Cannabis alters DNA methylation at maternally imprinted and autism candidate genes in spermatogenic cells.

IF 2.1 4区 医学 Q3 ANDROLOGY
Rose Schrott, Katherine W Greeson, Dillon King, Krista M Symosko Crow, Charles A Easley, Susan K Murphy
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引用次数: 10

Abstract

Cannabis use in the United States is increasing, with highest consumption among men at their peak reproductive years. We previously demonstrated widespread changes in sperm DNA methylation with cannabis exposure in humans and rats, including genes important in neurodevelopment. Here, we use an in vitro human spermatogenesis model to recapitulate chronic cannabis use and assess DNA methylation at imprinted and autism spectrum disorder (ASD) candidate genes in spermatogonial stem cell (SSC)- and spermatid-like cells. Methylation at maternally imprinted genes SGCE and GRB10 was significantly altered in SSC- and spermatid-like cells, respectively, while PEG3 was significantly differentially methylated in spermatid-like cells. Two of ten randomly selected ASD candidate genes, HCN1 and NR4A2, had significantly altered methylation with cannabis exposure in SSC-like cells. These results support our findings in human cohorts and provide a new tool with which to gain mechanistic insights into the association between paternal cannabis use and risk of ASD in offspring.

大麻改变了生精细胞中母体印记和自闭症候选基因的DNA甲基化。
大麻在美国的使用量正在增加,男性在生育高峰期的消费量最高。我们之前证明,在人类和大鼠中,随着大麻的暴露,精子DNA甲基化发生了广泛的变化,包括对神经发育重要的基因。在这里,我们使用体外人类精子发生模型来概括长期使用大麻的情况,并评估精原干细胞(SSC)和精子样细胞中印记和自闭症谱系障碍(ASD)候选基因的DNA甲基化。母印迹基因SGCE和GRB10的甲基化分别在SSC和精子细胞样细胞中显著改变,而PEG3在精子细胞样中显著差异甲基化。随机选择的十个ASD候选基因中有两个,HCN1和NR4A2,在SSC样细胞中随着大麻暴露而显著改变了甲基化。这些结果支持了我们在人类队列中的发现,并提供了一种新的工具,可以从机制上深入了解父亲使用大麻与后代ASD风险之间的关系。
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来源期刊
CiteScore
4.30
自引率
4.20%
发文量
27
审稿时长
>12 weeks
期刊介绍: Systems Biology in Reproductive Medicine, SBiRM, publishes Research Articles, Communications, Applications Notes that include protocols a Clinical Corner that includes case reports, Review Articles and Hypotheses and Letters to the Editor on human and animal reproduction. The journal will highlight the use of systems approaches including genomic, cellular, proteomic, metabolomic, bioinformatic, molecular, and biochemical, to address fundamental questions in reproductive biology, reproductive medicine, and translational research. The journal publishes research involving human and animal gametes, stem cells, developmental biology and toxicology, and clinical care in reproductive medicine. Specific areas of interest to the journal include: male factor infertility and germ cell biology, reproductive technologies (gamete micro-manipulation and cryopreservation, in vitro fertilization/embryo transfer (IVF/ET) and contraception. Research that is directed towards developing new or enhanced technologies for clinical medicine or scientific research in reproduction is of significant interest to the journal.
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