Purpose: The aim of this study was to investigate the effect of unoprostone isopropyl (UF-
021) on Ca2+ release-activated Ca2+ (CRAC) currents in cultured monkey trabecular meshwork (TM) cells and to compare the inhibitory effects on CRAC in cultured monkey ciliary
muscle (CM) cells.
Methods: Both TM and CM cells were isolated from monkey eyes, and each was grown in
monolayer cell cultures. To measure changes in intracellular Ca2+ concentrations ([Ca2+]i),
both types of cells were labeled with fluo-3 acetoxymethylester (AM) as a calcium indicator
for 30 min at 25°C and imaged with a confocal laser scanning microscope. After depletion of
the intracellular Ca2+ stores with 1 µM thapsigargin and 1 mM EGTA containing Ca2+-free external solution, exposure to 2 mM Ca2+-containing external solution induced a sudden increase
in [Ca2+]i, which was defined as the CRAC current.
Results: In both TM and CM cells, CRAC currents were observed and were well suppressed
by unoprostone-free acid (M1 metabolite). In the TM cells, 3 µM M1 metabolite suppressed
the CRAC current. In contrast, in the CM cells, the CRAC current was suppressed by 100 µM
M1 metabolite, but not by 10 µM or less. The half maximal inhibition concentration of M1
metabolite was 24.8 ± 9.8 µM in TM cells and 183 ± 30.6 µM in CM cells.
Conclusions: These findings indicate that there are CRAC channels in both TM and CM
cells, and the influx of [Ca2+]i through the CRAC channels is suppressed by M1 metabolite.
The inhibitory effect of M1 metabolite on CRAC currents was more prominent in TM cells
than in CM cells. Suppression of the Ca2+ influx through CRAC channels by M1 metabolite
is thought to regulate muscle tone in TM and CM cells. Therefore, CRAC inhibition by M1
metabolite may contribute to reduction of intraocular pressure.
