Bistable MAP Kinase Activity: A Plausible Mechanism Contributing to Maintenance of Late Long-Term Potentiation

TL;DR

This study models how bistable MAP kinase activity, stabilized by feedback loops, could sustain long-term potentiation and memory by maintaining persistent kinase activity despite molecular fluctuations.

Contribution

It demonstrates that positive feedback enhances the robustness of MAPK bistability, supporting its potential role in LTP maintenance and long-term memory.

Findings

Bistability is sensitive to Raf activity levels without feedback.

Positive feedback greatly stabilizes MAPK states against fluctuations.

Persistent MAPK activity may support long-term synaptic changes.

Abstract

Bistability of MAP kinase (MAPK) activity has been suggested to contribute to several cellular processes, including differentiation and long-term synaptic potentiation. A recent model (48) predicts bistability due to interactions of the kinases and phosphatases in the MAPK pathway, without feedback from MAPK to earlier reactions. Using this model and enzyme concentrations appropriate for neurons, we simulated bistable MAPK activity, but bistability only was present within a relatively narrow range of activity of Raf, the first pathway kinase. Stochastic fluctuations in molecule numbers eliminated bistability for small molecule numbers, such as are expected in the volume of a dendritic spine. However, positive feedback loops have been posited from MAPK up to Raf activation. One proposed loop in which MAPK directly activates Raf was incorporated into the model. We found that such feedback greatly enhanced the robustness of both stable states of MAPK activity to stochastic fluctuations and to parameter variations. Bistability was robust for molecule numbers plausible for a dendritic spine volume. The upper state of MAPK activity was resistant to inhibition of MEK activation for > 1 h, suggesting inhibitor experiments have not sufficed to rule out a role for persistent MAPK activity in LTP maintenance. These simulations suggest that persistent MAPK activity and consequent upregulation of translation may contribute to LTP maintenance and to long-term memory. Experiments using a fluorescent MAPK substrate may further test this hypothesis.