Cargando…

AII amacrine cells in the primate fovea contribute to photopic vision

The AII amacrine cell is known as a key interneuron in the scotopic (night-vision) pathway in the retina. Under scotopic conditions, rod signals are transmitted via rod bipolar cells to AII amacrine cells, which split the rod signal into the OFF (via glycinergic synapses) and the ON pathway (via gap...

Descripción completa

Detalles Bibliográficos
Autores principales: Strettoi, Enrica, Masri, Rania A., Grünert, Ulrike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219554/
https://www.ncbi.nlm.nih.gov/pubmed/30401922
http://dx.doi.org/10.1038/s41598-018-34621-2
_version_ 1783368677443239936
author Strettoi, Enrica
Masri, Rania A.
Grünert, Ulrike
author_facet Strettoi, Enrica
Masri, Rania A.
Grünert, Ulrike
author_sort Strettoi, Enrica
collection PubMed
description The AII amacrine cell is known as a key interneuron in the scotopic (night-vision) pathway in the retina. Under scotopic conditions, rod signals are transmitted via rod bipolar cells to AII amacrine cells, which split the rod signal into the OFF (via glycinergic synapses) and the ON pathway (via gap junctions). But the AII amacrine cell also has a “day job”: at high light levels when cones are active, AII connections with ON cone bipolar cells provide crossover inhibition to extend the response range of OFF cone bipolar cells. The question whether AII cells contribute to crossover inhibition in primate fovea (where rods and rod bipolar cells are rare or absent) has not been answered. Here, immunohistochemistry and three-dimensional reconstruction show that calretinin positive cells in the fovea of macaque monkeys and humans have AII morphology and connect to cone bipolar cells. The pattern of AII connections to cone bipolar cells is quantitatively similar to that of AII cells outside the fovea. Our results support the view that in mammalian retina AII cells first evolved to serve cone circuits, then later were co-opted to process scotopic signals subsequent to the evolution of rod bipolar cells.
format Online
Article
Text
id pubmed-6219554
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-62195542018-11-07 AII amacrine cells in the primate fovea contribute to photopic vision Strettoi, Enrica Masri, Rania A. Grünert, Ulrike Sci Rep Article The AII amacrine cell is known as a key interneuron in the scotopic (night-vision) pathway in the retina. Under scotopic conditions, rod signals are transmitted via rod bipolar cells to AII amacrine cells, which split the rod signal into the OFF (via glycinergic synapses) and the ON pathway (via gap junctions). But the AII amacrine cell also has a “day job”: at high light levels when cones are active, AII connections with ON cone bipolar cells provide crossover inhibition to extend the response range of OFF cone bipolar cells. The question whether AII cells contribute to crossover inhibition in primate fovea (where rods and rod bipolar cells are rare or absent) has not been answered. Here, immunohistochemistry and three-dimensional reconstruction show that calretinin positive cells in the fovea of macaque monkeys and humans have AII morphology and connect to cone bipolar cells. The pattern of AII connections to cone bipolar cells is quantitatively similar to that of AII cells outside the fovea. Our results support the view that in mammalian retina AII cells first evolved to serve cone circuits, then later were co-opted to process scotopic signals subsequent to the evolution of rod bipolar cells. Nature Publishing Group UK 2018-11-06 /pmc/articles/PMC6219554/ /pubmed/30401922 http://dx.doi.org/10.1038/s41598-018-34621-2 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Strettoi, Enrica
Masri, Rania A.
Grünert, Ulrike
AII amacrine cells in the primate fovea contribute to photopic vision
title AII amacrine cells in the primate fovea contribute to photopic vision
title_full AII amacrine cells in the primate fovea contribute to photopic vision
title_fullStr AII amacrine cells in the primate fovea contribute to photopic vision
title_full_unstemmed AII amacrine cells in the primate fovea contribute to photopic vision
title_short AII amacrine cells in the primate fovea contribute to photopic vision
title_sort aii amacrine cells in the primate fovea contribute to photopic vision
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219554/
https://www.ncbi.nlm.nih.gov/pubmed/30401922
http://dx.doi.org/10.1038/s41598-018-34621-2
work_keys_str_mv AT strettoienrica aiiamacrinecellsintheprimatefoveacontributetophotopicvision
AT masriraniaa aiiamacrinecellsintheprimatefoveacontributetophotopicvision
AT grunertulrike aiiamacrinecellsintheprimatefoveacontributetophotopicvision