Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Lou, Bingsheng, Zeng, Lei, Gao, Xinbo, Qian, Xiaobing, Li, Jing Jing, Gu, Xinyu, Liu, Zheng, Liu, Keli, Chen, Xun, Lin, Xiaofeng, Zhang, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
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
_version_ 1784797931682922496
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
work_keys_str_mv AT loubingsheng asinglecelltranscriptomicatlasofthehumanciliarybody
AT zenglei asinglecelltranscriptomicatlasofthehumanciliarybody
AT gaoxinbo asinglecelltranscriptomicatlasofthehumanciliarybody
AT qianxiaobing asinglecelltranscriptomicatlasofthehumanciliarybody
AT lijingjing asinglecelltranscriptomicatlasofthehumanciliarybody
AT guxinyu asinglecelltranscriptomicatlasofthehumanciliarybody
AT liuzheng asinglecelltranscriptomicatlasofthehumanciliarybody
AT liukeli asinglecelltranscriptomicatlasofthehumanciliarybody
AT chenxun asinglecelltranscriptomicatlasofthehumanciliarybody
AT linxiaofeng asinglecelltranscriptomicatlasofthehumanciliarybody
AT zhangfeng asinglecelltranscriptomicatlasofthehumanciliarybody
AT loubingsheng singlecelltranscriptomicatlasofthehumanciliarybody
AT zenglei singlecelltranscriptomicatlasofthehumanciliarybody
AT gaoxinbo singlecelltranscriptomicatlasofthehumanciliarybody
AT qianxiaobing singlecelltranscriptomicatlasofthehumanciliarybody
AT lijingjing singlecelltranscriptomicatlasofthehumanciliarybody
AT guxinyu singlecelltranscriptomicatlasofthehumanciliarybody
AT liuzheng singlecelltranscriptomicatlasofthehumanciliarybody
AT liukeli singlecelltranscriptomicatlasofthehumanciliarybody
AT chenxun singlecelltranscriptomicatlasofthehumanciliarybody
AT linxiaofeng singlecelltranscriptomicatlasofthehumanciliarybody
AT zhangfeng singlecelltranscriptomicatlasofthehumanciliarybody