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The Morphology and Intrinsic Excitability of Developing Mouse Retinal Ganglion Cells

The retinal ganglion cells (RGCs) have diverse morphology and physiology. Although some studies show that correlations between morphological properties and physiological properties exist in cat RGCs, these properties are much less distinct and their correlations are unknown in mouse RGCs. In this st...

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Autores principales: Qu, Juan, Myhr, Karen L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135603/
https://www.ncbi.nlm.nih.gov/pubmed/21765913
http://dx.doi.org/10.1371/journal.pone.0021777
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author Qu, Juan
Myhr, Karen L.
author_facet Qu, Juan
Myhr, Karen L.
author_sort Qu, Juan
collection PubMed
description The retinal ganglion cells (RGCs) have diverse morphology and physiology. Although some studies show that correlations between morphological properties and physiological properties exist in cat RGCs, these properties are much less distinct and their correlations are unknown in mouse RGCs. In this study, using three-dimensional digital neuron reconstruction, we systematically analyzed twelve morphological parameters of mouse RGCs as they developed in the first four postnatal weeks. The development of these parameters fell into three different patterns and suggested that contact from bipolar cells and eye opening might play important roles in RGC morphological development. Although there has been a general impression that the morphological parameters are not independent, such as RGCs with larger dendritic fields usually have longer but sparser dendrites, there was not systematic study and statistical analysis proving it. We used Pearson's correlation coefficients to determine the relationship among these morphological parameters and demonstrated that many morphological parameters showed high statistical correlation. In the same cells we also measured seven physiological parameters using whole-cell patch-clamp recording, focusing on intrinsic excitability. We previously reported the increase in intrinsic excitability in mouse RGCs during early postnatal development. Here we showed that strong correlations also existed among many physiological parameters that measure the intrinsic excitability. However, Pearson's correlation coefficient revealed very limited correlation across morphological and physiological parameters. In addition, principle component analysis failed to separate RGCs into clusters using combined morphological and physiological parameters. Therefore, despite strong correlations within the morphological parameters and within the physiological parameters, postnatal mouse RGCs had only limited correlation between morphology and physiology. This may be due to developmental immaturity, or to selection of parameters.
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spelling pubmed-31356032011-07-15 The Morphology and Intrinsic Excitability of Developing Mouse Retinal Ganglion Cells Qu, Juan Myhr, Karen L. PLoS One Research Article The retinal ganglion cells (RGCs) have diverse morphology and physiology. Although some studies show that correlations between morphological properties and physiological properties exist in cat RGCs, these properties are much less distinct and their correlations are unknown in mouse RGCs. In this study, using three-dimensional digital neuron reconstruction, we systematically analyzed twelve morphological parameters of mouse RGCs as they developed in the first four postnatal weeks. The development of these parameters fell into three different patterns and suggested that contact from bipolar cells and eye opening might play important roles in RGC morphological development. Although there has been a general impression that the morphological parameters are not independent, such as RGCs with larger dendritic fields usually have longer but sparser dendrites, there was not systematic study and statistical analysis proving it. We used Pearson's correlation coefficients to determine the relationship among these morphological parameters and demonstrated that many morphological parameters showed high statistical correlation. In the same cells we also measured seven physiological parameters using whole-cell patch-clamp recording, focusing on intrinsic excitability. We previously reported the increase in intrinsic excitability in mouse RGCs during early postnatal development. Here we showed that strong correlations also existed among many physiological parameters that measure the intrinsic excitability. However, Pearson's correlation coefficient revealed very limited correlation across morphological and physiological parameters. In addition, principle component analysis failed to separate RGCs into clusters using combined morphological and physiological parameters. Therefore, despite strong correlations within the morphological parameters and within the physiological parameters, postnatal mouse RGCs had only limited correlation between morphology and physiology. This may be due to developmental immaturity, or to selection of parameters. Public Library of Science 2011-07-13 /pmc/articles/PMC3135603/ /pubmed/21765913 http://dx.doi.org/10.1371/journal.pone.0021777 Text en Qu, Myhr. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Qu, Juan
Myhr, Karen L.
The Morphology and Intrinsic Excitability of Developing Mouse Retinal Ganglion Cells
title The Morphology and Intrinsic Excitability of Developing Mouse Retinal Ganglion Cells
title_full The Morphology and Intrinsic Excitability of Developing Mouse Retinal Ganglion Cells
title_fullStr The Morphology and Intrinsic Excitability of Developing Mouse Retinal Ganglion Cells
title_full_unstemmed The Morphology and Intrinsic Excitability of Developing Mouse Retinal Ganglion Cells
title_short The Morphology and Intrinsic Excitability of Developing Mouse Retinal Ganglion Cells
title_sort morphology and intrinsic excitability of developing mouse retinal ganglion cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135603/
https://www.ncbi.nlm.nih.gov/pubmed/21765913
http://dx.doi.org/10.1371/journal.pone.0021777
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