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ScRNA-seq of human fetal lung explants with R-SPONDIN Inhibition and human fetal lung primary tissue

ABSTRACT: scRNA-seq of human fetal lung explants with R-SPONDIN Inhibition and human fetal lung primary tissue

PROVIDER: PRJEB46033 | ENA |

REPOSITORIES: ENA

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			Action	DRS
		Other
	ERR6160190_1.fastq.gz	Fastqsanger.gz
	ERR6160190_2.fastq.gz	Fastqsanger.gz
	ERR6160191_1.fastq.gz	Fastqsanger.gz
	ERR6160191_2.fastq.gz	Fastqsanger.gz

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Project description:Fibroblast Growth Factor (FGF) signaling plays an important role in lung organogenesis. Over recent decades, FGF signaling in lung development has been extensively studied in animal models. However, little is known about the expression, localization and functional roles of FGF ligands during human fetal lung development. Therefore, we aimed to determine the expression and function of several FGF ligands and receptors in human lung development. Using in situ hybridization (ISH) and RNA-sequencing, we assessed their expression and distribution in native human fetal lung. Human fetal lung explants were treated with recombinant FGF7, FGF9 or FGF10 in air-liquid interface culture. Explants were analyzed grossly, to observe differences in branching pattern, as well as at the cellular and molecular level. ISH demonstrated that FGF7 is expressed in both the epithelium and mesenchyme; FGF9 is mainly localized in the distal epithelium, whereas FGF10 demonstrated diffuse expression throughout the parenchyma with some expression in the smooth muscle cells (SMCs). FGFR2 expression was high in both proximal and distal epithelial cells as well as the SMCs. FGFR3 was expressed mostly in the epithelial cells, with lower expression in the mesenchyme, while FGFR4 was highly expressed throughout the mesenchyme and in the distal epithelium. Using recombinant FGFs, we demonstrated that FGF7 and FGF9 had similar effects on human fetal lung as on mouse; however, FGF10 caused the human explants to expand and form cysts as opposed to inducing epithelial branching as seen in the mouse. In conjunction with decreased branching, treatment with recombinant FGF7, FGF9 and FGF10 also resulted in decreased double-positive SOX2/SOX9 progenitor cells, which are exclusively present in the distal epithelial tips in early human fetal lung. Although FGF ligand localization may be somewhat comparable between developing mouse and human lungs, their functional roles may differ substantially.

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ScRNA-seq of human fetal lung explants with R-SPONDIN Inhibition and human fetal lung primary tissue

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