正弦波
肝纤维化
纤维化
肝星状细胞
病理
门脉高压
肝纤维化
肝再生
血管
生物
医学
再生(生物学)
内科学
肝硬化
细胞生物学
作者
Lin Yuan,Z Liu,Meng‐Qi Dong,Weijie Zhou
出处
期刊:PubMed
日期:2022-12-20
卷期号:42 (12): 1907-1911
标识
DOI:10.12122/j.issn.1673-4254.2022.12.22
摘要
Although the portal vessels, liver sinusoids, and central vessels are known to contain microvessels with different structures and functions, their changes and roles in liver fibrogenesis have not been fully understood. Recent studies suggest that in mouse models of liver fibrogenesis, vascular changes can occur at a very early stage, and different liver vessels undergo different changes and play different roles, as shown by a decreased number of portal vessels, increased sinusoid capillarization and increased central vessels. The increase of portal vessels alleviates liver fibrosis, while the increase of central vessels and sinusoid capillarization aggravates liver fibrosis. A full understanding of the regulatory mechanisms of each of these vessels is vital for treatment of liver fibrosis. A combined regulation of different endothelial cell (EC) regulatory signaling pathways for vascular normalization may provide new strategies for liver fibrosis therapy. Further studies of the changes and functions of blood vessels in different liver diseases, liver development and regeneration may bring about important breakthroughs. This review summarizes the changes of 3 hepatic microvessels and their roles in liver fibrogenesis and propose the major directions of future studies in this field.
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