R. Rosin-arbesfeld et al., Actin-dependent membrane association of the APC tumour suppressor in polarized mammalian epithelial cells, EMBO J, 20(21), 2001, pp. 5929-5939
Adenomatous polyposis coli (APC) is mutated in most colorectal cancers. APC
downregulates nuclear beta -catenin, which is thought to be critical for i
ts tumour suppressor function. However, APC may have additional and separat
e functions at the cell periphery. Here, we examine polarized MDCK and WIF-
B hepatoma cells and find that APC is associated with their lateral plasma
membranes. This depends on the actin cytoskeleton but not on microtubules,
and drug wash-out experiments suggest that APC is delivered continuously to
the plasma membrane by a dynamic actin-dependent process. In polarized MDC
K cells, APC also clusters at microtubule tips in their basal-most regions.
Microtubule depolymerization causes APC to relocalize from these tips to t
he plasma membrane, indicating two distinct peripheral APC pools that are i
n equilibrium with each other in these cells. Truncations of APC such as th
ose found in APC mutant cancer cells can neither associate with the plasma
membrane nor with microtubule tips. The ability of APC to reach the cell pe
riphery may thus contribute to its tumour suppressor function in the intest
inal epithelium.