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Alpha retinal ganglion cells in pigmented mice retina: number and distribution

Purpose: To identify and characterize numerically and topographically the population of alpha retinal ganglion cells (αRGCs) and their subtypes, the sustained-response ON-center αRGCs (ONs-αRGCs), which correspond to the type 4 intrinsically photosensitive RGCs (M4-ipRGCs), the transient-response ON...

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Autores principales: Gallego-Ortega, Alejandro, Norte-Muñoz, María, Di Pierdomenico, Johnny, Avilés-Trigueros, Marcelino, de la Villa, Pedro, Valiente-Soriano, Francisco Javier, Vidal-Sanz, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9751430/
https://www.ncbi.nlm.nih.gov/pubmed/36530520
http://dx.doi.org/10.3389/fnana.2022.1054849
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author Gallego-Ortega, Alejandro
Norte-Muñoz, María
Di Pierdomenico, Johnny
Avilés-Trigueros, Marcelino
de la Villa, Pedro
Valiente-Soriano, Francisco Javier
Vidal-Sanz, Manuel
author_facet Gallego-Ortega, Alejandro
Norte-Muñoz, María
Di Pierdomenico, Johnny
Avilés-Trigueros, Marcelino
de la Villa, Pedro
Valiente-Soriano, Francisco Javier
Vidal-Sanz, Manuel
author_sort Gallego-Ortega, Alejandro
collection PubMed
description Purpose: To identify and characterize numerically and topographically the population of alpha retinal ganglion cells (αRGCs) and their subtypes, the sustained-response ON-center αRGCs (ONs-αRGCs), which correspond to the type 4 intrinsically photosensitive RGCs (M4-ipRGCs), the transient-response ON-center αRGCs (ONt-αRGCs), the sustained-response OFF-center αRGCs (OFFs-αRGCs), and the transient-response OFF-center αRGCs (OFFt-αRGCs) in the adult pigmented mouse retina. Methods: The αRGC population and its subtypes were studied in flat-mounted retinas and radial sections immunodetected against non-phosphorylated high molecular weight neurofilament subunit (SMI-32) or osteopontin (OPN), two αRGCs pan-markers; Calbindin, expressed in ONs-αRGCs, and amacrines; T-box transcription factor T-brain 2 (Tbr2), a key transcriptional regulator for ipRGC development and maintenance, expressed in ipRGCs and GABA-displaced amacrine cells; OPN4, an anti-melanopsin antibody; or Brn3a and Brn3c, markers of RGCs. The total population of RGCs was counted automatically and αRGCs and its subtypes were counted manually, and color-coded neighborhood maps were used for their topographical representation. Results: The total mean number of αRGCs per retina is 2,252 ± 306 SMI32(+)αRGCs and 2,315 ± 175 OPN(+)αRGCs (n = 10), representing 5.08% and 5.22% of the total number of RGCs traced from the optic nerve, respectively. αRGCs are distributed throughout the retina, showing a higher density in the temporal hemiretina. ONs-αRGCs represent ≈36% [841 ± 110 cells (n = 10)] of all αRGCs and are located throughout the retina, with the highest density in the temporal region. ONt-αRGCs represent ≈34% [797 ± 146 cells (n = 10)] of all αRGCs and are mainly located in the central retinal region. OFF-αRGCs represent the remaining 32% of total αRGCs and are divided equally between OFFs-αRGCs and OFFt-αRGCs [363 ± 50 cells (n = 10) and 376 ± 36 cells (n = 10), respectively]. OFFs-αRGCs are mainly located in the supero-temporal peripheral region of the retina and OFFt-αRGCs in the mid-peripheral region of the retina, especially in the infero-temporal region. Conclusions: The combination of specific antibodies is a useful tool to identify and study αRGCs and their subtypes. αRGCs are distributed throughout the retina presenting higher density in the temporal area. The sustained ON and OFF response subtypes are mainly located in the periphery while the transient ON and OFF response subtypes are found in the central regions of the retina.
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spelling pubmed-97514302022-12-16 Alpha retinal ganglion cells in pigmented mice retina: number and distribution Gallego-Ortega, Alejandro Norte-Muñoz, María Di Pierdomenico, Johnny Avilés-Trigueros, Marcelino de la Villa, Pedro Valiente-Soriano, Francisco Javier Vidal-Sanz, Manuel Front Neuroanat Neuroscience Purpose: To identify and characterize numerically and topographically the population of alpha retinal ganglion cells (αRGCs) and their subtypes, the sustained-response ON-center αRGCs (ONs-αRGCs), which correspond to the type 4 intrinsically photosensitive RGCs (M4-ipRGCs), the transient-response ON-center αRGCs (ONt-αRGCs), the sustained-response OFF-center αRGCs (OFFs-αRGCs), and the transient-response OFF-center αRGCs (OFFt-αRGCs) in the adult pigmented mouse retina. Methods: The αRGC population and its subtypes were studied in flat-mounted retinas and radial sections immunodetected against non-phosphorylated high molecular weight neurofilament subunit (SMI-32) or osteopontin (OPN), two αRGCs pan-markers; Calbindin, expressed in ONs-αRGCs, and amacrines; T-box transcription factor T-brain 2 (Tbr2), a key transcriptional regulator for ipRGC development and maintenance, expressed in ipRGCs and GABA-displaced amacrine cells; OPN4, an anti-melanopsin antibody; or Brn3a and Brn3c, markers of RGCs. The total population of RGCs was counted automatically and αRGCs and its subtypes were counted manually, and color-coded neighborhood maps were used for their topographical representation. Results: The total mean number of αRGCs per retina is 2,252 ± 306 SMI32(+)αRGCs and 2,315 ± 175 OPN(+)αRGCs (n = 10), representing 5.08% and 5.22% of the total number of RGCs traced from the optic nerve, respectively. αRGCs are distributed throughout the retina, showing a higher density in the temporal hemiretina. ONs-αRGCs represent ≈36% [841 ± 110 cells (n = 10)] of all αRGCs and are located throughout the retina, with the highest density in the temporal region. ONt-αRGCs represent ≈34% [797 ± 146 cells (n = 10)] of all αRGCs and are mainly located in the central retinal region. OFF-αRGCs represent the remaining 32% of total αRGCs and are divided equally between OFFs-αRGCs and OFFt-αRGCs [363 ± 50 cells (n = 10) and 376 ± 36 cells (n = 10), respectively]. OFFs-αRGCs are mainly located in the supero-temporal peripheral region of the retina and OFFt-αRGCs in the mid-peripheral region of the retina, especially in the infero-temporal region. Conclusions: The combination of specific antibodies is a useful tool to identify and study αRGCs and their subtypes. αRGCs are distributed throughout the retina presenting higher density in the temporal area. The sustained ON and OFF response subtypes are mainly located in the periphery while the transient ON and OFF response subtypes are found in the central regions of the retina. Frontiers Media S.A. 2022-12-01 /pmc/articles/PMC9751430/ /pubmed/36530520 http://dx.doi.org/10.3389/fnana.2022.1054849 Text en Copyright © 2022 Gallego-Ortega, Norte-Muñoz, Di Pierdomenico, Avilés-Trigueros, de la Villa, Valiente-Soriano and Vidal-Sanz. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Gallego-Ortega, Alejandro
Norte-Muñoz, María
Di Pierdomenico, Johnny
Avilés-Trigueros, Marcelino
de la Villa, Pedro
Valiente-Soriano, Francisco Javier
Vidal-Sanz, Manuel
Alpha retinal ganglion cells in pigmented mice retina: number and distribution
title Alpha retinal ganglion cells in pigmented mice retina: number and distribution
title_full Alpha retinal ganglion cells in pigmented mice retina: number and distribution
title_fullStr Alpha retinal ganglion cells in pigmented mice retina: number and distribution
title_full_unstemmed Alpha retinal ganglion cells in pigmented mice retina: number and distribution
title_short Alpha retinal ganglion cells in pigmented mice retina: number and distribution
title_sort alpha retinal ganglion cells in pigmented mice retina: number and distribution
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9751430/
https://www.ncbi.nlm.nih.gov/pubmed/36530520
http://dx.doi.org/10.3389/fnana.2022.1054849
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