Flow cytometric detection and identification of different leukocyte subpopulations in stallion semen

Abstract

AbstractTo improve accuracy in evaluating stallion ejaculates, an antibody‐based, flow cytometric assay for the detection and identification of leukocyte subpopulations (CD4‐, CD8‐, CD21‐, CD172a‐positive cells) in stallion semen (n = 12) was established. For establishment of the assay, native semen was supplemented with blood leukocytes (control: 20% leukocytes, 80% sperm cells) and analysed by flow cytometry. Adding antioxidants (ascorbic acid and butylated hydroxytoluol) to semen immediately after collection inhibited rapid death of lymphoid cells in sperm leukocyte mixtures. In control set‐ups, 27.85 ± 5.7% of events were positive for CD4, CD8, CD21 or CD172a, while in native semen samples, leukocytes were scarce (0.114 ± 0.134%). The most abundant leukocyte subpopulation in semen was of lymphoid origin (CD4‐positive cells [0.015 ± 0.02%]), whereas CD21‐positive cells (B cells; 0.001 ± 0.001%) were virtually absent in ejaculates of fertile stallions. This presented flow cytometric assay for the detection and identification of different leukocyte population in equine antioxidant‐treated ejaculates can be used as an additional tool for spermatological examination in stallions.