liver fibrosis;
proteomics;
non-parenchymal cells;
protein disulfide-isomerase associated protein 3;
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摘要:
Elucidation of the mechanisms of liver fibrogenesis is important to treat liver fibrosis. In this study, we established rat models of liver fibrosis with stages from 0–1, 2, and 3–4 to 4 at 2, 4, 6, and 8 weeks, respectively, by injection of pig serum. Liver fibrogenesis was detected by Masson’s trichrome staining. Rat non-parenchymal cells (NPCs) were enriched 4-fold by Percoll density gradient centrifugation. Protein extracts from NPCs were prepared at 4 and 8 weeks, separated by two-dimensional electrophoresis, and then stained with Coomassie Blue G-250. At 4 weeks, we identified 18 non-redundant differentially expressed proteins of which protein disulfide-isomerase associated protein 3 (PDIA3) and NDUV showed consistent expression at protein and mRNA levels from 4 to 8 weeks. PDIA3 was found to be down-regulated by Western blotting in the rat model and immunohistochemically in human liver. Our results revealed important aspects of the pathogenesis/progression of liver fibrosis and demonstrated important changes in protein expression levels of NPCs at various stages of liver fibrosis.
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First Department of Internal Medicine, Jikei University School of Medicine, Nishishinbashi, Mmato-ku, Tokyo,105, JapanFirst Department of Internal Medicine, Jikei University School of Medicine, Nishishinbashi, Mmato-ku, Tokyo,105, Japan
Homma, Sadamu
Nagamori, Seishi
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First Department of Internal Medicine, Jikei University School of Medicine, Nishishinbashi, Mmato-ku, Tokyo,105, JapanFirst Department of Internal Medicine, Jikei University School of Medicine, Nishishinbashi, Mmato-ku, Tokyo,105, Japan
Nagamori, Seishi
Hasumura, Satoshi
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First Department of Internal Medicine, Jikei University School of Medicine, Nishishinbashi, Mmato-ku, Tokyo,105, JapanFirst Department of Internal Medicine, Jikei University School of Medicine, Nishishinbashi, Mmato-ku, Tokyo,105, Japan
Hasumura, Satoshi
Fujise, Kiyotaka
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First Department of Internal Medicine, Jikei University School of Medicine, Nishishinbashi, Mmato-ku, Tokyo,105, JapanFirst Department of Internal Medicine, Jikei University School of Medicine, Nishishinbashi, Mmato-ku, Tokyo,105, Japan
Fujise, Kiyotaka
Sujino, Hajime
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First Department of Internal Medicine, Jikei University School of Medicine, Nishishinbashi, Mmato-ku, Tokyo,105, JapanFirst Department of Internal Medicine, Jikei University School of Medicine, Nishishinbashi, Mmato-ku, Tokyo,105, Japan
Sujino, Hajime
Kameda, Haruo
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First Department of Internal Medicine, Jikei University School of Medicine, Nishishinbashi, Mmato-ku, Tokyo,105, JapanFirst Department of Internal Medicine, Jikei University School of Medicine, Nishishinbashi, Mmato-ku, Tokyo,105, Japan
Kameda, Haruo
Kirino, Yuji
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Division of Morphology, Bio-Medical Research Laboratories, Jikei University School of Medicine, Nishishinbashi, Mmato-ku, Tokyo,105, JapanFirst Department of Internal Medicine, Jikei University School of Medicine, Nishishinbashi, Mmato-ku, Tokyo,105, Japan
Kirino, Yuji
Hataba, Yoshiaki
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Division of Morphology, Bio-Medical Research Laboratories, Jikei University School of Medicine, Nishishinbashi, Mmato-ku, Tokyo,105, JapanFirst Department of Internal Medicine, Jikei University School of Medicine, Nishishinbashi, Mmato-ku, Tokyo,105, Japan
Hataba, Yoshiaki
Suzuki, Teruo
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Division of Morphology, Bio-Medical Research Laboratories, Jikei University School of Medicine, Nishishinbashi, Mmato-ku, Tokyo,105, JapanFirst Department of Internal Medicine, Jikei University School of Medicine, Nishishinbashi, Mmato-ku, Tokyo,105, Japan