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Characterization of Pro-Fibrotic Signaling Pathways in Human Hepatic Organoids

ABSTRACT: Characterization of Pro-Fibrotic Signaling Pathways in Human Hepatic Organoids

PROVIDER: PRJNA948825 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR23972326_1.fastq.gz	Fastqsanger.gz
	SRR23972326_2.fastq.gz	Fastqsanger.gz
	SRR23972327_1.fastq.gz	Fastqsanger.gz
	SRR23972327_2.fastq.gz	Fastqsanger.gz
	SRR23972328_1.fastq.gz	Fastqsanger.gz

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Characterization of Pro-Fibrotic Signaling Pathways in Human Hepatic Organoids

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Project description:O-GlcNAcylation controls pro-fibrotic transcriptional regulatory signaling in hepatic stellate cells (HSCs)

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O-GlcNAcylation controls pro-fibrotic transcriptional regulatory signaling in hepatic stellate cells

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Project description:Activation of quiescent hepatic stellate cells (HSCs) into proliferative myofibroblasts drives extracellular cellular matrix (ECM) accumulation and liver fibrosis; nevertheless, transcriptional network that promotes such the process remains elusive. ZNF469, a putative C2H2 zinc finger protein, is found to be upregulated upon HSC activation; however, the molecular function of ZNF469 is completely unknown. Here, we show that knockdown of ZNF469 in primary human HSCs impaired proliferation, migration, and collagen production. Conversely, overexpression of ZNF469 in HSCs yielded the opposite results. TGFb promoted expression of ZNF469 in a Smad3-dependent manner where the binding of Smad3 was confirmed at the ZNF469 promoter. RNA-seq data of ZNF469-knockdown HSCs revealed the ECM-receptor interaction as the top affected pathway, and significant downregulation of various collagen and proteoglycan genes was observed. To explore the function of ZNF469, we cloned a full-length open reading frae (ORF) of ZNF469 with an epitope tag and identified a nuclear localization of the protein. ChIP assays revealed the presence of ZNF469 at the promoter of ECM genes, supporting its function as a transcription factor. Analysis of human fibrotic and cirrhotic tissues showed increased expression of ZNF469 and a positive correlation between expression levels of ZNF469 and ECM genes. Moreover, this observation was similar in other fibrotic organs, including heart, lung, and skin. Together, this study is the first to reveal the roles of ZNF469 as a pro-fibrotic factor in HSCs and suggests ZNF469 as a novel target for antifibrotic therapy.

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