FOCAL NODULAR HYPERPLASIA OF THE LIVER - COMPOSITION OF THE EXTRACELLULAR-MATRIX AND EXPRESSION OF CELL-CELL AND CELL-MATRIX ADHESION MOLECULES

被引:35
作者
SCOAZEC, JY
FLEJOU, JF
DERRICO, A
COUVELARD, A
KOZYRAKI, R
FIORENTINO, M
GRIGIONI, WF
FELDMANN, G
机构
[1] HOP BEAUJON,SERV CENT ANAT & CYTOL PATHOL,CLICHY,FRANCE
[2] POLICLIN S ORSOLA,IST ANAT & ISTOL PATOL,BOLOGNA,ITALY
关键词
FOCAL NODULAR HYPERPLASIA; LIVER; EXTRACELLULAR MATRIX; CELL ADHESION MOLECULES; IMMUNOHISTOCHEMISTRY;
D O I
10.1016/0046-8177(95)90274-0
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
We studied by immunohistochemistry 25 cases of focal nodular hyperplasia (FNH) to evaluate the composition of the extracellular matrix and the expression and distribution of endothelial cell-cell adhesion molecules and integrin receptors. The extracellular matrix of FNH retained the overall organization of that of normal liver. The matrix of central scars resembled that of portal tracts. The main difference was the presence of large vitronectin deposits, which might indicate the existence of local hemodynamic disturbances. The matrix lining the sinusoid-like vessels running in the hyperplastic parenchyma retained characteristic features of the normal perisinusoidal matrix, such as the presence of tenascin. In the zone surrounding the central scars, it contained large amounts of laminin, von Willebrand factor, and thrombospondin, suggesting the development of perisinusoidal fibrosis. Laminin deposition was accompanied by the induction of cell-cell adhesion molecules on adjacent endothelial cells and by the upregulation of specific integrin receptors on both hepatocytes and sinusoidal endothelial cells. In conclusion, our study: (1) reinforces the hypothesis that FNH is merely a hyperplastic response of liver parenchyma to local vascular abnormalities, and (2) shows that the lesions of perisinusoidal fibrosis associated with FNH are accompanied by the induction of integrin receptors on hepatocytes and sinusoidal endothelial cells. Copyright (C) 1995 by W.B. Saunders Company
引用
收藏
页码:1114 / 1125
页数:12
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