Expression and localization of aromatase during fetal mouse testis development
- Caroline Borday†1, 2, 3,
- Jorge Merlet†1, 2, 3,
- Chrystèle Racine1, 2, 3 and
- René Habert1, 2, 3Email author
© Borday et al.; licensee BioMed Central Ltd. 2013
Received: 9 June 2013
Accepted: 9 September 2013
Published: 1 December 2013
Both androgens and estrogens are necessary to ensure proper testis development and function. Studies on endocrine disruptors have highlighted the importance of maintaining the balance between androgens and estrogens during fetal development, when testis is highly sensitive to environmental disturbances. This balance is regulated mainly through an enzymatic cascade that converts irreversibly androgens into estrogens. The most important and regulated component of this cascade is its terminal enzyme: the cytochrome p450 19A1 (aromatase hereafter). This study was conducted to improve our knowledge about its expression during mouse testis development.
By RT-PCR and western blotting, we show that full-length aromatase is expressed as early as 12.5 day post-coitum (dpc) with maximal expression at 17.5 dpc. Two additional truncated transcripts were also detected by RT-PCR. Immunostaining of fetal testis sections and of gonocyte-enriched cell cultures revealed that aromatase is strongly expressed in fetal Leydig cells and at variable levels in gonocytes. Conversely, it was not detected in Sertoli cells.
This study shows for the first time that i) aromatase is expressed from the early stages of fetal testis development, ii) it is expressed in mouse gonocytes suggesting that fetal germ cells exert an endocrine function in this species and that the ratio between estrogens and androgens may be higher inside gonocytes than in the interstitial fluid. Furthermore, we emphasized a species-specific cell localization. Indeed, previous works found that in the rat aromatase is expressed both in Sertoli and Leydig cells. We propose to take into account this species difference as a new concept to better understand the changes in susceptibility to Endocrine Disruptors from one species to another.
Les androgènes et les oestrogènes sont indispensables au développement et aux fonctions du testicule. Le testicule est particulièrement sensible aux perturbateurs endocriniens pendant le développement fœtal et beaucoup de perturbateurs endocriniens agissent en modifiant la balance oestrogènes/androgènes. Physiologiquement, cette balance est régulée par une cascade enzymatique qui convertit irréversiblement les androgènes en oestrogènes. Le composant principal de cette cascade est le cytochrome p450 19A1 (appelé couramment aromatase). Le but de ce travail a été d’étudier l’expression de l’aromatase testiculaire au cours du développement fœtal chez la souris.
En utilisant une approche par RT-PCR et par western blot, nous avons montré que l’aromatase est exprimée dès 12,5 jours post-conception (jpc) et que l’expression est maximum à 17,5 jpc. Deux transcripts tronqués ont également été détectés par RT-PCR. La localisation cellulaire de l’aromatase a été étudiée par immunohistologie et par immunomarquage après séparation des cellules testiculaires. Cette enzyme est très fortement exprimée dans les cellules de Leydig fœtales. Elle est également exprimée dans les gonocytes mais plus faiblement et à un niveau variable selon les cellules. En revanche, elle est indétectable dans les cellules de Sertoli.
En conclusion, cette étude montre pour la première fois chez la souris que 1) l’aromatase est exprimée dès le début de l’ontogenèse testiculaire, 2) elle est exprimée dans les gonocytes suggérant que ces cellules interviennent dans l’endocrinologie testiculaire et que le rapport oestrogènes/androgènes est plus important dans les gonocytes que dans le liquide interstitiel. En outre, on sait que, chez le fœtus de rat l’aromatase est essentiellement exprimée par les cellules de Sertoli. Nous proposons de prendre en compte cette différence inter-espèces comme un nouveau concept pour comprendre les différences de sensibilité aux perturbateurs endocriniens d’une espèce à l’autre.
Ontogenesis of cytochrome P450 aromatase expression in the mouse testis during fetal development
C57BL/6 mice bred in our animal facility were housed under controlled photoperiod conditions (lights from 08:00 to 20:00 h) with commercial food and tap water supplied ad libitum, as previously described [1, 2]. The day after overnight mating was counted as 0.5 day post-coitum (dpc). The animal facility is licensed by the French Ministry of Agriculture (agreement N°B92-032-02). All animal experiments were supervised by Pr. René Habert (agreement delivered by the French Ministry of Agriculture for animal experimentation N°92-191) in compliance with the NIH Guide for Care and Use of Laboratory Animals.
Sequences of aromatase primers used in RT-PCR and qRT-PCR
RT-PCR all transcripts
To determine if aromatase is translated in mouse testis, western blot analysis was performed using a specific anti-aromatase antibody (MCA2077T, Serotec, France) (Figure 1D). Two proteins around 54 kDa and one around 27 kDa were detected. The protein of 54 kDa was also present in the ovary extract and it approximately corresponds to the aromatase expected size. We thus suppose that the two heaviest proteins derived from the full-length form of aromatase (T1) with the highest form corresponding to a testis-specific post-translational modification that remains to be identified. In order to understand the origin of the 27 kDa protein, we analysed sequences of the T2 and T3 variants. It revealed that the splicing of exon 3 in T2 would change the ORF and create a precocious codon stop leading to a probably not detected protein of 6 kDa. Splicing of exons 3 and 4 in T3 would not change the ORF allowing in theory the synthesis of a truncated protein of 46 kDa. No protein at this expected size was detected in the western blot (Figure 1D). However, the use of an alternative start codon located later in T2 and T3 sequences may lead to a protein of 27 kDa containing the C-terminal part of aromatase.
These findings are different from those of the only previously published paper on this topic showing that, in the mouse, aromatase expression starts at 17.5 dpc and reaches the highest level at day 1 post-partum . In our study, we detected aromatase expression as early as 12.5 dpc. This discrepancy probably results from the improvement of the methods of detection made since 1994. This is an important point because it shows that estrogens can be produced by mouse fetal testes very early and throughout development.
Our findings indicate that different aromatase transcripts are generated in fetal mouse testes. Previous studies in different mammalian species (including the mouse) reported that tissue-specific aromatase expression is driven by specific promoters [4–6]. Each tissue-specific promoter is associated with a specific untranslated first exon. In mice testis Golovine et al. have shown that aromatase transcripts may emerge from a specific promoter called Ptes . Our study showed that aromatase expression is also regulated at a second transcriptional level generating two additional truncated variants T2 and T3 by mRNA splicing. Our results suggest that there are several forms of aromatase protein however the nature and the physiological function of these isoforms remain to be investigated.
Aromatase cell localization in mouse fetal testes
In addition, our immunohistochemical analysis showed that aromatase was also expressed in gonocytes, but the intensity of the signal was not uniform: in some cells the signal was very strong, whereas in others it was faint or undetectable (Figure 2A, arrowheads). Similar results were previously described for Retinoic Acid Receptor alpha . As aromatase localization in germ cells was quite unexpected, aromatase immunostaining was also performed in enriched gonocyte cultures that were prepared from 17.5 dpc mouse testes as previously described . Similarly, aromatase was detected in some germ cell VASA-positive cells, a germ cell-specific marker (Figure 2B). This result identifies a sub-population of gonocytes with endocrine function. Aromatase expression was previously reported in adult rat and human germ cells [16, 17] and in pig gonocytes during development . Aromatase expression was also detected in gonocytes of human fetal testes .
In conclusion, aromatase cell localization in fetal testis appears to differ from one species to another and as consequence also the intracellular estrogen concentration. These differences should be taken into account to explain the variations in the susceptibility of fetal testis to estrogenic and anti-androgenic endocrine disruptors in different mammalian species that has been recently lightened .
We thank Véronique Neuville for animal care, Evelyne Moreau and Sebastien Messiaen for technical assistance, Aurélie Gouret for secretarial help and E. Andermarcher for editing the English manuscript.
This work was supported by Université Paris Diderot-Paris 7, CEA and INSERM. J.M. was supported by a fellowship from the Ministère de l’Education Nationale de la Recherche et de la Technologie. CB holds a position as Temporary Attached for Teaching and Research (ATER) at the Diderot-Paris 7 University.
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