The role of PKMζ in the maintenance of long-term memory: a review

Long-term memories are thought to be stored in neurones and synapses that undergo physical changes, such as long-term potentiation (LTP), and these changes can be maintained for long periods of time. A candidate enzyme for the maintenance of LTP is protein kinase Mzeta (PKM zeta), a constitutively active protein kinase C isoform that is elevated during LTP and long-term memory maintenance. This paper reviews the evidence and controversies surrounding the role of PKM zeta in the maintenance of long-term memory. PKM zeta maintains synaptic potentiation by preventing AMPA receptor endocytosis and promoting stabilisation of dendritic spine growth. Inhibition of PKM zeta, with zeta-inhibitory peptide (ZIP), can reverse LTP and impair established long-term memories. However, a deficit of memory retrieval cannot be ruled out. Furthermore, ZIP, and in high enough doses the control peptide scrambled ZIP, was recently shown to be neurotoxic, which may explain some of the effects of ZIP on memory impairment. PKM zeta knockout mice show normal learning and memory. However, this is likely due to compensation by protein-kinase C iota/lambda (PKC iota/lambda), which is normally responsible for induction of LTP. It is not clear how, or if, this compensatory mechanism is activated under normal conditions. Future research should utilise inducible PKM zeta knockdown in adult rodents to investigate whether PKM zeta maintains memory in specific parts of the brain, or if it represents a global memory maintenance molecule. These insights may inform future therapeutic targets for disorders of memory loss.

Automated summary

This paper reviews the role of PKM zeta in the maintenance of long-term memory, highlighting its mechanism in preventing AMPA receptor endocytosis for synaptic potentiation. While inhibition of PKM zeta can reverse LTP and impair established long-term memories, a deficit in memory retrieval cannot be ruled out.