δFosB differentially modulates nucleus accumbens direct and indirect pathway function

Abstract

Synaptic modifications in nucleus accumbens (NAc) medium spiny neurons (MSNs) play a key role in adaptive and pathological reward-dependent learning, including maladaptive responses involved in drug addiction. NAc MSNs participate in two parallel circuits, direct and indirect pathways that subserve distinct behavioral functions. Modification of NAc MSN synapses may occur inpart via changes in the transcriptional potential of certain genes in a cell type-specific manner. The transcription factor δFosB is one of the key proteins implicated in the gene expression changes in NAc caused by drugs of abuse, yet its effects on synaptic function in NAc MSNs are unknown. Here, we demonstrate that overexpression of δFosB decreased excitatory synaptic strength and likely increased silent synapses onto D1 dopamine receptor-expressing direct pathway MSNs in both the NAc shell and core. In contrast, δFosB likely decreased silent synapses onto NAc shell, but not core, D2 dopamine receptor-expressing indirect pathway MSNs. Analysis of NAc MSN dendritic spine morphology revealed that δFosB increased the density of immature spines in D1 direct but not D2 indirect pathway MSNs.Todetermine the behavioral consequences of cell type-specific actions of δFosB, we selectively overexpressed δFosB in D1 direct or D2 indirect MSNs in NAc in vivo and found that direct (but not indirect) pathway MSN expression enhances behavioral responses to cocaine. These results reveal that δFosB in NAc differentially modulates synaptic properties and reward-related behaviors in a cell type- and subregion-specific fashion.