Transforming Growth Factor Beta Recruits Persistent Mapk Signaling To Regulate Long-Term Memory Consolidation In Aplysia Californica

In this study, we explore the mechanistic relationship between growth factor signaling and kinase activity that supports the protein synthesis-dependent phase of long-term memory (LTM) consolidation for sensitization of Aplysia. Specifically, we examine LTM for tail shock-induced sensitization of the tail-elicited siphon withdrawal (T-SW) reflex, a form of memory that requires both (i) extracellular signal-regulated kinase (ERK1/2; MAPK) activity within identified sensory neurons (SNs) that mediate the T-SW and (ii) the activation of transforming growth factor beta (TGF beta) signaling. We now report that repeated tail shocks that induce intermediate-term (ITM) and LTM for sensitization, also induce a sustained post-training phase of MAPK activity in SNs (lasting at least 1 h). We identified two mechanistically distinct phases of post-training MAPK: (i) an immediate phase that does not require ongoing protein synthesis or TGFb signaling, and (ii) a sustained phase that requires both protein synthesis and extracellular TGF beta signaling. We find that LTM consolidation requires sustained MAPK, and is disrupted by inhibitors of protein synthesis and TGF beta signaling during the consolidation window. These results provide strong evidence that TGF beta signaling sustains MAPK activity as an essential mechanistic step for LTM consolidation.