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 |
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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. 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.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1006/bbrc.2001.6170</identifier><identifier>PMID: 11779195</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>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</subject><ispartof>Biochemical and biophysical research communications, 2002-01, Vol.290 (1), p.475-481</ispartof><rights>2002 Elsevier Science (USA)</rights><rights>(c)2002 Elsevier Science.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c384t-8326e3f8bdafddb04cf8aa65d76d0575d23c690e084699e8d4f3740b09baa0293</citedby><cites>FETCH-LOGICAL-c384t-8326e3f8bdafddb04cf8aa65d76d0575d23c690e084699e8d4f3740b09baa0293</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0006291X01961704$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11779195$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kaibori, Masaki</creatorcontrib><creatorcontrib>Inoue, Tomohisa</creatorcontrib><creatorcontrib>Oda, Michio</creatorcontrib><creatorcontrib>Naka, Daiji</creatorcontrib><creatorcontrib>Kawaguchi, Toshiya</creatorcontrib><creatorcontrib>Kitamura, Naomi</creatorcontrib><creatorcontrib>Miyazawa, Keiji</creatorcontrib><creatorcontrib>Kwon, A-Hon</creatorcontrib><creatorcontrib>Kamiyama, Yasuo</creatorcontrib><creatorcontrib>Okumura, Tadayoshi</creatorcontrib><title>Exogenously Administered HGF Activator Augments Liver Regeneration through the Production of Biologically Active HGF</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><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.</description><subject>Animals</subject><subject>Blotting, Western</subject><subject>Cell Division</subject><subject>DNA, Complementary - metabolism</subject><subject>Dose-Response Relationship, Drug</subject><subject>Hepatectomy</subject><subject>hepatocyte growth factor (HGF)</subject><subject>Hepatocyte Growth Factor - biosynthesis</subject><subject>Hepatocyte Growth Factor - blood</subject><subject>HGF precursor</subject><subject>HGF receptor/c-Met</subject><subject>HGF-activator</subject><subject>Humans</subject><subject>Liver - metabolism</subject><subject>Liver - physiology</subject><subject>partial hepatectomy</subject><subject>Phosphorylation</subject><subject>Precipitin Tests</subject><subject>Proliferating Cell Nuclear Antigen - metabolism</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Recombinant Proteins - metabolism</subject><subject>Regeneration</subject><subject>Serine Endopeptidases - metabolism</subject><subject>Serine Endopeptidases - pharmacology</subject><subject>Signal Transduction</subject><subject>Time Factors</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEtLxDAUhYMoOj62LiUrdx1v-s5yFF8woIiCu5Amt2OkbTRJB_33ps6AK1cXLt_54BxCThnMGUB50TROzVMANi9ZBTtkxoBDkjLId8kMIpGknL0ekEPv3yPF8pLvkwPGqoozXsxIuP6yKxzs6LtvutC9GYwP6FDTu9sbulDBrGWwji7GVY9D8HRp1ujoE8YQOhmMHWh4c3ZcvcWL9NFZParft23ppbGdXRklu8k-yXDyHpO9VnYeT7b3iLzcXD9f3SXLh9v7q8UyUVmdh6TO0hKztm60bLVuIFdtLWVZ6KrUUFSFTjNVckCoYyuOtc7brMqhAd5ICSnPjsj5xvvh7OeIPojeeIVdJweMjUXFsiJj-QTON6By1nuHrfhwppfuWzAQ085i2llMO4tp5xg425rHpkf9h2-HjUC9ATD2Wxt0wiuDg0JtHKogtDX_uX8A9K2N4w</recordid><startdate>20020111</startdate><enddate>20020111</enddate><creator>Kaibori, Masaki</creator><creator>Inoue, Tomohisa</creator><creator>Oda, Michio</creator><creator>Naka, Daiji</creator><creator>Kawaguchi, Toshiya</creator><creator>Kitamura, Naomi</creator><creator>Miyazawa, Keiji</creator><creator>Kwon, A-Hon</creator><creator>Kamiyama, Yasuo</creator><creator>Okumura, Tadayoshi</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20020111</creationdate><title>Exogenously Administered HGF Activator Augments Liver Regeneration through the Production of Biologically Active HGF</title><author>Kaibori, Masaki ; Inoue, Tomohisa ; Oda, Michio ; Naka, Daiji ; Kawaguchi, Toshiya ; Kitamura, Naomi ; Miyazawa, Keiji ; Kwon, A-Hon ; Kamiyama, Yasuo ; Okumura, Tadayoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c384t-8326e3f8bdafddb04cf8aa65d76d0575d23c690e084699e8d4f3740b09baa0293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animals</topic><topic>Blotting, Western</topic><topic>Cell Division</topic><topic>DNA, Complementary - metabolism</topic><topic>Dose-Response Relationship, Drug</topic><topic>Hepatectomy</topic><topic>hepatocyte growth factor (HGF)</topic><topic>Hepatocyte Growth Factor - biosynthesis</topic><topic>Hepatocyte Growth Factor - blood</topic><topic>HGF precursor</topic><topic>HGF receptor/c-Met</topic><topic>HGF-activator</topic><topic>Humans</topic><topic>Liver - metabolism</topic><topic>Liver - physiology</topic><topic>partial hepatectomy</topic><topic>Phosphorylation</topic><topic>Precipitin Tests</topic><topic>Proliferating Cell Nuclear Antigen - metabolism</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Recombinant Proteins - metabolism</topic><topic>Regeneration</topic><topic>Serine Endopeptidases - metabolism</topic><topic>Serine Endopeptidases - pharmacology</topic><topic>Signal Transduction</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kaibori, Masaki</creatorcontrib><creatorcontrib>Inoue, Tomohisa</creatorcontrib><creatorcontrib>Oda, Michio</creatorcontrib><creatorcontrib>Naka, Daiji</creatorcontrib><creatorcontrib>Kawaguchi, Toshiya</creatorcontrib><creatorcontrib>Kitamura, Naomi</creatorcontrib><creatorcontrib>Miyazawa, Keiji</creatorcontrib><creatorcontrib>Kwon, A-Hon</creatorcontrib><creatorcontrib>Kamiyama, Yasuo</creatorcontrib><creatorcontrib>Okumura, Tadayoshi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kaibori, Masaki</au><au>Inoue, Tomohisa</au><au>Oda, Michio</au><au>Naka, Daiji</au><au>Kawaguchi, Toshiya</au><au>Kitamura, Naomi</au><au>Miyazawa, Keiji</au><au>Kwon, A-Hon</au><au>Kamiyama, Yasuo</au><au>Okumura, Tadayoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Exogenously Administered HGF Activator Augments Liver Regeneration through the Production of Biologically Active HGF</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2002-01-11</date><risdate>2002</risdate><volume>290</volume><issue>1</issue><spage>475</spage><epage>481</epage><pages>475-481</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>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.</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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