Hernández-Avilés Camilo
Equine Fertility Laboratory, Department of Large Animal Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX, USA.
Methods Mol Biol. 2025;2954:241-259. doi: 10.1007/978-1-0716-4698-4_14.
Sperm quality analysis using computer-assisted sperm analysis (CASA) systems and fluorescence-based techniques has become common in the animal reproduction industry, particularly for large animals (i.e., bovine, porcine, equine). In this chapter, the methods commonly utilized in the author's laboratory to examine sperm motion characteristics via CASA and plasma membrane intactness by flow cytometry will be described. These include methods to properly dilute fresh (stallions, bulls, boars), cool-stored (stallions, boars), or frozen/thawed (stallions, bulls, boars) sperm for assessment of sperm motion characteristics using CASA, preparation of fluorochromes (SYBR-14/propidium iodide) utilized to distinguish between intact (i.e., viable or "live") versus non-intact (i.e., nonviable or "dead") sperm, and the analysis and interpretation of plasma membrane intactness using flow cytometry.
使用计算机辅助精子分析(CASA)系统和基于荧光的技术进行精子质量分析在动物繁殖行业中已很常见,特别是对于大型动物(即牛、猪、马)。在本章中,将描述作者实验室中通常用于通过CASA检查精子运动特征以及通过流式细胞术检查质膜完整性的方法。这些方法包括将新鲜(种马、公牛、公猪)、冷藏保存(种马、公猪)或冷冻/解冻(种马、公牛、公猪)的精子进行适当稀释,以便使用CASA评估精子运动特征;制备用于区分完整(即有活力或“活的”)与不完整(即无活力或“死的”)精子的荧光染料(SYBR-14/碘化丙啶);以及使用流式细胞术分析和解释质膜完整性。