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BERLINER STADTSYNODE Berliner Stadtsynode / Meyeren, Wilhelm von (Public Domain) ( - ) Title page ( - ) I. Regulativ ( - ) II. Geschäfts-Ordnung für die Berliner Stadtsynode ([7]) ColorChart ( -

New Tools for in Vitro Handling and Selection of Cryopreserved Sperm Samples in Equines

Cryopreserved sperm (SPZ) are used widely in domestic animals for assisted reproduction techniques (ART). However, cryopreservation procedures negatively affect SPZ quality, causing changes at the structural and molecular levels. Therefore, using cryopreserved SPZ for ART can decrease the efficiency of these techniques as well as the quality of the embryos obtained, being necessary to optimize the handling of this type of sample. Particularly in equines, ICSI is the most used technique for low-quality equine semen samples where SPZ is selected based on their motility and morphology. Physiologically, the oviduct epithelial cells (OEC) are involved in the selection of a population of SPZ suitable for oocyte fertilization, which is released from the oviduct due to the capacitation process. This work aimed to evaluate different conditions for the in vitro manipulation and incubation of equine cryopreserved SPZ and to establish an in vitro OEC culture to select an SPZ population with fertilizing capacity suitable for its use in ART in this species.Regarding the handling and the effect on the motility of post-thawed equine cryopreserved SPZ samples, we used non-capacitating Whitten´s medium, less effect on motility was observed through the time (120 min) when SPZ were incubated at concentrations of 30 mill/ml compared to lower concentrated samples (CASA, p<0.05). Also, the motility decreased by half with centrifugations at 200g longer than 1 min (p<0.05). On the other hand, we have established a culture model of OECs in vitro, in which we demonstrated the expression of epithelial markers (E-cadherin and cytokeratin) by both RT-PCR and immunofluorescence (IF). When we performed SPZ-OEC cocultures, we observed that the attached SPZs were motile and presented intact acrosome (PSA-FITC, IF), suggesting a selection by the oviductal model. Then, the co-cultures were incubated in capacitating conditions (capacitating Whitten´s medium) and the released SPZ population was recovered. Under these conditions, a greater number of live sperm (Hoechst258 assessed by IF), capacitated (activation of PKA and phosphorylation on tyrosine residues by IF), with progressive motility (CASA) and with the intact acrosome (PSA-FITC, IF) compared to the control was observed (p<0.05). Moreover, the decrease in motility through the time was less in these SPZ than in the cryopreserved SPZ incubated in the absence of OECs. This sperm population could be recovered for its use in different ART.Improvements in handling and selection of cryopreserved SPZ not only generate tools to solve the problem that IVF presents in equines, but would also improve efficiency in other ART such as ICSI, allowing the use of a population of higher quality gametes which it would positively impact the quality of the embryos obtained.Fil: Laiz Quiroga, Lucía Belén. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Biotecnológicas. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas; ArgentinaFil: Gimeno, Brenda Florencia. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Inmunología, Genética y Metabolismo. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Inmunología, Genética y Metabolismo; ArgentinaFil: Martínez León, Eduardo Antonio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Inmunología, Genética y Metabolismo. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Inmunología, Genética y Metabolismo; ArgentinaFil: Von Meyeren, Micaela. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas. - Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Biotecnológicas; ArgentinaFil: Mutto, Adrián Angel. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas. - Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Biotecnológicas; ArgentinaFil: Bariani, Maria Victoria. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Centro de Estudios Farmacológicos y Botánicos. Universidad de Buenos Aires. Facultad de Medicina. Centro de Estudios Farmacológicos y Botánicos; ArgentinaFil: Osycka Salut, Claudia Elena. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Centro de Estudios Farmacológicos y Botánicos. Universidad de Buenos Aires. Facultad de Medicina. Centro de Estudios Farmacológicos y Botánicos; ArgentinaIV Joint Meeting of The Biology Societies of ArgentinaMendozaArgentinaSociedad de Biología de CuyoSociedad Argentina de BiologíaSociedad de Biología de CórdobaSociedad de Biología de RosarioAsociación de Biología de Tucumá

Effects of in vitro interactions of oviduct epithelial cells with frozen–thawed stallion spermatozoa on their motility, viability and capacitation status

Cryopreservation by negatively affecting sperm quality decreases the efficiency of assisted reproduction techniques (ARTs). Thus, we first evaluated sperm motility at different conditions for the manipulation of equine cryopreserved spermatozoa. Higher motility was observed when spermatozoa were incubated for 30 min at 30 × 106 /mL compared to lower concentrations (p < 0.05) and when a short centrifugation at 200× g was performed (p < 0.05). Moreover, because sperm suitable for oocyte fertilization is released from oviduct epithelial cells (OECs), in response to the capacitation process, we established an in vitro OEC culture model to select a sperm population with potential fertilizing capacity in this species. We demonstrated E-cadherin and cytokeratin expression in cultures of OECs obtained. When sperm–OEC cocultures were performed, the attached spermatozoa were motile and presented an intact acrosome, suggesting a selection by the oviductal model. When co-cultures were incubated in capacitating conditions a greater number of alive (p < 0.05), capacitated (p < 0.05), with progressive motility (p < 0.05) and with the intact acrosome sperm population was observed (p < 0.05) suggesting that the sperm population released from OECs in vitro presents potential fertilizing capacity. Improvements in handling and selection of cryopreserved sperm would improve efficiencies in ARTs allowing the use of a population of higher-quality sperm.Fil: Gimeno, Brenda Florencia. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas. - Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Biotecnológicas; ArgentinaFil: Bariani, Maria Victoria. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas. - Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Biotecnológicas; ArgentinaFil: Laiz Quiroga, Lucía Belén. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas. - Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Biotecnológicas; ArgentinaFil: Martínez León, Eduardo Antonio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Inmunología, Genética y Metabolismo. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Inmunología, Genética y Metabolismo; ArgentinaFil: Von Meyeren, Micaela. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas. - Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Biotecnológicas; ArgentinaFil: Rey, Osvaldo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Inmunología, Genética y Metabolismo. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Inmunología, Genética y Metabolismo; ArgentinaFil: Mutto, Adrián Angel. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas. - Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Biotecnológicas; ArgentinaFil: Osycka Salut, Claudia Elena. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas. - Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Biotecnológicas; Argentin