Immunofluorescence of c-myc-tagged hSlo and the
truncated mutant hSlo-S0–S6. Permanently transfected
MDCK cells were grown on coverslips, treated with 12 mM sodium butyrate
for 48 h, and fixed with 4% paraformaldehyde. Nonpermeabilized
cells (a) and cells permeabilized with 0.2% Triton
X-100 (b and c) were subjected to
indirect immunofluorescence staining with anti-c-myc monoclonal
antibody. hSlo shows a predominantly apical distribution
(a and b), with a scant immune reaction
inside the cell. Instead, the truncated mutant bearing a deletion after
S6 (hSlo-S0–S6) showed no staining at the cell surface
in nonpermeabilized cells (not shown), but revealed an intense
intracellular reticular pattern characteristic of the ER in
permeabilized cells (c).