| Project/Area Number |
13670579
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Gastroenterology
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| Research Institution | The Institute of Physical and Chemical Research |
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Principal Investigator |
KOJIMA Soichi RIKEN, Molecular Cellular Pathology Research Unit, Research Unit Leader, 分子細胞病態学研究ユニット, 研究ユニットリーダー (10202061)
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| Co-Investigator(Kenkyū-buntansha) |
OKUNO Masataka Gifu Univ Schi of Med, The 1st Dept of Int Med, Associate Professor, 医学部・第一内科, 助教授 (10204140)
SUZUKI Yasuhiro RIKEN, Mol Cell Pathol Res Unit, Contract Researcher, 分子細胞病態学研究ユニット, 協力研究員 (60332277)
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| Project Period (FY) |
2001 – 2003
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| Project Status |
Completed (Fiscal Year 2003)
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| Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2003: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 2002: ¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 2001: ¥1,200,000 (Direct Cost: ¥1,200,000)
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| Keywords | Hepatic Fibrosis / Cirrhosis / Impaired Liver Regeneration / TGF-β Activation / Plasmin / Plasma Kallikrein / Protease Inhibitor / Hepatic Stellate Cells / Cutting Edge Antibody / 肝硬変 |
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| Research Abstract |
Transforming growth factor-β(TGF-β), a potent fibrogenic and growth-suppressing cytokine, is composed of two different gene products, and secreted as latent form. It must be activated before binding to receptors and exerting its activities. Latent TGF-β is physiologically activated by specific cleavage of latency-associated peptide (LAP) portion with proteases such as plasmin (PLN) or plasma kallikrein (PLK). In the current study, using animal models, we have established that TGF-β is secreted and activated either by PLN in liver fibrosis/cirrhosis or by PLK in impaired liver regeneration, and therefore that inhibition of the activation with protease inhibitors including FOY305 (camostat mesilate) prevents the development of the diseases. We then determined different cleavage sites by PLN and PLK in LAP portion and raised antibodies in rabbits by immunizing LAP sequence peptides beginning from or ending at these cleavage sites. Purified antibody against N-terminus of PLK-cleaved site specifically recognized PLK-cleaved LAP, but not uncleaved LAP, and weakly recognized PLN-cleaved LAP in Western Blot. Liver sections from LPS-pretreated and partial hepatectomized mice were specifically immunostained with this antibody as well as anti-active TGF-β antibody. The anti-cleaved LAP antibody also weakly but significantly stained liver sections from patients with fulminant hepatitis compared to pre-immune antibody, suggesting that PLK-dependent activation reaction may occur to produce active TGF-β, which suppresses regeneration of the patient liver. In addition, we discovered a compound CXZ, which interferes with TGF-β signaling and thus exerts a synergism in suppressing the activation of hepatic stellate cells with the protease inhibitor, suggesting a promising combination therapy of CXZ and protease inhibitors against the liver diseases.
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