Molecular constraints on synaptic tagging and maintenance of long-term potentiation: a predictive model

• Published in: PLoS computational biology Vol. 8; no. 8; p. e1002620
• Main Authors: Smolen, Paul, Baxter, Douglas A, Byrne, John H
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 01.08.2012; Public Library of Science (PLoS)
• Subjects: Biology; Computational biology; Experiments; Feedback; Hippocampus (Brain); Humans; Kinases; Long-Term Potentiation; Mathematics; Models, Biological; Molecular dynamics; Neurosciences; Physiological aspects; Protein biosynthesis; Protein Kinase C - metabolism; Protein synthesis; Proteins; Stochastic Processes; Synapses - enzymology; Synapses - physiology; Tetanus; United States; Stochastic Processes; Models, Biological; Humans; Synapses; Long-Term Potentiation; Protein Kinase C
• ISSN: 1553-7358; 1553-734X; 1553-7358
• DOI: 10.1371/journal.pcbi.1002620

Protein synthesis-dependent, late long-term potentiation (LTP) and depression (LTD) at glutamatergic hippocampal synapses are well characterized examples of long-term synaptic plasticity. Persistent increased activity of protein kinase M ζ (PKMζ) is thought essential for maintaining LTP. Additional spatial and temporal features that govern LTP and LTD induction are embodied in the synaptic tagging and capture (STC) and cross capture hypotheses. Only synapses that have been "tagged" by a stimulus sufficient for LTP and learning can "capture" PKMζ. A model was developed to simulate the dynamics of key molecules required for LTP and LTD. The model concisely represents relationships between tagging, capture, LTD, and LTP maintenance. The model successfully simulated LTP maintained by persistent synaptic PKMζ, STC, LTD, and cross capture, and makes testable predictions concerning the dynamics of PKMζ. The maintenance of LTP, and consequently of at least some forms of long-term memory, is predicted to require continual positive feedback in which PKMζ enhances its own synthesis only at potentiated synapses. This feedback underlies bistability in the activity of PKMζ. Second, cross capture requires the induction of LTD to induce dendritic PKMζ synthesis, although this may require tagging of a nearby synapse for LTP. The model also simulates the effects of PKMζ inhibition, and makes additional predictions for the dynamics of CaM kinases. Experiments testing the above predictions would significantly advance the understanding of memory maintenance.