Relationship between caspase activity and apoptotic markers in human sperm in response to hydrogen peroxide and progesterone

Apoptosis plays an essential role in normal spermatogenesis, but deregulations of this biological process, which is closely associated with male infertility, have been found. Whereas calcium homeostasis is a key regulator of cell survival, sustained elevation of intracellular calcium plays a role in...

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Detalles Bibliográficos
Autores: Lozano Cordero, Graciela María, Bejarano Hernando, Ignacio, Espino Palma, Javier, González Flores, David, Ortiz Ruiz, Águeda, García Malpartida, Juan Francisco, Rodríguez Moratinos, Ana Beatriz, Pariente Llanos, José Antonio
Tipo de recurso: artículo
Fecha de publicación:2009
País:España
Institución:Universidad de Cantabria (UC)
Repositorio:UCrea Repositorio Abierto de la Universidad de Cantabria
Idioma:inglés
OAI Identifier:oai:repositorio.unican.es:10902/38792
Acceso en línea:https://hdl.handle.net/10902/38792
Access Level:acceso abierto
Palabra clave:Apoptosis
Caspases
Phosphatidylserine exposure
Spermatozoa
TUNEL
Descripción
Sumario:Apoptosis plays an essential role in normal spermatogenesis, but deregulations of this biological process, which is closely associated with male infertility, have been found. Whereas calcium homeostasis is a key regulator of cell survival, sustained elevation of intracellular calcium plays a role in apoptosis. The aim of this research was to determine the role of two different calcium mobilizing agents, hydrogen peroxide (H2O2) and the physiological agonist progesterone, on the apoptosis process of human ejaculated spermatozoa. Translocation of membrane phosphatidylserine was examined with an annexin V binding assay, DNA damage was detected by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labelling (TUNEL assay) and caspase-3 activity was assessed using a fluorometric assay. After incubation of spermatozoa for 1 h with either 10 µM H2O2 or 20 µM of progesterone, there was a significant increase in both caspase-3 activity and the percentage of annexin V-positive cells. Similarly, the TUNEL results were significantly higher 1 h after incubation with either 10 µM H2O2 or 20 µM of progesterone. In fact, progesterone-treated cells showed a three-fold increase (from 17.6 to 52.9%) of TUNEL-positive cells compared to untreated cells, while H2O2-treated cells exhibited a two-fold increase (from 17.6 to 37.9%). In sum, our results suggest that spermatozoa treated with calcium mobilizing agents, such as H2O2 and progesterone, seem to undergo an apoptosis process that is dependent on caspase-3 activation.