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Effects of Estrogen on Tight Junctional Resistance in Cultured Human Umbilical Vein Endothelial CellsDepartments of Reproductive Biology, Pathology, and Physiology and Biophysic, Case Western Reserve University School of Medicine. Cleverand, Ohio; Department of Ob-Gyn, Division of Reproductive Endocrinology and Infertility, USC/LAC, Women's and Children's Hospital, Room IM2, 1240 North Mission Road, Los Angeles. CA 90033
Departments of Reproductive Biology, Pathology, and Physiology and Biophysic, Case Western Reserve University School of Medicine, Cleverand, Ohio
Departments of Reproductive Biology, Pathology. and Physiology and Biophysic, Case Western Reserve University School of Medicine, Cleverand, Ohio; University MacDonald Women's Hospital, University Hospitals of Cleveland, 11100 Euclid Avenue, Cleveland, OH 44106 gig{at}po.cwru.edu Objective: To study the effects of estrogen on transendothelial paracellular permeability in women. Methods: Human umbilical vein endothelial cells (HUVEC) obtained from women were grown on filters. The paracellular permeability characteristics were determined in terms of changes in the prmeability to the polar acid pyranine (Ppyr) and as changes in the transendothelial electrical resistance (RTE). Tight junctional resistance characteristics were assayed by lowering luminal NaCl and measuring the dilution potential, and were expressed as the ratio of monion mobility uCl/uNa (cation selectivity). Results: Low extracellular calcium and hyperosmolarity increased Ppyr and decreased RTE. The former but not the latter condition abolished the endothelium-specific cation selectivity. Treatment with 10 nM of estradiol-17ß had no effect on RTE, but it increased the cation selectivity. The effect of estradiol required 1-6 hours' incubation with the hormone; it was dose dependent and saturable, with a median effective concentration of estradiol of 1 nM. Diethylstilbestrol, but not estriol, could mimic the effect of estradiol, and the estrogen rectpro antagonist ICI-182,780 blocked it. Conclusion: Cultured HUVEC cells from patent tight junctions. Estrogens increase the cation selectivity across HUVEC cultures. The effect of estrogen may be mediated by an estrogen receptor. These effects may be important for vasculoprotection in cases of sudden changes in ions levels across the capillary wall, such as ischemia or reperfusion.
Key Words: Tight junctions paracellular permeability sex hormones microcirculation
Journal of the Society for Gynecologic Investigation, Vol. 5, No. 5,
260-270 (1998) |
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