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Accueil Tous les numéros Volume 32 / Numéro 2 (Février 2016) Med Sci (Paris), 32 2 (2016) 198-203 Références
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Numéro
Med Sci (Paris)
Volume 32, Numéro 2, Février 2016
Page(s) 198 - 203
Section M/S Revues
DOI https://doi.org/10.1051/medsci/20163202014
Publié en ligne 2 mars 2016
  1. Pellestor F. Âge maternel et anomalies chromosomiques dans les ovocytes humains. Med Sci (Paris) 2004 ; 20 : 691–696. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  2. Jones KT Mammalian egg activation: from Ca2+ spiking to cell cycle progression. Reproduction 2005 ; 130 : 813–823. [CrossRef] [PubMed] [Google Scholar]
  3. Krauchunas AR, Wolfner MF. Molecular changes during egg activation. Curr Top Dev Biol 2013 ; 102 : 267–292. [CrossRef] [PubMed] [Google Scholar]
  4. Amdani SN, Yeste M, Jones C, Coward K. Sperm factors and oocyte activation: current controversies and considerations. Biol Reprod 2015 ; 93 : 50. [CrossRef] [PubMed] [Google Scholar]
  5. Saunders CM, Larman MG, Parrington J, et al. PLC zeta: a sperm-specific trigger of Ca2+ oscillations in eggs and embryo development. Development 2002 ; 129 : 3533–3544. [PubMed] [Google Scholar]
  6. Yoon SY, Eum JH, Lee JE, et al. Recombinant human phospholipase C zeta 1 induces intracellular calcium oscillations and oocyte activation in mouse and human oocytes. Hum Reprod 2012 ; 27 : 1768–1780. [CrossRef] [PubMed] [Google Scholar]
  7. Kouchi Z, Fukami K, Shikano T, et al. Recombinant phospholipase C zeta has high Ca2+ sensitivity and induces Ca2+oscillations in mouse eggs. J Biol Chem 2004 ; 279 : 10408–10412. [CrossRef] [PubMed] [Google Scholar]
  8. Viaud J, Payrastre B. Les phosphoinositides : ces lipides qui coordonnent la dynamique cellulaire. Med Sci (Paris) 2015 ; 31 : 996–1005. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  9. Hajnóczky G, Thomas AP. Minimal requirements for calcium oscillations driven by the IP3 receptor. EMBO J 1997 ; 16 : 3533–3543. [CrossRef] [PubMed] [Google Scholar]
  10. Yoon SY, Jellerette T, Salicioni AM, et al. Human sperm devoid of PLC Zeta1 fail to induce Ca2+ release and are unable to initiate the first step of embryo development. J Clin Invest 2008 ; 118 : 3671–3681. [CrossRef] [PubMed] [Google Scholar]
  11. Kashir J, Konstantinidis M, Jones C, et al. A maternally inherited autosomal point mutation in human phospholipase C zeta (PLCζ) leads to male infertility. Hum Reprod 2012 ; 27 : 222–231. [CrossRef] [PubMed] [Google Scholar]
  12. Yoon HJ, Kim HJ, Bae IH, et al. An effective method for improving outcomes in patients with a fertilization defect. Clin Exp Reprod Med 2014 ; 41 : 137–139. [CrossRef] [PubMed] [Google Scholar]
  13. Aarabi M, Balakier H, Bashar S, et al. Sperm-derived WW domain-binding protein, PAWP, elicits calcium oscillations and oocyte activation in humans and mice. FASEB J 2014 ; 28 : 4434–4440. [CrossRef] [PubMed] [Google Scholar]
  14. Wu AT, Sutovsky P, Manandhar G, et al. PAWP, a sperm-specific WW domain-binding protein, promotes meiotic resumption and pronuclear development during fertilization. J Biol Chem 2007 ; 282 : 12164–12175. [CrossRef] [PubMed] [Google Scholar]
  15. Nomikos M, Sanders JR, Theodoridou M, et al. Sperm-specific post-acrosomal WW-domain binding protein (PAWP) does not cause Ca2+ release in mouse oocytes. Mol Hum Reprod 2014 ; 20 : 938–947. [CrossRef] [PubMed] [Google Scholar]
  16. Ravel C, Siffroi JP. Y chromosome and spermatogenesis. Gynecol Obstet Fertil 2009 ; 37 : 901–907. [CrossRef] [PubMed] [Google Scholar]
  17. Chianese C, Fino MG, Riera Escamilla A, et al. Comprehensive investigation in patients affected by sperm macrocephaly and globozoospermia. Andrology 2015 ; 3 : 203–212. [CrossRef] [PubMed] [Google Scholar]
  18. Ravel C, Chantot-Bastaraud S, Siffroi JP, et al. Tail stump syndrome associated with chromosomal translocation in two brothers attempting intracytoplasmic sperm injection. Fertil Steril 2006 ; 86 : 719.e1-7. [CrossRef] [PubMed] [Google Scholar]
  19. De Braekeleer M, Nguyen MH, Morel F, Perrin A. Genetic aspects of monomorphic teratozoospermia: a review. J Assist Reprod Genet 2015 ; 32 : 615–623. [CrossRef] [PubMed] [Google Scholar]
  20. Escoffier J, Yassine S, Lee HC, et al. Subcellular localization of phospholipase Cζ in human sperm and its absence in DPY19L2-deficient sperm are consistent with its role in oocyte activation. Mol Hum Reprod 2015 ; 21 : 157–168. [CrossRef] [PubMed] [Google Scholar]
  21. Yassine S, Escoffier J, Martinez G, et al. Dpy19l2-deficient globozoospermic sperm display altered genome packaging and DNA damage that compromises the initiation of embryo development. Mol Hum Reprod 2015 ; 21 : 169–185. [CrossRef] [PubMed] [Google Scholar]
  22. Vanden Meerschaut F, Leybaert L, Nikiforaki D, et al. Diagnostic and prognostic value of calcium oscillatory pattern analysis for patients with ICSI fertilization failure. Hum Reprod 2013 ; 28 : 87–98. [CrossRef] [PubMed] [Google Scholar]
  23. Wolf JP, Ziyyat A, Ciapa B. ICSI et signalisation calcique. Med Sci (Paris) 2007 ; 23 : 475–477. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  24. Halet G, Marangos P, Fitzharris G, Carroll J. Ca2+ oscillations at fertilization in mammals. Biochem Soc Trans 2003 ; 31 : 907–911. [CrossRef] [PubMed] [Google Scholar]
  25. Ecker DJ, Stein P, Xu Z, et al. Long-term effects of culture of preimplantation mouse embryos on behavior. Proc Natl Acad Sci USA 2004 ; 101 : 1595–1600. [CrossRef] [Google Scholar]
  26. Fernandez-Gonzalez R, Moreira PN, Perez-Crespo M, et al. Long-term effects of mouse intracytoplasmic sperm injection with DNA-fragmented sperm on health and behavior of adult offspring. Biol Reprod 2008 ; 78 : 761–772. [CrossRef] [PubMed] [Google Scholar]
  27. Fernandez-Gonzale R, Ramirez MA, Pericuesta E, et al. Histone modifications at the blastocyst Axin1(Fu) locus mark the heritability of in vitro culture-induced epigenetic alterations in mice. Biol Reprod 2010 ; 83 : 720–727. [CrossRef] [PubMed] [Google Scholar]
  28. Tesarik J, Testart J. Treatment of sperm-injected human oocytes with Ca2+ ionophore supports the development of Ca2+ oscillations. Biol Reprod 1994 ; 51 : 385–391. [CrossRef] [PubMed] [Google Scholar]
  29. Hoshi K, Yanagida K, Yazawa H, et al. Intracytoplasmic sperm injection using immobilized or motile human spermatozoon. Fertil Steril 1995 ; 63 : 1241–1245. [PubMed] [Google Scholar]
  30. Yanagida K, Morozumi K, Katayose H, et al. Successful pregnancy after ICSI with strontium oocyte activation in low rates of fertilization. Reprod Biomed Online 2006 ; 13 : 801–806. [CrossRef] [PubMed] [Google Scholar]
  31. Kyono K, Kumagai S, Nishinaka C, et al. Birth and follow-up of babies born following ICSI using SrCl2 oocyte activation. Reprod Biomed Online 2008 ; 17 : 53–58. [CrossRef] [PubMed] [Google Scholar]
  32. Vanden Meerschaut F, Nikiforaki D, Heindryckx B, De Sutter P. Assisted oocyte activation following ICSI fertilization failure. Reprod Biomed Online 2014 ; 28 : 560–571. [CrossRef] [PubMed] [Google Scholar]
  33. Rexhaj E, Paoloni-Giacobino A, Rimoldi SF, et al. Mice generated by in vitro fertilization exhibit vascular dysfunction and shortened life span. J Clin Invest 2013 ; 123 : 5052–5060. [CrossRef] [PubMed] [Google Scholar]
  34. Yoon HJ, Bae IH, Kim HJ, et al. Analysis of clinical outcomes with respect to spermatozoan origin after artificial oocyte activation with a calcium ionophore. J Assist Reprod Genet 2013 ; 30 : 1569–1575. [CrossRef] [PubMed] [Google Scholar]
  35. Takisawa T, Doshida M, Hattori H, et al. Effect of oocyte activation by calcium ionophore A23187 or strontium chloride in patients with low fertilization rates and follow-up of babies. Hum Reprod 2011 ; 26 : P-141. [Google Scholar]
  36. Sato Y, Nakamura Y, Sakamoto E, et al. Follow up of children following new technology: TESE, IVM, and oocyte activation. Hum Reprod 2011 ; 26 : P-394. [Google Scholar]
  37. Vanden Meerschaut F, D’Haeseleer E, Gysels H, et al. Neonatal and neurodevelopmental outcome of children aged 3–10 years born following assisted oocyte activation. Reprod Biomed Online 2014 ; 28 : 54–63. [CrossRef] [PubMed] [Google Scholar]
  38. Deemeh MR, Tavalaee M, Nasr-Esfahani MH. Health of children born through artificial oocyte activation: a pilot study. Reprod Sci 2015 ; 22 : 322–328. [CrossRef] [PubMed] [Google Scholar]
  39. Ebner T, Montag M; Oocyte Activation Study Group, et al. Live birth after artificial oocyte activation using a ready-to-use ionophore: a prospective multicentre study. Reprod Biomed Monline 2015 ; 30 : 359–365. [CrossRef] [Google Scholar]
  40. Heindryckx B, Van der Elst J, De Sutter P, Dhont M. Treatment option for sperm- or oocyte-related fertilization failure: assisted oocyte activation following diagnostic heterologous ICSI. Hum Reprod 2005 ; 20 : 2237–2241. [CrossRef] [PubMed] [Google Scholar]
  41. Moaz MN, Khattab S, Foutouh IA, Mohsen EA. Chemical activation of oocytes in different types of sperm abnormalities in cases of low or failed fertilization after ICSI: a prospective pilot study. Reprod Biomed Online 2006 ; 13 : 791–794. [CrossRef] [PubMed] [Google Scholar]
  42. Heindryckx B, De Gheselle S, Gerris J, et al. Efficiency of assisted oocyte activation as a solution for failed intracytoplasmic sperm injection. Reprod Biomed Online 2008 ; 17 : 662–668. [CrossRef] [PubMed] [Google Scholar]
  43. Kyono K, Kumagai S, Nishinaka C, et al. Birth and follow-up of babies born following ICSI using SrCl2 oocyte activation. Reprod Biomed Online 2008 ; 17 : 53–58. [CrossRef] [PubMed] [Google Scholar]
  44. Borges E Jr, de Almeida Ferreira Braga DP, de Sousa Bonetti TC, et al. Artificial oocyte activation with calcium ionophore A23187 in intracytoplasmic sperm injection cycles using surgically retrieved spermatozoa. Fertil Steril 2009 ; 92 : 131–136. [CrossRef] [PubMed] [Google Scholar]
  45. Ebner T, Köster M, Shebl O, et al. Application of a ready-to-use calcium ionophore increases rates of fertilization and pregnancy in severe male factor infertility. Fertil Steril 2012 ; 98 : 1432–1437. [CrossRef] [PubMed] [Google Scholar]
  46. Montag M, Köster M, van der Ven K, et al. The benefit of artificial oocyte activation is dependent on the fertilization rate in a previous treatment cycle. Reprod Biomed Online 2012 ; 24 : 521–526. [CrossRef] [PubMed] [Google Scholar]
  47. Kuentz P, Vanden Meerschaut F, Elinati E, et al. Assisted oocyte activation overcomes fertilization failure in globozoospermic patients regardless of the DPY19L2 status. Hum Reprod 2013 ; 28 : 1054–1061. [CrossRef] [PubMed] [Google Scholar]
  48. Ebner T, Oppelt P, Wöber M, et al. Treatment with Ca2+ ionophore improves embryo development and outcome in cases with previous developmental problems: a prospective multicenter study. Hum Reprod 2015 ; 30 : 97–102. [CrossRef] [PubMed] [Google Scholar]

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