Department of Neurobiology, Duke University Medical Center, Durham, North Carolina.
Department of Neurobiology, Duke University Medical Center, Durham, North Carolina; Department of Neurology, Duke University Medical Center, Durham, North Carolina; Department of Cell Biology, Duke University Medical Center, Durham, North Carolina; Duke Institute for Brain Sciences, Duke University Medical Center, Durham, North Carolina.
Biol Psychiatry. 2024 Nov 1;96(9):694-707. doi: 10.1016/j.biopsych.2024.02.003. Epub 2024 Feb 10.
Experience-dependent functional adaptation of nucleus accumbens (NAc) circuitry underlies the development and expression of reward-motivated behaviors. Parvalbumin-expressing GABAergic (gamma-aminobutyric acidergic) interneurons (PVINs) within the NAc are required for this process. Perineuronal nets (PNNs) are extracellular matrix structures enriched around PVINs that arise during development and have been proposed to mediate brain circuit stability. However, their function in the adult NAc is largely unknown. Here, we studied the developmental emergence and adult regulation of PNNs in the NAc of male and female mice and examined the cellular and behavioral consequences of reducing the PNN component brevican in NAc PVINs.
We characterized the expression of PNN components in mouse NAc using immunofluorescence and RNA in situ hybridization. We lowered brevican in NAc PVINs of adult mice using an intersectional viral and genetic method and quantified the effects on synaptic inputs to NAc PVINs and reward-motivated learning.
PNNs around NAc PVINs were developmentally regulated and appeared during adolescence. In the adult NAc, PVIN PNNs were also dynamically regulated by cocaine. Transcription of the gene that encodes brevican was regulated in a cell type- and isoform-specific manner in the NAc, with the membrane-tethered form of brevican being highly enriched in PVINs. Lowering brevican in NAc PVINs of adult mice decreased their excitatory inputs and enhanced both short-term novel object recognition and cocaine-induced conditioned place preference.
Regulation of brevican in NAc PVINs of adult mice modulates their excitatory synaptic drive and sets experience thresholds for the development of motivated behaviors driven by rewarding stimuli.
伏隔核(NAc)电路的经验依赖性功能适应是奖励动机行为的发展和表达的基础。NAc 中的表达囊泡相关蛋白(parvalbumin)的 GABA 能(γ-氨基丁酸能)中间神经元(PVINs)是这个过程所必需的。周围神经节苷脂(perineuronal nets,PNNs)是一种细胞外基质结构,在发育过程中丰富了 PVINs,并被提出介导大脑回路的稳定性。然而,它们在成年 NAc 中的功能在很大程度上是未知的。在这里,我们研究了雄性和雌性小鼠 NAc 中 PNNs 的发育出现和成年调节,并研究了降低 NAc PVINs 中 PNN 成分短蛋白聚糖(brevican)对细胞和行为的影响。
我们使用免疫荧光和 RNA 原位杂交技术来描述小鼠 NAc 中 PNN 成分的表达。我们使用一种交叉病毒和遗传方法来降低成年小鼠 NAc PVINs 中的 brevican,并量化了对 NAc PVINs 突触输入和奖励动机学习的影响。
NAc PVINs 周围的 PNNs 是发育调节的,并在青春期出现。在成年 NAc 中,可卡因也可以动态调节 PVIN 的 PNN。编码 brevican 的基因在 NAc 中的转录以细胞类型和同工型特异性的方式被调节,其中 brevican 的膜结合形式在 PVINs 中高度富集。降低成年小鼠 NAc PVINs 中的 brevican 会减少其兴奋性输入,并增强短期新物体识别和可卡因诱导的条件性位置偏好。
成年小鼠 NAc PVINs 中 brevican 的调节调节了它们的兴奋性突触驱动,并为受奖励刺激驱动的动机行为的发展设定了经验阈值。