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Am J Physiol Cell Physiol 285: C642-C651, 2003. First published April 30, 2003; doi:10.1152/ajpcell.00587.2002
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MEMBRANE TRANSPORTERS, ION CHANNELS, AND PUMPS

Control of ascorbic acid efflux in rat luteal cells: role of intracellular calcium and oxygen radicals

John R. Pepperell,1,2 D. Marshall Porterfield,3 David L. Keefe,1 Harold R. Behrman,2 and Peter J. S. Smith3

3BioCurrents Research Center, Marine Biological Laboratory, Woods Hole, Massachusetts 02543; 1Department of Obstetrics/Gynecology, Women and Infants Hospital of Rhode Island, Providence, Rhode Island 02905; and 2Department of Obstetrics/Gynecology, Yale Medical School, New Haven, Connecticut 06511

Submitted 16 December 2002 ; accepted in final form 17 April 2003

In luteal cells, prostaglandin (PG)F2a mobilizes intracellular calcium concentration ([Ca]i), generates reactive oxygen species (ROS), depletes ascorbic acid (AA) levels, inhibits steroidogenesis, and ultimately induces cell death. We investigated the hypothesis that [Ca]i mobilization stimulates ROS, which results in depletion of cellular AA in rat luteal cells. We used a self-referencing AA-selective electrode that noninvasively measures AA flux at the extended boundary layer of single cells and fluorescence microscopy with fura 2 and dichlorofluorescein diacetate (DCF-DA) to measure [Ca]i and ROS, respectively. Menadione, a generator of intracellular superoxide radical (), PGF2a, and calcium ionophore were shown to increase [Ca]i and stimulate intracellular ROS. With calcium ionophore and PGF2a, but not menadione, the generation of ROS was dependent on extracellular calcium influx. In unstimulated cells there was a net efflux of AA of 121.5 ± 20.3 fmol · cm1 · s1 (mean ± SE, n = 8), but in the absence of extracellular calcium the efflux was significantly reduced (10.3 ± 4.9 fmol · cm1 · s1; n = 5, P < 0.05). PGF2a and menadione stimulated AA efflux, but calcium ionophore had no significant effect. These data suggest two AA regulatory mechanisms: Under basal conditions, AA efflux is calcium dependent and may represent recycling and maintenance of an antioxidant AA gradient at the plasma membrane. Under luteolytic hormone and/or oxidative stress, AA efflux is stimulated that is independent of extracellular calcium influx or generation of ROS. Although site-specific mobilization of calcium pools and ROS cannot be ruled out, the release of AA by PGF2a-stimulated luteal cells may occur through other signaling pathways.

luteolysis; apoptosis; self-referencing microelectrode



Address for reprint requests and other correspondence: J. R. Pepperell, Dept. of Pathology, Women & Infants Hospital of Rhode Island, 101 Dudley St., Providence, RI 02905 (E-mail: jpeppere{at}wihri.org).




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