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Updated: Aug 18, 2026

Human Egg Maturity Assessment and Its Clinical Application
Published on: August 19, 2019
Effects of maturation conditions on spindle morphology in porcine MII oocytes
Satoshi Ueno1, Mayuko Kurome, Hideto Ueda
1Laboratory of Developmental Engineering, Department of Life Science, School of Agriculture, Meiji University, Kawasaki, Japan. cf50405@isc.meiji.ac.jp
Abstract:
Incomplete cytoplasmic maturation of in vitro matured (IVM) oocytes has been known to cause microtubule and microfilament alterations, which may result in abnormal pronuclear formation and failed embryonic development. We examined the influences of maturation conditions on meiotic spindle morphology at metaphase of meiosis II (MII) in porcine oocytes. Porcine oocytes were matured under various conditions, i.e., in vitro or in vivo, with different amounts of cumulus cells, with or without hormonal supplements, and with various exposure durations to the hormones, to examine the effects on spindle morphology in MII oocytes by immunofluorescence under confocal laser microscopy. Interpolar spindle length (microm) and spindle area (microm2) were compared among these maturation conditions. The spindle length was significantly shorter in IVM oocytes compared to those matured in vivo. Oocytes collected from cumulus oocyte complexes (COCs), which were poor in cumulus cells, showed smaller spindle areas than those from cumulus-rich COCs. The spindle length and area were both significantly reduced in oocytes grown without hormonal supplements. When oocytes were grown with hormonal supplements for either 6 or 22 hours for the first half of culture, there was no difference in the spindle morphology between these oocytes. These results suggested that maturation conditions significantly influence morphogenesis of MII spindles in porcine oocytes. Oocytes matured in poor conditions were more likely to have a shorter spindle length (long axis) and smaller spindle areas.
Insights
Maturation conditions significantly impact spindle morphology in porcine oocytes. Poor in vitro maturation (IVM) conditions lead to shorter spindle length and smaller spindle areas, affecting embryonic development.
Area of Science:
- Reproductive Biology
- Cell Biology
- Developmental Biology
Background:
- In vitro matured (IVM) oocytes often exhibit incomplete cytoplasmic maturation.
- This can lead to microtubule and microfilament alterations, impacting pronuclear formation and embryonic development.
- Meiotic spindle morphology is crucial for successful oocyte maturation and subsequent development.
Purpose of the Study:
- To investigate the influence of various maturation conditions on meiotic spindle morphology in porcine oocytes at metaphase of meiosis II (MII).
- To compare spindle length and area under different in vitro and in vivo maturation protocols.
- To identify specific maturation factors affecting spindle organization.
Main Methods:
- Porcine oocytes were matured in vitro and in vivo under varying conditions.
- Conditions included different amounts of cumulus cells, presence/absence of hormonal supplements, and hormone exposure durations.
- Spindle morphology (interpolar spindle length and spindle area) was assessed using immunofluorescence and confocal laser microscopy.
Main Results:
- In vitro matured (IVM) oocytes had significantly shorter spindle lengths compared to in vivo matured oocytes.
- Oocytes from cumulus oocyte complexes (COCs) with fewer cumulus cells showed smaller spindle areas.
- Oocytes matured without hormonal supplements exhibited significantly reduced spindle length and area.
- Hormone exposure duration (6 vs. 22 hours) did not significantly affect spindle morphology.
Conclusions:
- Maturation conditions critically influence the morphogenesis of MII spindles in porcine oocytes.
- Suboptimal maturation conditions, such as those with poor cumulus cell support or lack of hormonal supplementation, result in abnormal spindle morphology.
- These spindle alterations may contribute to the reduced developmental potential observed in oocytes matured in vitro under suboptimal conditions.
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