Résumé
The mucociliary function of the bronchial epithelium ensures the continuous clearance of the respiratory system. This function relies on two main elements: mucus properties and cilia beating coordination. We work on high speed optical microscopy videos of Human bronchial epithelium from ALI (Air-liquid interface) cultures. We present here a technique based on the tracking of each cilium and on the spatiotemporal analysis of the obtained trajectories. To relate each cilium to its corresponding cell, a clustering method is used. The spatiotemporal coordination can than be quantified both, inside and in-between ciliated cells. In addition the physical parameters can be mapped to observe the heterogeneity of the cilia activity and compare different pathologies.