The Phase Lag between Agonist-Induced Oscillatory Ca2+ and IP3 Signals Does Not Imply Causality (December 2015).

Abstract

Activated phospholipase C (PLC*) generates 1,4,5-triphosphate (IP₃) and diacylglycerol (DAG) from phosphatidyl inositol (PIP₂). The DAG remains in the plasma membrane and co-activates conventional protein kinase C (PKC) with Ca²⁺. We have developed a mathematical model for the activation of the Ca²⁺-dependent PKC and its negative feedback on phospholipase C (PLC) and coupled it to the De Young-Keizer model for IP₃ mediated Ca²⁺ oscillations. The model describes the cascade of reactions for the translocation of PKC to plasma membrane, and simulates activation of Ca²⁺ and diacylglycerol (DAG) oscillations. The model demonstrates that oscillations in Ca²⁺ and DAG are possible with or without a positive Ca²⁺ feedback on phospholipase C consistent with experiment. In many experimental studies, the timing of the peaks of the Ca²⁺ and IP₃ oscillations have been used to suggest causality, i.e. that the IP₃ oscillations cause the Ca²⁺ oscillations. The model is used to explore this question. To this end, the positive and negative feedback between Ca²⁺ and IP₃ production are modulated, resulting in changes to the phase lag between the peaks in [Ca²⁺]_cyt and [IP]_cyt. The model simulates a possible experimental protocol that can be used to differentiate whether or not the positive feedback of Ca²⁺ on PLC is needed for the oscillations.