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J. Biol. Chem., Vol. 255, Issue 3, 1000-1007, Feb, 1980
RW Ruddon, CA Hanson, AH Bryan, GJ Putterman, EL White, F Perini, KS Meade and PH Aldenderfer
The synthesis and secretion of human chorionic gonadotropin (hCG) subunits
have been studied by pulse-chase techniques in JAR choriocarcinoma cells,
which produce both the alpha and beta subunits of hCG "eutopically," that
is, as part of their expected repertoire of gene products, and in three
cell lines that produce either alpha or beta subunit "ectopically." JAR
cells contain two intracellular forms of the alpha subunit (Mr = 15,000 and
18,000) and of the beta subunit (Mr = 18,000 and 24,000) but do not
accumulate fully processed, "mature" alpha (Mr = 22,000) or beta (Mr =
34,000) subunits during chase of pulse-labeled cells. Mature subunits,
however, are secreted into the culture medium during this time. Thus,
secretion of mature subunits appears to occur rapidly after processing of
the intracellular forms. Two cell lines that ectopically secrete alpha but
not beta subunit, ChaGo bronchogenic carcinoma cells and HeLa S3 cervical
carcinoma cells, also contain the Mr = 15,000 and 18,000 intracellular
forms of alpha subunit and appear to accumulate mature alpha subunit
intracellularly. The CBT cell line, derived from a glioblastoma multiforme,
produces the Mr = 18,000 and 24,000 intracellular forms of beta subunit
with no evidence for alpha subunit synthesis or secretion. These four cell
lines should provide "biologic reagents" for the further study of alpha and
beta subunit processing and secretion.
Synthesis and secretion of human chorionic gonadotropin subunits by cultured human malignant cells
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