Department of Anatomical Science, Hirosaki University Graduate School of Medicine, Hirosaki 036-8562, Japan.
Hum Reprod. 2011 May;26(5):978-86. doi: 10.1093/humrep/der047. Epub 2011 Feb 28.
The aims of this study were to establish whether individual differences exist in the frequency and size of vacuoles found in human sperm and to ascertain whether such vacuoles are involved in causing DNA damage.
Morphologically normal sperm were obtained from 15 IVF and 2 ICSI patients and 3 fertile donors. (i) Sperm heads were analyzed for the presence of vacuoles under a 1000× differential interference contrast microscope. (ii) In three patients and two donor samples, structural chromosomal damage was evaluated in normal sperm containing large vacuoles and selected at 1000× magnification for injection into mouse oocytes. (iii) In 10 patients and two donor samples, confocal laser microscopy detected DNA damage in sperm-exhibiting large vacuoles and stained with an in situ cell death detection kit.
(i) Vacuoles were observed in almost all normal sperm from patient and donor ejaculates and were mainly located at the tip or middle area of the sperm heads. However, average incidence of normal sperm exhibiting large vacuoles was 4.6 and 4.2% in the patient and donor groups, respectively. (ii) Sperm chromosome assays did not reveal any differences in the incidence of structural chromosome aberrations between sperm exhibiting large vacuoles and those without them (9.1 versus 4.1%). (iii) No significant difference in frequency of TUNEL-positive cells was found between normal sperm with large vacuoles and those without them in the samples examined. Among 227 sperm exhibiting large vacuoles, only 7 cells were TUNEL positive.
The results showed that large vacuoles were not responsible for DNA damage, suggesting that intra-cytoplasmic injection of morphologically selected sperm may not be required for patients who produce high-quality semen.
本研究旨在确定人类精子中是否存在空泡的频率和大小的个体差异,并确定这些空泡是否与 DNA 损伤有关。
从 15 名 IVF 和 2 名 ICSI 患者和 3 名生育能力正常的供体中获得形态正常的精子。(i)在 1000×相差显微镜下分析精子头是否有空泡。(ii)在 3 名患者和 2 名供体样本中,评估含有大空泡的正常精子中的结构染色体损伤,并在 1000×放大倍数下选择用于注射到小鼠卵母细胞中。(iii)在 10 名患者和 2 名供体样本中,通过共聚焦激光显微镜检测具有大空泡的精子中的 DNA 损伤,并使用原位细胞死亡检测试剂盒进行染色。
(i)几乎所有来自患者和供体精液的正常精子都观察到空泡,主要位于精子头部的尖端或中部。然而,在患者和供体组中,分别有 4.6%和 4.2%的正常精子表现出大空泡。(ii)精子染色体分析未发现表现出大空泡的精子与无大空泡的精子之间结构染色体异常的发生率有任何差异(9.1%与 4.1%)。(iii)在所检查的样本中,具有大空泡的正常精子与无大空泡的精子之间 TUNEL 阳性细胞的频率没有显著差异。在 227 个具有大空泡的精子中,只有 7 个细胞 TUNEL 阳性。
结果表明,大空泡与 DNA 损伤无关,这表明对于产生高质量精液的患者,可能不需要进行形态选择的精子胞质内注射。