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Journal of Clinical Endocrinology & Metabolism Vol. 44, No. 6 1032-1037
doi:10.1210/jcem-44-6-1032
Copyright © 1977 by the Endocrine Society.
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Prostaglandin F2{alpha} Binding Sites in Human Corpora Lutea

CH. V. RAO, LARRY P. GRIFFIN and FRED R. CARMAN, JR.

Department of Obstetrics and Gynecology, University of Louisville, School of Medicine Louisville, Kentucky 40202

The specific binding of 3H-prostaglandin (PG) F2{alpha} to homogenates of human corpora lutea of the cycle and ectopic pregnancy was examined. Corpora lutea of ectopic pregnancy bound significantly (P < 0.01) higher amounts of added 3H-PGF2{alpha} than those of the luteal phase of the menstrual cycle. The 3H-PGF2{alpha} binding sites in corpora lutea of ectopic pregnancy were further characterized. The specific 3H-PGF2{alpha} binding to all corpora lutea was biphasic: all contained sites of 10–8M Kd, two also had sites of Kd < 10–8M while the other contained sites of 10–9M Kd. PGs competed for 3H-PGF2a binding in the following order: PGF2{alpha} > 15(S)15 methyl PGF2{alpha} > PGF1{alpha} > PGE2 > PGE1 > PGB1 > PGA1. Binding was time and temperature dependent; maximum binding was obtained by 1 h at 22 C; at 38 C, the initial binding was high but rapidly declined after 30 min of incubation. A cationic requirement for 3H-PGF2{alpha} binding is suggested by the findings that the addition of EDTA severely reduced the binding which was reversed by concomittant addition of Ca2% to the medium. Preincubation of homogenates with proteolytic enzymes drastically reduced the binding, suggesting that the binding sites are protein in nature.

Supported by grants from the Population Council, M75.16 and from NIH, HD09557

This work was presented in part at the Fifty-eighth Annual Meeting of the Endocrine Society (24).

Received September 20, 1976.




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Copyright © 1977 by The Endocrine Society