Efimova Olga A, Pendina Anna A, Tikhonov Andrei V, Parfenyev Sergey E, Mekina Irina D, Komarova Evgeniia M, Mazilina Mariia A, Daev Eugene V, Chiryaeva Olga G, Galembo Ilona A, Krapivin Mikhail I, Glotov Oleg S, Stepanova Irina S, Shlykova Svetlana A, Kogan Igor Yu, Gzgzyan Alexander M, Kuznetzova Tatyana V, Baranov Vladislav S
D.O. Ott Research Institute of Obstetrics, Gynecology and Reproductology, St. Petersburg, Russia.
St. Petersburg State University, St. Petersburg, Russia.
Oncotarget. 2017 Jun 1;8(51):88294-88307. doi: 10.18632/oncotarget.18331. eCollection 2017 Oct 24.
We performed immunofluorescent analysis of DNA hydroxymethylation and methylation in human testicular spermatogenic cells from azoospermic patients and ejaculated spermatozoa from sperm donors and patients from infertile couples. In contrast to methylation which was present throughout spermatogenesis, hydroxymethylation was either high or almost undetectable in both spermatogenic cells and ejaculated spermatozoa. On testicular cytogenetic preparations, 5-hydroxymethylcytosine was undetectable in mitotic and meiotic chromosomes, and was present exclusively in interphase spermatogonia Ad and in a minor spermatid population. The proportions of hydroxymethylated and non-hydroxymethylated diploid and haploid nuclei were similar among samples, suggesting that the observed alterations of 5-hydroxymethylcytosine patterns in differentiating spermatogenic cells are programmed. In ejaculates, a few spermatozoa had high 5-hydroxymethylcytosine level, while in the other ones hydroxymethylation was almost undetectable. The percentage of highly hydroxymethylated (5-hydroxymethylcytosine-positive) spermatozoa varied strongly among individuals. In patients from infertile couples, it was higher than in sperm donors (<0.0001) and varied in a wider range: 0.12-21.24% versus 0.02-0.46%. The percentage of highly hydroxymethylated spermatozoa correlated strongly negatively with the indicators of good semen quality - normal morphology (=-0.567, <0.0001) and normal head morphology (=-0.609, <0.0001) - and strongly positively with the indicator of poor semen quality: sperm DNA fragmentation (=0.46, =0.001). Thus, the immunocytochemically detected increase of 5hmC in individual spermatozoa is associated with infertility in a couple and with deterioration of sperm parameters. We hypothesize that this increase is not programmed, but represents an induced abnormality and, therefore, it can be potentially used as a novel indicator of semen quality.
我们对无精子症患者的人类睾丸生精细胞以及精子捐献者和不育夫妇患者的射出精子进行了DNA羟甲基化和甲基化的免疫荧光分析。与在整个精子发生过程中都存在的甲基化不同,羟甲基化在生精细胞和射出精子中要么很高,要么几乎检测不到。在睾丸细胞遗传学标本上,有丝分裂和减数分裂染色体中检测不到5-羟甲基胞嘧啶,仅存在于间期精原细胞Ad和少量精子细胞群体中。样本中羟甲基化和非羟甲基化二倍体及单倍体细胞核的比例相似,这表明在分化的生精细胞中观察到的5-羟甲基胞嘧啶模式变化是程序性的。在射出精液中,少数精子的5-羟甲基胞嘧啶水平很高,而在其他精子中羟甲基化几乎检测不到。高度羟甲基化(5-羟甲基胞嘧啶阳性)精子的百分比在个体间差异很大。在不育夫妇患者中,该比例高于精子捐献者(<0.0001),且变化范围更广:0.12 - 21.24% 对 0.02 - 0.46%。高度羟甲基化精子的百分比与精液质量良好指标(正常形态(=-0.567,<0.0001)和正常头部形态(=-0.609,<0.0001))呈强烈负相关,与精液质量差的指标(精子DNA碎片化(=0.46,=0.001))呈强烈正相关。因此,免疫细胞化学检测到的单个精子中5hmC的增加与夫妇不育以及精子参数恶化有关。我们推测这种增加不是程序性的,而是代表一种诱导性异常,因此,它有可能作为精液质量的一种新指标。