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Characterization of Retinal Development in 13-Lined Ground Squirrels
PURPOSE: The cone-dominant, 13-lined ground squirrel (13-LGS) retina mimics the human central retina, but a thorough examination of retinal development in this species has not been reported. Here, the embryonic and postnatal development of the 13-LGS retina was studied to further characterize 13-LGS...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Association for Research in Vision and Ophthalmology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9695149/ https://www.ncbi.nlm.nih.gov/pubmed/36409292 http://dx.doi.org/10.1167/tvst.11.11.17 |
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author | Kandoi, Sangeetha Martinez, Cassandra Merriman, Dana K. Lamba, Deepak A. |
author_facet | Kandoi, Sangeetha Martinez, Cassandra Merriman, Dana K. Lamba, Deepak A. |
author_sort | Kandoi, Sangeetha |
collection | PubMed |
description | PURPOSE: The cone-dominant, 13-lined ground squirrel (13-LGS) retina mimics the human central retina, but a thorough examination of retinal development in this species has not been reported. Here, the embryonic and postnatal development of the 13-LGS retina was studied to further characterize 13-LGS as a practical alternative animal model for investigating cone-based vision in health and disease. METHODS: The spatiotemporal expression of key progenitor and cell type markers was examined in retinas from defined embryonic and postnatal stages using immunohistochemistry. Postnatal gene expression changes were validated by quantitative PCR. RESULTS: The 13-LGS neuroblastic layer expressed key progenitor markers (Sox2, Vsx2, Pax6, and Lhx2) at E18. Sequential cell fate determination evidenced by the first appearance of cell-type-specific marker labeling was at embryonic stage 18 (E18) with ganglion cells (Brn-3A, HuC/D) and microglia (Iba1); at E22.5 with photoreceptor progenitors (Otx2, recoverin) followed shortly by horizontal and amacrine cells (Lhx1, Oc1) at E24 to E25.5; and at postnatal stage 15 (P15) with bipolar cells (Vsx1, CaBP5) and Müller glia cells (GS, Rlbp1). Photoreceptor maturation indicated by opsin-positive outer segments and peanut agglutinin (PNA) labeling of cone sheaths was completed at the time of eye opening (P21–P24). CONCLUSIONS: The timeline and order of retinal cell development in the 13-LGS generally matches that recorded from other mammalian models but with a stark variation in the proportion of various cell types due to cone-dense photoreceptors. TRANSLATIONAL RELEVANCE: This thorough examination of an emerging translationally relevant cone-dominant specie provides a baseline for future disease modeling and stem cell approach studies of human vision. |
format | Online Article Text |
id | pubmed-9695149 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Association for Research in Vision and Ophthalmology |
record_format | MEDLINE/PubMed |
spelling | pubmed-96951492022-11-26 Characterization of Retinal Development in 13-Lined Ground Squirrels Kandoi, Sangeetha Martinez, Cassandra Merriman, Dana K. Lamba, Deepak A. Transl Vis Sci Technol Retina PURPOSE: The cone-dominant, 13-lined ground squirrel (13-LGS) retina mimics the human central retina, but a thorough examination of retinal development in this species has not been reported. Here, the embryonic and postnatal development of the 13-LGS retina was studied to further characterize 13-LGS as a practical alternative animal model for investigating cone-based vision in health and disease. METHODS: The spatiotemporal expression of key progenitor and cell type markers was examined in retinas from defined embryonic and postnatal stages using immunohistochemistry. Postnatal gene expression changes were validated by quantitative PCR. RESULTS: The 13-LGS neuroblastic layer expressed key progenitor markers (Sox2, Vsx2, Pax6, and Lhx2) at E18. Sequential cell fate determination evidenced by the first appearance of cell-type-specific marker labeling was at embryonic stage 18 (E18) with ganglion cells (Brn-3A, HuC/D) and microglia (Iba1); at E22.5 with photoreceptor progenitors (Otx2, recoverin) followed shortly by horizontal and amacrine cells (Lhx1, Oc1) at E24 to E25.5; and at postnatal stage 15 (P15) with bipolar cells (Vsx1, CaBP5) and Müller glia cells (GS, Rlbp1). Photoreceptor maturation indicated by opsin-positive outer segments and peanut agglutinin (PNA) labeling of cone sheaths was completed at the time of eye opening (P21–P24). CONCLUSIONS: The timeline and order of retinal cell development in the 13-LGS generally matches that recorded from other mammalian models but with a stark variation in the proportion of various cell types due to cone-dense photoreceptors. TRANSLATIONAL RELEVANCE: This thorough examination of an emerging translationally relevant cone-dominant specie provides a baseline for future disease modeling and stem cell approach studies of human vision. The Association for Research in Vision and Ophthalmology 2022-11-21 /pmc/articles/PMC9695149/ /pubmed/36409292 http://dx.doi.org/10.1167/tvst.11.11.17 Text en Copyright 2022 The Authors https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License. |
spellingShingle | Retina Kandoi, Sangeetha Martinez, Cassandra Merriman, Dana K. Lamba, Deepak A. Characterization of Retinal Development in 13-Lined Ground Squirrels |
title | Characterization of Retinal Development in 13-Lined Ground Squirrels |
title_full | Characterization of Retinal Development in 13-Lined Ground Squirrels |
title_fullStr | Characterization of Retinal Development in 13-Lined Ground Squirrels |
title_full_unstemmed | Characterization of Retinal Development in 13-Lined Ground Squirrels |
title_short | Characterization of Retinal Development in 13-Lined Ground Squirrels |
title_sort | characterization of retinal development in 13-lined ground squirrels |
topic | Retina |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9695149/ https://www.ncbi.nlm.nih.gov/pubmed/36409292 http://dx.doi.org/10.1167/tvst.11.11.17 |
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