M. Depreter et al., Maturation of the liver-specific peroxisome versus laminin, collagen IV and integrin expression, BIO CELL, 90(9), 1998, pp. 641-652
The interaction of cells with extracellular matrix components contributes t
o their specific differentiation. We studied hepatic peroxisomes and their
changing features during embryonic development, and we immunolocalized in t
he same tissue the extracellular matrix components laminin and collagen IV
as well as the integrin receptor subunits alpha(1), alpha(2), beta(1) and b
eta(4). Rat and human embryonic liver peroxisome expression were studied at
the light- and electron-microscopic level by means of localizing catalase-
, D-amino acid oxidase- and polyamine oxidase activities and by means of th
e immunocytochemistry of six peroxisomal proteins. The successive import of
catalase and the peroxisomal beta-oxidation enzymes, the late appearance o
f the other enzymes, and the gradual increase of peroxisomal size and numbe
r to adult values occurred as asynchronous events. Although still immature,
peroxisomes were recognized at every stage examined and coexisted with lam
inin and collagen TV in both species. The PI integrin subunit was immunodet
ected as early as at 12.5 days in rat. It was concluded that these extracel
lular matrix factors may be important for the differentiation of liver pare
nchyma from the liverbud stage onwards. However, the stepwise maturation of
the liver-specific peroxisome suggests the involvement of many other regul
ating factors. ((C) Elsevier, Paris).