Sorbitol plays a major role in the maintenance of cell volume and functiona
l integrity of several renal cells. Sorbitol synthesis takes place in inner
collecting duct cells, whereas sorbitol dehydrogenase activity, which cata
lyzes the degradation of sorbiotol to fructose, could mainly be detected in
renal inner medullary interstitial cells. Therefore, we supposed that inte
rstitial cells would require a sorbitol transport into the cells. However,
such a transport system has not yet been described. Therefore, we have char
acterized the uptake of sorbitol in immortalized interstitial TK-173 cells,
which were derived from human renal fibroblasts. Comparable to fresh isola
ted renal fibroblasts of the rat, immortalized TK-173 cells have a high sor
bitol dehydrogenase activity. In this report, a temperature-dependent sorbi
tol uptake with saturation kinetics could be detected in immortalized TK-17
3 cells. The transport is characterized by a high velocity (V-max 84 mmol/l
x h) and an apparent K-m of 10 mmol/l. The sorbitol uptake is independent
of membrane potential, sodium, and chloride. Altogether, the physiological
characteristics of this sorbitol transport are different from those of the
osmotically regulated sorbitol efflux from epithelial cells. These results
provide evidence that TK-173 cells derived from renal fibroblasts have a sp
ecific sorbitol transport. Furthermore, these data suggest a cooperation be
tween epithelial and interstitial cells concerning osmoregulation. Copyrigh
t (C) 2001 S. Karger AG, Basel.