# CG-RecNet: a gated and attention-fused deep learning framework for label-free classification of neural stem cell differentiation via imaging flow cytometry

**Authors:** Qinzi Li, Fang Liu, Junyu Zhou, Xuanjian Zou, Chenlin Gao, Jingze Li

PMC · DOI: 10.3389/fcell.2026.1767574 · Frontiers in Cell and Developmental Biology · 2026-02-16

## TL;DR

CG-RecNet is a deep learning model that classifies neural stem cell differentiation using imaging flow cytometry without the need for invasive labeling.

## Contribution

CG-RecNet introduces a novel architecture combining cross-channel attention and gated CNNs for label-free NSC lineage classification.

## Key findings

- CG-RecNet achieved 96.40% accuracy in classifying NSC differentiation lineages.
- The model outperformed baselines by 1.82% and accurately identified minority oligodendrocytes without oversampling.
- Grad-CAM analysis showed the model focuses on biologically relevant features like neurite outgrowth.

## Abstract

Precise and longitudinal monitoring of Neural Stem Cell (NSC) differentiation is pivotal for advancing regenerative medicine. However, traditional identification methods rely on invasive immunochemical staining, which terminates cell viability and precludes real-time analysis.

To address these limitations, we propose CG-RecNet, a specialized deep learning framework for accurate, label-free classification of NSC differentiation lineages—specifically neurons, astrocytes, and oligodendrocytes—directly from brightfield imaging flow cytometry (IFC) data. The architecture integrates a LinAngular Cross-Channel Attention (LinAngular-XCA) Fusion Module to capture global morphological dependencies and a Gated Convolutional Neural Network (GatedCNN) Block to suppress background noise.

Validation on rat embryonic NSCs indicates that CG-RecNet achieves an overall accuracy of 96.40% and a macro-average AUC of 0.9979, representing a 1.82% improvement over established baselines. Notably, the model achieved high precision in identifying the minority oligodendrocyte lineage without synthetic oversampling.

Grad-CAM analysis indicates that the model’s attention aligns with biologically relevant hallmarks, such as neurite outgrowth and soma texture. CG-RecNet provides a reliable, non-invasive, and qualitatively interpretable tool for neural stem cell research.

## Linked entities

- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** GFAP (glial fibrillary acidic protein) [NCBI Gene 2670] {aka ALXDRD}, RBFOX3 (RNA binding fox-1 homolog 3) [NCBI Gene 146713] {aka FOX-3, FOX3, HRNBP3, NEUN}, SHH (sonic hedgehog signaling molecule) [NCBI Gene 6469] {aka HHG1, HLP3, HPE3, MCOPCB5, SMMCI, ShhNC}, APC (APC regulator of Wnt signaling pathway) [NCBI Gene 324] {aka BTPS2, DESMD, DP2, DP2.5, DP3, GS}, OLIG2 (oligodendrocyte transcription factor 2) [NCBI Gene 10215] {aka BHLHB1, OLIGO2, PRKCBP2, RACK17, bHLHe19}, SUCO (SUN domain containing ossification factor) [NCBI Gene 51430] {aka C1orf9, CH1, OPT, SLP1}
- **Diseases:** toxicity (MESH:D064420), demyelinating diseases (MESH:D003711), MS (MESH:D009103), neuronal loss (MESH:D009410), AD (MESH:D000544), PD (MESH:D010300), traumatic injuries (MESH:D014947), neurodegenerative conditions (MESH:D019636), inflammatory (MESH:D007249), NSC (MESH:D000092423), Neurological disorders (MESH:D009461), neurological diseases (MESH:D020271)
- **Chemicals:** RA (MESH:D014212)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12950795/full.md

## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC12950795/full.md

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Source: https://tomesphere.com/paper/PMC12950795