RT info:eu-repo/semantics/article
T1 Mitochondrial activity and forward scatter vary in necrotic, apoptotic and membrane-intact spermatozoan subpopulations
A1 Martínez Pastor, Felipe
A1 Fernández Santos, María Rocío
A1 Olmo de Medina, Enrique del
A1 Domínguez Rebolledo, Álvaro Efrén
A1 Esteso, Milagros
A1 Montoro, Vidal
A1 Garde López-Brea, Julián
A2 Biologia Celular
K1 Veterinaria
K1 Cell volume
K1 Flow cytometry
K1 Membrane changes
K1 Mitochondrial membrane potential
K1 Sperm death
K1 YO-PRO-1
AB 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.
PB CSIRO
YR 2019
FD 2019-04-17
LK http://hdl.handle.net/10612/10346
UL http://hdl.handle.net/10612/10346
NO Reproduction, Fertility and Development, 2008, vol. 20, n. 5
NO P. 547-556
DS BULERIA. Repositorio Institucional de la Universidad de León
RD 27-abr-2024