Role of GPR55 receptor in bovine sperm capacitation

Author:

Lottero‐Leconte Raquel1,Lara Angela1,Plaza Jessica2,Arroyo‐Salvo Camila1ORCID,Bogetti María Eugenia1,Rivolta Amada Eugenia Ynsaurralde3,Dellavalle Franco3,Sengiali Fiamma2,Cetica Pablo24,Rio Sofía1,Zalazar Lucia5,Cesari Andreína5ORCID,Miragaya Marcelo2,Morado Sergio24,Perez‐Martinez Silvina1ORCID

Affiliation:

1. Centro de Estudios Farmacológicos y Botánicos (CEFYBO) Facultad de Medicina‐Universidad de Buenos Aires (UBA/CONICET) Buenos Aires Argentina

2. Facultad de Ciencias Veterinarias, Instituto de Investigación y Tecnología en Reproducción Animal (INITRA) Universidad de Buenos Aires Buenos Aires Argentina

3. Laboratorio de Biotecnología de la Reproducción. Instituto Nacional de Tecnología Agropecuaria (INTA) Mercedes‐Corrientes Argentina

4. Instituto de Investigaciones en Producción Animal (INPA) CONICET‐Universidad de Buenos Aires Buenos Aires Argentina

5. Instituto de Investigaciones Biológicas CONICET, Universidad Nacional de Mar del Plata (IIB/UNMdP) Mar del Plata Argentina

Abstract

AbstractBackgroundEndocannabinoids like anandamide (AEA), among other lipids, are recognized signaling molecules that participate in reproductive events.ObjectivesOur aims were to characterize orphan G protein‐coupled receptor (GPR55) presence; investigate GPR55 activation by AEA and determine GPR55 role in the bovine sperm function.Materials and methodsGPR55 presence was assessed by immunocytochemistry. Protein kinase A (pPKA) and PKC (pPKC) substrates, pERK1/2, G/F‐actin were determined by Western blotting, activation of RAC‐1 by pull‐down assay, F‐actin and acrosomal exocytosis by fluorescence microscopy, sperm motility by optic microscopy and computer‐aided sperm analysis and fertilizing ability by in vitro fertilization (IVF).ResultsWe detected GPR55 in spermatozoa at T0, after incubation in non‐capacitating and capacitating (presence of AEA) conditions and upon release from oviductal epithelia. AEA induced an increase in pPKA and pPKC, while CID16020046 (CID), selective GPR55 antagonist, prevented this effect. Incubation with H89, PKA inhibitor, significantly decreased pPKC, while Gö6983, a PKC inhibitor, partially reduced pPKA. pPKA remained elevated at 15‐ and 45‐min incubation, while pPKC decreased at 15 and increased at 45 min. CID prevented pPKC increase at 5 and 45 min and decreased pPKA at 45 min. RAC‐1 and F‐actin increase induced by AEA was prevented by CID. Variations in two progressive motility kinematic parameters were observed with AEA and/or CID. Sperm pretreatment with AEA increased the rate of cleaved embryos and CID prevented this effect.DiscussionWe demonstrated that GPR55 activation by AEA induces time‐dependent signaling pathways involving pPKA and pPKC during bovine sperm capacitation. AEA regulates actin polymerization through GPR55 activation, suggesting the receptor participates in cytoskeleton remodeling, and yielded higher IVF rates. Also, sperm pre‐incubation with molecules like AEA involved in capacitation could improve the embryo development.ConclusionWe have demonstrated GPR55 presence in bovine spermatozoa. The regulation of PKA and PKC and of molecules associated with cytoskeletal dynamics, such as RAC‐1 and actin, by GPR55 is closely related to sperm motility and acrosomal exocytosis.

Funder

Universidad de Buenos Aires

Publisher

Wiley

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