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Epigenetic transgenerational inheritance of testis pathology and Sertoli cell epimutations: generational origins of male infertility

机译:睾丸病理学和睾丸支持细胞的表观遗传后代遗传:男性不育的世代起源

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摘要

Male reproductive health has been in decline for decades with dropping sperm counts and increasing infertility, which has created a significant societal and economic burden. Between the 1970s and now, a general decline of over 50% in sperm concentration has been observed in the population. Environmental toxicant-induced epigenetic transgenerational inheritance has been shown to affect testis pathology and sperm count. Sertoli cells have an essential role in spermatogenesis by providing physical and nutritional support for developing germ cells. The current study was designed to further investigate the transgenerational epigenetic changes in the rat Sertoli cell epigenome and transcriptome that are associated with the onset of testis disease. Gestating female F0 generation rats were transiently exposed during the period of fetal gonadal sex determination to the environmental toxicants, such as dichlorodiphenyltrichloroethane (DDT) or vinclozolin. The F1 generation offspring were bred (i.e. intercross within the lineage) to produce the F2 generation grand-offspring that were then bred to produce the transgenerational F3 generation (i.e. great-grand-offspring) with no sibling or cousin breeding used. The focus of the current study was to investigate the transgenerational testis disease etiology, so F3 generation rats were utilized. The DNA and RNA were obtained from purified Sertoli cells isolated from postnatal 20-day-old male testis of F3 generation rats. Transgenerational alterations in DNA methylation, noncoding RNA, and gene expression were observed in the Sertoli cells from vinclozolin and DDT lineages when compared to the control (vehicle exposed) lineage. Genes associated with abnormal Sertoli cell function and testis pathology were identified, and the transgenerational impacts of vinclozolin and DDT were determined. Alterations in critical gene pathways, such as the pyruvate metabolism pathway, were identified. Observations suggest that ancestral exposures to environmental toxicants promote the epigenetic transgenerational inheritance of Sertoli cell epigenetic and transcriptome alterations that associate with testis abnormalities. These epigenetic alterations appear to be critical factors in the developmental and generational origins of testis pathologies and male infertility.
机译:几十年来,随着精子数量的减少和不育的增加,男性生殖健康一直在下降,这给社会和经济造成了沉重负担。从1970年代到现在,在人群中普遍观察到精子浓度下降了50%以上。研究表明,环境毒物诱导的表观遗传转基因遗传会影响睾丸的病理和精子数量。睾丸支持细胞通过为发育生殖细胞提供物理和营养支持,在精子发生中起重要作用。本研究旨在进一步研究大鼠睾丸支持细胞的表观基因组和转录组中与睾丸疾病发作有关的跨代表观遗传学变化。妊娠雌性F0代大鼠在确定胎儿的性腺性别期间暂时暴露于环境毒物,例如二氯二苯基三氯乙烷(DDT)或长效氯唑啉。繁殖F1代后代(即在谱系内杂交)以产生F2代大后代,然后繁殖以产生不使用兄弟姐妹或表亲的跨代F3代(即重祖代)。当前研究的重点是研究跨代睾丸疾病的病因,因此采用了F3代大鼠。 DNA和RNA获自纯化的Sertoli细胞,该细胞从F3代大鼠的出生后20天大的雄性睾丸中分离出来。与对照(暴露于车辆的)谱系相比,在长春新碱和DDT谱系的Sertoli细胞中观察到了DNA甲基化,非编码RNA和基因表达的世代变化。确定了与支持细胞功能异常和睾丸病理异常相关的基因,并确定了长春氯唑林和滴滴涕的转基因影响。关键的基因途径,如丙酮酸代谢途径,发生了改变。观察表明,祖先暴露于环境毒物会促进与睾丸异常有关的支持细胞表观遗传和转录组改变的表观遗传跨代遗传。这些表观遗传学改变似乎是睾丸病理学和男性不育的发展和世代起源的关键因素。

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