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
Hauptverfasser: Armbrust, Thomas, Batusic, Danko, Ringe, Burkhardt, Ramadori, Giuliano
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container_end_page 1054
container_issue 5
container_start_page 1042
container_title Journal of hepatology
container_volume 26
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
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Indications for mast cell participation in development of liver fibrosis</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Armbrust, Thomas ; Batusic, Danko ; Ringe, Burkhardt ; Ramadori, Giuliano</creator><creatorcontrib>Armbrust, Thomas ; Batusic, Danko ; Ringe, Burkhardt ; Ramadori, Giuliano</creatorcontrib><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><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. 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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. 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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. 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source MEDLINE; Elsevier ScienceDirect Journals
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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