Metabolic responses of Sertoli cells in culture to various concentrations of follicle stimulating hormone and cholera toxin

1978 ◽  
Vol 56 (9) ◽  
pp. 875-879 ◽  
Author(s):  
Irving B. Fritz ◽  
Michael D. Griswold ◽  
B. Gregory Louis ◽  
Jennifer H. Dorrington

The concentration of cholera toxin required for half-maximal stimulation of cAMP production by Sertoli cell enriched cultures (4.48 × 10−2 μg/ml) is greater than that required for half-maximal stimulation of 17β-estradiol synthesis from testosterone (2.34 × 10−4 μg/ml), [3H]thymidine incorporation into DNA (1.48 × 10−5μg/ml), or androgen binding protein production (2.43 × 10−6 μg/ml). The same relative dose response hierarchy was obtained with respect to stimulation of Sertoli cells with follicle stimulating hormone (FSH) preparations. Again, highest concentrations were required to elicit maximal cAMP production. The data are discussed in relation to an apparent paradox: If cAMP is the mediating 'second messenger' following stimulation by FSH or cholera toxin, why should highest concentrations of these agents be required to elicit 50% of maximal cAMP levels?

1978 ◽  
Vol 89 (1) ◽  
pp. 166-172 ◽  
Author(s):  
T. J. Weiss ◽  
D. T. Armstrong ◽  
J. E. A. McIntosh ◽  
R. F. Seamark

ABSTRACT Theca and granulosa tissues isolated from sheep ovarian follicles of different sizes were incubated in the presence of human chorionic gonadotrophin (HCG; 5 IU/ml) or follicle stimulating hormone (FSH; 5 μg NIH-FSH-S11/ml) for 40 min. Changes in the total amounts of cyclic 3′,5′-adenosine monophosphate (cAMP) were used as an index of the responsiveness of these preparations to the hormones. Thecal tissue of both large (4–6 mm in diameter) and small (1–3 mm) follicles responded similarly to gonadotrophins. Granulosa cells from small follicles failed to respond to stimulation by HCG. FSH, however, consistently increased cAMP production in comparison with controls or cells treated with HCG. Granulosa cells of large follicles responded to both HCG and FSH.


Author(s):  
O. N Nwankudu

Follicle Stimulating Hormone (FSH) is a polypeptide hormone secreted by the cells of the anterior pituitary whose primary function is stimulation of ovarian follicle to grow and mature in females. Additionally, FSH stimulates the granulosa cells in the ovarian follicle to synthesize aromatase which converts androgen produced by the thecal cells to estradiol. Estradiol in the blood primes the hypothalamus to produce stronger pulses of Gonadotropin Releasing Hormone (GnRH) leading to secretion of Luteinizing hormone (LH). Then, LH causes ovulation and the developmentof corpus luteum. But, in the males, FSH stimulates the Sertoli cells to secret Androgen Binding Protein (ABP) which concentrates local testosterone leading to stimulation of spermatogenesis. However, FSH has been identified in many angiogenic vasculature of many tumors. The review tries to bring out FSH in reproduction and pathology as well as reveal certain solutions which may be useful in infertility and oncogenic therapy.


1993 ◽  
Vol 155 (1) ◽  
pp. 68-74 ◽  
Author(s):  
Pellegrino Rossi ◽  
Susanna Dolci ◽  
Cristina Albanesi ◽  
Paola Grimaldi ◽  
Rossana Ricca ◽  
...  

1991 ◽  
Vol 125 (3) ◽  
pp. 280-285 ◽  
Author(s):  
J. Alan Talbot ◽  
Ann Lambert ◽  
Robert Mitchell ◽  
Marek Grabinski ◽  
David C. Anderson ◽  
...  

Abstract We have investigated the role of Ca2+ in the control of FSH-induced estradiol secretion by Sertoli cells isolated from 8-10 days old rats. Exogenous Ca2+ (4-8 mmol/1) inhibited FSH-stimulated E2 secretion such that, with 8 mmol/l Ca2+ and FSH (8 IU/l) E2 secretion decreased from 2091±322 to 1480±84 pmol/l (p<0.002), whilst chelation of Ca2+ in the culture medium with EGTA (3 mmol/l) increased E2 secretion from 360±45 to 1242±133 pmol/l) in the absence of FSH. Further, EGTA (3 mmol/l) markedly potentiated FSH (8 IU/l), forskolin (1 μmol/l) and dibutyryl cAMP (1 mmol/l)-stimulated E2 secretion. Addition of the Ca2+ ionophores, ionomycin (2-5 μmol/l) and A23187 (2 μmol/l), inhibited FSH (8 IU/l)-stimulated E2 secretion by >80%. The effect of ionomycin was totally reversible, whereas that of A23187 was irreversible. Ionomycin (5 μmol/l) had no effect on EGTA-induced E2 secretion in the absence of FSH, but reduced EGTA-provoked E2 secretion by 59% in the presence of FSH (8 IU/l). Similarly, forskolin- and dibutyryl cAMP-provoked E2 production was inhibited 46-50% by ionomycin (5 μmol/l). We conclude that FSH-induced E2 secretion from immature rat Sertoli cells is modulated by intra- and extracellular Ca2+.


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