Related Experiment Videos
The effects of cooling human oocytes
A H Sathananthan1, A Trounson, L Freemann
1Centre for Early Human Development, Monash Medical Centre, Clayton, Victoria, Australia.
Human Reproduction (Oxford, England)
|November 1, 1988
Summary
Cooling human oocytes to 0°C disrupts meiotic spindles, even with cryoprotectant dimethyl sulfoxide (DMSO). This simple cooling damages microtubules, affecting oocyte structure and chromosome arrangement.
Area of Science:
- Reproductive Biology
- Cell Biology
- Cryobiology
Background:
- Human oocyte cryopreservation is crucial for fertility treatments.
- Understanding the effects of low temperatures on oocyte structure is vital for improving cryopreservation success rates.
Purpose of the Study:
- To investigate the impact of cooling on the meiotic spindle and overall structure of preovulatory human oocytes.
- To evaluate the cryoprotective efficacy of dimethyl sulfoxide (DMSO) against cooling-induced damage.
Main Methods:
- Human oocytes were cooled to 0°C at 1°C/min, with or without DMSO.
- Oocytes were held at 0°C for 20 or 60 minutes.
- Transmission electron microscopy (TEM) was used to examine oocyte structure and meiotic spindles at 0°C or 8°C, with controls at 22°C or 37°C.
Main Results:
- Cooling to 0°C caused significant disassembly of meiotic spindles due to microtubule depolymerization, irrespective of DMSO presence.
- DMSO offered minimal stabilization; cooled oocytes showed disorganized spindles and abnormal chromosome arrangement.
- Other cellular components like endoplasmic reticulum and mitochondria were also adversely affected in some cooled oocytes and cumulus cells.
Conclusions:
- Human oocyte meiotic spindles are highly sensitive to simple cooling, even at 0°C.
- Dimethyl sulfoxide (DMSO) does not provide substantial stabilization to meiotic spindles during cooling.
- These findings highlight the vulnerability of oocytes to thermal stress and inform strategies for improving oocyte cryopreservation.