Angiotensin II Activates IκB Kinase Phosphorylation of RelA at Ser536 to Promote Myofibroblast Survival and Liver Fibrosis

被引:111
作者
Oakley, Fiona [1 ]
Teoh, Victoria [2 ]
Ching-A-Sue, Gemma [2 ]
Bataller, Ramon [3 ]
Colmenero, Jordi [3 ]
Jonsson, Julie R. [4 ]
Eliopoulos, Aristides G. [5 ]
Watson, Martha R. [1 ]
Manas, Derek [1 ]
Mann, Derek A. [1 ]
机构
[1] Univ Newcastle, Inst Cellular Med, Liver Res Grp, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
[2] Univ Southampton, Liver Grp, Southampton, Hants, England
[3] Hosp Clin Barcelona, Liver Unit, Inst Invest Biomed August Pi & Sunyer, Inst Clin Malalties Digest & Metab, Barcelona, Spain
[4] Univ Queensland, Princess Alexandra Hosp, Sch Med, Southern Div, Brisbane, Qld 4072, Australia
[5] Univ Crete, Sch Med, Div Basic Sci, Mol & Cellular Biol Lab, Iraklion, Greece
基金
英国医学研究理事会;
关键词
HEPATIC STELLATE CELLS; APOPTOSIS; P65; EXPRESSION; FIBROGENESIS; RESOLUTION; SYSTEM; INFLAMMATION; PROGRESSION; INHIBITION;
D O I
10.1053/j.gastro.2009.02.081
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & AimS: The transcription factor nuclear factor-kappa B (NF)-kappa B promotes survival of hepatic myofibroblasts and fibrogenesis through poorly defined mechanisms. We investigated the activities of angiotensin II and I kappa B kinase (IKK) in regulation of NF-kappa B activity and the role of these proteins in liver fibrosis in rodents and humans. Methods: Phosphorylation of the NF-kappa B subunit RelA at serine 536 (P-Ser(536)-RelA) was detected by immunoblot and immunohistochemical analyses. P-Ser(536)-RelA function was assessed using vectors that expressed mutant forms of RelA, cell-permeable blocking peptides, and assays for RelA nuclear transport and apoptosis. Levels of P-Ser(536)-RelA were compared with degree of fibrosis in liver sections from chronically injured rats and patients with hepatitis C virus-mediated fibrosis who had been treated with the AT1 antagonist losartan. Results: Constitutive P-Ser(536)-RelA is a feature of human hepatic myofibroblasts, both in vitro and in situ in diseased livers. Autocrine angiotensin II stimulated IKK-mediated phosphorylation of RelA at Ser(536), which was required for nuclear transport and transcriptional activity of NF-kappa B. Inhibition of angiotensin II, the angiotensin II receptor type 1 (AT1), or IKK blocked Ser(536) phosphorylation and stimulated myofibroblast apoptosis. Treatment of fibrotic rodent liver with the angiotensin converting enzyme (ACE) inhibitor captopril or the IKK inhibitor sulphasalazine resulted in loss of P-Ser(536)-RelA-positive myofibroblasts and fibrosis regression. In human liver samples, increased numbers of P-Ser(536)-RelA-positive cells were associated with fibrosis that regressed following exposure to losartan. Conclusions: An autocrine pathway that includes angiotensin II, IKK, and P-Ser(536)-RelA regulates myofibroblast survival and can be targeted to stimulate therapeutic regression of liver fibrosis.
引用
收藏
页码:2334 / 2344
页数:11
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