In porcine thyroid cells, thyroglobulin sulfation is controlled by thyrotro
pin (TSH) and iodide, which contribute to regulating the intracellular sulf
ate concentration, as we previously established. Here, we studied the trans
port of sulfate and its regulation by these two effectors. Kinetic studies
were performed after [S-35] sulfate was added to either the basal or apical
medium of cell monolayers cultured without any effectors, or with TSH with
or without iodide. The basolateral uptake rates were about tenfold higher
than the apical uptake rates. TSH increased the basolateral and apical upta
ke values (by 24 and 9%, respectively, compared with unstimulated cells), a
nd iodide inhibited these effects of TSH. On the basis of results of the pu
lse-chase experiments, the basolateral and apical effluxes appeared to be w
ell balanced in unstimulated cells and in cells stimulated by both TSH and
iodide: similar to 40-50% of the intracellular radioactivity was released i
nto each medium, whereas in the absence of iodide, 70% of the intracellular
radioactivity was released on the basolateral side. The rates of transepit
helial sulfate transport were increased by TSH compared with unstimulated c
ells, and these effects decreased in response to iodide. These results sugg
est that TSH and iodide may each control the sulfate transport process on t
wo sides of the polarized cells, and that the absence of iodide in the TSH-
stimulated cells probably results in an unbalanced state of sulfate transpo
rt.