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Developmental potential of biopsied mouse blastocysts.
1Centre for Reproductive Medicine, Vrije Universiteit Brussel, Belgium.
The Journal of Experimental Zoology
|November 1, 1990
Summary
Trophectoderm cell biopsy in hatching mouse blastocysts impairs in vitro implantation and early development. Biopsy, particularly of polar trophectoderm cells, significantly reduces the chances of reaching the egg cylinder stage, impacting embryo viability.
Area of Science:
- Embryology
- Developmental Biology
- Reproductive Science
Background:
- Preimplantation embryo health is crucial for successful pregnancy.
- Cellular biopsy of early embryos is a technique explored for diagnostic purposes.
- Trophectoderm cells contribute to implantation and early embryonic development.
Purpose of the Study:
- To evaluate the impact of trophectoderm cell biopsy on mouse blastocyst in vitro implantation.
- To assess the effect of biopsy on early egg cylinder formation.
- To determine the viability and developmental potential of biopsied blastocysts.
Main Methods:
- Mouse blastocysts were cultured in vitro after hCG administration.
- Hatching was induced or occurred spontaneously.
- Trophectoderm cells were removed using micromanipulation.
- Embryo viability was assessed using FDA staining.
- In vitro implantation and egg cylinder formation were evaluated.
Main Results:
- Biopsy of trophectoderm cells from hatching blastocysts impaired in vitro implantation.
- Zona pellucida shedding and implantation rates were reduced post-biopsy.
- Biopsy of polar trophectoderm cells significantly decreased the number of embryos reaching the egg cylinder stage.
- FDA staining indicated reduced viability in biopsied embryos.
Conclusions:
- Trophectoderm cell biopsy negatively affects the implantation potential and early development of mouse blastocysts.
- The extent of impairment is notable, especially when polar trophectoderm cells are targeted.
- These findings highlight potential risks associated with embryonic cell biopsy in assisted reproductive technologies.