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Department of Molecular Cell Biology, The Weizmann Institute of Science (K.H., A.D., C. S.-L., A.A.), Rehovot 76100, Israel; Department of Obstetrics and Gynecology, Kaplan Hospital (A.B.), Rehovot 76100, Israel; Department of Obstetrics and Gynecology, Fukui Medical University (K.H., Y.Y., F.K.), Fukui 910-1193, Japan; and Department of Oncology, Hadassah-Hebrew University Hospital (I.V.), Jerusalem 91120, Israel
Address all correspondence and requests for reprints to: Abraham Amsterdam, Department of Molecular Cell Biology, Weigmann Institute of Scince, Rehovot 761000, Israel. E-mail: lhamster{at}weizmann
We have established immortalized human granulosa cells by triple
transfection of primary cells obtained from in vitro
fertilization patients with SV40 DNA, Ha-ras oncogene,
and a temperature sensitive (ts) mutant of the tumor suppressor gene
p53 (p53val135). Forty-one clones were isolated, and their
steroidogenic responses were analyzed. While all the cell lines
proliferate rapidly and show only traces of progesterone production,
upon stimulation with 50 µM of forskolin (FK), which
elevates intracellular cAMP, they become steroidogenic as evidenced by
progesterone production. The steroidogenic response of the cell lines
was stable even after 20 generations and several cycles of freezing and
thawing. A highly responsive cell line (HO-23) was further examined for
characteristics of the steroidogenic response. Cells stimulated with FK
and 8-Br-cAMP produced high levels of pregnenolone, progesterone, and
20
-hydroxy-4-pregnen-3-one (20
-OH-progesterone) comparable with
amounts produced by highly differentiated primary human
granulosa-luteal cells. Hydrocortisone and dexamethasone highly augment
the cAMP-stimulated progesterone production, whereas testosterone and
PRL enhanced cAMP-induced progesterone synthesis only moderately.
Estradiol, insulin-like growth factor I, and insulin showed no
significant effect on cAMP-induced steroidogenesis. The phorbol ester
TPA, and basic fibroblast growth factor, dramatically suppress
cAMP-induced production of progesterone, whereas bovine corneal
endothelial cell ECM (BCE/ECM) enhanced cAMP-induced progesterone and
antagonized basic fibroblast growth factor suppression of cAMP-induced
steroidogenesis. Steroidogenic factor 1 (Ad4BP/SF-1) was expressed in
control cells, and its expression was augmented by FK, whereas the
steroidogenic acute regulatory protein showed low expression in the
nonstimulated cells but was clearly elevated upon cAMP stimulation and
was slightly decreased by TPA in cAMP-stimulated cells. Expression of
the electron carrier adrenodoxin (ADX), which is a part of the
cytochrome P450scc enzyme system, was very low in nonstimulated cells
but was dramatically elevated in FK- and 8-Br-cAMP-stimulated cells,
whereas no reduction of ADX was evident in cells costimulated with FK
and TPA. Immunocytochemical studies revealed a weak staining of ADX in
mitochrondria of nonstimulated cells and intensive staining in highly
clustered mitochondria of FK- or 8-Br-cAMP-stimulated cells. Only
moderate reduction in ADX staining was evident in cells costimulated
with FK and TPA. These unique cell lines can provide a useful model for
the investigation of induced steroidogenesis in human granulosa cells.
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