阿特拉津会破坏层粘连蛋白的形成,并减少柽柳睾丸早期分化过程中的睾丸细胞数量。

IF 3.7 3区 生物学 Q1 DEVELOPMENTAL BIOLOGY Reproduction Pub Date : 2024-06-28 Print Date: 2024-08-01 DOI:10.1530/REP-23-0504
Yu Chen, Jaiden Lay, Geoffrey Shaw, Gerard A Tarulli, Marilyn B Renfree
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引用次数: 0

摘要

除草剂阿特拉津由于具有干扰内分泌的活性,已于 2003 年在欧洲被禁用,但仍在广泛使用。胎儿睾丸脐带中层粘蛋白结构的完整性需要雌激素信号,但成人过度接触异雌激素会导致睾丸发育不良。然而,异雌激素是否会影响发育中睾丸的层粘连蛋白形成,目前还没有研究。在这里,我们研究了阿特拉津在有袋类犭胥鼠早期发育过程中的影响,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影响进行了比较。有袋小袋鼠与所有有袋类动物一样,产下的幼鼠都是后生的,因此可以在雄性程序窗口期(产后第 20-40 天)直接对发育中的幼鼠进行治疗。从第20天到第40天,雄性小袋鼠每天口服阿特拉津(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)。处理后第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、AMH和SF1的mRNA表达。直接接触阿特拉津、氟他胺、17β-雌二醇和氟维司群都会破坏睾丸中的层粘连蛋白,但对睾丸中的波形蛋白分布没有影响。在第 40-50 天和第 20-40 天分别检测时,阿特拉津会减少生殖细胞和 Sertoli 细胞的数量。氟他胺和氟维司群都减少了生殖细胞和Sertoli细胞的数量。阿特拉津还会下调SRY的表达并影响SOX9的核转位。我们的研究结果表明,阿特拉津会在关键的雄性编程窗口期损害睾丸的正常分化。
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Atrazine disorganises laminin formation and reduces cell numbers in the tammar testis during early differentiation.

In brief: 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.

Abstract: 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.

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来源期刊
Reproduction
Reproduction 生物-发育生物学
CiteScore
7.40
自引率
2.60%
发文量
199
审稿时长
4-8 weeks
期刊介绍: Reproduction is the official journal of the Society of Reproduction and Fertility (SRF). It was formed in 2001 when the Society merged its two journals, the Journal of Reproduction and Fertility and Reviews of Reproduction. Reproduction publishes original research articles and topical reviews on the subject of reproductive and developmental biology, and reproductive medicine. The journal will consider publication of high-quality meta-analyses; these should be submitted to the research papers category. The journal considers studies in humans and all animal species, and will publish clinical studies if they advance our understanding of the underlying causes and/or mechanisms of disease. Scientific excellence and broad interest to our readership are the most important criteria during the peer review process. The journal publishes articles that make a clear advance in the field, whether of mechanistic, descriptive or technical focus. Articles that substantiate new or controversial reports are welcomed if they are noteworthy and advance the field. Topics include, but are not limited to, reproductive immunology, reproductive toxicology, stem cells, environmental effects on reproductive potential and health (eg obesity), extracellular vesicles, fertility preservation and epigenetic effects on reproductive and developmental processes.
期刊最新文献
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