PDGF-BB is involved in HIF-1?/CXCR4/CXCR7 axis promoting capillarization of hepatic sinusoidal endothelial cells

Background: The activation of HIF-1 alpha/CXCR4 pathway in liver sinusoidal endothelial cells (LSECs) could downregulate CXCR7, leading to the capillarization of LSECs to promote hepatic fibrosis. However, the mechanism between CXCR4 and CXCR7 is still undefined. The aim is to investigate the role of PDGF-BB in the dedifferentiation of LSECs and hepatic stellate cells (HSCs) activation. Methods: The activation of HIF-1 alpha/CXCR4 pathway in two kinds of liver fibrosis models were observed. The effects of HIF-1 alpha, CXCR4, PDGF-BB on the dedifferentiation of LSECs were investigated by using the inhibitors of HIF-1 alpha, CXCR4 or PDGFR-I3 separately or transfecting with a CXCR4 knockdown lentiviral vector. In addition, the relationship between LSECs and HSCs was demonstrated by co-culture of LSECs and HSCs using the transwell chamber. Results: CXCR4 upregulation and CXCR7 downregulation were accompanied by LSECs capillari-zation and HSCs activation both in CCl4-induced and BDL-induced fibrotic liver. In vitro, down -regulation of HIF-1 alpha significantly descreased CXCR4 and CD31 expression, and enhanced the expressions of CXCR7, CD44 and LYVE1. Downregulation of CXCR4 in LSECs significantly downregulated PDGF-BB, PDGFR-I3 and CD31, and enhanced CXCR7, CD44 and LYVE1 expres-sion, while the expression of HIF-1 alpha did not change significantly. STI571, a PDGF receptor in-hibitor, could significantly downregulate PDGFR-I3 and increase the expression of CXCR7 to inhibit the dedifferentiation of LSECs. In addition, alleviateion the dedifferentiation of LSECs could decrease the expression of PDGFR-I3 of HSCs, then inhibiting the activation of HSCs. Conclusions: This study revealed that HIF-1 alpha/CXCR4/PDGF-BB/CXCR7 axis promoted the dedif-ferentiation of LSECs, consequently triggering HSCs activation and liver fibrosis.