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Biology subjects

Hufgard, S.

Publications and source records attributed to Hufgard, S..

2 recordsLinked to original sources

Classifying Calcium Imaging Dynamics with Deep Learning: Multi-Frequency Analysis through Quantile-Based Time-Series Network Representations

To address the limitations of calcium imaging data, we propose a segmentation-agnostic deep learning framework that integrates Quantile-Based Time-Series Network (QTN) representations with convolutional neural networks to classify neuronal dynamics across multiple spatial resolutions and acquisition frequencies. By transforming fluorescence traces into compact, fixed-size matrices derived from quantile transitions, the method standardizes inputs across recordings while markedly reducing dimensionality and computational cost. Several QTN variants were systematically evaluated, demonstrating strong and consistent classification performance across both whole-image and grid-based preprocessing strategies. Notably, the framework maintained high accuracy under reduced temporal resolution and controlled noise perturbations, confirming that discrimination arises from meaningful temporal patterns rather than artifacts. This study establishes a robust, scalable, and generalizable approach for analyzing calcium imaging dynamics, paving the way for efficient, segmentation-independent characterization of neuronal activity in pharmacological and systems neuroscience applications.

cell biology↗

Human cerebral organoids model tumor infiltration and migration supported by astrocytes in an autologous setting

Efforts to achieve precise and efficient tumor targeting of highly malignant brain tumors are constrained by the dearth of appropriate models to study the effects and potential side effects of radiation, chemotherapy, and immunotherapy on the most complex human organ, the brain. We established a cerebral organoid model of brain tumorigenesis in an autologous setting by overexpressing c-MYC as one of the most common oncogenes in brain tumors. GFP+/c-MYChigh cells were isolated from tumor organoids and used in two different culture approaches: assembloids comprising of a normal cerebral organoid with a GFP+/c-MYChigh tumor sphere and co-culture of cerebral organoid slices at air-liquid interface with GFP+/c-MYChigh cells. GFP+/c-MYChigh cells used in both approaches exhibited tumor-like properties, including overexpression of the c-MYC oncogene, high proliferative and invasive potential, and an immature phenotype as evidenced by increased expression of Ki-67, VIM, and CD133. Organoids and organoid slices served as suitable scaffolds for infiltrating tumor-like cells. Using our highly reproducible and powerful model system that allows long-term culture, we demonstrated that the migratory and infiltrative potential of tumor-like cells is shaped by the environment in which glia cells provide support to tumor-like cells.

cell biology↗