Liver sinusoidal endothelial cells as potential drivers of liver fibrosis (Review)

被引:6
|
作者
Gao, Jiaqin [1 ,2 ]
Zuo, Bin [1 ,2 ]
He, Yang [1 ]
机构
[1] Soochow Univ, Affiliated Hosp 1, Jiangsu Inst Hematol, Natl Hlth Commiss,Key Lab Thrombosis & Hemostasis, 188 Shizi St, Suzhou 215006, Jiangsu, Peoples R China
[2] Soochow Univ, Minist Educ Engn, Cyrus Tang Hematol Ctr, Collaborat Innovat Ctr Hematol,Ctr Hematol Dis, Suzhou 215123, Jiangsu, Peoples R China
关键词
liver fibrosis; liver sinusoidal endothelial cells; crosstalk; capillarization; endothelial dysfunction; HEPATIC-FIBROSIS; PORTAL-HYPERTENSION; HEDGEHOG PATHWAY; RAT-LIVER; PLATELETS; INFLAMMATION; ANGIOGENESIS; ACTIVATION; DIFFERENTIATION; DEFENESTRATION;
D O I
10.3892/mmr.2024.13164
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Liver fibrosis due to viral or metabolic chronic liver diseases is a major challenge of global health. It is a critical pre-stage condition of severe hepatopathy, characterized by excessive accumulation of extracellular matrix components and ongoing chronic inflammation. To date, early prevention of liver fibrosis remains challenging. As the most abundant non-parenchymal hepatic cell population, liver sinusoidal endothelial cells (LSECs) are stabilizers that maintain the intrahepatic environment. Notably, LSECs dysfunction appears to be implicated in the progression of liver fibrosis via numerous mechanisms. Following sustained liver injury, they lose their fenestrae (cytoplasmic pores) and change their crosstalk with other cellular interactions in the hepatic blood environment. LSEC-targeted therapy has shown promising effects on fibrosis resolution, opening up new opportunities for anti-fibrotic therapy. In light of this, the present study summarized changes in LSECs during liver fibrosis and their interactions with hepatic milieu, as well as possible therapeutic approaches that specially target LSECs.
引用
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页数:10
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