AI Article Synopsis

  • Meiotic maturation is essential for oocyte development and successful fertilization, and understanding this process can enhance research and reproductive technologies.
  • The study introduces a computational framework that uses machine learning to analyze oocyte images and identify morphological characteristics from various species via a Fiji plugin.
  • Key findings include the identification of specific features like zona pellucida texture and cytoplasmic particle size to predict maturation potential, with implications for both mouse and human oocytes.

Article Abstract

Meiotic maturation is a crucial step of oocyte formation, allowing its potential fertilization and embryo development. Elucidating this process is important for both fundamental research and assisted reproductive technology. However, few computational tools based on non-invasive measurements are available to characterize oocyte meiotic maturation. Here, we develop a computational framework to phenotype oocytes based on images acquired in transmitted light. We trained neural networks to segment the contour of oocytes and their zona pellucida using oocytes from diverse species. We defined a comprehensive set of morphological features to describe an oocyte. These steps were implemented in an open-source Fiji plugin. We present a feature-based machine learning pipeline to recognize oocyte populations and determine morphological differences between them. We first demonstrate its potential to screen oocytes from different strains and automatically identify their morphological characteristics. Its second application is to predict and characterize the maturation potential of oocytes. We identify the texture of the zona pellucida and cytoplasmic particle size as features to assess mouse oocyte maturation potential and tested whether these features were applicable to the developmental potential of human oocytes. This article has an associated First Person interview with the first author of the paper.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9377708PMC
http://dx.doi.org/10.1242/jcs.260281DOI Listing

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