Motility factors, e.g. SF/HGF (scatter factor/hepatocyte growth factor) or
AMF (autocrine motility factor) can influence the migration of tumor cells
in vitro and may facilitate invasive growth and metastases in vivo. The pro
duction of motility factors was studied in cell lines derived from human ch
olangiocarcinomas. Culture supernatants from 5 different cholangiocarcinoma
cell lines (EGI-1, RPMI 7451, MZ CHA-1, MZ CHA-2 and MZ CHA-3) were analyz
ed in scatter assays with NRK and MDCK cells as indicator cells which react
with cellular migration in the presence of motility factors. Culture super
natants from 4 of the 5 cell lines investigated induced migration of the in
dicator cells thus demonstrating the production of motility factors. Three
of the cell lines (MZ CHA-1, MZ CHA-2, RPMI 7451) produced a factor with a
molecular weight ranging between 50 and 100 kDa, EGI-1 cells secreted a fac
tor with a molecular weight >100 kDa. None of the factors was identical to
HGF as demonstrated by the lacking reactivity in a HGF specific ELISA and b
y the inability to induce scattering of HPAF indicator cells like HGF. Simi
lar to SF/HGF, the activity of the EGI-1 factor was inhibited by the proteo
glycan heparin and stimulated the chemotactic cell migration, but in contra
st to SF/HGF it could not induce invasive growth of NRK cells. The producti
on of scatter factors could be involved in tumor progression and formation
of metastases of cholangiocarcinomas.