Integrins play a pivotal role in organogenesis, by mediating the inter
actions between differentiating cells and the extracellular matrix. We
analyzed the expression of integrins and their ligands during human l
iver organogenesis. The expression of beta 1, beta 3, and beta 4 integ
rins and the distribution of several extracellular matrix proteins wer
e studied by immunoperoxidase in fetal liver samples from 5 to 40 week
s' gestation. Hepatoblasts expressed only the beta 1, alpha I, alpha 5
, alpha 6, and alpha 9 integrin chains. Fetal hepatocytes, emerging at
the 8th week of gestation, initially retained the same combination of
integrins, but presented a progressive decrease in their expression l
evels. After 15 weeks' gestation, the expression levels of beta 1, alp
ha 1, alpha 5, and alpha 9 reached levels comparable to those observed
in the adult state. alpha 6 expression became undetectable after 30 w
eeks' gestation. As compared to hepatoblasts, intrahepatic biliary epi
thelial cells, differentiating at the 8th week of gestation in the duc
tal plate, were characterized by the progressive loss of alpha 1, the
marked induction of alpha 6, and the de novo acquisition of the beta 4
, alpha 2, and alpha 3 integrin chains. The disappearance of integrin
receptors for laminin on hepatocytes was associated with the rarefacti
on of laminin in the perisinusoidal matrix, whereas their induction on
biliary epithelial cells was associated with laminin deposition at th
e point of contact with the ductal plate. In conclusion, integrins lik
ely play an important role in the differentiation of the epithelial ce
ll populations of the liver.