STUDIES ON THE MICROHETEROGENEITY OF CHORIONIC-GONADOTROPIN SECRETED BY THE HUMAN CYTOTROPHOBLAST IN CULTURE

被引:14
作者
ULLOAAGUIRRE, A
MENDEZ, JP
CRAVIOTO, A
GROTJAN, E
DAMIANMATSUMURA, P
ESPINOZA, R
机构
[1] Department of Reproductive Biology, National Institute of Nutrition Salvador Zubiran, Tlalpan 14000, Mexico D.F.
[2] Department of Animal Science, University of Nebraska, Lincoln, NE
[3] Department of Reproductive Biology, Universidad Autonoma Metropolitana-Iztapalapa, Mexico D.F.
关键词
Culture; Cytotrophoblast; Differentiation; HCG;
D O I
10.1093/oxfordjournals.humrep.a137164
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
In the present study, we investigated the biological characteristics of different molecular forms of chorionic gonadotrophin (HCG) secreted by the human cytotrophoblast during its morphological and functional differentiation in culture. Highly purified cytotrophoblasts were prepared from term placentae and cultured for 24 to 96 h in the absence or presence of 8-bromo-3',5'-cAMP. Media were collected at 24 h intervals and the secreted isofonms of HCG were then separated by polyacrylamlde gel isoelectric focusing (pH range 8.0-3.0) and quantified by radloimmunoassay. The secretion of HCG was significantly increased by 8-bromo-cAMP (from 23.5 ± 6.3 ng/ml at 24 h to 1619 ± 835.8 ng/ml at 96 h; controls, 9.3 ± 0.1 ng/ml at 24 h and 26.6 ± 3.5 ng/ml at 96 h, X&macr; ± SD). Analysis of media concentrates from cAMP-stimulated cultures by isoelectric focusing revealed the presence of several distinct peaks of HCG within the pH range of 7.3-4.8; major peaks consistently exhibited isoelectric points (pI) of 7.3-7.0 (peak 1), 5.6-5.4 (peak 2) and 5.1-4.8 (peak 3). The relative HCG content of the most acidic peak (as % of total on gel) progressively increased with time of exposure to the cAMP analogue (from 19.8 ± 1.6% at 24 h to 34.4 ± 4.3% at 96 h, X&macr; ± SEM, P < 0.01). HCG recovered from peak 1 exhibited the highest receptor-binding capacity and in-vitro biological potency. Removal of sialic acid residues from purified HCG (pI of 5.2) by neuraminidase digestion resulted in the production of several peaks of immunoactive HCG with less acidic pIs (6.5, 6.7, 6.9 and 7.1). Only in those concentrates from control media at 72 and 96 h was it possible to identify some peaks of HCG immunoactivity after isoelectric focusing. These components exhibited pIs of 7.8-5.2 and were dissimilarly distributed over the 24 h period analysed. These results demonstrate that the human cytotrophoblast in vitro secretes chorionic gonadotrophin in different molecular forms, thus indicating that some of the previously identified forms of HCG in serum are actually produced by the placenta and then released to the periphery. © 1990 Oxford University Press.
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页码:661 / 669
页数:9
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共 41 条
[1]  
Adams T.E., Adams B.M., Watson J.G., Secretory dynamics of bioactive and immunoactive LH during the oestrous cycle in the sheep, J. Reprod. Fertil, 79, pp. 555-563, (1987)
[2]  
Bex F.J., Corbin A., Luteinizing hormone-releasing hormone (LHRH) and LHRH agonist termination of pregnancy in hypo- physectomized rats: Extrapituitary site of action, Endocrinology, 10, pp. 273-280, (1981)
[3]  
Birken S., Armstrong E.G., Kolks M.A.G., Cole L.A., Agosto G.M., Knchevsky A., Vaitukaitis J.L., Canfield R.E., Structure of the human chorionic gonadotropin b-subunit fragment from pregnancy urine, Endocrinology, 12, pp. 572-583, (1988)
[4]  
Blithe D.L., Akar A.H., Wehmann R.E., Nisula B.C., Purification of β -core fragment from pregnancy urine and demonstration that its carbohydrate moieties differ from those of native human chorionic gonadotropin-β. Endocrinology, Endocrinology, 12, (1988)
[5]  
Blum W.F.P., Riegelbauer G.K., Gupta D., Heterogeneity of rat FSH by chromatofocusing: Studies on in-vitro bioactivity of pituitary FSH forms and effect of neuraminidase treatment, J. Endocrinol, 17, (1985)
[6]  
Brossmer R., Merz W.E., Hilgenfeldt U., Separation of purified human chorionic gonadotropin into single bands by isoelectric focusing and their characterization, FEBS Lett, 18, pp. 112-114, (1971)
[7]  
Charming C.P., Sakai C.N., Bahl O.P., Role of carbohydrate residues of human chorionic gonadotropin in binding and stimulation of adenosine 3', 5'-monophosphate accumulation by porcine granulosa cells, Endocrinology, 10, pp. 341-348, (1978)
[8]  
Cole L.A., Birken S., Origin and occurrence of human chorionic gonadotropin β-subunit core fragment. Mol, Endocrinol, (1988)
[9]  
Dearden L., Ockleford C.D., Structure of human trophoblast: Correlation with function, Biology of Trophoblast, (1983)
[10]  
De Lean A.P., Munson P.J., Rodbard D., Simultaneous analysis of families of sigmoidal curves: Application to bioassay, radioligand assay and physiological dose—response curves, Am. J. Physiol, 23, pp. EE97-E102, (1978)