A single-cell transcriptomic dataset of pluripotent stem cell-derived astrocytes via NFIB/SOX9 overexpression

Astrocytes, the predominant glial cells in the central nervous system, play essential roles in maintaining brain function. Reprogramming induced pluripotent stem cells (iPSCs) to become astrocytes through overexpression of the transcription factors, NFIB and SOX9, is a rapid and efficient approach for studying human neurological diseases and identifying therapeutic targets. However, the precise differentiation path and molecular signatures of induced astrocytes remain incompletely understood. Accordingly, we performed single-cell RNA sequencing analysis on 64,736 cells to establish a comprehensive atlas of NFIB/SOX9-directed astrocyte differentiation from human iPSCs. Our dataset provides detailed information about the path of astrocyte differentiation, highlighting the stepwise molecular changes that occur throughout the differentiation process. This dataset serves as a valuable reference for dissecting uncharacterized transcriptomic features of NFIB/SOX9-induced astrocytes and investigating lineage progression during astrocyte differentiation. Moreover, these findings pave the way for future studies on neurological diseases using the NFIB/SOX9-induced astrocyte model.

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Publication Details

Journal
Scientific Data
Published
2024-09-10
DOI
https://doi.org/10.1038/s41597-024-03823-x
Citations
3
Primary Topic
RNA regulation and disease
Type
article
Field-Weighted Citation Impact
0.70

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article

A single-cell transcriptomic dataset of pluripotent stem cell-derived astrocytes via NFIB/SOX9 overexpression

Chunyan Liao, Suming Chen, Jacque Pak Kan Ip, Yu Chen et al.
3 citations
Scientific Data
RNA regulation and disease
0.70
article

A single-cell transcriptomic dataset of pluripotent stem cell-derived astrocytes via NFIB/SOX9 overexpression

Chunyan Liao, Suming Chen, Jacque Pak Kan Ip, Yu Chen, Ye Tao, Yi Ran, Mingfeng Guan, Yao Zhu
article en
3 citations

Abstract

Astrocytes, the predominant glial cells in the central nervous system, play essential roles in maintaining brain function. Reprogramming induced pluripotent stem cells (iPSCs) to become astrocytes through overexpression of the transcription factors, NFIB and SOX9, is a rapid and efficient approach for studying human neurological diseases and identifying therapeutic targets. However, the precise differentiation path and molecular signatures of induced astrocytes remain incompletely understood. Accordingly, we performed single-cell RNA sequencing analysis on 64,736 cells to establish a comprehensive atlas of NFIB/SOX9-directed astrocyte differentiation from human iPSCs. Our dataset provides detailed information about the path of astrocyte differentiation, highlighting the stepwise molecular changes that occur throughout the differentiation process. This dataset serves as a valuable reference for dissecting uncharacterized transcriptomic features of NFIB/SOX9-induced astrocytes and investigating lineage progression during astrocyte differentiation. Moreover, these findings pave the way for future studies on neurological diseases using the NFIB/SOX9-induced astrocyte model.

Scientific DataVol. 11(1)
Chinese University of Hong Kong (HK), Chinese Academy of Sciences (CN), Hong Kong University of Science and Technology (HK), HKUST Shenzhen Research Institute (CN), Chinese University of Hong Kong, Shenzhen (CN), Shenzhen Institutes of Advanced Technology (CN), University of Chinese Academy of Sciences (CN), University of Hong Kong (HK)
National Natural Science Foundation of China, Ministry of Science and Technology of the People's Republic of China, Guangdong Science and Technology Department, Science, Technology and Innovation Commission of Shenzhen Municipality
Zero hunger
Openalex Percentile: Top 30%
RNA regulation and disease
0.70
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