Mechanisms underlying divergent relationships between Ca2+and YAP/TAZ signaling

Yes-associated protein (YAP) and its homolog TAZ are transducers of several biochemical and biomechanical signals, serving to integrate multiplexed inputs from the microenvironment into higher-level cellular functions such as proliferation, differentiation, apoptosis, migration, and hemostasis. Emerging evidence suggests that Ca 2+ is a key second messenger that closely connects microenvironmental input signals and YAP/TAZ regulation. However, studies that directly modulate Ca 2+ have reported contradictory YAP/TAZ responses: In some studies, a reduction in Ca 2+ influx increases the activity of YAP/TAZ, while in others, an increase in Ca 2+ influx activates YAP/TAZ. Importantly, Ca 2+ and YAP/TAZ exhibit distinct spatiotemporal dynamics, making it difficult to unravel their connections from a purely experimental approach. In this study, we developed a network model of Ca 2+ -mediated YAP/TAZ signaling to investigate how temporal dynamics and crosstalk of signaling pathways interacting with Ca 2+ can alter YAP/TAZ response, as observed in experiments. By including six signaling modules (e.g., GPCR, IP3-Ca 2+ , Kinases, RhoA, F-actin, and Hippo-YAP/TAZ) that interact with Ca 2+ , we investigated both transient and steady-state cell response to Angiotensin II and thapsigargin stimuli. The model predicts stimuli, Ca 2+ transient, and frequency-dependent relationships between Ca 2+ and YAP/TAZ primarily mediated by signaling species like cPKC, DAG, CaMKII, and F-actin. Model results illustrate the role of Ca 2+ dynamics and CaMKII bistable response in switching the direction of changes in Ca 2+ -induced YAP/TAZ activity for different stimuli. Frequency-dependent YAP/TAZ response revealed the competition between upstream regulators of LATS1/2, leading to the YAP/TAZ non-monotonic response to periodic GPCR stimulation. This study provides new insights into the underlying mechanisms responsible for the controversial Ca 2+ -YAP/TAZ relationship observed in experiments.