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Wu, B.-S.

Publications and source records attributed to Wu, B.-S..

2 recordsLinked to original sources

CASTLE: a training-free foundation-model pipeline for cross-species behavioral classification

Accurately and efficiently quantifying animal behavior at scale without intensive manual labeling is a long-standing challenge for neuroscience and ethology. Keypoint-based tracking emphasizes simplicity and efficiency but loses the richness of posture and context, while emerging foundation models capture pixel-level details, yet often require nontrivial efforts of retraining and can be more sensitive to backgrounds or lighting. Here, we present CASTLE, a training-free pipeline that addresses all these issues by synergistically combining foundation models for segmentation, tracking, and feature extraction. By isolating regions-of-interest (ROI), CASTLE first generates "focused (ROI-masked)" and orientation-invariant latent features, capturing rich postural details in zero-shot, fine-tuning-free manners. Following ROI isolation, CASTLE, through an interactive "Behavior Microscope" module, supports hierarchical clustering, for progressive, human-in-the-loop embedding and clustering. This enables raw-image-assisted discovery of behavioral classes without predefined categories. Across mice, Drosophila and C. elegans, CASTLE matches expert class annotations (>90%), reveals disease-relevant phenotypes in Parkinsonian mouse models. By eliminating purpose-specific model training and providing a raw-image-informed accessible workflow, CASTLE offers a scalable framework for interpretable, cross-species behavioral phenotyping.

neuroscience↗

Mixed Selectivity of Subthalamic Nucleus Neurons in Encoding Motor and Reward Behaviors

The subthalamic nucleus (STN) plays a critical role in modulating motor and cognitive functions within the basal ganglia, with its dysfunction being implicated in movement disorders such as Parkinsons disease. However, the behavioral representations of individual STN neurons remain incompletely understood. Using in vivo two-photon calcium imaging in behaving mice, we systematically mapped the activity of single STN neurons across diverse behavioral contexts, including locomotion, licking, and reward-driven actions. Our findings reveal that STN neurons exhibit mixed selectivity, encoding multiple behaviors with distinct temporal dynamics and excitatory or inhibitory response patterns. This mixed selectivity allows the STN to robustly encode motor parameters such as locomotion speed and licking intensity while integrating contextual information from different behavioral states. Comparisons with the adjacent zona incerta (ZI) revealed distinct encoding properties: while both regions represent locomotion, STN neurons more faithfully track motor states, whereas ZI neurons exhibit prolonged calcium events with weaker movement correlations. Population-level analysis showed STN activity in a low-dimensional neural manifold, with components linked to movement velocity and licking intensity. Notably, locomotion encoding in STN was context-dependent, diverging when movements were internally generated versus reward-modulated. Together, these findings highlight the specialized yet flexible role of the STN in integrating motor and reward-related signals, supporting a framework in which STN neurons contribute to motor control through multiplexed and context-dependent encoding. This work provides new insights into the functional organization of basal ganglia circuits and has implications for understanding STNs role in both physiological and pathological conditions.

neuroscience↗