We report for the first time that cultured lens epithelial cell layers and
rabbit lenses in vitro transport fluid. Layers of the alpha TN4 mouse cell
line and bovine cell cultures were grown to confluence on permeable membr a
ne inserts. Fluid movement across cultured layers and excised rabbit lenses
was determined by volume clamp (37 degrees C). Cultured layers transported
fluid from their basal to their apical sides against a pressure head of 3
cmH(2)O. Rates were (in mu l . h(-1) . cm(-2)) 3.3 +/- 0.3 for alpha TN4 ce
lls (n = 27) and 4.7 +/- 1.0 for bovine layers (n = 6). Quinidine, a blocke
r of K+ channels, and p-chloromercuribenzenesulfonate and HgCl2, inhibitors
of aquaporins, inhibited fluid transport. Rabbit lenses transported fluid
from their anterior to their posterior sides; against a 2.5-cmH(2)O pressur
e head at 10.3 +/- 0.62 mu l . h(-1) . lens(-1) (n = 5) and along the same
pressure head at 12.5 +/- 1.1 mu l . h(-1) . lens(-1) (n = 6). We calculate
that this flow could wash the lens extracellular space by convection about
once every 2 h and therefore might contribute to lens homeostasis and tran
sparency.