Heng K, Anand-Ivell R, Teerds K, Ivell R
School of Medical Science, University of Adelaide, SA, Australia.
Int J Androl. 2012 Jun;35(3):353-63. doi: 10.1111/j.1365-2605.2011.01231.x. Epub 2011 Dec 13.
The manner by which endocrine-disrupting xenobiotics, such as phthalates, can induce changes in the development of the male reproductive system still remains largely unknown. Herein, we have explored the application of ethane dimethane sulphonate (EDS) to eliminate adult-type Leydig cells in the mature rat testis, leading to their regeneration from resident stem cells, as a novel system to investigate the effects of dibutyl phthalate (DBP) and diethylstilbestrol (DES) on adult-type Leydig cell differentiation. The advantage of this model is that one can study adult-type Leydig cell differentiation in vivo divorced from the concomitant endocrine development of puberty. In these preliminary studies, we show that both DBP and/or DES, given for 2 or 4 days following EDS application, indeed affect Leydig cell differentiation in the adult testis, largely by increasing early Leydig cell proliferation and possibly thereby delaying early differentiation. In particular, on day 27 post-EDS, a time-point when the differentiation trajectory appears to be most discriminating, we observe that both DBP and/or DES cause a fourfold increase in Leydig cell density, and a significant increase in the expression of the Leydig cell-specific marker transcripts INSL3, LH receptor, Cyp17a1 and Cyp 11a1. In conclusion, both DBP and DES are able to affect adult-type Leydig cells during their differentiation to cause a significant perturbation in their ultimate functional capacity.
内分泌干扰性外源性物质,如邻苯二甲酸盐,可诱导雄性生殖系统发育变化的具体方式在很大程度上仍不为人知。在此,我们探索了应用乙烷二甲磺酸盐(EDS)消除成熟大鼠睾丸中的成年型睾丸间质细胞,使其从驻留干细胞再生,作为一种研究邻苯二甲酸二丁酯(DBP)和己烯雌酚(DES)对成年型睾丸间质细胞分化影响的新系统。该模型的优势在于能够在脱离青春期伴随内分泌发育的情况下,在体内研究成年型睾丸间质细胞的分化。在这些初步研究中,我们发现,在应用EDS后给予DBP和/或DES 2天或4天,确实会影响成年睾丸中睾丸间质细胞的分化,主要是通过增加早期睾丸间质细胞增殖,并可能由此延迟早期分化。特别是在EDS处理后的第27天,这是一个分化轨迹似乎最具区分性的时间点,我们观察到DBP和/或DES均使睾丸间质细胞密度增加了四倍,并且睾丸间质细胞特异性标志物转录本INSL3、促黄体生成素受体、Cyp17a1和Cyp 11a1的表达显著增加。总之,DBP和DES在成年型睾丸间质细胞分化过程中均能够对其产生影响,从而对其最终功能能力造成显著干扰。