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Reproduction, Fertility and Development Reproduction, Fertility and Development Society
Vertebrate reproductive science and technology
RESEARCH ARTICLE (Open Access)

Identifying the composition of large vesicles in the cytoplasm of oocytes

Karen L. Reader https://orcid.org/0000-0002-5253-0666 A * , Isabella G. Pratt A , Georgia L. Lawson A and Robert J. Woolley B
+ Author Affiliations
- Author Affiliations

A Department of Pathology, University of Otago, Dunedin, New Zealand.

B Confocal Microscopy Unit, Research Infrastructure Centre, University of Otago, Dunedin, New Zealand.

* Correspondence to: karen.reader@otago.ac.nz

Handling Editor: Marc Yeste

Reproduction, Fertility and Development 37, RD24131 https://doi.org/10.1071/RD24131
Submitted: 14 August 2024  Accepted: 26 November 2024  Published online: 17 December 2024

© 2025 The Author(s) (or their employer(s)). Published by CSIRO Publishing. This is an open access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND)

Abstract

Context

Oocyte vesicles, or vacuoles, have been described using transmission electron microscopy in most species. In sheep and cow oocytes, vesicles constitute up to 30% of the cytoplasm, their volume decreases during maturation and is lower in poorer quality oocytes, suggesting they are important for oocyte competence. However, the composition and function of these organelles is unknown.

Aim

This study aimed to ascertain the content of oocyte vesicles and examine the effect of different fixation methods on the size and preservation of these organelles.

Methods

Sheep oocytes were centrifuged to segregate organelles then stained with organelle-specific fluorescent dyes (Nile Red, LysoTracker, Fluo-4-AM and TMRM) and imaged by live cell confocal microscopy. The oocytes were fixed with either glutaraldehyde or paraformaldehyde and prepared for electron microscopy to confirm the distribution of organelles and compare ultrastructure and organelle size.

Key results

Nile Red staining has identified that vesicles contain lipid that is different to that in the osmium-stained lipid droplets observed by electron microscopy. Lipid droplets and vesicles were significantly smaller when prepared for electron microscopy compared to live cell imaging. Organelles were less likely to be fully segregated following centrifugation in oocytes prior to maturation (20%) compared to oocytes after maturation (77%; P < 0.0001).

Conclusions

Oocyte vesicles are lipid storing organelles that may be important for oocyte quality.

Implications

This study highlights the importance of lipid for oocyte quality and the need for further research to identify the optimal fatty acid content for in vitro maturation media and oocyte competence.

Keywords: confocal microscopy, electron microscopy, lipid, oocyte quality, vesicles.

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