The Effect of ATP INDUCED CALCIUM DYNAMICS ON EPITHELIAL TO MESENCHYMAL TRANSITIONS

Cells respond to a multitude of external triggers by a limited number of signaling pathways activated by receptors on plasma membrane, such as receptor tyrosine kinases (RTKs) or G protein-coupled receptors (GPCRs). These pathways do not simply convey the downstream signal, but instead the signal is very often processed by encoding and integrated with the current state of the cell. A traditional transcriptional analysis tends to provide an averaged output measured in a population, what often masks the behavior of individual cells. However, with recent single cell techniques developments, it is possible to investigate transcription in individual living cells. This contributed tremendously to the understanding of development and progression of many diseases including cancer. The more we understand about this high complexity of signaling mechanisms and multitude of cellular safety countermeasures, the more we see cancer as a microevolution state of “rebellious cells” (cells entering the fate opposite to the one intended) following a patch through a discreet system. This thesis specifically focused on the temporal aspect of signaling in the context of the epithelia-to-mensenchymal transition (EMT) by combining single cell experiments and bioinformatics analysis. We investigated cellular signaling changes in response to different dynamical profiles of the stimuli. In particular, we used the HMLER cell line, which is a metastatic breast cancer model for the epithelial to mesenchymal transition. By applying stochastic or oscillatory pulses of extracellular ATP-induced Ca2+ signals with different interspike intervals, we were investigating different transcription states from those evoked by constant ATP-induced Ca2+ dose responses. In order to precisely apply those stimulation profiles, we have developed and established a perfusion system. This device allows to treat population of cells simultaneously with the exact same dynamical profiles. Cells treated by these well contr