Rajkumar K, Bigsby R, Lieberman R, Gerschenson L E
Endocrinology. 1983 Apr;112(4):1490-8. doi: 10.1210/endo-112-4-1490.
Uteroglobin (UG) is a secretory protein produced by the rabbit endometrium and its production is increased during cell differentiation which occurs during early pregnancy or pseudopregnancy. In the present study, the optimal conditions for UG production by rabbit endometrial epithelial cells in culture were examined. Metabolic labeling studies showed the incorporation of [35S]methionine into UG molecules by the endometrial epithelial cells in culture. Accumulation of UG in culture media was linear for at least a period of 24 h. These cells do not catabolize exogenously added radiolabeled UG. Endometrial cells obtained from virgin female rabbits at different times after the administration of human CG (hCG) and put in culture were found to make different amounts of UG. The maximal UG production was found in cells taken from pseudopregnant rabbits 4 days after hCG administration. Cycloheximide (28 micrograms/ml) inhibited the production of UG by the cells in culture whereas actinomycin-D (5 micrograms/ml) and cordycipin (50 micrograms/ml) increased its production. Inhibition of DNA synthesis by hydroxyurea (10(-3) M) did not affect the UG production. The production of UG was significantly less when cells were cultured on attached or floating collagen gels as compared to cells grown on plastic Petri dishes. The amino acid content of Ham's F-12 medium was shown to be adequate for maximal UG production; lowering this amino acid concentration decreased the amount of UG accumulated in the medium over a 24-h period. Increasint the number of cultured cells per dish resulted in an increased UG production per cell.
子宫珠蛋白(UG)是一种由兔子宫内膜产生的分泌蛋白,在妊娠早期或假孕期间细胞分化过程中其产量会增加。在本研究中,检测了兔子宫内膜上皮细胞在培养条件下产生UG的最佳条件。代谢标记研究表明,培养的子宫内膜上皮细胞可将[35S]甲硫氨酸掺入UG分子中。UG在培养基中的积累在至少24小时内呈线性。这些细胞不会分解外源性添加的放射性标记UG。从给予人绒毛膜促性腺激素(hCG)后不同时间的未孕雌性兔获取子宫内膜细胞并进行培养,发现它们产生的UG量不同。在hCG给药后4天从假孕兔获取的细胞中发现UG产量最高。环己酰亚胺(28微克/毫升)抑制培养细胞产生UG,而放线菌素-D(5微克/毫升)和虫草素(50微克/毫升)则增加其产量。羟基脲(10^(-3) M)抑制DNA合成并不影响UG的产生。与在塑料培养皿中生长的细胞相比,当细胞在附着或漂浮的胶原凝胶上培养时,UG的产量明显较低。结果表明,Ham's F-12培养基中的氨基酸含量足以实现UG的最大产量;降低该氨基酸浓度会减少24小时内培养基中积累的UG量。增加每个培养皿中培养细胞的数量会导致每个细胞的UG产量增加。