Angiogenesis and liver fibrogenesis

被引:1
|
作者
di Bonzo, Lorenzo Valfre
Novo, Erica
Cannito, Stefania
Busletta, Chiara
Paternostro, Claudia
Povero, Davide
Parola, Maurizio [1 ]
机构
[1] Univ Turin, Dip Med & Oncol Sperimentale, I-10125 Turin, Italy
关键词
Liver angiogenesis; Hepatic stellate cells; Hepatic myofibroblasts; VEGF; Pro-angiogenic cytokines; ENDOTHELIAL GROWTH-FACTOR; HEPATIC STELLATE CELLS; HYPOXIA-INDUCED VEGF; RAT-LIVER; FACTOR EXPRESSION; VESSEL FORMATION; PROANGIOGENIC CYTOKINES; INHIBITOR TNP-470; MESSENGER-RNA; DNA-SYNTHESIS;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Angiogenesis is a dynamic, hypoxia-stimulated and growth factor-dependent process, eventually leading to the formation of new vessels from pre-existing blood vessels. In the last decade experimental and clinical studies have described the occurrence of hepatic angiogenesis in a number of different pathophysiological conditions, including those involving inflammatory, fibrotic and ischemic features. In particular, the literature evidence indicates that hepatic angiogenesis is strictly associated with, and may even favour fibrogenic progression of chronic inflammatory liver diseases of different aetiology. In this review, current "in vivo" and "in vitro" evidence supporting the potential pathogenetic role of angiogenesis in chronic liver diseases will be reviewed in an attempt to outline cellular and molecular mechanisms involved, with a specific emphasis on the crucial role of hypoxic conditions and hepatic stellate cells (HSCs), particularly when activated to the myofibroblast-like pro-fibrogenic phenotype.
引用
收藏
页码:1323 / 1341
页数:19
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