2014
DOI: 10.1016/j.ygcen.2013.11.001
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Application of intracytoplasmic sperm injection (ICSI) for fertilization and development in birds

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Cited by 8 publications
(4 citation statements)
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“…Indeed, the volume of quail egg cytoplasm is more than 1-2 µL, whereas that of the mouse is approximately 200 pL. 9 Egg-activating proteins equivalent to 100-200 sperm are required for fertilization and full-term development to hatching in quails, which supports the strong correlation between egg size and polyspermy (Birkhead et al 1994;Mizushima 2012Shimada et al 2014;Kang et al 2015).…”
Section: Egg Size and Sperm Numbermentioning
confidence: 90%
See 1 more Smart Citation
“…Indeed, the volume of quail egg cytoplasm is more than 1-2 µL, whereas that of the mouse is approximately 200 pL. 9 Egg-activating proteins equivalent to 100-200 sperm are required for fertilization and full-term development to hatching in quails, which supports the strong correlation between egg size and polyspermy (Birkhead et al 1994;Mizushima 2012Shimada et al 2014;Kang et al 2015).…”
Section: Egg Size and Sperm Numbermentioning
confidence: 90%
“…This finding suggests that the fertilization rate increases when the number of sperm incorporated into an egg is higher. In addition, the direct injection of sperm into the cytoplasm of a mature quail egg, namely, an intracytoplasmic sperm injection (ICSI), directly revealed that a single sperm was insufficient for a high rate of fertilization and subsequent blastoderm development (approximately 20%; Hrabia et al 2003;Takagi et al 2007a;Mizushima 2008Mizushima , 2009Mizushima , 2012Shimada et al 2014;Kang et al 2015). It has been proposed that the purpose of polyspermy is to increase the opportunity of a sperm nucleus migrating to the center of the germinal disc and making contact with the female nucleus because the surface area of the avian germinal disc in relation to that of sperm is very large.…”
mentioning
confidence: 99%
“…In the chicken, CRISPR/Cas9 has been used to knock out genes in somatic cells of the developing embryo [ 16 ], but no germline modifications have been reported. In birds, direct injection of constructs into the zygote and SCNT approaches are impractical, owing to the structure of the zygote, the opacity of the oocyte, and the difficulty in retrieving, manipulating, and culturing early embryos to term [ 17 , 18 ]. Direct in vivo transfection of germline cells in embryos by lipofection is an alternative strategy to introduce constructs but the efficiency of transfection is low [ 19 , 20 ].…”
Section: Introductionmentioning
confidence: 99%
“…Thus, the relatively simple straightforward one-cell embryo microinjection procedures of generating genome edited mammalian embryos or SCNT cannot be easily replicated in birds as the early stage embryo is not accessible. Recent advances, however, have been made manipulating the early stage of ovum using intracytoplasmic sperm injection (ICSI) for fertilisation 24 and a surrogate shell for incubation. 25 However, this ICSI method has yet to be used for GE as few hatchlings were obtained from the ICSI embryos.…”
Section: Ge Of Bird Speciesmentioning
confidence: 99%