Exogenously Administered HGF Activator Augments Liver Regeneration through the Production of Biologically Active HGF

Hepatocyte growth factor (HGF) plays a crucial role in the recovery of injured liver. Liver functions are mostly impaired in patients with liver diseases including cirrhosis. However, a significant amount of inactive HGF precursor (proHGF) is reported in the plasma of these patients. proHGF is prote...

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Veröffentlicht in:Biochemical and biophysical research communications 2002-01, Vol.290 (1), p.475-481
Hauptverfasser: Kaibori, Masaki, Inoue, Tomohisa, Oda, Michio, Naka, Daiji, Kawaguchi, Toshiya, Kitamura, Naomi, Miyazawa, Keiji, Kwon, A-Hon, Kamiyama, Yasuo, Okumura, Tadayoshi
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container_title Biochemical and biophysical research communications
container_volume 290
creator Kaibori, Masaki
Inoue, Tomohisa
Oda, Michio
Naka, Daiji
Kawaguchi, Toshiya
Kitamura, Naomi
Miyazawa, Keiji
Kwon, A-Hon
Kamiyama, Yasuo
Okumura, Tadayoshi
description Hepatocyte growth factor (HGF) plays a crucial role in the recovery of injured liver. Liver functions are mostly impaired in patients with liver diseases including cirrhosis. However, a significant amount of inactive HGF precursor (proHGF) is reported in the plasma of these patients. proHGF is proteolytically converted to an active form (mature HGF) by HGF-activator. Thus conversion of proHGF into mature HGF presumably contributes to the recovery of liver functions. In this study, rats with a partial hepatectomy were used, as proHGF is accumulated in the remnant liver. Recombinant human HGF-activator was administered via the portal vein to investigate the effect on molecular forms of HGF and its biological signaling. rhHGF-activator promptly converted proHGF into mature HGF, reaching maximal levels at 5–10 min after the injection, while the decreased proHGF was quickly recovered to the initial levels in the liver. The HGF receptor/c-Met was found to be autophosphorylated in the liver treated with rhHGF-activator. Further, the proliferating cell nuclear antigen labeling index and the liver regeneration rate were significantly higher in rhHGF-activator group than in control animals. These results indicate that exogenously administered HGF-activator produces a biologically active HGF from its precursor form and increases the potential for liver regeneration in vivo.
doi_str_mv 10.1006/bbrc.2001.6170
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Liver functions are mostly impaired in patients with liver diseases including cirrhosis. However, a significant amount of inactive HGF precursor (proHGF) is reported in the plasma of these patients. proHGF is proteolytically converted to an active form (mature HGF) by HGF-activator. Thus conversion of proHGF into mature HGF presumably contributes to the recovery of liver functions. In this study, rats with a partial hepatectomy were used, as proHGF is accumulated in the remnant liver. Recombinant human HGF-activator was administered via the portal vein to investigate the effect on molecular forms of HGF and its biological signaling. rhHGF-activator promptly converted proHGF into mature HGF, reaching maximal levels at 5–10 min after the injection, while the decreased proHGF was quickly recovered to the initial levels in the liver. The HGF receptor/c-Met was found to be autophosphorylated in the liver treated with rhHGF-activator. Further, the proliferating cell nuclear antigen labeling index and the liver regeneration rate were significantly higher in rhHGF-activator group than in control animals. 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Liver functions are mostly impaired in patients with liver diseases including cirrhosis. However, a significant amount of inactive HGF precursor (proHGF) is reported in the plasma of these patients. proHGF is proteolytically converted to an active form (mature HGF) by HGF-activator. Thus conversion of proHGF into mature HGF presumably contributes to the recovery of liver functions. In this study, rats with a partial hepatectomy were used, as proHGF is accumulated in the remnant liver. Recombinant human HGF-activator was administered via the portal vein to investigate the effect on molecular forms of HGF and its biological signaling. rhHGF-activator promptly converted proHGF into mature HGF, reaching maximal levels at 5–10 min after the injection, while the decreased proHGF was quickly recovered to the initial levels in the liver. The HGF receptor/c-Met was found to be autophosphorylated in the liver treated with rhHGF-activator. 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Further, the proliferating cell nuclear antigen labeling index and the liver regeneration rate were significantly higher in rhHGF-activator group than in control animals. These results indicate that exogenously administered HGF-activator produces a biologically active HGF from its precursor form and increases the potential for liver regeneration in vivo.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>11779195</pmid><doi>10.1006/bbrc.2001.6170</doi><tpages>7</tpages></addata></record>
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subjects Animals
Blotting, Western
Cell Division
DNA, Complementary - metabolism
Dose-Response Relationship, Drug
Hepatectomy
hepatocyte growth factor (HGF)
Hepatocyte Growth Factor - biosynthesis
Hepatocyte Growth Factor - blood
HGF precursor
HGF receptor/c-Met
HGF-activator
Humans
Liver - metabolism
Liver - physiology
partial hepatectomy
Phosphorylation
Precipitin Tests
Proliferating Cell Nuclear Antigen - metabolism
Rats
Rats, Sprague-Dawley
Recombinant Proteins - metabolism
Regeneration
Serine Endopeptidases - metabolism
Serine Endopeptidases - pharmacology
Signal Transduction
Time Factors
title Exogenously Administered HGF Activator Augments Liver Regeneration through the Production of Biologically Active HGF
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