BIOFITER Research Group, Environmental Sciences Institute (IUCA), Department of Animal Production and Food Sciences, University of Zaragoza, Huesca 22071, Spain.
Department of Computer Science, University of Zaragoza, Zaragoza 50018, Spain.
Asian J Androl. 2020 Nov-Dec;22(6):578-582. doi: 10.4103/aja.aja_2_20.
To date, sperm morphometric studies have assessed whole sperm populations without considering sperm function. The aim of this study was to evaluate the relationship of sperm membrane and acrosomal integrity with sperm morphometry in liquid semen samples collected from bulls. To this end, sperm morphometry was performed on cryopreserved semen samples from 16 bulls by a combination of fluorescent dyes, including Hoechst 33343, carboxyfluorescein diacetate, and propidium iodide. This allowed discrimination of different subpopulations on the basis of sperm membrane and acrosomal integrity and analysis of the morphometrics of the sperm head, nucleus, and acrosome using a specific plug-in module created on ImageJ. Acrosomal integrity was related to sperm morphometry as the heads of spermatozoa with a damaged acrosome were significantly smaller than those with a normal acrosome (P < 0.001). In the case of spermatozoa with an intact acrosome, those with a damaged plasma membrane had a larger sperm head and acrosome than spermatozoa with an intact plasma membrane (P < 0.001). No significant differences in the sperm head size were observed between sperm subpopulations without an acrosome or in the nuclear sperm morphometry of the different subpopulations. There was a positive correlation between the sperm motility values of the samples and the morphometric parameters for intact spermatozoa. These correlations were particularly strong for the morphometric parameters of the sperm acrosome. We conclude that there are clear differences in the sperm morphometry depending on the status of the sperm membrane and acrosome and this should be considered when performing this kind of analysis.
迄今为止,精子形态计量学研究评估了整个精子群体,而没有考虑精子功能。本研究的目的是评估精子膜和顶体完整性与公牛液态精液样本精子形态计量之间的关系。为此,使用荧光染料(包括 Hoechst 33343、羧基荧光素二乙酸酯和碘化丙啶)对 16 头公牛的冷冻精液样本进行了精子形态计量分析。这使得能够根据精子膜和顶体完整性区分不同的亚群,并使用 ImageJ 上创建的特定插件模块分析精子头部、核和顶体的形态计量学。顶体完整性与精子形态计量有关,因为顶体受损的精子头部明显小于顶体正常的精子头部(P<0.001)。对于顶体完整的精子,顶体受损的精子头部和顶体比顶体完整的精子更大(P<0.001)。没有顶体或不同亚群的核精子形态计量的精子亚群之间,精子头部大小没有显著差异。样本的精子运动值与完整精子的形态计量参数之间存在正相关。这些相关性对于精子顶体的形态计量参数尤为强烈。我们得出结论,根据精子膜和顶体的状态,精子形态计量存在明显差异,在进行这种分析时应考虑到这一点。