The process of programmable cell death, i.e., apoptosis, physiologically occurs during development and aging and as a homeostatic mechanism to maintain cell populations in tissues. Apoptosis also happens as a defense mechanism in immune reactions or when cells are damaged by disease or external stimuli (drugs). Due to its complexity and the fact that apoptosis fate resolves in a very short time (a few hours in general), apoptosis mechanisms have been extensively studied only recently with the advent of advanced time-lapse microscopy. Timing related to apoptosis stages is strongly correlated to many factors including cell type, drug dose, cell microenvironment, and related cross-talks whose knowledge is too little to predict apoptosis duration. Such times are of fundamental importance since they linked with drug efficacy, immunotherapy treatment, cancer-immune interaction effectiveness. In light of this, by exploiting video analysis, deep learning algorithms, and multiple linear regression, we presented a platform to examine the apoptosis and blebbing times with very high accuracy and precision levels. More in detail, we artificially generated, through a computer vision analysis platform, synthetic apoptosis videos with randomly variated apoptosis timing profiles. By using a pre-trained Convolutional Neural Network (CNN) architecture within the so-called transfer learning procedure, we encoded each frame of the video into a list of numerical descriptors. Automatic examination of apoptosis timing profiles was then accomplished by training a multivariate linear regression (MLR) model. An extended version of the work will present further advancement of this research by considering real videos of dying cells and additional confounding effects.
Mencattini, A., Casti, P., Filippi, J., D(')Orazio, M., Cardarelli, S., Antonelli, G., et al. (2022). Robust examination of cell apoptosis timing in presence of noisy environment. In 2022 IEEE International Symposium on Medical Measurements and Applications (MeMeA): proceedings (pp.1-5). New York : IEEE [10.1109/MeMeA54994.2022.9856514].
Robust examination of cell apoptosis timing in presence of noisy environment
Mencattini, A.;Casti, P.;Filippi, J.;D(')Orazio, M.;Cardarelli, S.;Antonelli, G.;Martinelli, E.
2022-01-01
Abstract
The process of programmable cell death, i.e., apoptosis, physiologically occurs during development and aging and as a homeostatic mechanism to maintain cell populations in tissues. Apoptosis also happens as a defense mechanism in immune reactions or when cells are damaged by disease or external stimuli (drugs). Due to its complexity and the fact that apoptosis fate resolves in a very short time (a few hours in general), apoptosis mechanisms have been extensively studied only recently with the advent of advanced time-lapse microscopy. Timing related to apoptosis stages is strongly correlated to many factors including cell type, drug dose, cell microenvironment, and related cross-talks whose knowledge is too little to predict apoptosis duration. Such times are of fundamental importance since they linked with drug efficacy, immunotherapy treatment, cancer-immune interaction effectiveness. In light of this, by exploiting video analysis, deep learning algorithms, and multiple linear regression, we presented a platform to examine the apoptosis and blebbing times with very high accuracy and precision levels. More in detail, we artificially generated, through a computer vision analysis platform, synthetic apoptosis videos with randomly variated apoptosis timing profiles. By using a pre-trained Convolutional Neural Network (CNN) architecture within the so-called transfer learning procedure, we encoded each frame of the video into a list of numerical descriptors. Automatic examination of apoptosis timing profiles was then accomplished by training a multivariate linear regression (MLR) model. An extended version of the work will present further advancement of this research by considering real videos of dying cells and additional confounding effects.| File | Dimensione | Formato | |
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