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Liver fibrosis: Pathophysiology, pathogenetic targets and clinical issues
被引:844
作者:
Parola, Maurizio
[1
]
Pinzani, Massimo
[2
]
机构:
[1] Univ Torino, Unit Expt Med & Clin Pathol, Dept Clin & Biol Sci, Corso Raffaello 30, I-10125 Turin, Italy
[2] Royal Free Hosp, Div Med, UCL Inst Liver & Digest Hlth, London, England
关键词:
Hepatic myofibroblasts;
Hepatic stellate cells;
Liver fibrosis;
Liver biopsy;
Transient elestography;
HEPATIC STELLATE CELLS;
TISSUE GROWTH-FACTOR;
C VIRUS CORE;
EPITHELIAL-MESENCHYMAL TRANSITION;
SINUSOIDAL ENDOTHELIAL-CELLS;
NATURAL-KILLER-CELLS;
FATTY LIVER;
NONALCOHOLIC STEATOHEPATITIS;
KUPFFER CELLS;
EXTRACELLULAR VESICLES;
D O I:
10.1016/j.mam.2018.09.002
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The progression of chronic liver diseases (CLD), irrespective of etiology, involves chronic parenchymal injury, persistent activation of inflammatory response as well as sustained activation of liver fibrogenesis and wound healing response. Liver fibrogenesis, is a dynamic, highly integrated molecular, cellular and tissue process responsible for driving the excess accumulation of extracellular matrix (ECM) components (i.e., liver fibrosis) sustained by an eterogeneous population of hepatic myofibroblasts (MFs). The process of liver fibrogenesis recognizes a number of common and etiology-independent mechanisms and events but it is also significantly influenced by the specific etiology, as also reflected by peculiar morphological patterns of liver fibrosis development. In this review we will analyze the most relevant established and/or emerging pathophysiological issues underlying CLD progression with a focus on the role of critical hepatic cell populations, mechanisms and signaling pathways involved, as they represent potential therapeutic targets, to finally analyze selected and relevant clinical issues.
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页码:37 / 55
页数:19
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