Bocca Claudia, Novo Erica, Miglietta Antonella, Parola Maurizio
Unit of Experimental Medicine and Clinical Pathology, Department of Clinical and Biological Sciences, School of Medicine, University of Torino, Torino, Italy.
Cell Mol Gastroenterol Hepatol. 2015 Jul 13;1(5):477-488. doi: 10.1016/j.jcmgh.2015.06.011. eCollection 2015 Sep.
Pathologic angiogenesis appears to be intrinsically associated with the fibrogenic progression of chronic liver diseases, which eventually leads to the development of cirrhosis and related complications, including hepatocellular carcinoma. Several laboratories have suggested that this association is relevant for chronic liver disease progression, with angiogenesis proposed to sustain fibrogenesis. This minireview offers a synthesis of relevant findings and opinions that have emerged in the last few years relating liver angiogenesis to fibrogenesis. We discuss liver angiogenesis in normal and pathophysiologic conditions with a focus on the role of hypoxia and hypoxia-inducible factors and assess the evidence supporting a clear relationship between angiogenesis and fibrogenesis. A section is dedicated to the critical interactions between liver sinusoidal endothelial cells and either quiescent hepatic stellate cells or myofibroblast-like stellate cells. Finally, we introduce the unusual, dual (profibrogenic and proangiogenic) role of hepatic myofibroblasts and emerging evidence supporting a role for specific mediators like vasohibin and microparticles and microvesicles.
病理性血管生成似乎与慢性肝病的纤维化进展内在相关,而慢性肝病最终会导致肝硬化及相关并发症的发生,包括肝细胞癌。多个实验室指出,这种关联与慢性肝病的进展相关,血管生成被认为维持了纤维化过程。这篇小型综述综合了过去几年中出现的有关肝脏血管生成与纤维化关系的相关研究结果和观点。我们讨论正常和病理生理条件下的肝脏血管生成,重点关注缺氧和缺氧诱导因子的作用,并评估支持血管生成与纤维化之间明确关系的证据。有一部分专门讨论肝窦内皮细胞与静止肝星状细胞或肌成纤维细胞样星状细胞之间的关键相互作用。最后,我们介绍肝肌成纤维细胞不同寻常的双重(促纤维化和促血管生成)作用,以及支持血管抑制素和微粒及微泡等特定介质发挥作用的新证据。