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DOI 10.1016/j.gendis.2025.101610

Медицинская библиотека · Genes & diseases · 2025

Integrated analysis of single-cell RNA-seq and ATAC-seq in lens epithelial cells: Unveiling the role of ATF6 as a key transcription factor.

Lu Huiping, Liu Xianyang, Zhou Qian, Li Ruonan, Zuo Hangjia, Hu Ke, Tian Meng, Wang Hong, Li Jianqiao, Li Na, Hou Shengping

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Аннотация

Lens epithelium, a fundamental biological structure pivotal for maintaining normal vision, can be disrupted, leading to the development of cataracts. The epithelial-mesenchymal transition has been proven to be the key factor of secondary cataract progression. However, the underlying mechanism of epithelial-mesenchymal transition in lens epithelial cells remains unclear. In this study, we conducted a comprehensive analysis and classification annotation of single-cell transcriptomic sequencing (scRNA-seq) data. This data was derived from fetal eye tissues of ages ranging from 9 to 23 weeks, sourced from our previously published research. Trajectory analysis showed a differentiation trend from epithelial cell to fiber cell. Furthermore, an integrative analysis of accessible-chromatin sequencing (scATAC-seq) and single-cell RNA sequencing (scRNA-seq) data revealed that the transcription factor ATF6 may play a pivotal role in maintaining the homeostasis of lens epithelial cells. Subsequent in vitro experiments revealed that inhibition of ATF6 could alleviate epithelial-mesenchymal fibrosis by reducing STAT3 phosphorylation. Collectively, our study presents an atlas of lens epithelial cell development at the single-cell resolution, uncovering evidence that heightened ATF6 activity could potentially promote epithelial-mesenchymal transition in lens epithelial cells.

Для цитирования: Lu Huiping, Liu Xianyang, Zhou Qian, Li Ruonan, Zuo Hangjia, Hu Ke, Tian Meng, Wang Hong, Li Jianqiao, Li Na, Hou Shengping. Integrated analysis of single-cell RNA-seq and ATAC-seq in lens epithelial cells: Unveiling the role of ATF6 as a key transcription factor.. Genes & diseases. 2025. DOI: 10.1016/j.gendis.2025.101610.
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