights in the structure-function relationship of neural circuits.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 17 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 17 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 4 24%
Student > Postgraduate 3 18%
Student > Master 2 12%
Student > Ph. D. Student 2 12%
Librarian 1 6%
Other 2 12%
Unknown 3 18%
Readers by discipline Count As %
Neuroscience 6 35%
Agricultural and Biological Sciences 2 12%
Medicine and Dentistry 2 12%
Biochemistry, Genetics and Molecular Biology 1 6%
Veterinary Science and Veterinary Medicine 1 6%
Other 1 6%
Unknown 4 24%