Tahmasbpour Marzouni Eisa, Ilkhani Hanieh, Beigi Harchegani Asghar, Shafaghatian Hossein, Layali Issa, Shahriary Alireza
Laboratory of Regenerative Medicine and Biomedical Innovations, Pasteur Institute of Iran, Tehran, Iran.
Islamic Azad University, Pharmaceutical Sciences Branch, Tehran, Iran.
Int J Fertil Steril. 2022 Jan;16(1):1-9. doi: 10.22074/IJFS.2021.138499.1032.
Recent studies have indicated that epigenetic alterations are critical for normal function and development of spermatozoa during the fertilization process. This review will focus on the latest advances in epigenome profiling of the chromatin modifications during sperm development, as well as the potential roles of epigenetic mechanisms in the context of male infertility. In this review, all data were collected from published studies that considered the effect of epigenetic abnormalities on human spermatogenesis, sperm parameters quality, fertilization process, embryo development and live births. The database PubMed was searched for all experimental and clinical studies using the Keywords "epigenetic modifications", "male infertility", "spermatogenesis", "embryo development" and "reproductive function". Post-translational modifications of histone, DNA methylations and chromatin remodeling are among the most common forms of epigenetic modifications that regulate all stages of spermatogenesis and fertilization process. Incorrect epigenetic modifications of certain genes involved in the spermatogenesis and sperm maturation may be a main reason of male reproductive disorder and infertility. Most importantly, abnormal patterns of epigenetic modifications or transgenerational phenotypes and miRNAs expression may be transmitted from one generation to the next through assisted reproductive techniques (ART) and cause an increased risk of birth defects, infertility and congenital anomalies in children. Epigenetic modifications must be considered as a one of the main factors of unexplained male infertility etiology. Due to high risk of transmitting incorrect primary imprints to offspring, there is a need for more research into epigenetic alterations in couples who benefit of ART support.
最近的研究表明,表观遗传改变对于受精过程中精子的正常功能和发育至关重要。本综述将聚焦于精子发育过程中染色质修饰的表观基因组分析的最新进展,以及表观遗传机制在男性不育背景下的潜在作用。在本综述中,所有数据均收集自已发表的研究,这些研究考虑了表观遗传异常对人类精子发生、精子参数质量、受精过程、胚胎发育和活产的影响。使用关键词“表观遗传修饰”、“男性不育”、“精子发生”、“胚胎发育”和“生殖功能”在数据库PubMed中搜索所有实验和临床研究。组蛋白的翻译后修饰、DNA甲基化和染色质重塑是调节精子发生和受精过程所有阶段的最常见表观遗传修饰形式。参与精子发生和精子成熟的某些基因的表观遗传修饰错误可能是男性生殖障碍和不育的主要原因。最重要的是,表观遗传修饰的异常模式或跨代表型以及miRNA表达可能通过辅助生殖技术(ART)从一代传递到下一代,并增加儿童出生缺陷、不育和先天性异常的风险。表观遗传修饰必须被视为不明原因男性不育病因的主要因素之一。由于将不正确的原始印记传递给后代的风险很高,因此需要对受益于ART支持的夫妇的表观遗传改变进行更多研究。