Mast cells distribution in human liver disease and experimental rat liver fibrosis. Indications for mast cell participation in development of liver fibrosis
Background/Aims: The development of liver fibrosis due to chronic liver diseases is thought to be mediated by inflammatory cells releasing fibrogenic mediators that activate fat-storing cells (Ito-cells). Recently, the involvement of mast cells in fibrogenesis has been suggested. We studied the dist...
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Veröffentlicht in: | Journal of hepatology 1997-05, Vol.26 (5), p.1042-1054 |
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creator | Armbrust, Thomas Batusic, Danko Ringe, Burkhardt Ramadori, Giuliano |
description | Background/Aims: The development of liver fibrosis due to chronic liver diseases is thought to be mediated by inflammatory cells releasing fibrogenic mediators that activate fat-storing cells (Ito-cells). Recently, the involvement of mast cells in fibrogenesis has been suggested. We studied the distribution of these cells in normal human liver and human nonfibrotic and fibrotic liver disease as well as in normal rat liver and acutely and chronically injured rat liver (CCl
4 model).
Methods: Mast cells were identified by histochemical and immunohistochemical methods. The immunoreactivity of liver and comparatively of rat peritoneal mast cells to the serpins alpha1-antitrypsin, alpha1-antichymotrypsin and antithrombin III was also studied.
Results: In normal human and rat liver, mast cells were rarely found in portal tracts, and there was no change in cell numbers in nonfibrotic human or acutely injured rat livers. In contrast, cirrhotic human and rat livers contained numerous mast cells in the portal tracts and the fibrous septa. They exhibited strong immunoreactivity to the serpins, as did rat peritoneal mast cells.
Conclusions: The results indicate that in the late stages of liver fibrogeneis, mast cells may be involved by diplaying protease inhibitory activity in the fibrotic septa. |
doi_str_mv | 10.1016/S0168-8278(97)80113-4 |
format | Article |
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4 model).
Methods: Mast cells were identified by histochemical and immunohistochemical methods. The immunoreactivity of liver and comparatively of rat peritoneal mast cells to the serpins alpha1-antitrypsin, alpha1-antichymotrypsin and antithrombin III was also studied.
Results: In normal human and rat liver, mast cells were rarely found in portal tracts, and there was no change in cell numbers in nonfibrotic human or acutely injured rat livers. In contrast, cirrhotic human and rat livers contained numerous mast cells in the portal tracts and the fibrous septa. They exhibited strong immunoreactivity to the serpins, as did rat peritoneal mast cells.
Conclusions: The results indicate that in the late stages of liver fibrogeneis, mast cells may be involved by diplaying protease inhibitory activity in the fibrotic septa.</description><identifier>ISSN: 0168-8278</identifier><identifier>EISSN: 1600-0641</identifier><identifier>DOI: 10.1016/S0168-8278(97)80113-4</identifier><identifier>PMID: 9186835</identifier><identifier>CODEN: JOHEEC</identifier><language>eng</language><publisher>Oxford: Elsevier B.V</publisher><subject>Animals ; Biological and medical sciences ; Cirrhosis ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Liver - cytology ; Liver - pathology ; Liver Cirrhosis - etiology ; Liver Cirrhosis - pathology ; Liver Cirrhosis, Experimental - pathology ; Liver disease ; Liver Diseases - pathology ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Mast cells ; Mast Cells - metabolism ; Mast Cells - pathology ; Mast Cells - physiology ; Medical sciences ; Other diseases. Semiology ; Peritoneum - cytology ; Peritoneum - metabolism ; Rats ; Rats, Wistar ; Reference Values ; Serine Proteinase Inhibitors - metabolism</subject><ispartof>Journal of hepatology, 1997-05, Vol.26 (5), p.1042-1054</ispartof><rights>1997</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c507t-c3d068a51f28c4b5b77394f5b5cdcad266d44a8423b8b92fac483eaec336879d3</citedby><cites>FETCH-LOGICAL-c507t-c3d068a51f28c4b5b77394f5b5cdcad266d44a8423b8b92fac483eaec336879d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0168-8278(97)80113-4$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2676412$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9186835$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Armbrust, Thomas</creatorcontrib><creatorcontrib>Batusic, Danko</creatorcontrib><creatorcontrib>Ringe, Burkhardt</creatorcontrib><creatorcontrib>Ramadori, Giuliano</creatorcontrib><title>Mast cells distribution in human liver disease and experimental rat liver fibrosis. Indications for mast cell participation in development of liver fibrosis</title><title>Journal of hepatology</title><addtitle>J Hepatol</addtitle><description>Background/Aims: The development of liver fibrosis due to chronic liver diseases is thought to be mediated by inflammatory cells releasing fibrogenic mediators that activate fat-storing cells (Ito-cells). Recently, the involvement of mast cells in fibrogenesis has been suggested. We studied the distribution of these cells in normal human liver and human nonfibrotic and fibrotic liver disease as well as in normal rat liver and acutely and chronically injured rat liver (CCl
4 model).
Methods: Mast cells were identified by histochemical and immunohistochemical methods. The immunoreactivity of liver and comparatively of rat peritoneal mast cells to the serpins alpha1-antitrypsin, alpha1-antichymotrypsin and antithrombin III was also studied.
Results: In normal human and rat liver, mast cells were rarely found in portal tracts, and there was no change in cell numbers in nonfibrotic human or acutely injured rat livers. In contrast, cirrhotic human and rat livers contained numerous mast cells in the portal tracts and the fibrous septa. They exhibited strong immunoreactivity to the serpins, as did rat peritoneal mast cells.
Conclusions: The results indicate that in the late stages of liver fibrogeneis, mast cells may be involved by diplaying protease inhibitory activity in the fibrotic septa.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cirrhosis</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Liver - cytology</subject><subject>Liver - pathology</subject><subject>Liver Cirrhosis - etiology</subject><subject>Liver Cirrhosis - pathology</subject><subject>Liver Cirrhosis, Experimental - pathology</subject><subject>Liver disease</subject><subject>Liver Diseases - pathology</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Mast cells</subject><subject>Mast Cells - metabolism</subject><subject>Mast Cells - pathology</subject><subject>Mast Cells - physiology</subject><subject>Medical sciences</subject><subject>Other diseases. Semiology</subject><subject>Peritoneum - cytology</subject><subject>Peritoneum - metabolism</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Reference Values</subject><subject>Serine Proteinase Inhibitors - metabolism</subject><issn>0168-8278</issn><issn>1600-0641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1u1TAQhS0EKreFR6jkBUKwSGvHjuOsEKr4qVTUBbC2JvZYGCVOsJOr8i48bJPe9C7YdGMvzjfnjOYQcs7ZBWdcXX5fHl3ostbvmvq9ZpyLQj4jO64YK5iS_DnZHZGX5DTn34wxwRp5Qk4arpUW1Y78-wZ5oha7LlMX8pRCO09hiDRE-mvuIdIu7DGtGkJGCtFRvBsxhR7jBB1NMG2ID20acsgX9Dq6YGG1ydQPifaPGXSENAUbRnjMcLjHbhhXMzr4_5xekRceuoyvt_-M_Pz86cfV1-Lm9sv11cebwlasngorHFMaKu5LbWVbtXUtGumrtrLOgiuVclKClqVodduUHqzUAgGtEErXjRNn5O3Bd0zDnxnzZPqQ130h4jBnUzesEorxBawOoF32ywm9GZdDQPprODNrK-ahFbOe3DS1eWjFyGXufAuY2x7dcWqrYdHfbDpkC51PEG3IR6xU9dJnuWAfDhgux9gHTCbbgNGiCwntZNwQnljkHqnTrVU</recordid><startdate>19970501</startdate><enddate>19970501</enddate><creator>Armbrust, Thomas</creator><creator>Batusic, Danko</creator><creator>Ringe, Burkhardt</creator><creator>Ramadori, Giuliano</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><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>19970501</creationdate><title>Mast cells distribution in human liver disease and experimental rat liver fibrosis. Indications for mast cell participation in development of liver fibrosis</title><author>Armbrust, Thomas ; Batusic, Danko ; Ringe, Burkhardt ; Ramadori, Giuliano</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c507t-c3d068a51f28c4b5b77394f5b5cdcad266d44a8423b8b92fac483eaec336879d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cirrhosis</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Liver - cytology</topic><topic>Liver - pathology</topic><topic>Liver Cirrhosis - etiology</topic><topic>Liver Cirrhosis - pathology</topic><topic>Liver Cirrhosis, Experimental - pathology</topic><topic>Liver disease</topic><topic>Liver Diseases - pathology</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Mast cells</topic><topic>Mast Cells - metabolism</topic><topic>Mast Cells - pathology</topic><topic>Mast Cells - physiology</topic><topic>Medical sciences</topic><topic>Other diseases. Semiology</topic><topic>Peritoneum - cytology</topic><topic>Peritoneum - metabolism</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Reference Values</topic><topic>Serine Proteinase Inhibitors - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Armbrust, Thomas</creatorcontrib><creatorcontrib>Batusic, Danko</creatorcontrib><creatorcontrib>Ringe, Burkhardt</creatorcontrib><creatorcontrib>Ramadori, Giuliano</creatorcontrib><collection>Pascal-Francis</collection><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>Journal of hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Armbrust, Thomas</au><au>Batusic, Danko</au><au>Ringe, Burkhardt</au><au>Ramadori, Giuliano</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mast cells distribution in human liver disease and experimental rat liver fibrosis. Indications for mast cell participation in development of liver fibrosis</atitle><jtitle>Journal of hepatology</jtitle><addtitle>J Hepatol</addtitle><date>1997-05-01</date><risdate>1997</risdate><volume>26</volume><issue>5</issue><spage>1042</spage><epage>1054</epage><pages>1042-1054</pages><issn>0168-8278</issn><eissn>1600-0641</eissn><coden>JOHEEC</coden><abstract>Background/Aims: The development of liver fibrosis due to chronic liver diseases is thought to be mediated by inflammatory cells releasing fibrogenic mediators that activate fat-storing cells (Ito-cells). Recently, the involvement of mast cells in fibrogenesis has been suggested. We studied the distribution of these cells in normal human liver and human nonfibrotic and fibrotic liver disease as well as in normal rat liver and acutely and chronically injured rat liver (CCl
4 model).
Methods: Mast cells were identified by histochemical and immunohistochemical methods. The immunoreactivity of liver and comparatively of rat peritoneal mast cells to the serpins alpha1-antitrypsin, alpha1-antichymotrypsin and antithrombin III was also studied.
Results: In normal human and rat liver, mast cells were rarely found in portal tracts, and there was no change in cell numbers in nonfibrotic human or acutely injured rat livers. In contrast, cirrhotic human and rat livers contained numerous mast cells in the portal tracts and the fibrous septa. They exhibited strong immunoreactivity to the serpins, as did rat peritoneal mast cells.
Conclusions: The results indicate that in the late stages of liver fibrogeneis, mast cells may be involved by diplaying protease inhibitory activity in the fibrotic septa.</abstract><cop>Oxford</cop><pub>Elsevier B.V</pub><pmid>9186835</pmid><doi>10.1016/S0168-8278(97)80113-4</doi><tpages>13</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Cirrhosis Female Gastroenterology. Liver. Pancreas. Abdomen Humans Liver - cytology Liver - pathology Liver Cirrhosis - etiology Liver Cirrhosis - pathology Liver Cirrhosis, Experimental - pathology Liver disease Liver Diseases - pathology Liver. Biliary tract. Portal circulation. Exocrine pancreas Mast cells Mast Cells - metabolism Mast Cells - pathology Mast Cells - physiology Medical sciences Other diseases. Semiology Peritoneum - cytology Peritoneum - metabolism Rats Rats, Wistar Reference Values Serine Proteinase Inhibitors - metabolism |
title | Mast cells distribution in human liver disease and experimental rat liver fibrosis. Indications for mast cell participation in development of liver fibrosis |
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