Kleiman Sandra E, Yogev Leah, Lehavi Ofer, Yavetz Haim, Hauser Ron
Institute for the Study of Fertility, Lis Maternity Hospital, Tel Aviv Sourasky Medical Center, Sackler Faculty of Medicine, Tel Aviv University, 6 Weizman Street, Tel Aviv, 6423906, Israel.
J Assist Reprod Genet. 2016 Jun;33(6):807-14. doi: 10.1007/s10815-016-0698-0. Epub 2016 Mar 19.
Mature sperm cells can be found in testicular specimens extracted from azoospermic men with non-mosaic Klinefelter syndrome (KS). The present study evaluates the expression of various known molecular markers of spermatogenesis in a population of men with KS and assesses the ability of those markers to predict spermatogenesis.
Two groups of men with non-obstructive azoospermia who underwent testicular sperm-retrieval procedures were included in the study: 31 had non-mosaic KS (KS group) and 91 had normal karyotype (NK group). Each group was subdivided into mixed atrophy (containing some mature sperm cells) or Sertoli cell only syndrome according to testicular histology and cytology observations. Semi-quantitative histological morphometric analysis (interstitial hyperplasia and hyalinization, tubules with cells and abnormal thickness of the basement membrane) and expression of spermatogenetic markers (DAZ, RBM, BOLL, and CDY1) were evaluated and compared among those subgroups.
Clear differences in the histological morphometry and spermatogenetic marker expression were noted between the KS and NK groups. There was a significant difference in the expression of spermatogenetic markers between the subgroups of the NK group (as expected), while no difference could be discerned between the two subgroups in the KS group.
We conclude that molecular spermatogenetic markers have a pattern of expression in men with KS that is distinctively different from that of men with NK, and that it precludes and limits their use for predicting spermatogenesis in the former. It is suggested that this difference might be due to the specific highly abnormal histological morphometric parameters in KS specimens.
在从非嵌合型克兰费尔特综合征(KS)的无精子症男性中提取的睾丸标本中可发现成熟精子细胞。本研究评估了KS男性群体中各种已知精子发生分子标志物的表达情况,并评估了这些标志物预测精子发生的能力。
两组接受睾丸取精手术的非梗阻性无精子症男性纳入本研究:31例患有非嵌合型KS(KS组),91例核型正常(NK组)。根据睾丸组织学和细胞学观察结果,每组再分为混合性萎缩(含有一些成熟精子细胞)或仅支持细胞综合征。对这些亚组进行半定量组织形态计量分析(间质增生和透明变性、有细胞的小管以及基底膜厚度异常)以及精子发生标志物(DAZ、RBM、BOLL和CDY1)表达的评估和比较。
KS组和NK组在组织形态计量和精子发生标志物表达方面存在明显差异。NK组亚组之间精子发生标志物的表达存在显著差异(如预期),而KS组的两个亚组之间没有差异。
我们得出结论,精子发生分子标志物在KS男性中的表达模式与NK男性明显不同,这排除并限制了它们在前者中用于预测精子发生的用途。提示这种差异可能是由于KS标本中特定的高度异常的组织形态计量参数所致。