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    Título
    Mitochondrial activity and forward scatter vary in necrotic, apoptotic and membrane-intact spermatozoan subpopulations
    Autor
    Martínez Pastor, FelipeAutoridad BuleriaORCID
    Fernández Santos, María Rocío
    Olmo de Medina, Enrique del
    Domínguez Rebolledo, Álvaro Efrén
    Esteso, Milagros
    Montoro, Vidal
    Garde López-Brea, Julián
    Facultad/Centro
    Facultad de Ciencias Biologicas y Ambientales
    Área de conocimiento
    Biologia Celular
    Datos de la obra
    Reproduction, Fertility and Development, 2008, vol. 20, n. 5
    Editor
    CSIRO
    Fecha
    2008-04-28
    Abstract
    In the present study, we have related mitochondrial membrane potential (ΔΨm) and forward scatter (FSC) to apoptotic-related changes in spermatozoa. Thawed red deer spermatozoa were incubated in synthetic oviductal fluid medium (37°C, 5% CO2), with or without antioxidant (100 μm Trolox). At 0, 3, 6 and 9 h, aliquots were assessed for motility and were stained with a combination of Hoechst 33342, propidium ioide (PI), YO-PRO-1 and Mitotracker Deep Red for flow cytometry. The proportion of spermatozoa YO-PRO-1+ and PI+ (indicating a damaged plasmalemma; DEAD) increased, whereas that of YO-PRO-1– and PI– (INTACT) spermatozoa decreased. The proportion of YO-PRO-1+ and PI– spermatozoa (altered plasmalemma; APOPTOTIC) did not change. Both DEAD and APOPTOTIC spermatozoa had low ΔΨm. Most high-ΔΨm spermatozoa were INTACT, and their proportion decreased with time. The FSC signal also differed between different groups of spermatozoa, in the order APOPTOTIC > DEAD > INTACT/low ΔΨm > INTACT/high ΔΨm; however, the actual meaning of this difference is not clear. APOPTOTIC spermatozoa seemed motile at 0 h, but lost motility with time. Trolox only slightly improved the percentage of INTACT spermatozoa (P < 0.05). The population of APOPTOTIC spermatozoa in the present study may be dying cells, possibly with activated cell death pathways (loss of ΔΨm). We propose that the sequence of spermatozoon death here would be: (1) loss of ΔΨm; (2) membrane changes (YO-PRO-1+ and PI–); and (3) membrane damage (PI+). INTACT spermatozoa with low ΔΨm or altered FSC may be compromised cells. The present study is the first that directly relates membrane integrity, apoptotic markers and mitochondrial status in spermatozoa. The results of the present study may help us understand the mechanisms leading to loss of spermatozoon viability after thawing.
    Materia
    Veterinaria
    Palabras clave
    Cell volume
    Flow cytometry
    Membrane changes
    Mitochondrial membrane potential
    Sperm death
    YO-PRO-1
    Peer review
    SI
    URI
    http://hdl.handle.net/10612/10346
    Versión del editor
    http://www.publish.csiro.au/RD/RD08002
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