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Personne :
Bergeron, Annick

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Bergeron

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Annick

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Université Laval. Département des sciences animales

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ncf13730940

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Voici les éléments 1 - 4 sur 4
  • PublicationRestreint
    Signal transduction pathways in oocyte maturation
    (John Wiley & Sons Inc., 2017-01-01) Khan, Daulat Raheem; Bergeron, Annick; Santiquet, Nicolas; Richard, François J.
  • PublicationRestreint
    Active 3'–5' cyclic nucleotide phosphodiesterases are present in detergent-resistant membranes of mural granulosa cells
    (CSIRO, 2016-01-04) Bergeron, Annick; Richard, François J.; Guillemette, Christine; Sirard, Marc-André
    Lipids rafts are specialised membrane microdomains involved in cell signalling that can be isolated as detergent-resistant membranes (DRMs). The second messenger cyclic AMP (cAMP) has a central role in cell signalling in the ovary and its degradation is carried out by the phosphodiesterase (PDE) enzyme family. We hypothesised that PDEs could be functionally present in the lipid rafts of porcine mural granulosa cell membranes. PDE6C, PDE8A and PDE11A were detected by dot blot in the DRMs and the Triton-soluble fraction of the mural granulosa cells membrane and the cytosol. As shown by immunocytochemistry, PDEs showed clear immunostaining in mural granulosa cell membranes and the cytosol. Interestingly, cAMP-PDE activity was 18 times higher in the DRMs than in the Triton-soluble fraction of cell membranes and was 7.7 times higher in the cytosol than in the DRMs. cAMP-PDE activity in mural granulosa cells was mainly contributed by the PDE8 and PDE11 families. This study shows that PDEs from the PDE8 and PDE11 families are present in mural granulosa cells and that the cAMP-PDE activity is mainly contributed by the cytosol. In the cell membrane, the cAMP-PDE activity is mainly contributed by the DRMs. In addition, receptors for prostaglandin E2 and LH, two G-protein-coupled receptors, are present in lipid rafts and absent from the non-raft fraction of the granulosa cell membrane. These results suggest that in these cells, the lipid rafts exist as a cell-signalling platform and PDEs are one of the key enzyme families present in the raft.
  • PublicationRestreint
    Papaverine-sensitive phosphodiesterase activity is measured in bovine spermatozoa
    (Wiley, 2016-11-16) Vigneault, Christian; Poulin, Marie-Pier; Bergeron, Annick; Leclerc, Pierre; Richard, François J.; Sullivan, Robert; Hébert, Audrey; Guillemette, Christine; Aragon, Juan Pablo; Laroche, A.; Blondin, Patrick.
    Cyclic adenosine monophosphate (cAMP) plays a crucial role as a signaling molecule for capacitation, motility, and acrosome reaction in mammalian spermatozoa. It is well‐known that cAMP degradation by phosphodiesterase (PDE) enzyme has a major impact on sperm functions. This study was undertaken to characterize cAMP‐PDE activity in bovine spermatozoa. Total cAMP‐PDE activity in cauda epididymal and ejaculated spermatozoa was 543.2 ± 49.5 and 1252.6 ± 86.5 fmoles/min/106 spermatozoa, respectively. Using different family‐specific PDE inhibitors, we showed that in cauda epididymal and ejaculated spermatozoa, the major cAMP‐PDE activity was papaverine‐sensitive (44.5% and 57.5%, respectively, at 400 nm, papaverine is a specific inhibitor of the PDE10 family). These data are supporting the functional presence of PDE10 in bovine spermatozoa and were further confirmed by western blot to be PDE10A. Using immunocytochemistry, we showed immunoreactive signal for PDE10A present on the post‐acrosomal region of the head and on the flagella of ejaculated spermatozoa. Using papaverine, we showed that it promotes tyrosine phosphorylation of sperm proteins, phosphorylation of Erk1 and Erk2, and Ca²+ release from Ca²+ store. These results suggest that PDE10 is functionally present in bovine spermatozoa and is affecting different molecular events involved in capacitation, most probably by cAMP local regulation.
  • PublicationRestreint
    Characterization of cAMP-phosphodiesterase activity in bovine seminal plasma
    (American Society of Andrology, 2016-08-27) Bergeron, Annick; Richard, François J.; Sullivan, Robert; Hébert, Audrey; Guillemette, Christine; Aragon, Juan Pablo; Blondin, Patrick.
    The second messenger cyclic adenosine monophosphate (cAMP) has a central role in sperm physiology. Extracellular cAMP can besequentially degraded into 50AMP and adenosine by ecto-phosphodiesterases (ecto-PDE) and ecto-nucleotidases, a phenomenoncalled extracellular cAMP-adenosine pathway. As cAMP-adenosine pathway is involved in sperm capacitation, we hypothesize thatextracellular PDEs are functionally present in seminal plasma. Exclusively measuring cAMP-PDE activity, total activity in bovineseminal plasma was 10.1 1.5 fmoles/min/lg. Using different family-specific PDE inhibitors, we showed that in seminal plasma,the major cAMP-PDE activity was papaverine sensitive (47.5%). These data support the presence of PDE10 in bovine seminal plasmaand was further confirmed by western blot. In epididymal fluid, total cAMP-PDE activity was 48.2 14.8 fmoles/min/lg and weshowed that the major cAMP-PDE activity was 3-isobutyl-methylxanthine insensitive and thus ascribed to PDE8 family. PDE10AmRNAs were found in the testis, epididymis, and seminal vesicles. cAMP-PDE activity is present in bovine seminal plasma and epi-didymal fluid. The results suggest a role for ecto-PDEs present in those fluids in the signaling pathways involved in sperm functions.