# Deep learning models to map osteocyte networks from confocal microscopy can successfully distinguish between young and aged bone

**Authors:** Simon D. Vetter, Charles A. Schurman, Tamara Alliston, Gregory Slabaugh, Stefaan W. Verbruggen

PMC · DOI: 10.1371/journal.pcbi.1013914 · PLOS Computational Biology · 2026-01-27

## TL;DR

This study uses deep learning to quickly analyze osteocyte networks in bone tissue, distinguishing between young and aged samples efficiently.

## Contribution

The study introduces a deep learning approach to automate osteocyte network analysis, drastically reducing analysis time.

## Key findings

- A deep learning model segmented osteocyte networks in 10 seconds versus 130 hours manually.
- The model could distinguish between young and aged mouse bone samples.
- The model partially captured degeneration from genetic modifications.

## Abstract

Osteocytes, the most abundant and mechanosensitive cells in bone tissue, play a pivotal role in bone homeostasis and mechano-responsiveness, orchestrating the delicate balance between bone formation and resorption under daily activity. Studying osteocyte connectivity and understanding their intricate arrangement within the lacunar canalicular network is essential for unravelling bone physiology, which is significantly disrupted during ageing. Much work has been carried out to investigate this relationship, often involving high resolution microscopy of discrete fragments of this network, alongside advanced computational modelling of individual cells. However, traditional methods of segmenting and measuring osteocyte connectomics are time-consuming and labour-intensive, often hindered by human subjectivity and limited throughput. In this study, we explored the application of deep learning and computer vision techniques to automate the segmentation and measurement of osteocyte connectomics, enabling more efficient and accurate analysis. For this specific application, once trained, the analysis was completed within 10 seconds, compared to manual segmentation time of 130 hours. We compared a number of state-of-the-art computer vision models (U-Nets and Vision Transformers) to successfully segment the osteocyte network, finding that an Attention U-Net model can accurately segment and measure 81.8% of osteocytes and 42.1% of dendritic processes, when compared to manual labelling. While further development is required, we demonstrated that this degree of accuracy is already sufficient to distinguish between bones of young (2-month-old) and aged (36-month-old) mice, as well as partially capturing the degeneration induced by genetic modification of osteocytes. Comparison of the model predictions with manual measurements showed no significant difference, indicating that, with additional training, such deep learning algorithms could be trained to human-level accuracy when measuring the osteocyte network. By harnessing the power of these advanced technologies, further developments will likely shed light on the complexities of osteocyte networks with ever-increasing efficiency.

Osteocytes make up the vast majority of our bone cells, and are spread in a complex network throughout our bone tissue, making them difficult to visualize and time-consuming to measure. This study applied cutting edge machine learning techniques to confocal microscopy scans of the osteocyte network, cutting analysis time down from 130 hours to 10 seconds. Interestingly, the models were sufficiently accurate to distinguish between bones of young and aged mice. Similarly, the models partially captured the degeneration induced by key genetic mutations. This study presents a powerful new tool to analyse bone structure at the cellular scale.

## Linked entities

- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Tgfbr2 (transforming growth factor, beta receptor II) [NCBI Gene 21813] {aka 1110020H15Rik, DNIIR, RIIDN, TBR-II, TbetaR-II, TbetaRII}, Tgfbr1 (transforming growth factor, beta receptor I) [NCBI Gene 21812] {aka ALK5, Alk-5, ESK2, TGFR-1, TbetaR-I, TbetaRI}, Bglap2 (bone gamma-carboxyglutamate protein 2) [NCBI Gene 12097] {aka BGP2, Bglap1, Bgp, Og2, mOC-B}
- **Diseases:** inflammatory (MESH:D007249), osteoporosis (MESH:D010024)
- **Chemicals:** PBS (MESH:D007854), sucrose (MESH:D013395), EDTA (MESH:D004492), phalloidin (MESH:D010590), Alexa Fluor 488-Phalloidin (-), glucose (MESH:D005947), DAPI (MESH:C007293), OCT (MESH:C051883)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090], Ovis aries (domestic sheep, species) [taxon 9940]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12875574/full.md

## References

61 references — full list in the complete paper: https://tomesphere.com/paper/PMC12875574/full.md

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Source: https://tomesphere.com/paper/PMC12875574