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Endocrinology, doi:10.1210/endo-106-3-849
Endocrinology Vol. 106, No. 3 849-858
Copyright © 1980 by the Endocrine Society.
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De Novo Synthesis and Secretion of Heterogeneous Forms of Human Chorionic Gonadotropin and Its Free {alpha}-Subunit in the Human Choriocarcinoma Clonal Cell Line JEG-3

DONNA J. DEAN, BRUCE D. WEINTRAUB and SAUL W. ROSEN

Clinical Endocrinology Branch, National Institute of Arthritis, Metabolism, and Digestive Diseases, National Institutes of Health Bethesda, Maryland 20205

Address requests for reprints to: Dr. Donna J. Dean, Clinical Endocrinology Branch, National Institutes of Health, Building 10, Room 8N315, Bethesda, Maryland 20205.

Abstract

The clonal human choriocarcinoma cell line JEG-3 secretes hCG and heterogeneous forms of its free {alpha}-subunit. We have studied the relationship of these forms in de novo biosynthesis experiments. Cells at near confluence were labeled with [35S]methionine by continuous (10-min to 24-h exposure) and by pulse-chase (5-min exposure, 10-min to 4-h chase) techniques. Media and cell lysates, chromatographed on Sephadex G-100 or, after reduction, electrophoresed on 12–20% gradient sodium dodecyl sulfate-polyacrylamide slab gels (SDSPAGE), were analyzed by immunoprecipitation with antisera to hCG-{alpha} and hCG-β. The intracellular labeled free {alpha}-subunit observed in lysates at all time points of either continuous or pulsechase experiments was the same size or was slightly smaller on G-100 (apparent mol wt, 21,600 ± 3,900) than urinary standard {alpha}-subunit (CR119{alpha}; apparent mol wt, 22,700 ± 1,500) and also somewhat smaller on SDS-PAGE (apparent mol wt, 19,400 ± 600) than urinary standard {alpha}-subunit (apparent mol wt, 20,200 ± 1,100). However, the predominant form of secreted free asubunit, at chase times as early as 30 min, migrated with a higher apparent molecular weight in both systems (SDS-PAGE, 22,100 ± 400; G-100,29,300 ± 2,700). We have not observed this secreted large free {alpha}-subunit in the cell lysate, and our data suggest that the small intracellular {alpha}-subunit is a precursor of the larger secreted {alpha}-subunit and not vice versa. The β-subunit of secreted hCG was somewhat larger (apparent mol wt, 31,500 ± 1,000) on SDS-PAGE than standard β-subunit (CR119-2β- and CR115β-; apparent mol wt, 29,900 ± 1,900). Secreted intact hCG migrated with urinary standard hCG (CR119) on G-100, but analysis of 35S-labeled intracellular hCG was complicated by co-precipitating large mol wt proteins. De novo synthesis and secretion of a large form of free {alpha}-subunit as well as a large β-subunit in hCG may be due to posttranslational oligosaccharide addition during the secretory process. (Endocrinology 106: 849, 1980)

Received April 4, 1979.







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