Rondanino Christine, Duchesne Véronique, Escalier Denise, Jumeau Fanny, Verhaeghe France, Peers Marie-Claire, Mitchell Valérie, Rives Nathalie
EA 4308 'Gamétogenèse et qualité du gamète', Rouen, France; Laboratoire de Biologie de la Reproduction - CECOS, CHU - Hôpitaux de Rouen, Institut de Recherche et d'Innovation Biomédicale, Université de Rouen, Rouen, France.
EA 4308 'Gamétogenèse et qualité du gamète', Rouen, France; Laboratoire de Biologie de la Reproduction - CECOS, CHU - Hôpitaux de Rouen, Institut de Recherche et d'Innovation Biomédicale, Université de Rouen, Rouen, France.
Reprod Biomed Online. 2015 Jul;31(1):89-99. doi: 10.1016/j.rbmo.2015.04.002. Epub 2015 Apr 16.
The decapitated sperm defect is a rare type of teratozoospermia responsible for male infertility. Spermatozoa from patients affected by this syndrome are used for intracytoplasmic sperm injection (ICSI) although little is known about their DNA integrity. This study evaluated sperm nuclear alterations in four patients and ten fertile men (control group). Sperm samples were examined by light, transmission electron and high-magnification contrast microscopy and analysed after terminal deoxynucleotidyltransferase-mediated dUTP nick end labelling, aniline blue staining and fluorescence in-situ hybridization. Spermatozoa from patients presented varying degrees of decapitation, along with morphological and ultrastructural head abnormalities. Whereas the proportion of spermatozoa with fragmented DNA and numerical chromosome abnormalities was similar in patients 1-3 and controls, the percentage of spermatozoa with hypocondensed chromatin was higher in patients 1-3 than in fertile men. Patient 4 presented a distinct phenotype, with an increased proportion of flagellated spermatozoa with DNA strand breaks as well as increased aneuploidy and diploidy rates compared with controls and with patients 1-3. No successful pregnancy resulted from ICSI although embryos were obtained for three patients. The morphological defects and the nuclear alterations observed in spermatozoa of patients with the decapitated sperm syndrome may have contributed to ICSI failures.
断头精子缺陷是一种导致男性不育的罕见畸形精子症类型。尽管对受该综合征影响患者的精子DNA完整性知之甚少,但来自这些患者的精子仍被用于卵胞浆内单精子注射(ICSI)。本研究评估了4例患者和10名生育能力正常男性(对照组)的精子核改变情况。通过光学显微镜、透射电子显微镜和高倍对比显微镜对精子样本进行检查,并在末端脱氧核苷酸转移酶介导的dUTP缺口末端标记、苯胺蓝染色和荧光原位杂交后进行分析。患者的精子呈现出不同程度的断头现象,同时伴有头部形态和超微结构异常。虽然患者1 - 3与对照组精子中DNA片段化和染色体数目异常的比例相似,但患者1 - 3中染色质凝聚不足的精子百分比高于生育能力正常男性。患者4呈现出独特的表型,与对照组以及患者1 - 3相比,有鞭毛的精子中DNA链断裂的比例增加,非整倍体和二倍体率也增加。尽管为3例患者获取了胚胎,但ICSI未成功妊娠。断头精子综合征患者精子中观察到的形态缺陷和核改变可能导致了ICSI失败。