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通过 NCAM 调节小鼠前额叶皮层篮状中间神经元突触和行为的发育

Developmental Regulation of Basket Interneuron Synapses and Behavior through NCAM in Mouse Prefrontal Cortex.

机构信息

Department of Biochemistry and Biophysics, University of North Carolina School of Medicine at Chapel Hill, Chapel Hill, NC 27599, USA.

Department of Otolaryngology/Head and Neck Surgery, and Cell Biology and Physiology, University of North Carolina School of Medicine at Chapel Hill, Chapel Hill, NC 27599, USA.

出版信息

Cereb Cortex. 2020 Jun 30;30(8):4689-4707. doi: 10.1093/cercor/bhaa074.

Abstract

Parvalbumin (PV)-expressing basket interneurons in the prefrontal cortex (PFC) regulate pyramidal cell firing, synchrony, and network oscillations. Yet, it is unclear how their perisomatic inputs to pyramidal neurons are integrated into neural circuitry and adjusted postnatally. Neural cell adhesion molecule NCAM is expressed in a variety of cells in the PFC and cooperates with EphrinA/EphAs to regulate inhibitory synapse density. Here, analysis of a novel parvalbumin (PV)-Cre: NCAM F/F mouse mutant revealed that NCAM functions presynaptically in PV+ basket interneurons to regulate postnatal elimination of perisomatic synapses. Mutant mice exhibited an increased density of PV+ perisomatic puncta in PFC layer 2/3, while live imaging in mutant brain slices revealed fewer puncta that were dynamically eliminated. Furthermore, EphrinA5-induced growth cone collapse in PV+ interneurons in culture depended on NCAM expression. Electrophysiological recording from layer 2/3 pyramidal cells in mutant PFC slices showed a slower rise time of inhibitory synaptic currents. PV-Cre: NCAM F/F mice exhibited impairments in working memory and social behavior that may be impacted by altered PFC circuitry. These findings suggest that the density of perisomatic synapses of PV+ basket interneurons is regulated postnatally by NCAM, likely through EphrinA-dependent elimination, which is important for appropriate PFC network function and behavior.

摘要

脑啡肽(PV)表达的篮状细胞中间神经元调节前额叶皮层(PFC)中的锥体神经元的放电、同步和网络振荡。然而,其对锥体神经元的胞体输入是如何整合到神经回路中并在出生后进行调整的尚不清楚。神经细胞粘附分子 NCAM 在 PFC 中的多种细胞中表达,并与 EphrinA/EphAs 合作调节抑制性突触密度。在这里,对新型脑啡肽(PV)-Cre:NCAM F/F 小鼠突变体的分析表明,NCAM 在 PV+篮状细胞中间神经元中发挥突触前作用,以调节出生后胞体周围突触的消除。突变小鼠在 PFC 第 2/3 层中表现出 PV+胞体周围突触及密度增加,而在突变脑片中的实时成像显示动态消除的突触及数量减少。此外, EphrinA5 在培养的 PV+中间神经元中诱导的生长锥塌陷依赖于 NCAM 的表达。突变 PFC 切片中第 2/3 层锥体神经元的电生理记录显示抑制性突触电流的上升时间较慢。PV-Cre:NCAM F/F 小鼠在工作记忆和社交行为方面表现出障碍,这可能受到改变的 PFC 回路的影响。这些发现表明,PV+篮状细胞中间神经元的胞体周围突触密度通过 NCAM 进行出生后调节,可能通过 EphrinA 依赖性消除进行调节,这对于适当的 PFC 网络功能和行为很重要。

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