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Expression of fibrillin-1 in focal nodular hyperplasia of the liver: a role in microcirculation adaptability

INTRODUCTION: It has been suggested that the elastic network plays an important role in the tissue response to mechanical stress. The components of the elastic network have been poorly studied in liver diseases. Therefore, in this work, the expression and distribution of fibrillin-1 and elastin were...

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Autores principales: Lepreux, Sébastien, Desmouliere, Alexis, Rosenbaum, Jean, Balabaud, Charles, Bioulac-Sage, Paulette
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409448/
https://www.ncbi.nlm.nih.gov/pubmed/14960209
http://dx.doi.org/10.1186/1476-5926-2-S1-S57
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author Lepreux, Sébastien
Desmouliere, Alexis
Rosenbaum, Jean
Balabaud, Charles
Bioulac-Sage, Paulette
author_facet Lepreux, Sébastien
Desmouliere, Alexis
Rosenbaum, Jean
Balabaud, Charles
Bioulac-Sage, Paulette
author_sort Lepreux, Sébastien
collection PubMed
description INTRODUCTION: It has been suggested that the elastic network plays an important role in the tissue response to mechanical stress. The components of the elastic network have been poorly studied in liver diseases. Therefore, in this work, the expression and distribution of fibrillin-1 and elastin were studied in hepatic focal nodular hyperplasia and compared with surrounding liver and hepatocellular adenoma. METHODS: Immunohistochemical studies for fibrillin-1 and elastin were performed on unfixed cryostat sections of focal nodular hyperplasia (22 cases), hepatocellular adenoma (15 cases) and surrounding liver (34 cases). RESULTS: Surrounding normal liver showed only a continuous, thin and regular immunostaining of fibrillin-1 in the space of Disse, whereas elastin was nearly absent. In focal nodular hyperplasia, fibrillin-1 was more strongly expressed in the perisinusoidal space, compared with surrounding liver; in contrast, in adenomas fibrillin-1 immunostaining was irregular and very low in perisinusoidal space, more intense in peliotic areas. CONCLUSIONS: In focal nodular hyperplasia, the increased microfibrillar network containing fibrillin-1 in the space of Disse could reflect an adaptation of the sinusoidal wall to an increased arterial blood flow in sinusoids. In hepatocellular adenoma, the different patterns of fibrillin-1 could be related to the heterogeneity of the arterial vascularization and to the frequent necrotico-hemorrhagic changes. This study comparing the elastic network in two types of lesions with vascularization abnormalities and in the surrounding liver provides interesting new data for understanding the structural role of fibrillin-1 in the space of Disse.
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spelling pubmed-24094482008-06-05 Expression of fibrillin-1 in focal nodular hyperplasia of the liver: a role in microcirculation adaptability Lepreux, Sébastien Desmouliere, Alexis Rosenbaum, Jean Balabaud, Charles Bioulac-Sage, Paulette Comp Hepatol Proceedings INTRODUCTION: It has been suggested that the elastic network plays an important role in the tissue response to mechanical stress. The components of the elastic network have been poorly studied in liver diseases. Therefore, in this work, the expression and distribution of fibrillin-1 and elastin were studied in hepatic focal nodular hyperplasia and compared with surrounding liver and hepatocellular adenoma. METHODS: Immunohistochemical studies for fibrillin-1 and elastin were performed on unfixed cryostat sections of focal nodular hyperplasia (22 cases), hepatocellular adenoma (15 cases) and surrounding liver (34 cases). RESULTS: Surrounding normal liver showed only a continuous, thin and regular immunostaining of fibrillin-1 in the space of Disse, whereas elastin was nearly absent. In focal nodular hyperplasia, fibrillin-1 was more strongly expressed in the perisinusoidal space, compared with surrounding liver; in contrast, in adenomas fibrillin-1 immunostaining was irregular and very low in perisinusoidal space, more intense in peliotic areas. CONCLUSIONS: In focal nodular hyperplasia, the increased microfibrillar network containing fibrillin-1 in the space of Disse could reflect an adaptation of the sinusoidal wall to an increased arterial blood flow in sinusoids. In hepatocellular adenoma, the different patterns of fibrillin-1 could be related to the heterogeneity of the arterial vascularization and to the frequent necrotico-hemorrhagic changes. This study comparing the elastic network in two types of lesions with vascularization abnormalities and in the surrounding liver provides interesting new data for understanding the structural role of fibrillin-1 in the space of Disse. BioMed Central 2004-01-14 /pmc/articles/PMC2409448/ /pubmed/14960209 http://dx.doi.org/10.1186/1476-5926-2-S1-S57 Text en Copyright © 2004 Lepreux et al; licensee BioMed Central Ltd This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Proceedings
Lepreux, Sébastien
Desmouliere, Alexis
Rosenbaum, Jean
Balabaud, Charles
Bioulac-Sage, Paulette
Expression of fibrillin-1 in focal nodular hyperplasia of the liver: a role in microcirculation adaptability
title Expression of fibrillin-1 in focal nodular hyperplasia of the liver: a role in microcirculation adaptability
title_full Expression of fibrillin-1 in focal nodular hyperplasia of the liver: a role in microcirculation adaptability
title_fullStr Expression of fibrillin-1 in focal nodular hyperplasia of the liver: a role in microcirculation adaptability
title_full_unstemmed Expression of fibrillin-1 in focal nodular hyperplasia of the liver: a role in microcirculation adaptability
title_short Expression of fibrillin-1 in focal nodular hyperplasia of the liver: a role in microcirculation adaptability
title_sort expression of fibrillin-1 in focal nodular hyperplasia of the liver: a role in microcirculation adaptability
topic Proceedings
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409448/
https://www.ncbi.nlm.nih.gov/pubmed/14960209
http://dx.doi.org/10.1186/1476-5926-2-S1-S57
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