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The rod signaling pathway in marsupial retinae

The retinal rod pathway, featuring dedicated rod bipolar cells (RBCs) and AII amacrine cells, has been intensely studied in placental mammals. Here, we analyzed the rod pathway in a nocturnal marsupial, the South American opossum Monodelphis domestica to elucidate whether marsupials have a similar r...

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Autores principales: Lutz, Nicolas D., Lemes, Emina, Krubitzer, Leah, Collin, Shaun P., Haverkamp, Silke, Peichl, Leo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6114508/
https://www.ncbi.nlm.nih.gov/pubmed/30157204
http://dx.doi.org/10.1371/journal.pone.0202089
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author Lutz, Nicolas D.
Lemes, Emina
Krubitzer, Leah
Collin, Shaun P.
Haverkamp, Silke
Peichl, Leo
author_facet Lutz, Nicolas D.
Lemes, Emina
Krubitzer, Leah
Collin, Shaun P.
Haverkamp, Silke
Peichl, Leo
author_sort Lutz, Nicolas D.
collection PubMed
description The retinal rod pathway, featuring dedicated rod bipolar cells (RBCs) and AII amacrine cells, has been intensely studied in placental mammals. Here, we analyzed the rod pathway in a nocturnal marsupial, the South American opossum Monodelphis domestica to elucidate whether marsupials have a similar rod pathway. The retina was dominated by rods with densities of 338,000–413,000/mm². Immunohistochemistry for the RBC-specific marker protein kinase Cα (PKCα) and the AII cell marker calretinin revealed the presence of both cell types with their typical morphology. This is the first demonstration of RBCs in a marsupial and of the integration of RBCs and AII cells in the rod signaling pathway. Electron microscopy showed invaginating synaptic contacts of the PKCα-immunoreactive bipolar cells with rods; light microscopic co-immunolabeling for the synaptic ribbon marker CtBP2 confirmed dominant rod contacts. The RBC axon terminals were mostly located in the innermost stratum S5 of the inner plexiform layer (IPL), but had additional side branches and synaptic varicosities in strata S3 and S4, with S3-S5 belonging to the presumed functional ON sublayer of the IPL, as shown by immunolabeling for the ON bipolar cell marker Gγ13. Triple-immunolabeling for PKCα, calretinin and CtBP2 demonstrated RBC synapses onto AII cells. These features conform to the pattern seen in placental mammals, indicating a basically similar rod pathway in M. domestica. The density range of RBCs was 9,900–16,600/mm(2), that of AII cells was 1,500–3,260/mm(2). The numerical convergence (density ratio) of 146–156 rods to 4.7–6.0 RBCs to 1 AII cell is within the broad range found among placental mammals. For comparison, we collected data for the Australian nocturnal dunnart Sminthopsis crassicaudata, and found it to be similar to M. domestica, with rod-contacting PKCα-immunoreactive bipolar cells that had axon terminals also stratifying in IPL strata S3-S5.
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spelling pubmed-61145082018-09-17 The rod signaling pathway in marsupial retinae Lutz, Nicolas D. Lemes, Emina Krubitzer, Leah Collin, Shaun P. Haverkamp, Silke Peichl, Leo PLoS One Research Article The retinal rod pathway, featuring dedicated rod bipolar cells (RBCs) and AII amacrine cells, has been intensely studied in placental mammals. Here, we analyzed the rod pathway in a nocturnal marsupial, the South American opossum Monodelphis domestica to elucidate whether marsupials have a similar rod pathway. The retina was dominated by rods with densities of 338,000–413,000/mm². Immunohistochemistry for the RBC-specific marker protein kinase Cα (PKCα) and the AII cell marker calretinin revealed the presence of both cell types with their typical morphology. This is the first demonstration of RBCs in a marsupial and of the integration of RBCs and AII cells in the rod signaling pathway. Electron microscopy showed invaginating synaptic contacts of the PKCα-immunoreactive bipolar cells with rods; light microscopic co-immunolabeling for the synaptic ribbon marker CtBP2 confirmed dominant rod contacts. The RBC axon terminals were mostly located in the innermost stratum S5 of the inner plexiform layer (IPL), but had additional side branches and synaptic varicosities in strata S3 and S4, with S3-S5 belonging to the presumed functional ON sublayer of the IPL, as shown by immunolabeling for the ON bipolar cell marker Gγ13. Triple-immunolabeling for PKCα, calretinin and CtBP2 demonstrated RBC synapses onto AII cells. These features conform to the pattern seen in placental mammals, indicating a basically similar rod pathway in M. domestica. The density range of RBCs was 9,900–16,600/mm(2), that of AII cells was 1,500–3,260/mm(2). The numerical convergence (density ratio) of 146–156 rods to 4.7–6.0 RBCs to 1 AII cell is within the broad range found among placental mammals. For comparison, we collected data for the Australian nocturnal dunnart Sminthopsis crassicaudata, and found it to be similar to M. domestica, with rod-contacting PKCα-immunoreactive bipolar cells that had axon terminals also stratifying in IPL strata S3-S5. Public Library of Science 2018-08-29 /pmc/articles/PMC6114508/ /pubmed/30157204 http://dx.doi.org/10.1371/journal.pone.0202089 Text en © 2018 Lutz et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Lutz, Nicolas D.
Lemes, Emina
Krubitzer, Leah
Collin, Shaun P.
Haverkamp, Silke
Peichl, Leo
The rod signaling pathway in marsupial retinae
title The rod signaling pathway in marsupial retinae
title_full The rod signaling pathway in marsupial retinae
title_fullStr The rod signaling pathway in marsupial retinae
title_full_unstemmed The rod signaling pathway in marsupial retinae
title_short The rod signaling pathway in marsupial retinae
title_sort rod signaling pathway in marsupial retinae
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6114508/
https://www.ncbi.nlm.nih.gov/pubmed/30157204
http://dx.doi.org/10.1371/journal.pone.0202089
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