Nuffield Department of Obstetrics and Gynaecology, Level 3, Women's Centre, John Radcliffe Hospital, Headington, Oxford OX3 9DU, UK.
Hum Reprod. 2012 Nov;27(11):3150-60. doi: 10.1093/humrep/des312. Epub 2012 Aug 31.
Does motile sperm organelle morphology examination (MSOME) affect levels and localization patterns of the oocyte activation factor phospholipase C zeta (PLCζ) in globozoospermic sperm with and without an acrosomal bud?
MSOME identified round-headed globozoospermic sperm with increased levels of PLCζ relative to sperm from the same sample that did not undergo MSOME, and identified novel patterns of PLCζ localization in sperm exhibiting an acrosomal bud.
Absence or reduction in the level of PLCζ in the sperm head, abnormal localization patterning, or defective functional ability as a result of PLCζ gene mutation, have been linked to certain types of human male factor infertility in which oocyte activation is deficient. It has been determined that a subpopulation of sperm (1%) from a patient exhibiting 100% globozoospermia presented with an acrosome bud upon MSOME. A cycle of intracytoplasmic morphologically selected sperm injection, carried out with sperm exhibiting an acrosomal bud led to pregnancy and birth of a healthy baby boy, without the use of assisted oocyte activation (AOA).
STUDY DESIGN, SIZE, DURATION: Immunofluorescent analysis of PLCζ in globozoospermic sperm from three patients, before and after MSOME.
PARTICIPANTS/MATERIALS, SETTING, METHODS: Quantitative immunofluorescence was used to investigate PLCζ levels and localization patterns in individual sperm (n = 1 patient) identified by MSOME and isolated by micromanipulation, and presenting with and without the acrosomal bud. A secondary aim was to investigate levels and localization patterns of PLCζ in sperm before and after MSOME from two other globozoospermic men.
Non-globozoospermic control sperm exhibited characteristic localization patterns of PLCζ immunofluorescence. Completely round-headed globozoospermic sperm from patients 1-3 were either devoid of PLCζ immunofluorescence, or exhibited an abnormal, punctate, pattern of PLCζ localization. PLCζ immunofluorescence in sperm exhibiting an acrosomal bud was observed in the midpiece with varying fluorescent intensity and was detected in 28.5% of such sperm. The majority of sperm with an acrosomal bud (43.0%) exhibited punctate patterns of PLCζ localization within the sperm head. A further 28.5% of sperm exhibited PLCζ in both the head and the midpiece. Total levels of PLCζ, and the proportions of sperm exhibiting PLCζ immunoreactivity, showed significant variance (P ≤ 0.05) amongst control [45.8 arbitrary units (a.u.) and 95.7%, respectively], non-MSOME-selected (25.9 a.u. and 46.1%, respectively) and MSOME-selected globozoospermic sperm (33.4 a.u. and 65.0%, respectively). Total levels of PLCζ immunofluorescence, and proportions of sperm exhibiting PLCζ immunoreactivity, in control sperm was significantly higher (P≤ 0.05) compared with non-MSOME-selected sperm, but not significantly different from MSOME-selected sperm.
LIMITATIONS, REASONS FOR CAUTION: The low numbers of sperm analysed may not be ideal for conclusive statistical analysis. Evaluation of the effects of MSOME on morphologically normal sperm would confirm conclusions.
The present findings provide hope for the future treatment of globozoospermia without the need for AOA, and provide further evidence for the clinical application of PLCζ as a therapeutic and prognostic tool.
STUDY FUNDING/COMPETING INTEREST(S): The research described herein was funded by the Nuffield Department of Obstetrics and Gynaecology, University of Oxford. The authors report no conflict of interest.
在有和没有顶体芽的圆头型玻璃化精子中,运动精子细胞器形态检查(MSOME)是否会影响卵母细胞激活因子磷脂酶 C ζ(PLCζ)的水平和定位模式?
MSOME 鉴定出具有相对较高 PLCζ水平的圆头型玻璃化精子,而未经 MSOME 处理的同一样本中的精子则没有,并且鉴定出在具有顶体芽的精子中 PLCζ 定位的新模式。
在卵母细胞激活不足的某些类型的人类男性不育症中,精子头部的 PLCζ 水平降低或减少、异常定位模式或由于 PLCζ 基因突变导致功能缺陷,与某些类型的人类男性不育症有关。已经确定,在表现出 100%玻璃化的患者的精子亚群(1%)中,经 MSOME 处理后,精子表现出顶体芽。与未进行卵母细胞激活辅助(AOA)的情况下,使用表现出顶体芽的精子进行的胞质内形态选择精子注射周期导致了健康男婴的妊娠和出生。
研究设计、规模、持续时间:对来自三名患者的玻璃化精子进行 PLCζ 的免疫荧光分析,分别在 MSOME 前后进行。
参与者/材料、设置、方法:使用定量免疫荧光技术研究通过 MSOME 鉴定和通过微操作分离的单个精子(n = 1 名患者)中的 PLCζ 水平和定位模式,这些精子表现出和不表现出顶体芽。次要目标是研究两名其他玻璃化患者的精子在 MSOME 前后的 PLCζ 水平和定位模式。
非玻璃化精子表现出 PLCζ 免疫荧光的特征性定位模式。来自患者 1-3 的完全圆头型玻璃化精子要么没有 PLCζ 免疫荧光,要么表现出异常的点状 PLCζ 定位模式。在具有顶体芽的精子中观察到 PLCζ 免疫荧光在中段,荧光强度不同,并在 28.5%的此类精子中检测到。大多数具有顶体芽的精子(43.0%)在精子头部表现出点状 PLCζ 定位模式。进一步的 28.5%的精子在头部和中段都显示出 PLCζ。PLCζ 的总水平,以及表现出 PLCζ 免疫反应性的精子比例,在对照组[45.8 个任意单位(a.u.)和 95.7%,分别]、非 MSOME 选择的精子(25.9 a.u.和 46.1%,分别)和 MSOME 选择的玻璃化精子(33.4 a.u.和 65.0%,分别)之间表现出显著差异(P ≤ 0.05)。PLCζ 免疫荧光的总水平,以及表现出 PLCζ 免疫反应性的精子比例,在对照组精子中明显高于(P≤0.05)非 MSOME 选择的精子,但与 MSOME 选择的精子无显著差异。
局限性、谨慎的原因:分析的精子数量可能不适合进行结论性的统计分析。评估 MSOME 对形态正常精子的影响将证实这些结论。
本研究结果为未来无需 AOA 治疗玻璃化精子提供了希望,并为 PLCζ 作为治疗和预后工具的临床应用提供了进一步的证据。
研究资金/利益冲突:本文所述的研究由牛津大学纳菲尔德妇产科系资助。作者没有报告任何利益冲突。