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A single-cell transcriptome atlas of the aging human and macaque retina
The human retina is a complex neural tissue that detects light and sends visual information to the brain. However, the molecular and cellular processes that underlie aging primate retina remain unclear. Here, we provide a comprehensive transcriptomic atlas based on 119 520 single cells of the foveal...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288367/ https://www.ncbi.nlm.nih.gov/pubmed/34691611 http://dx.doi.org/10.1093/nsr/nwaa179 |
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author | Yi, Wenyang Lu, Yufeng Zhong, Suijuan Zhang, Mei Sun, Le Dong, Hao Wang, Mengdi Wei, Min Xie, Haohuan Qu, Hongqiang Peng, Rongmei Hong, Jing Yao, Ziqin Tong, Yunyun Wang, Wei Ma, Qiang Liu, Zeyuan Ma, Yuqian Li, Shouzhen Yin, Chonghai Liu, Jianwei Ma, Chao Wang, Xiaoqun Wu, Qian Xue, Tian |
author_facet | Yi, Wenyang Lu, Yufeng Zhong, Suijuan Zhang, Mei Sun, Le Dong, Hao Wang, Mengdi Wei, Min Xie, Haohuan Qu, Hongqiang Peng, Rongmei Hong, Jing Yao, Ziqin Tong, Yunyun Wang, Wei Ma, Qiang Liu, Zeyuan Ma, Yuqian Li, Shouzhen Yin, Chonghai Liu, Jianwei Ma, Chao Wang, Xiaoqun Wu, Qian Xue, Tian |
author_sort | Yi, Wenyang |
collection | PubMed |
description | The human retina is a complex neural tissue that detects light and sends visual information to the brain. However, the molecular and cellular processes that underlie aging primate retina remain unclear. Here, we provide a comprehensive transcriptomic atlas based on 119 520 single cells of the foveal and peripheral retina of humans and macaques covering different ages. The molecular features of retinal cells differed between the two species, suggesting distinct regional and species specializations of the human and macaque retinae. In addition, human retinal aging occurred in a region- and cell-type-specific manner. Aging of human retina exhibited a foveal to peripheral gradient. MYO9A(−) rods and a horizontal cell subtype were greatly reduced in aging retina, indicating their vulnerability to aging. Moreover, we generated a dataset showing the cell-type- and region-specific gene expression associated with 55 types of human retinal disease, which provides a foundation to understanding of the molecular and cellular mechanisms underlying human retinal diseases. Such datasets are valuable to understanding of the molecular characteristics of primate retina, as well as molecular regulation of aging progression and related diseases. |
format | Online Article Text |
id | pubmed-8288367 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-82883672021-10-21 A single-cell transcriptome atlas of the aging human and macaque retina Yi, Wenyang Lu, Yufeng Zhong, Suijuan Zhang, Mei Sun, Le Dong, Hao Wang, Mengdi Wei, Min Xie, Haohuan Qu, Hongqiang Peng, Rongmei Hong, Jing Yao, Ziqin Tong, Yunyun Wang, Wei Ma, Qiang Liu, Zeyuan Ma, Yuqian Li, Shouzhen Yin, Chonghai Liu, Jianwei Ma, Chao Wang, Xiaoqun Wu, Qian Xue, Tian Natl Sci Rev Molecular Biology & Genetics The human retina is a complex neural tissue that detects light and sends visual information to the brain. However, the molecular and cellular processes that underlie aging primate retina remain unclear. Here, we provide a comprehensive transcriptomic atlas based on 119 520 single cells of the foveal and peripheral retina of humans and macaques covering different ages. The molecular features of retinal cells differed between the two species, suggesting distinct regional and species specializations of the human and macaque retinae. In addition, human retinal aging occurred in a region- and cell-type-specific manner. Aging of human retina exhibited a foveal to peripheral gradient. MYO9A(−) rods and a horizontal cell subtype were greatly reduced in aging retina, indicating their vulnerability to aging. Moreover, we generated a dataset showing the cell-type- and region-specific gene expression associated with 55 types of human retinal disease, which provides a foundation to understanding of the molecular and cellular mechanisms underlying human retinal diseases. Such datasets are valuable to understanding of the molecular characteristics of primate retina, as well as molecular regulation of aging progression and related diseases. Oxford University Press 2020-08-25 /pmc/articles/PMC8288367/ /pubmed/34691611 http://dx.doi.org/10.1093/nsr/nwaa179 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of China Science Publishing & Media Ltd. https://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/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Molecular Biology & Genetics Yi, Wenyang Lu, Yufeng Zhong, Suijuan Zhang, Mei Sun, Le Dong, Hao Wang, Mengdi Wei, Min Xie, Haohuan Qu, Hongqiang Peng, Rongmei Hong, Jing Yao, Ziqin Tong, Yunyun Wang, Wei Ma, Qiang Liu, Zeyuan Ma, Yuqian Li, Shouzhen Yin, Chonghai Liu, Jianwei Ma, Chao Wang, Xiaoqun Wu, Qian Xue, Tian A single-cell transcriptome atlas of the aging human and macaque retina |
title | A single-cell transcriptome atlas of the aging human and macaque retina |
title_full | A single-cell transcriptome atlas of the aging human and macaque retina |
title_fullStr | A single-cell transcriptome atlas of the aging human and macaque retina |
title_full_unstemmed | A single-cell transcriptome atlas of the aging human and macaque retina |
title_short | A single-cell transcriptome atlas of the aging human and macaque retina |
title_sort | single-cell transcriptome atlas of the aging human and macaque retina |
topic | Molecular Biology & Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288367/ https://www.ncbi.nlm.nih.gov/pubmed/34691611 http://dx.doi.org/10.1093/nsr/nwaa179 |
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