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Mouse Retinal Phenotyping

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Cover of 'Mouse Retinal Phenotyping'

Table of Contents

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    Book Overview
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    Chapter 1 Morphological Survey from Neurons to Circuits of the Mouse Retina
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    Chapter 2 Measuring Retinal Function in the Mouse
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    Chapter 3 Modeling Retinal Diseases Using Genetic Approaches in Mice
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    Chapter 4 Cell Culture Analysis of the Phagocytosis of Photoreceptor Outer Segments by Primary Mouse RPE Cells
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    Chapter 5 Two-Photon Microscopy (TPM) and Fluorescence Lifetime Imaging Microscopy (FLIM) of Retinal Pigment Epithelium (RPE) of Mice In Vivo
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    Chapter 6 RPE Visual Cycle and Biochemical Phenotypes of Mutant Mouse Models
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    Chapter 7 Use of Direct Current Electroretinography for Analysis of Retinal Pigment Epithelium Function in Mouse Models
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    Chapter 8 Disruption of Rhodopsin Dimerization in Mouse Rod Photoreceptors by Synthetic Peptides Targeting Dimer Interface
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    Chapter 9 Experimental Approaches for Defining the Role of the Ca2+-Modulated ROS-GC System in Retinal Rods of Mouse
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    Chapter 10 Microglia Analysis in Retinal Degeneration Mouse Models
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    Chapter 11 Determination of Mitochondrial Oxygen Consumption in the Retina Ex Vivo: Applications for Retinal Disease
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    Chapter 12 Analysis of Feedback Signaling from Horizontal Cells to Photoreceptors in Mice
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    Chapter 13 Assessment of the Absolute Excitatory Level of the Retina by Flicker ERG
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    Chapter 14 Ex Vivo Functional Evaluation of Synaptic Transmission from Rods to Rod Bipolar Cells in Mice
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    Chapter 15 Functional and Morphological Analysis of OFF Bipolar Cells
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    Chapter 16 Immunohistochemical Phenotyping of Mouse Amacrine Cell Subtypes
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    Chapter 17 Phenotyping of Gap-Junctional Coupling in the Mouse Retina
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    Chapter 18 Ganglion Cell Assessment in Rodents with Retinal Degeneration
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    Chapter 19 Morphological Identification of Melanopsin-Expressing Retinal Ganglion Cell Subtypes in Mice
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    Chapter 20 Functional Assessment of Melanopsin-Driven Light Responses in the Mouse: Multielectrode Array Recordings
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    Chapter 21 In Vitro Assays for Mouse Müller Cell Phenotyping Through microRNA Profiling in the Damaged Retina
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    Chapter 22 Analysis of Retinal Vascular Plexuses and Interplexus Connections
Attention for Chapter 12: Analysis of Feedback Signaling from Horizontal Cells to Photoreceptors in Mice
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Chapter title
Analysis of Feedback Signaling from Horizontal Cells to Photoreceptors in Mice
Chapter number 12
Book title
Mouse Retinal Phenotyping
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-7720-8_12
Pubmed ID
Book ISBNs
978-1-4939-7719-2, 978-1-4939-7720-8
Authors

Arlene A. Hirano, Xue Liu, Nicholas C. Brecha, Steven Barnes

Abstract

Genetic manipulation of horizontal cells using a Connexin57-iCre mouse (Cx57-iCre) line combined with calcium imaging is proving to be a valuable method to study horizontal cell feedback inhibition onto photoreceptor terminals. While it is accepted that horizontal cells provide lateral inhibitory feedback to photoreceptors, the cellular mechanisms that underlie this feedback inhibition remain only partially elucidated. Feedback inhibition of photoreceptors acts via modulation of their voltage-gated calcium channels at their synaptic terminal. Calcium imaging of photoreceptors in retinal slices, therefore, reflects the impact of inhibitory feedback from horizontal cells. The development of a Cx57-iCre mouse line permits genetic manipulation of horizontal cells. In wild-type mouse retina, depolarization of horizontal cells by kainate provokes a decrease in photoreceptor Ca2+i, whereas hyperpolarization by NBQX elicits an increase in photoreceptor Ca2+i. These responses indicate increased feedback inhibition occurred when horizontal cells are depolarized, and decreased feedback inhibition, when hyperpolarized. This system was used to test the role of GABA release from horizontal cells in feedback inhibition by the selective elimination of VGAT/VIAAT, the inhibitory amino acid transmitter transporter that loads GABA into the synaptic vesicles of horizontal cells. Combined with calcium imaging of photoreceptors in retinal slices, the knockout of specific proteins, e.g., VGAT, provides a robust technique to test the role of GABA in feedback inhibition by horizontal cells.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 6 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 6 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 3 50%
Professor 1 17%
Student > Bachelor 1 17%
Researcher 1 17%
Readers by discipline Count As %
Neuroscience 4 67%
Agricultural and Biological Sciences 1 17%
Biochemistry, Genetics and Molecular Biology 1 17%