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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.
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页码:2334 / 2344
页数:11
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