In response to treatment with 17 beta-estradiol, MCF-7 human breast carcino
ma cells undergo a marked rearrangement of the F-actin cytoskeleton. The mo
st conspicuous aspect of this rearrangement is the formation of an extensiv
e array of lamellipodial structures which are situated beneath cell cluster
s. Treatment of cells with 17 beta-estradiol in the presence of the anti-es
trogen ICI182,780 suppressed the development of the lamellipodial structure
s, indicating that this cytoskeletal rearrangement is mediated by the estro
gen receptor. Time-lapse, video-enhanced, differential interference contras
t microscopy reveals that the lamellipodial structures are actively motile
beneath cell clusters. Furthermore, the lamellipodial structures form few f
ocal contacts with the underlying substrate of the coverslip, as evidenced
by either interference reflection microscopy or staining for the focal cont
act protein talin, indicating: that these structures are not strongly adher
ed to the substratum. Immunofluorescence localization of E-cadherin indicat
es that this cell-cell adhesion receptor is present within these structures
as either adhesion plaque- or point contact-like depositions. These findin
gs implicate the cadherin-based cell-cell adhesion system in supporting tum
or cell motility over adjacent cell surfaces via discrete adhesive structur
es which are associated with motile lamellipodia.