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Mouse Round Spermatid Injection
Published on: January 26, 2024
Methodology matters: IVF versus ICSI and embryonic gene expression.
Phillip J Bridges1, Myoungkun Jeoung, Heyoung Kim
1Division of Clinical and Reproductive Sciences, University of Kentucky, Lexington, KY 40536, USA.
Reproductive Biomedicine Online
|June 14, 2011
Summary
Intracytoplasmic sperm injection (ICSI) and ICSI with artificial oocyte activation (ICSI-A) alter gene expression in blastocysts compared to in vitro fertilization (IVF). These genetic changes may explain adverse outcomes associated with assisted reproduction treatments.
Area of Science:
- Reproductive biology
- Developmental biology
- Genomics
Background:
- Assisted reproduction treatments (ART), particularly intracytoplasmic sperm injection (ICSI), are associated with adverse outcomes.
- The underlying genetic causes of these adverse effects remain largely unknown.
Purpose of the Study:
- To investigate gene expression differences in blastocysts created via ICSI and ICSI with artificial oocyte activation (ICSI-A) compared to conventional in vitro fertilization (IVF).
- To provide genetic insights that could aid in diagnosing or treating ART-related adverse effects and refine ART techniques.
Main Methods:
- Murine blastocysts were generated using ICSI, ICSI-A, and IVF.
- Microarray analysis was employed to assess gene expression profiles.
- Differential gene expression and affected biological pathways were identified.
Main Results:
- Significant differences in gene expression were observed: 197 genes between ICSI and IVF blastocysts (P < 0.01).
- 132 genes differed between ICSI-A and IVF blastocysts (P < 0.01).
- 65 genes differed between ICSI-A and ICSI blastocysts (P < 0.01).
- Procedural-induced genetic changes in specific pathways showed correlation with known adverse consequences.
Conclusions:
- ICSI and ICSI-A significantly alter blastocyst gene expression compared to IVF.
- These genetic alterations may underlie adverse outcomes observed in ART.
- Further research into procedure-specific genetic dysfunction is warranted.
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