scholarly journals Effects of Follicle-Stimulating Hormone on Intermediate Filaments and Cell Division of Sertoli Cells of Fetal Rat Testis in Culture.

1998 ◽  
Vol 60 (1) ◽  
pp. 35-39 ◽  
Author(s):  
Motoki SASAKI ◽  
Masako YAMAMOTO ◽  
Kazuyoshi ARISHIMA ◽  
Yasunobu EGUCHI
Neonatology ◽  
2000 ◽  
Vol 78 (1) ◽  
pp. 48-52 ◽  
Author(s):  
Motoki Sasaki ◽  
Masako Yamamoto ◽  
Kazuyoshi Arishima ◽  
Yasunobu Eguchi

Endocrinology ◽  
1993 ◽  
Vol 133 (5) ◽  
pp. 2313-2318 ◽  
Author(s):  
L Lecerf ◽  
V Rouiller-Fabre ◽  
C Levacher ◽  
C Gautier ◽  
J M Saez ◽  
...  

Endocrinology ◽  
1982 ◽  
Vol 110 (5) ◽  
pp. 1535-1541 ◽  
Author(s):  
MASATOSHI MITA ◽  
J. MICHAEL PRICE ◽  
PETER F. HALL

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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