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A single-cell transcriptomic atlas of the human ciliary body
The ciliary body critically contributes to the ocular physiology with multiple responsibilities in the production of aqueous humor, vision accommodation and intraocular immunity. Comparatively little work, however, has revealed the single-cell molecular taxonomy of the human ciliary body required fo...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9512889/ https://www.ncbi.nlm.nih.gov/pubmed/36163311 http://dx.doi.org/10.1007/s00018-022-04559-w |
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author | Lou, Bingsheng Zeng, Lei Gao, Xinbo Qian, Xiaobing Li, Jing Jing Gu, Xinyu Liu, Zheng Liu, Keli Chen, Xun Lin, Xiaofeng Zhang, Feng |
author_facet | Lou, Bingsheng Zeng, Lei Gao, Xinbo Qian, Xiaobing Li, Jing Jing Gu, Xinyu Liu, Zheng Liu, Keli Chen, Xun Lin, Xiaofeng Zhang, Feng |
author_sort | Lou, Bingsheng |
collection | PubMed |
description | The ciliary body critically contributes to the ocular physiology with multiple responsibilities in the production of aqueous humor, vision accommodation and intraocular immunity. Comparatively little work, however, has revealed the single-cell molecular taxonomy of the human ciliary body required for studying these functionalities. In this study, we report a comprehensive atlas of the cellular and molecular components of human ciliary body as well as their interactions using single-cell RNA sequencing (scRNAseq). Cluster analysis of the transcriptome of 14,563 individual ciliary cells from the eyes of 3 human donors identified 14 distinct cell types, including the ciliary epithelium, smooth muscle, vascular endothelial cell, immune cell and other stromal cell populations. Cell-type discriminative gene markers were also revealed. Unique gene expression patterns essential for ciliary epithelium-mediated aqueous humor inflow and ciliary smooth muscle contractility were identified. Importantly, we discovered the transitional states that probably contribute to the transition of ciliary macrophage into retina microglia and verified no lymphatics in the ciliary body. Moreover, the utilization of CellPhoneDB allowed us to systemically infer cell–cell interactions among diverse ciliary cells including those that potentially participate in the pathogenesis of glaucoma and uveitis. Altogether, these new findings provide insights into the regulation of intraocular pressure, accommodation reflex and immune homeostasis under physiological and pathological conditions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00018-022-04559-w. |
format | Online Article Text |
id | pubmed-9512889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-95128892022-09-28 A single-cell transcriptomic atlas of the human ciliary body Lou, Bingsheng Zeng, Lei Gao, Xinbo Qian, Xiaobing Li, Jing Jing Gu, Xinyu Liu, Zheng Liu, Keli Chen, Xun Lin, Xiaofeng Zhang, Feng Cell Mol Life Sci Original Article The ciliary body critically contributes to the ocular physiology with multiple responsibilities in the production of aqueous humor, vision accommodation and intraocular immunity. Comparatively little work, however, has revealed the single-cell molecular taxonomy of the human ciliary body required for studying these functionalities. In this study, we report a comprehensive atlas of the cellular and molecular components of human ciliary body as well as their interactions using single-cell RNA sequencing (scRNAseq). Cluster analysis of the transcriptome of 14,563 individual ciliary cells from the eyes of 3 human donors identified 14 distinct cell types, including the ciliary epithelium, smooth muscle, vascular endothelial cell, immune cell and other stromal cell populations. Cell-type discriminative gene markers were also revealed. Unique gene expression patterns essential for ciliary epithelium-mediated aqueous humor inflow and ciliary smooth muscle contractility were identified. Importantly, we discovered the transitional states that probably contribute to the transition of ciliary macrophage into retina microglia and verified no lymphatics in the ciliary body. Moreover, the utilization of CellPhoneDB allowed us to systemically infer cell–cell interactions among diverse ciliary cells including those that potentially participate in the pathogenesis of glaucoma and uveitis. Altogether, these new findings provide insights into the regulation of intraocular pressure, accommodation reflex and immune homeostasis under physiological and pathological conditions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00018-022-04559-w. Springer International Publishing 2022-09-26 2022 /pmc/articles/PMC9512889/ /pubmed/36163311 http://dx.doi.org/10.1007/s00018-022-04559-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Lou, Bingsheng Zeng, Lei Gao, Xinbo Qian, Xiaobing Li, Jing Jing Gu, Xinyu Liu, Zheng Liu, Keli Chen, Xun Lin, Xiaofeng Zhang, Feng A single-cell transcriptomic atlas of the human ciliary body |
title | A single-cell transcriptomic atlas of the human ciliary body |
title_full | A single-cell transcriptomic atlas of the human ciliary body |
title_fullStr | A single-cell transcriptomic atlas of the human ciliary body |
title_full_unstemmed | A single-cell transcriptomic atlas of the human ciliary body |
title_short | A single-cell transcriptomic atlas of the human ciliary body |
title_sort | single-cell transcriptomic atlas of the human ciliary body |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9512889/ https://www.ncbi.nlm.nih.gov/pubmed/36163311 http://dx.doi.org/10.1007/s00018-022-04559-w |
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