Extracellular Matrix and Liver Disease

被引:120
|
作者
Arriazu, Elena [1 ]
Ruiz de Galarreta, Marina [2 ]
Cubero, Francisco Javier [3 ]
Varela-Rey, Marta [4 ]
Pilar Perez de Obanos, Maria [5 ]
Leung, Tung Ming [6 ]
Lopategi, Aritz [7 ]
Benedicto, Aitor [1 ]
Abraham-Enachescu, Ioana [1 ]
Nieto, Natalia [1 ]
机构
[1] Mt Sinai Sch Med, Dept Med, Div Liver Dis, New York, NY 10029 USA
[2] Univ Navarra, Dept Biochem & Genet, Pamplona, Spain
[3] Rhein Westfal TH Aachen, Univ Hosp, Dept Med 3, D-52062 Aachen, Germany
[4] Ciberehd, CIC bioGUNE, Derio, Spain
[5] Digna Biotech, Pamplona, Spain
[6] Suny Downstate Med Ctr, Dept Cell Biol, Brooklyn, NY 11203 USA
[7] IDIBAPS Esther Koplowitz Ctr, Barcelona, Spain
关键词
HEPATIC STELLATE-CELLS; GROWTH-FACTOR-BETA; GENE-EXPRESSION PROFILES; NECROSIS-FACTOR-ALPHA; MESSENGER-RNA LEVELS; NF-KAPPA-B; OXIDATIVE-STRESS; KUPFFER CELLS; TNF-ALPHA; NONALCOHOLIC STEATOHEPATITIS;
D O I
10.1089/ars.2013.5697
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
Significance: The extracellular matrix (ECM) is a dynamic microenvironment that undergoes continuous remodeling, particularly during injury and wound healing. Chronic liver injury of many different etiologies such as viral hepatitis, alcohol abuse, drug-induced liver injury, obesity and insulin resistance, metabolic disorders, and autoimmune disease is characterized by excessive deposition of ECM proteins in response to persistent liver damage. Critical Issues: This review describes the main collagenous and noncollagenous components from the ECM that play a significant role in pathological matrix deposition during liver disease. We define how increased myofibroblasts (MF) from different origins are at the forefront of liver fibrosis and how liver cell-specific regulation of the complex scarring process occurs. Recent Advances: Particular attention is paid to the role of cytokines, growth factors, reactive oxygen species, and newly identified matricellular proteins in the regulation of fibrillar type I collagen, a field to which our laboratory has significantly contributed over the years. We compile data from recent literature on the potential mechanisms driving fibrosis resolution such as MF' apoptosis, senescence, and reversal to quiescence. Future Directions: We conclude with a brief description of how epigenetics, an evolving field, can regulate the behavior of MF and of how new "omics'' tools may advance our understanding of the mechanisms by which the fibrogenic response to liver injury occurs.
引用
收藏
页码:1078 / 1097
页数:20
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