Yániz J L, Palacín I, Caycho K S, Soler C, Silvestre M A, Santolaria P
TECNOGAM Research Group, Environmental Sciences Institute (IUCA), Department of Animal Production and Food Sciences, University of Zaragoza, 22071, Huesca, Spain.
Department of Cellular Biology, Functional Biology and Physical Anthropology, University of Valencia, 46100, Burjassot, Valencia, Spain.
Reprod Fertil Dev. 2018 Jun;30(6):919-923. doi: 10.1071/RD17441.
The aim of the present study was to determine whether there is an association between the kinematic sperm subpopulations and fluorescent groups in bulls using a new fluorescent staining method that allows classification of spermatozoa into groups depending on their acrosomal and membrane integrity, as well as functional status, without inhibiting sperm motility. Cryopreserved semen samples from 10 Holstein bulls were used in the study. A multiparametric analysis of results obtained by the ISAS 3Fun kit (Proiser) was performed. The different fluorescent groups were detected and their motility characteristics evaluated using ISAS software. Clustering procedures using the kinematic data resulted in the classification of spermatozoa into three kinematic sperm subpopulations. The distribution of kinematic sperm subpopulations was different between the fluorescent sperm groups (P<0.001), although the correlation between them was low (r=0.113; P<0.01).
本研究的目的是,使用一种新的荧光染色方法来确定公牛的运动精子亚群与荧光组之间是否存在关联,该方法可根据精子的顶体和膜完整性以及功能状态将精子分类为不同组,且不会抑制精子活力。本研究使用了来自10头荷斯坦公牛的冷冻精液样本。对ISAS 3Fun试剂盒(Proiser)获得的结果进行了多参数分析。使用ISAS软件检测不同的荧光组并评估其运动特征。利用运动数据进行聚类程序,将精子分为三个运动精子亚群。荧光精子组之间运动精子亚群的分布不同(P<0.001),尽管它们之间的相关性较低(r=0.113;P<0.01)。