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Regulation of inositol phosphate levels by prostaglandins in cultured endometrial cells

Journal Article · · J. Cell. Physiol.; (United States)
Stimulation of cultured rabbit endometrial cells by one of the rabbit endometrial cell culture proliferation factors, prostaglandin F/sub 2//sub ..cap alpha../ (PGF/sub 2//sub ..cap alpha../), resulted in a very rapid increase in the intracellular levels of (/sup 3/H)-inositol triphosphate (IP/sub 3/), (/sup 3/H)-inositol biphosphate (IP/sub 2/), and (/sup 3/H)-inositol monophosphate (IP/sub 1/) in cells prelabeled with (/sup 3/H)-inositol. These increases in inositol phosphate levels were detected in periods of stimulation as short as 30 seconds, reached a maximum by 1 1/2-2 min and declined to control levels by 6-10 min. The stimulation was dose-dependent with maximal increases observed near 10/sup -6/ M PGF/sub 2//sub ..cap alpha../. The cholinergic agent, carbachol, also led to time and dose-independent increases in IP/sub 3/. Lithium, cadmium, silver, copper, and zinc ions had no effect either on the breakdown of IP/sub 3/ or on the accumulation of IP/sub 1/. In contrast, vanadate at 10/sup -6/ or 10/sup -5/ M did lead to a decrease in the breakdown of IP/sub 1/ and a concomitant increase in IP/sub 1/, IP/sub 2/, and IP/sub 3/. PGF/sub 2//sub ..cap alpha../ was found previously to induce an increase in rabbit endometrial cell DNA synthesis which was inhibited by concomitant or prior addition of prostaglandin E/sub 1/ (PGE/sub 1/). PGE/sub 1/, in a dose-dependent manner, was found to inhibit the observed IP/sub 3/ increase by PGF/sub 2//sub ..cap alpha../ at 1 1/2 min of stimulation. PGF/sub 2//sub ..cap alpha../ treated and control cultures did not differ in cAMP 3 or cGMP levels, cellular /sup 45/Ca uptake, nor cellular /sup 22/Na uptake. The authors propose that P/sub 3/ may be one of the intracellular messenger(s) synthesized following the treatment of rabbit endometrial cell cultures with the proliferation agent PGF/sub 2//sub ..cap alpha../ and that it may play a crucial role with cAMP in growth regulation.
Research Organization:
Univ. of Colorado Health Sciences Center, Denver
OSTI ID:
6898682
Journal Information:
J. Cell. Physiol.; (United States), Journal Name: J. Cell. Physiol.; (United States) Vol. 128:1; ISSN JCLLA
Country of Publication:
United States
Language:
English

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