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Iterative transcription factor screening enables rapid generation of microglia-like cells from human iPSC - TFiMGLs are responsive to disease-relevant stimuli

ABSTRACT: Iterative transcription factor screening enables rapid generation of microglia-like cells from human iPSC - TFiMGLs are responsive to disease-relevant stimuli

PROVIDER: PRJNA1214809 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR32095153_1.fastq.gz	Fastqsanger.gz
	SRR32095153_2.fastq.gz	Fastqsanger.gz
	SRR32095154_1.fastq.gz	Fastqsanger.gz
	SRR32095154_2.fastq.gz	Fastqsanger.gz
	SRR32095155_1.fastq.gz	Fastqsanger.gz

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Iterative transcription factor screening enables rapid generation of microglia-like cells from human iPSC - TFiMGLs are responsive to disease-relevant stimuli

Project description:Differentiation of induced pluripotent stem cells (iPSCs) into specialized cell types is essential for uncovering cell-type specific molecular mechanisms and interrogating cellular function. Transcription factor (TF) screens have enabled efficient production of a few cell types; however, engineering cell types that require complex TF combinations remains challenging. Here, we report an iterative, high-throughput single-cell TF screening method that enables identification of TF combinations for specialized cell differentiation, which we validated by differentiating human microglia-like cells. We found that the expression of six TFs, SPI1, CEBPA, FLI1, MEF2C, CEBPB, and IRF8, is sufficient to differentiate human iPSC into cells with transcriptional and functional similarity to primary human microglia within 4 days.

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Iterative transcription factor screening enables rapid generation of microglia-like cells from human iPSC -Single cell transcriptome timecourse analysis of TFiMGLs after SCF-MCI (SPI1, FLI1, CEBPA, CEBPB, IRF8, and Mef2C) induction.

Project description:Transcription factor (TF) screens have enabled efficient production of a few cell types; however, engineering cell types that require complex TF combinations remains challenging. Here, we report an iterative, high-throughput single-cell TF screening method that enables identification of TF combinations for specialized cell differentiation, which we validated by differentiating human microglia-like cells. We found that the expression of six TFs, SPI1, CEBPA, FLI1, MEF2C, CEBPB, and IRF8, is sufficient to differentiate human iPSC into cells with transcriptional and functional similarity to primary human microglia within 4 days.

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Bulk RNA-seq of iPSC-derived macrophages exposed to disease-relevant stimuli

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