scholarly journals Status of the down-regulated canine testis using two different GNRH agonist implants in comparison with the juvenile testis

Reproduction ◽  
2013 ◽  
Vol 146 (6) ◽  
pp. 517-526 ◽  
Author(s):  
S Goericke-Pesch ◽  
M Gentil ◽  
A Spang ◽  
M P Kowalewski ◽  
K Failing ◽  
...  

Testicular function in the dog was down-regulated using two different GNRH agonist implants, with adult and juvenile testes serving as controls. Treatment resulted in an increased percentage of the interstitial area and decreased area of Leydig cell nuclei. Expression of StAR and the steroidogenic enzymes cytochrome P450 side-chain cleavage enzyme (P450scc, CYP11A1) and cytochrome P450 17α-hydroxylase-17,20-lyase (P450c17, CYP17A1) in Leydig cells was blocked at the mRNA and protein level, showing no differences between the two agonists. Staining for androgen receptor (AR) by immunohistochemistry was positive in Sertoli, Leydig and peritubular cells and some spermatogonia, with in situ hybridization confirming expression in Sertoli cells. At the mRNA level, expression of AR was not affected; however, translation was blocked (reduced percentage of AR-positive Sertoli cells), with the number of nuclei in basal position being decreased. In the juvenile testes, mRNA expression of StAR, CYP11A1 and CYP17A1 was higher compared with the other groups but distinctly lower for the AR. At the protein level, the expression was at the limit of detection for StAR; AR-positive Sertoli cells were not detected. Our observations show that the down-regulated testis is different from the juvenile one rather resembling the testicular status in seasonal breeders out of season.

1996 ◽  
Vol 109 (4) ◽  
pp. 773-776 ◽  
Author(s):  
A.C. Chandley ◽  
R.M. Speed ◽  
A.R. Leitch

Using whole chromosome painting probes for human chromosomes 3,7,8,13,17 and 21 and X and the probe pHY2.1 for the Y chromosome coupled with fluorescent in situ hybridization (FISH) analysis, the distribution of chromosomes is reported in nuclei of Sertoli cells of the adult testis and in stimulated blood lymphocytes. The distribution of chromosomes in the two cell types is significantly different. A strong tendency for each pair of homologues to pair is inferred from the observation of only a single detectable signal in the majority of Sertoli cell nuclei. The sex chromosomes, by contrast, give two clearly separated signals. Interphase nuclei in dividing blood lymphocytes, analysed as controls, also show mainly two separated signals for all non-acrocentric autosomal pairs, but acrocentric pairs no. 13 and 21 show some tendency to associate, probably reflecting satellite association.


Endocrinology ◽  
1999 ◽  
Vol 140 (4) ◽  
pp. 1936-1944 ◽  
Author(s):  
Minoru Takase ◽  
Kazuyoshi Ukena ◽  
Takeshi Yamazaki ◽  
Shiro Kominami ◽  
Kazuyoshi Tsutsui

2002 ◽  
Vol 19 (6) ◽  
pp. 673-678 ◽  
Author(s):  
Hideki Endo ◽  
Kazuo Okanoya ◽  
Thomas J. Park ◽  
Motoki Sasaki ◽  
Kentaro Tanemura ◽  
...  

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