# Metabolic Comparison of Mature and Immature Bovine Cumulus–Oocyte Complexes with Standardization of Bioenergetic Assessment

**Authors:** Cristina Algieri, Emilia Attolini, Eleonora Iacono, Salvatore Nesci, Barbara Merlo

PMC · DOI: 10.3390/biom16020317 · Biomolecules · 2026-02-18

## TL;DR

This study compares the metabolism of immature and mature bovine egg complexes and finds that mature eggs rely more on mitochondria for energy.

## Contribution

The study establishes standardized conditions for measuring metabolism in bovine egg complexes during in vitro maturation.

## Key findings

- Mature bovine egg complexes show increased mitochondrial ATP production compared to immature ones.
- HSOF medium and adhesion with fibronectin or concanavalin A improve metabolic measurements in immature complexes.
- Metabolic profiles are significantly affected by adhesion conditions and medium choice.

## Abstract

This study compared the bioenergetic profiles of immature and in vitro–matured bovine cumulus–oocyte complexes (COCs) using Seahorse extracellular flux technology, with the aim of establishing standardized conditions for real-time metabolic assessment during in vitro maturation (IVM). Groups of five COCs were analysed prior to maturation and after 22 h of IVM using the Seahorse XFp Analyzer to measure oxygen consumption rate (OCR, pmoL/min) and extracellular acidification rate (ECAR, mpH/min), providing dynamic readouts of oxidative phosphorylation and glycolysis that extend beyond conventional endpoint assays. To optimize assay performance, three media were first evaluated: TCM199, DMEM/F12, and HEPES-buffered synthetic oviductal fluid (HSOF). HSOF yielded the most reliable readings for immature COCs, whereas TCM199 provided superior conditions for mature COCs. Adhesion strategies were then tested by comparing uncoated wells with wells coated with fibronectin, concanavalin A, or Matrigel®. Sequential injections of oligomycin and rotenone plus antimycin A enabled partitioning of mitochondrial and glycolytic contributions to ATP production. COC maturation was associated with a clear metabolic shift from glycolysis toward oxidative metabolism. Immature COCs displayed a predominantly glycolytic phenotype, while mature COCs showed increased active mitochondrial ATP production. Adhesion conditions markedly affected the detected metabolic profile: concanavalin A and fibronectin supported effective attachment and were associated with robust energy metabolism, whereas Matrigel® and poor adhesion were linked to quiescent profiles with low OCR and ECAR signals. Together, these data define practical assay parameters for extracellular flux analysis of COCs and highlight the increasing reliance on mitochondrial function as a hallmark of oocyte maturation, supporting improved metabolic phenotyping for IVM optimization.

## Linked entities

- **Species:** Bos taurus (taxon 9913)

## Full-text entities

- **Genes:** EGFR (epidermal growth factor receptor) [NCBI Gene 407217], Fn1 (fibronectin 1) [NCBI Gene 14268] {aka E330027I09, Fn, Fn-1}, EGF (epidermal growth factor) [NCBI Gene 530315], epidermal growth factor [NCBI Gene 521832], IGF1 (insulin like growth factor 1) [NCBI Gene 281239] {aka IGF-1, IGF-I}, FN1 (fibronectin 1) [NCBI Gene 280794] {aka FN}
- **Diseases:** injury to (MESH:D014947), tumor (MESH:D009369), hypoxic (MESH:D002534)
- **Chemicals:** Oxygen (MESH:D010100), pyruvate (MESH:D019289), cGMP (MESH:D006152), PVA (MESH:C063253), ADP (MESH:D000244), pentose phosphate (MESH:D010428), lactate (MESH:D019344), mineral oil (MESH:D008899), F12 (MESH:C007782), nucleotides (MESH:D009711), bisbenzimide (MESH:D006690), water (MESH:D014867), kanamycin (MESH:D007612), glycin (MESH:D005998), silicone (MESH:D012828), proton (MESH:D011522), HEPES (MESH:D006531), NaHCO3 (MESH:D017693), Rot (-), polyvinyl alcohol (MESH:D011142), Hoechst 33342 (MESH:C017807), AA (MESH:D000596), antimycin A (MESH:D000968), L-cysteine (MESH:D003545), lipid (MESH:D008055), ATP (MESH:D000255), CO2 (MESH:D002245), glutathione (MESH:D005978), rot (MESH:D012402), glutamine (MESH:D005973), Glucose (MESH:D005947), olig (MESH:D009840), ROS (MESH:D017382), PBS (MESH:D007854), LH (MESH:D007986)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Bos taurus (bovine, species) [taxon 9913]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12938731/full.md

## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938731/full.md

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Source: https://tomesphere.com/paper/PMC12938731