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Biology subjects

Umirbaeva, A.

Publications and source records attributed to Umirbaeva, A..

2 recordsLinked to original sources

Deep Learning-enabled Sperm Morphology Analysis of Bovine Sperm for label-free Imaging Flow Cytometry

Data analysis of sperm morphology is critical for evaluating bull fertility, yet it is often performed using light microscopy and staining techniques in a highly subjective and manual manner. In this study, we introduce a scalable, high-resolution approach combining label-free Imaging Flow Cytometry (IFC) with deep learning for automated classification of bovine sperm morphology. We analyzed 436,374 single-cell images obtained from three prominent bull breeds in Kazakhstan - Kazakh Whitehead, Auliekol, and Simmental from fresh and cryopreserved sperm - providing a uniquely large and diverse dataset. The dataset was used for training and evaluation of deep learning models, among which the convolutional neural network (CNN) MobileNetV4 yielded superior results, achieving 92.3% accuracy and a 0.91 F1-score after training with a Layer-wise Pretraining and Fine-Tuning (LP-FT) strategy. The model classified spermatozoa into eight distinct morphological categories. The CNN-based pipeline ensured consistent, observer-independent classification across all samples. Testing across different conditions and breeds resulted in a 5-10% drop in generalization performance, highlighting the impact of domain-specific biases and underscoring the need for larger, standardized datasets. The proportion of morphologically abnormal spermatozoa varied between seasons and after cryopreservation. This study highlights the advantages of integrating IFC and artificial intelligence (AI) algorithms for robust, high-throughput, and objective label- free spermatozoa morphology assessment in fresh and cryopreserved sperm, offering a promising tool for improving fertility diagnostics and breeding strategies in veterinary practice.

systems biology↗

Super homotypic targeting by exosome surface engineering

Homotypic targeting is the inherent ability of cells for preferential interaction with cells of similar or identical types, a phenomenon commonly seen in cell adhesion, tissue formation, and immune responses. Unfortunately, its full potential remains largely untapped. Here we introduce an approach to drastically boost the homotypic targeting capabilities of cells via exosomes (nanoscale extracellular vesicles secreted by cells). By engineering exosome surfaces with lanthanides, we amplify specific cell-exosome interactions by more than 25-fold, significantly accelerating the selective capture of exosomes by cells of the same lineage. This substantial enhancement in cellular homophilicity opens up an entirely new class of applications, two of which we showcase here with unprecedented performance: using cells to detect specific exosomes and using exosomes to detect specific cells. The concept of "super homotypic targeting" offers enormous potential to transform cancer diagnostics, immunotherapy, targeted drug delivery, tissue engineering, and vaccine development.

cell biology↗