ICSI-generated mouse zygotes exhibit altered calcium oscillations, inositol 1,4,5-trisphosphate receptor-1 down-regulation, and embryo development

Mol Hum Reprod. 2003 Sep;9(9):523-33. doi: 10.1093/molehr/gag072.

Abstract

ICSI bypasses not only fusion of the gametes but also a series of signalling events that occur in the sperm prior to and during interaction with the oocyte's vestments. The effect of this altered encounter of the gametes on the fertilization-associated intracellular calcium ([Ca2+]i) oscillations has not been thoroughly investigated. Here, ICSI and IVF were performed using gametes from two mouse strains, B6D2F1 and CD1, and in-vitro development, pattern of [Ca2+]i oscillations and down-regulation of inositol 1,4,5-trisphosphate receptor-1 (IP3R-1) in the produced embryos were compared. ICSI and IVF resulted in comparable rates of activation and pre-implantation development. However, ICSI-generated zygotes cleaved at a slower rate, had lower cell numbers and lower hatching rates. The deleterious effects of ICSI could not be exclusively attributed to the injury by the injection since sham-injected IVF zygotes only exhibited delayed progression to the blastocyst stage. ICSI and IVF induced similar initial [Ca2+]i responses, although ICSI zygotes exhibited shorter durations of [Ca2+]i oscillations and showed diminished degradation of IP3R-1. Importantly, sperm manipulation affected the pattern of oscillations, which further decreased pre-implantation developmental rates. Our results demonstrate that ICSI-induced [Ca2+]i responses are not equivalent to those initiated by IVF and that this may have developmental consequences.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Blastocyst / metabolism
  • Calcium / metabolism
  • Calcium Channels / metabolism*
  • Calcium Signaling*
  • Cell Membrane / metabolism
  • Down-Regulation*
  • Embryo, Mammalian / embryology*
  • Embryo, Mammalian / metabolism*
  • Embryonic and Fetal Development
  • Female
  • Inositol 1,4,5-Trisphosphate Receptors
  • Male
  • Mice
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Sperm Injections, Intracytoplasmic*
  • Spermatozoa / cytology
  • Spermatozoa / metabolism
  • Zygote / metabolism*

Substances

  • Calcium Channels
  • Inositol 1,4,5-Trisphosphate Receptors
  • Receptors, Cytoplasmic and Nuclear
  • Calcium