The change of taurine transport in variable stress states through the inner blood-retinal barrier using in vitro model

Abstract

Taurine is the most abundant free amino acid in the retina and transported into retina via taurine transporter (TauT) at the inner blood-retinal barrier (iBRB). In the present study, we investigated whether the taurine transport at the iBRB is regulated by oxidative stress or disease-like state in a conditionally immortalized rat retinal capillary endothelial cell line (TR-iBRB) used as an in vitro model of iBRB. First, [3H]taurine uptake and efflux by TR-iBRB were regulated in the presence of extracellular Ca2+. [ 3H]Taurine uptake was inhibited and efflux was enhanced under Ca 2+ free condition in the cells. In addition, oxidative stress inducing agents such as tumor necrosis factor-α (TNF-α), lipopolysaccharide (LPS), diethyl maleate (DEM) and glutamate increased [ 3H]taurine uptake and decreased [3H]taurine efflux in TR-iBRB cells. Whereas, 3-morpholinosydnonimine (SIN-1), which is known to NO donor decreased [3H]taurine uptake. Lastly, TR-iBRB cells exposed to high glucose (25 mM) medium and the [3H]taurine uptake was reduced about 20% at the condition. Also, [3H]taurine uptake was decreased by cytochalasin B, which is known to glucose transport inhibitor. In conclusion, taurine transport in TR-iBRB cells is regulated diversely at extracellular Ca2+, oxidative stress and hyperglycemic condition. It suggested that taurine would play a role as a retinal protector in diverse disease states.