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The distribution of the preferred directions of the ON–OFF direction selective ganglion cells in the rabbit retina requires refinement after eye opening

The ON–OFF direction selective ganglion cells (DSGCs) in the mammalian retina respond differentially for an object moving in different directions. DSGCs can be further segregated into four functional subtypes, namely those responsible for the detection of motion in the superior, inferior, anterior,...

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Autores principales: Chan, Ya-Chien, Chiao, Chuan-Chin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3831909/
https://www.ncbi.nlm.nih.gov/pubmed/24303104
http://dx.doi.org/10.1002/phy2.13
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author Chan, Ya-Chien
Chiao, Chuan-Chin
author_facet Chan, Ya-Chien
Chiao, Chuan-Chin
author_sort Chan, Ya-Chien
collection PubMed
description The ON–OFF direction selective ganglion cells (DSGCs) in the mammalian retina respond differentially for an object moving in different directions. DSGCs can be further segregated into four functional subtypes, namely those responsible for the detection of motion in the superior, inferior, anterior, and posterior directions of the visual field. Although it has been known that the basic neural circuit of direction selectivity is established at around the time of eye opening, it is less known if the four DSGC subtypes can be unambiguously distinguished at this time and whether their preferred directions are aligned with four canonical axes at this developmental stage. By examining the preferred directions of DSGCs in P10-12 rabbit retinas and characterizing their distribution pattern, we have shown that the preferred directions of DSGCs at around the time of eye opening are not distinctly segregated but rather are diffusely distributed along the four canonical axes. Similar results were found in the mouse retina by reanalyzing previously published data. Furthermore, taking into account the fact that the direction tuning strength of DSGCs at P10-12 is weaker than that in adults, this was found not to be correlated with their preferred directions, which suggests that the maturations of direction selectivity and preferred direction are independent processes. In addition, we also found that the subtypes of DSGCs, which do not display tracer coupling pattern in the adult, show extensive coupling at P10-12. Taken together, the present study supports that the significant refinement after eye opening is required for the development of the four functional DSGC subtypes in the rabbit retina.
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spelling pubmed-38319092013-12-03 The distribution of the preferred directions of the ON–OFF direction selective ganglion cells in the rabbit retina requires refinement after eye opening Chan, Ya-Chien Chiao, Chuan-Chin Physiol Rep Original Research The ON–OFF direction selective ganglion cells (DSGCs) in the mammalian retina respond differentially for an object moving in different directions. DSGCs can be further segregated into four functional subtypes, namely those responsible for the detection of motion in the superior, inferior, anterior, and posterior directions of the visual field. Although it has been known that the basic neural circuit of direction selectivity is established at around the time of eye opening, it is less known if the four DSGC subtypes can be unambiguously distinguished at this time and whether their preferred directions are aligned with four canonical axes at this developmental stage. By examining the preferred directions of DSGCs in P10-12 rabbit retinas and characterizing their distribution pattern, we have shown that the preferred directions of DSGCs at around the time of eye opening are not distinctly segregated but rather are diffusely distributed along the four canonical axes. Similar results were found in the mouse retina by reanalyzing previously published data. Furthermore, taking into account the fact that the direction tuning strength of DSGCs at P10-12 is weaker than that in adults, this was found not to be correlated with their preferred directions, which suggests that the maturations of direction selectivity and preferred direction are independent processes. In addition, we also found that the subtypes of DSGCs, which do not display tracer coupling pattern in the adult, show extensive coupling at P10-12. Taken together, the present study supports that the significant refinement after eye opening is required for the development of the four functional DSGC subtypes in the rabbit retina. Blackwell Publishing Ltd 2013-07 2013-06-26 /pmc/articles/PMC3831909/ /pubmed/24303104 http://dx.doi.org/10.1002/phy2.13 Text en © 2013 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Original Research
Chan, Ya-Chien
Chiao, Chuan-Chin
The distribution of the preferred directions of the ON–OFF direction selective ganglion cells in the rabbit retina requires refinement after eye opening
title The distribution of the preferred directions of the ON–OFF direction selective ganglion cells in the rabbit retina requires refinement after eye opening
title_full The distribution of the preferred directions of the ON–OFF direction selective ganglion cells in the rabbit retina requires refinement after eye opening
title_fullStr The distribution of the preferred directions of the ON–OFF direction selective ganglion cells in the rabbit retina requires refinement after eye opening
title_full_unstemmed The distribution of the preferred directions of the ON–OFF direction selective ganglion cells in the rabbit retina requires refinement after eye opening
title_short The distribution of the preferred directions of the ON–OFF direction selective ganglion cells in the rabbit retina requires refinement after eye opening
title_sort distribution of the preferred directions of the on–off direction selective ganglion cells in the rabbit retina requires refinement after eye opening
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3831909/
https://www.ncbi.nlm.nih.gov/pubmed/24303104
http://dx.doi.org/10.1002/phy2.13
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