Collagen XVIII is localized in sinusoids and basement membrane zones and expressed by hepatocytes and activated stellate cells in fibrotic human liver

Type XVIII collagen is a recently discovered nonfibrillar collagen associated with basement membranes in mice and expressed at high levels in human liver. We studied the origin, distribution, and RNA levels of type XVIII collagen in normal and fibrotic human livers by in situ hybridization, immunohi...

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Veröffentlicht in:Hepatology (Baltimore, Md.) Md.), 1998-07, Vol.28 (1), p.98-107
Hauptverfasser: Musso, Orlando, Rehn, Marko, Saarela, Janna, Théret, Nathalie, Liétard, Jocelyne, Hintikka, Elina, Lotrian, Dominique, Campion, Jean‐Pierre, Pihlajaniemi, Taina, Clément, Bruno
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container_start_page 98
container_title Hepatology (Baltimore, Md.)
container_volume 28
creator Musso, Orlando
Rehn, Marko
Saarela, Janna
Théret, Nathalie
Liétard, Jocelyne
Hintikka, Elina
Lotrian, Dominique
Campion, Jean‐Pierre
Pihlajaniemi, Taina
Clément, Bruno
description Type XVIII collagen is a recently discovered nonfibrillar collagen associated with basement membranes in mice and expressed at high levels in human liver. We studied the origin, distribution, and RNA levels of type XVIII collagen in normal and fibrotic human livers by in situ hybridization, immunohistochemistry, and Northern and dot blots and compared procollagen α1(XVIII) RNA levels with those of procollagen α1(IV) and laminin γ1, the two major components of liver basement membranes. In normal liver, type XVIII collagen was heavily deposited in perisinusoidal spaces and basement membrane zones. The major source of type XVIII collagen was hepatocytes and, to a lesser extent, endothelial, biliary epithelial, and vascular smooth muscle cells and peripheral nerves. In cirrhosis, type XVIII collagen formed a thick deposit along capillarized sinusoids. Grain counts after in situ hybridization showed myofibroblasts to increase their expression 13‐fold in active and twofold in quiescent fibrosis, whereas hepatocytes increased their expression only twofold in both active and quiescent fibrosis. Activated stellate cells in vitro expressed type XVIII collagen at high levels. These data indicate that type XVIII collagen is a component of the perisinusoidal space and is associated with basement membrane remodeling. Hepatocytes and activated stellate cells are important sources of type XVIII collagen in normal and fibrotic liver respectively, which suggests tissue‐specific regulation of its expression.
doi_str_mv 10.1002/hep.510280115
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We studied the origin, distribution, and RNA levels of type XVIII collagen in normal and fibrotic human livers by in situ hybridization, immunohistochemistry, and Northern and dot blots and compared procollagen α1(XVIII) RNA levels with those of procollagen α1(IV) and laminin γ1, the two major components of liver basement membranes. In normal liver, type XVIII collagen was heavily deposited in perisinusoidal spaces and basement membrane zones. The major source of type XVIII collagen was hepatocytes and, to a lesser extent, endothelial, biliary epithelial, and vascular smooth muscle cells and peripheral nerves. In cirrhosis, type XVIII collagen formed a thick deposit along capillarized sinusoids. Grain counts after in situ hybridization showed myofibroblasts to increase their expression 13‐fold in active and twofold in quiescent fibrosis, whereas hepatocytes increased their expression only twofold in both active and quiescent fibrosis. Activated stellate cells in vitro expressed type XVIII collagen at high levels. These data indicate that type XVIII collagen is a component of the perisinusoidal space and is associated with basement membrane remodeling. Hepatocytes and activated stellate cells are important sources of type XVIII collagen in normal and fibrotic liver respectively, which suggests tissue‐specific regulation of its expression.</description><identifier>ISSN: 0270-9139</identifier><identifier>EISSN: 1527-3350</identifier><identifier>DOI: 10.1002/hep.510280115</identifier><identifier>PMID: 9657102</identifier><identifier>CODEN: HPTLD9</identifier><language>eng</language><publisher>Philadelphia, PA: W.B. Saunders</publisher><subject>Basement Membrane - metabolism ; Biological and medical sciences ; Cells, Cultured ; Collagen - metabolism ; Gastroenterology. Liver. Pancreas. 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Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Liver - cytology</topic><topic>Liver - metabolism</topic><topic>Liver Cirrhosis - metabolism</topic><topic>Liver Cirrhosis - pathology</topic><topic>Liver Cirrhosis - physiopathology</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Medical sciences</topic><topic>Other diseases. 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We studied the origin, distribution, and RNA levels of type XVIII collagen in normal and fibrotic human livers by in situ hybridization, immunohistochemistry, and Northern and dot blots and compared procollagen α1(XVIII) RNA levels with those of procollagen α1(IV) and laminin γ1, the two major components of liver basement membranes. In normal liver, type XVIII collagen was heavily deposited in perisinusoidal spaces and basement membrane zones. The major source of type XVIII collagen was hepatocytes and, to a lesser extent, endothelial, biliary epithelial, and vascular smooth muscle cells and peripheral nerves. In cirrhosis, type XVIII collagen formed a thick deposit along capillarized sinusoids. Grain counts after in situ hybridization showed myofibroblasts to increase their expression 13‐fold in active and twofold in quiescent fibrosis, whereas hepatocytes increased their expression only twofold in both active and quiescent fibrosis. Activated stellate cells in vitro expressed type XVIII collagen at high levels. These data indicate that type XVIII collagen is a component of the perisinusoidal space and is associated with basement membrane remodeling. Hepatocytes and activated stellate cells are important sources of type XVIII collagen in normal and fibrotic liver respectively, which suggests tissue‐specific regulation of its expression.</abstract><cop>Philadelphia, PA</cop><pub>W.B. Saunders</pub><pmid>9657102</pmid><doi>10.1002/hep.510280115</doi><tpages>10</tpages></addata></record>
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source MEDLINE; Wiley Journals; EZB-FREE-00999 freely available EZB journals
subjects Basement Membrane - metabolism
Biological and medical sciences
Cells, Cultured
Collagen - metabolism
Gastroenterology. Liver. Pancreas. Abdomen
Humans
Liver - cytology
Liver - metabolism
Liver Cirrhosis - metabolism
Liver Cirrhosis - pathology
Liver Cirrhosis - physiopathology
Liver. Biliary tract. Portal circulation. Exocrine pancreas
Medical sciences
Other diseases. Semiology
Procollagen - genetics
Reference Values
RNA, Messenger - metabolism
Tissue Distribution
title Collagen XVIII is localized in sinusoids and basement membrane zones and expressed by hepatocytes and activated stellate cells in fibrotic human liver
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