Role of Wasp and the small GTPases RhoA, RhoB, and Cdc42 during capacitation and acrosome reaction in spermatozoa of English guinea pigs


Por: Delgado-Buenrostro, Norma L., Mujica, Adela, Chiquete-Felix, Natalia, Deciga-Alcaraz, Alejandro, Medina-Reyes, Estefany I., Uribe-Carvajal, Salvador, Chirino, Yolanda I.

Publicada: 1 oct 2016
Resumen:
Cytoskeleton remodeling is necessary for capacitation and the acrosome reaction in spermatozoa. F-actin is located in the acrosome and equatorial region during capacitation, but is relocated in the post-acrosomal region during the acrosome reaction in spermatozoa from bull, rat, mice, and guinea pig. Actin polymerization and relocalization are generally regulated by small GTPases that activate Wasp protein, which coordinates with Arp2/3, profilin I, and profilin II to complete cytoskeletal remodeling. This sequence of events is not completely described in spermatozoa, though. Therefore, the aim of this study was to determine if Wasp interacts with small GTPases (RhoA, RhoB, and Cdc42) and proteins (Arp2/3, profilin I, and profilin II) that co-localize with F-actin during capacitation and the acrosome reaction in English guinea pig spermatozoa obtained from the vas deferens. The spermatozoa were capacitated in calcium-free medium, incubated with an activator or an inhibitor of GTPases, and then induced to acrosome react using calcium. The distribution patterns of F-actin were compared to the patterns of Wasp and its putative interaction partners: Wasp and RhoB, but not RhoA or Cdc42, localization overlap with F-actin during capacitation and the acrosome reaction. Activation of small GTPases localized RhoB to the post-acrosomal region whereas their inhibition prevented acrosome exocytosis. Arp2/3 and profilin II appear to interact with Wasp in the post-acrosomal region and flagellum, while profilin I and Wasp could be found in the equatorial region. Thus, Wasp and F-actin distribution overlap during capacitation and acrosome reaction, and small GTPases play an important role in cytoskeleton remodeling during these processes in spermatozoa. Mol. Reprod. Dev. 83: 927-937, 2016 (c) 2016 Wiley Periodicals, Inc.

Filiaciones:
Univ Nacl Autonoma Mexico, Unidad Biomed UBIMED, Fac Estudios Super Iztacala, Tlalnepantla 54090, Estado De Mexic, Mexico
Univ Nacl Autonoma Mexico, Secc Bioquim & Farmacol Humana, Fac Estudios Super Cuautitlan, Cuautitlan 54743, Estado De Mexic, Mexico
Inst Politecn Nacl, Ctr Invest & Estudios Avanzados, Dept Biol Celular, Mexico City 07360, DF, Mexico
Univ Nacl Autonoma Mexico, Inst Fisiol Celular, Mexico City 04510, DF, Mexico
Univ Nacl Autonoma Mexico, Programa Doctorado Ciencias Biomed, Mexico City 07360, DF, Mexico
ISSN: 1040452X
Editorial
WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, NJ 07030 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 83 Número: 10
Páginas: 927-937
WOS Id: 000387015400010
ID de PubMed: 27182927

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