4.6 Article Proceedings Paper

NOX in liver fibrosis

期刊

ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS
卷 462, 期 2, 页码 266-272

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.abb.2007.04.016

关键词

liver fibrosis; hepatic stellate cells; NADPH oxidase (NOX); reactive oxygen species (ROS); angiotensin II; PDGF; apoptotic bodies; p47(phox) component; Rac1 component

资金

  1. NIDDK NIH HHS [R01 DK072237-05, R01 DK072237] Funding Source: Medline

向作者/读者索取更多资源

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 11 (Ang 11) 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 p47(phox) knockout mice provided evidence for a central role of NADPH oxidase in the regulation of HSC-activity and liver fibrosis. In addition to the p47(phox) component, only Racl has been identified as a functional active component of the NADPH oxidase complex in HSCs. Published by Elsevier Inc.

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