An automated method to discover true events and classification of intracellular Ca 2+ profiles for endothelium in situ injury assay

• Published in: Frontiers in physiology Vol. 14; p. 1161023
• Main Authors: Sánchez-Tecuatl, Marcial, Moccia, Francesco, Martínez-Carballido, Jorge F, Berra-Romani, Roberto
• Format: Journal Article
• Language: English
• Published: Switzerland 2023
• Subjects: automated method; endothelium; intracellular Ca2; true event identification; signal processing; signal feature
• ISSN: 1664-042X; 1664-042X

Endothelial cells (ECs), being located at the interface between flowing blood and vessel wall, maintain cardiovascular homeostasis by virtue of their ability to integrate chemical and physical cues through a spatio-temporally coordinated increase in their intracellular Ca concentration ([Ca ]i). Endothelial heterogeneity suggests the existence of spatially distributed functional clusters of ECs that display different patterns of intracellular Ca response to extracellular inputs. Characterizing the overall Ca activity of the endothelial monolayer in situ requires the meticulous analysis of hundreds of ECs. This complex analysis consists in detecting and quantifying the true Ca events associated to extracellular stimulation and classifying their intracellular Ca profiles (ICPs). The injury assay technique allows exploring the Ca -dependent molecular mechanisms involved in angiogenesis and endothelial regeneration. However, there are true Ca events of nearly undetectable magnitude that are almost comparable with inherent instrumental noise. Moreover, undesirable artifacts added to the signal by mechanical injury stimulation complicate the analysis of intracellular Ca activity. In general, the study of ICPs lacks uniform criteria and reliable approaches for assessing these highly heterogeneous spatial and temporal events. Herein, we present an approach to classify ICPs that consists in three stages: 1) identification of Ca candidate events through thresholding of a feature termed left-prominence; 2) identification of non-true events, known as artifacts; and 3) ICP classification based upon event temporal location. The performance assessment of true-events identification showed competitive sensitivity = [0.9995, 0.9831], specificity = [0.9946, 0.7818] and accuracy = [0.9978, 0.9579] improvements of 2x and 14x, respectively, compared with other methods. The ICP classifier enhanced by artifact detection showed 0.9252 average accuracy with the ground-truth sets provided for validation. Results indicate that our approach ensures sturdiness to experimental protocol maneuvers, besides it is effective, simple, and configurable for different studies that use unidimensional time dependent signals as data. Furthermore, our approach would also be effective to analyze the ICPs generated by other cell types, other dyes, chemical stimulation or even signals recorded at higher frequency.