Title of article :
NOX in liver fibrosis
Author/Authors :
De Minicis، نويسنده , , Samuele and Brenner، نويسنده , , David A.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2007
Pages :
7
From page :
266
To page :
272
Abstract :
NADPH oxidase is a multi-protein complex producing reactive oxygen species (ROS) both in phagocytic cells, being essential in host defense, and in non-phagocytic cells, regulating intracellular signalling. In the liver, NADPH oxidase plays a central role in fibrogenesis. A functionally active form of the NADPH oxidase is expressed not only in Kupffer cells (phagocytic cell type) but also in hepatic stellate cells (HSCs) (non-phagocytic cell type), suggesting a role of the non-phagocytic NADPH oxidase in HSC activation. Consistent with this concept, profibrogenic agonists such as Angiotensin II (Ang II) and platelet derived growth factor (PDGF), or apoptotic bodies exert their activity through NADPH oxidase-activation in HSCs. Both pharmacological inhibition with DPI and genetic studies using p47phox knockout mice provided evidence for a central role of NADPH oxidase in the regulation of HSC-activity and liver fibrosis. In addition to the p47phox component, only Rac1 has been identified as a functional active component of the NADPH oxidase complex in HSCs.
Keywords :
Apoptotic bodies , Rac1 component , p47phox component , Liver fibrosis , Hepatic Stellate Cells , NADPH oxidase (NOX) , Reactive Oxygen Species (ROS) , angiotensin II , PDGF
Journal title :
Archives of Biochemistry and Biophysics
Serial Year :
2007
Journal title :
Archives of Biochemistry and Biophysics
Record number :
1628635
Link To Document :
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