Scuola Normale Superiore, Neurobiology Laboratory, Piazza dei Cavalieri Pisa 56100 Italy.
J Physiol. 2012 Oct 1;590(19):4777-87. doi: 10.1113/jphysiol.2012.234237. Epub 2012 Jun 6.
There is evidence that developmental-like plasticity can be reactivated in the adult visual cortex. Although activity-dependent transcription factors underlying the process of plasticity reactivation are currently unknown, recent studies point towards NPAS4 as a candidate gene for the occurrence of plasticity in the adult visual system. Here, we addressed whether NPAS4 is involved in the reinstatement of plasticity by using the monocular deprivation protocol and long-term fluoxetine treatment as a pharmacological strategy that restores plasticity in adulthood. A combination of molecular assays for gene expression and epigenetic analysis, gene delivery by lentiviral infection, shRNA interference and electrophysiology as a functional read-out, revealed a previously unknown role for the transcription factor NPAS4 in the regulation of adult visual cortical plasticity. We found that NPAS4 overexpression restores ocular dominance plasticity in adult naıve animals whereas NPAS4 down-regulation prevents the plastic outcome caused by fluoxetine in adulthood.Our findings lead the way to the identification of novel therapeutic targets for pathological conditions where reorganization of neuronal networks would be beneficial in adult life.
有证据表明,发育样可塑性可以在成年视觉皮层中重新激活。虽然目前尚不清楚可塑性重新激活背后的活性依赖性转录因子,但最近的研究指向 NPAS4 作为成年视觉系统中发生可塑性的候选基因。在这里,我们通过使用单眼剥夺方案和长期氟西汀治疗作为恢复成年期可塑性的药理学策略,来研究 NPAS4 是否参与了可塑性的恢复。分子表达谱分析和表观遗传分析、慢病毒感染的基因传递、shRNA 干扰和电生理学作为功能读出的组合,揭示了转录因子 NPAS4 在调节成年视觉皮质可塑性中的一个以前未知的作用。我们发现,NPAS4 的过表达恢复了成年未成熟动物的眼优势可塑性,而 NPAS4 的下调则阻止了氟西汀在成年期引起的可塑性结果。我们的发现为识别新的治疗靶点铺平了道路,这些靶点可用于在成年期对神经元网络进行重组有益的病理状况。