Chen Yu, Lay Jaiden, Shaw Geoffrey, Tarulli Gerard A, Renfree Marilyn B
School of BioSciences, The University of Melbourne, Victoria, Australia.
Reproduction. 2024 Jun 28;168(2). doi: 10.1530/REP-23-0504. Print 2024 Aug 1.
Atrazine, like oestrogen, disorganises laminin formation and reduces the number of germ cells and Sertoli cells in the developing testes of the tammar wallaby. This study suggests that interfering with the balance of androgen and oestrogen affects the integrity of laminin structure and testis differentiation.
The herbicide atrazine was banned in Europe in 2003 due to its endocrine disrupting activity but remains widely used. The integrity of the laminin structure in fetal testis cords requires oestrogen signalling but overexposure to xenoestrogens in the adult can cause testicular dysgenesis. However, whether xenoestrogens affect laminin formation in developing testes has not been investigated. Here we examined the effects of atrazine in the marsupial tammar wallaby during early development and compare it with the effects of the anti-androgen flutamide, oestrogen, and the oestrogen degrader fulvestrant. The tammar, like all marsupials, gives birth to altricial young, allowing direct treatment of the developing young during the male programming window (day 20-40 post partum (pp)). Male pouch young were treated orally with atrazine (5 mg/kg), flutamide (10 mg/kg), 17β-oestradiol (2.5 mg/kg) and fulvestrant (1 mg/kg) daily from day 20 to 40 pp. Distribution of laminin, vimentin, SOX9 and DDX4, cell proliferation and mRNA expression of SRY, SOX9, AMH, and SF1 were examined in testes at day 50 post partum after the treatment. Direct exposure to atrazine, flutamide, 17β-oestradiol, and fulvestrant all disorganised laminin but had no effect on vimentin distribution in testes. Atrazine reduced the number of germ cells and Sertoli cells when examined at day 40-50 pp and day 20 to 40 pp, respectively. Both flutamide and fulvestrant reduced the number of germ cells and Sertoli cells. Atrazine also downregulated SRY expression and impaired SOX9 nuclear translocation. Our results demonstrate that atrazine can compromise normal testicular differentiation during the critical male programming window.
阿特拉津与雌激素一样,会破坏层粘连蛋白的形成,并减少发育中的袋鼠睾丸中的生殖细胞和支持细胞数量。这项研究表明,干扰雄激素和雌激素的平衡会影响层粘连蛋白结构的完整性和睾丸分化。
除草剂阿特拉津由于其内分泌干扰活性于2003年在欧洲被禁用,但仍被广泛使用。胎儿睾丸索中层粘连蛋白结构的完整性需要雌激素信号传导,但成年后过度暴露于外源性雌激素会导致睾丸发育不全。然而,外源性雌激素是否会影响发育中的睾丸中层粘连蛋白的形成尚未得到研究。在这里,我们研究了阿特拉津在有袋类动物袋鼠早期发育过程中的作用,并将其与抗雄激素氟他胺、雌激素和雌激素降解剂氟维司群的作用进行比较。与所有有袋类动物一样,袋鼠产下的幼崽发育不全,这使得在雄性编程窗口(产后第20 - 40天)期间可以直接处理发育中的幼崽。从产后第20天到第40天,每天给雄性育儿袋幼崽口服阿特拉津(5毫克/千克)、氟他胺(10毫克/千克)、17β - 雌二醇(2.5毫克/千克)和氟维司群(1毫克/千克)。在处理后的产后第50天,检测睾丸中层粘连蛋白、波形蛋白、SOX9和DDX4的分布、细胞增殖以及SRY、SOX9、抗苗勒氏管激素(AMH)和类固醇生成因子1(SF1)的mRNA表达。直接暴露于阿特拉津、氟他胺、17β - 雌二醇和氟维司群都会破坏层粘连蛋白,但对睾丸中波形蛋白的分布没有影响。分别在产后第40 - 50天和第20至40天检查时,阿特拉津减少了生殖细胞和支持细胞的数量。氟他胺和氟维司群都减少了生殖细胞和支持细胞的数量。阿特拉津还下调了SRY表达并损害了SOX9的核转位。我们的结果表明,在关键的雄性编程窗口期间,阿特拉津会损害正常的睾丸分化。