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They first elucidated that ISL relieved liver fibrosis by inducing HSCs ferroptosis through repressing GPX4 expression and increasing the expression of transferrin receptor (TFR) and divalent metal transporter 1 (DMT1), thus producing a large number of ROS ( in vivo and in vitro , block the sphingosine kinases/sphingosine-1-phosphate/IL-17 signaling pathway and regulate the expression of -SMA by inhibiting the phosphorylation of STAT3 at the downstream signal to finally reverse HSCs activation and hepatic fibrosis (Liu et al., 2023)

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Schopf, L

Science 348 , 636637 (2015)