Deciphering the heterogeneity of differentiating hPSC-derived corneal limbal stem cells through single-cell RNA sequencing

被引:0
|
作者
Vattulainen, Meri [1 ]
Smits, Jos G. A. [2 ,3 ]
Arts, Julian A. [2 ]
Cunha, Dulce Lima [2 ]
Ilmarinen, Tanja [1 ]
Skottman, Heli [1 ]
Zhou, Huiqing [2 ,3 ]
机构
[1] Tampere Univ, Fac Med & Hlth Technol, Tampere, Finland
[2] Radboud Univ Nijmegen, Radboud Inst Mol Life Sci, Fac Sci, Dept Mol Dev Biol, Nijmegen, Netherlands
[3] Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlands
来源
STEM CELL REPORTS | 2024年 / 19卷 / 07期
关键词
GENE-EXPRESSION; EPITHELIUM; PAX6;
D O I
10.1016/j.stemcr.2024.06.001
中图分类号
Q813 [细胞工程];
学科分类号
摘要
A comprehensive understanding of the human pluripotent stem cell (hPSC) differentiation process stands as a prerequisite for the development of hPSC-based therapeutics. In this study, single-cell RNA sequencing (scRNA-seq) was performed to decipher the heterogeneity during differentiation of three hPSC lines toward corneal limbal stem cells (LSCs). The scRNA-seq data revealed nine clusters encompassing the entire differentiation process, among which five followed the anticipated differentiation path of LSCs. The remaining four clusters were previously undescribed cell states that were annotated as either mesodermal-like or undifferentiated subpopulations, and their prevalence was hPSC line dependent. Distinct cluster-specific marker genes identified in this study were confirmed by immunofluorescence analysis and employed to purify hPSC-derived LSCs, which effectively minimized the variation in the line-dependent differentiation efficiency. In summary, scRNA-seq offered molecular insights into the heterogeneity of hPSC-LSC differentiation, allowing a data-driven strategy for consistent and robust generation of LSCs, essential for future advancement toward clinical translation.
引用
收藏
页码:1010 / 1023
页数:14
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