Abstract
A cultured rat ovarian cell line (31 A-F(2)) was used to study the effect of growth factors (epidermal growth factor [EGF] and fibroblast growth factor [FGF]), a survival factor (ovarian growth factor [OGF]), a hormone (insulin), and an iron-binding protein (transferring) on cell proliferation and steroid production under defined culture conditions. EGF and insulin were shown to be mitogenic (half-maximal response at 0.12 nM and 0.11 muM, respectively) for 31A-F(2) cells incubated in serum-free medium. EGF induced up to three doublings in the cell population, whereas insulin induced an average of one cell population doubling. FGF, OGF, and transferrin were found not to have any prominent effect on cell division when incubated individually with 31A-F(2) cells in serum-free medium. However, a combination of EGF, OGF, insulin, and transferrin stimulated cell division to the same approximate extent as cells incubated in the presence of 5 percent fetal calf serum. EGF or insulin did not significantly affect total cell cholesterol levels (relative to cells incubated in serum-free medium) when incubated individually with 31A-F(2) cells. However, cell cholesterol levels were increased by the addition of OGF (250 percent), FGF (370 percent), or a combination of insulin and EGF (320 percent). Progesterone secretion from 31A-F(2) cells was enhanced by EGF (25 percent), FGF (80 percent), and insulin (115 percent). However, the addition of a mitogenic mixture of EGF, OGF, insulin, and transferrin suppressed progesterone secretion 150 percent) below that of control cultures. These studies have permitted us to determine that EGF and insulin are mitogenic factors that are required for the growth of 31A-F(2) cells and that OGF and transferrin are positive cofactors that enhance growth. Also, additional data suggest that cholesterol and progesterone production in 31A-F(2) cells can be regulated by peptide growth factors and the hormone insulin.
Full Text
The Full Text of this article is available as a PDF (605.8 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Baker J. B., Barsh G. S., Carney D. H., Cunningham D. D. Dexamethasone modulates binding and action of epidermal growth factor in serum-free cell culture. Proc Natl Acad Sci U S A. 1978 Apr;75(4):1882–1886. doi: 10.1073/pnas.75.4.1882. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cantley T. C., Garverick H. A., Bierschwal C. J., Martin C. E., Youngquist R. S. Hormonal responses of dairy cows with ovarian cysts to GnRH. J Anim Sci. 1975 Dec;41(6):1666–1673. doi: 10.2527/jas1975.4161666x. [DOI] [PubMed] [Google Scholar]
- Channing C. P., Tsafriri A. Mechanism of action of luteinizing hormone and follicle-stimulating hormone on the ovary in vitro. Metabolism. 1977 Apr;26(4):413–468. doi: 10.1016/0026-0495(77)90108-1. [DOI] [PubMed] [Google Scholar]
- Channing C. P., Tsai V., Sachs D. Role of insulin, thyroxin and cortisol in luteinization of porcine granulosa cells grown in chemically defined media. Biol Reprod. 1976 Sep;15(2):235–247. doi: 10.1095/biolreprod15.2.235. [DOI] [PubMed] [Google Scholar]
- Clark J. L., Jones K. I., Gospodarowicz D., Sato G. H. Growth response to hormones by a new rat ovary cell line. Nat New Biol. 1972 Apr 12;236(67):180–181. doi: 10.1038/newbio236180a0. [DOI] [PubMed] [Google Scholar]
- Gospodarowicz D., Ill C. R., Birdwell C. R. Effects of fibroblast and epidermal growth factors on ovarian cell proliferation in vitro. I. Characterization of the response of granulosa cells to FGF and EGF. Endocrinology. 1977 Apr;100(4):1108–1120. doi: 10.1210/endo-100-4-1108. [DOI] [PubMed] [Google Scholar]
- Gospodarowicz D., Ill C. R., Birdwell C. R. Effects of fibroblast and epidermal growth factors on ovarian cell proliferation in vitro. II. Proliferative response of luteal cells to FGF but not EGF. Endocrinology. 1977 Apr;100(4):1121–1128. doi: 10.1210/endo-100-4-1121. [DOI] [PubMed] [Google Scholar]
- Gospodarowicz D., Moran J. S. Growth factors in mammalian cell culture. Annu Rev Biochem. 1976;45:531–558. doi: 10.1146/annurev.bi.45.070176.002531. [DOI] [PubMed] [Google Scholar]
- Hayashi I., Larner J., Sato G. Hormonal growth control of cells in culture. In Vitro. 1978 Jan;14(1):23–30. doi: 10.1007/BF02618171. [DOI] [PubMed] [Google Scholar]
- Jordan A. W., 3rd, Caffrey J. L., Niswender G. D. Catecholamine-induced stimulation of progesterone and adenosine 3',5'-monophosphate production by dispersed ovine luteal cells. Endocrinology. 1978 Aug;103(2):385–392. doi: 10.1210/endo-103-2-385. [DOI] [PubMed] [Google Scholar]
- Kowal J. ACTH and the metabolism of adrenal cell cultures. Recent Prog Horm Res. 1970;26:623–687. doi: 10.1016/b978-0-12-571126-5.50020-0. [DOI] [PubMed] [Google Scholar]
- Levine E. M., Thomas L., McGregor D., Hayflick L., Eagle H. Altered nucleic acid metabolism in human cell cultures infected with mycoplasma. Proc Natl Acad Sci U S A. 1968 Jun;60(2):583–589. doi: 10.1073/pnas.60.2.583. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rudel L. L., Morris M. D. Determination of cholesterol using o-phthalaldehyde. J Lipid Res. 1973 May;14(3):364–366. [PubMed] [Google Scholar]
- Thorneycroft I. H., Stone S. C. Radioimmunoassay of serum progesterone in women receiving oral contraceptive steroids. Contraception. 1972 Feb;5(2):129–146. doi: 10.1016/0010-7824(72)90024-8. [DOI] [PubMed] [Google Scholar]
- Wyche J. H., Noteboom W. D. Requirement of a specific factor for the multiplication of ovarian cells in serum-free medium. Exp Cell Res. 1977 Nov;110(1):135–141. doi: 10.1016/0014-4827(77)90279-8. [DOI] [PubMed] [Google Scholar]
- Zeleznik A. J., Hillier S. G., Knazek R. A., Ross G. T., Coon H. G. Production of long term steroid-producing granulosa cell cultures by cell hybridization. Endocrinology. 1979 Jul;105(1):156–162. doi: 10.1210/endo-105-1-156. [DOI] [PubMed] [Google Scholar]
- Zlatkis A., Zak B. Study of a new cholesterol reagent. Anal Biochem. 1969 Apr 11;29(1):143–148. doi: 10.1016/0003-2697(69)90017-7. [DOI] [PubMed] [Google Scholar]
