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非典型粘附G蛋白偶联受体ADGRA1控制海马体抑制性回路功能。

The atypical adhesion GPCR ADGRA1 controls hippocampal inhibitory circuit function.

作者信息

Tosun Baris, Orput Elizabeth, Bui Duy Lan Huong, Sando Richard C

机构信息

Department of Pharmacology, Vanderbilt Brain Institute, Vanderbilt University, Nashville, TN 37240 USA.

出版信息

bioRxiv. 2025 Jul 30:2025.07.30.667713. doi: 10.1101/2025.07.30.667713.

Abstract

Neural circuits contain a diverse array of inhibitory interneurons that control information processing. The cell surface receptors and signaling pathways that modulate cell type specific inhibitory synaptic function are unclear. Here, we identify the atypical adhesion GPCR ADGRA1 as essential for hippocampal PV and SST inhibitory synaptic function. ADGRA1 is selectively enriched in hippocampal PV and SST interneurons and localizes to a subset of synapses. ADGRA1 deletion in PV and SST interneurons impairs inhibitory synaptic inputs onto Dentate Gyrus granule cells and generates deficits in learning and memory. ADGRA1 engages several downstream G proteins, notably Gα13, a pathway important for the establishment of hippocampal PV interneuron synaptic networks. These results identify an orphan receptor pathway selective for specific inhibitory synapse subtypes and expand our understanding of the signaling mechanisms that establish hippocampal inhibitory circuits.

摘要

神经回路包含各种各样控制信息处理的抑制性中间神经元。调节细胞类型特异性抑制性突触功能的细胞表面受体和信号通路尚不清楚。在此,我们确定非典型粘附GPCR ADGRA1对海马体中PV和SST抑制性突触功能至关重要。ADGRA1选择性地富集于海马体的PV和SST中间神经元,并定位于一部分突触。PV和SST中间神经元中ADGRA1的缺失会损害齿状回颗粒细胞上的抑制性突触输入,并导致学习和记忆缺陷。ADGRA1与几种下游G蛋白相互作用,特别是Gα13,这是一条对海马体PV中间神经元突触网络建立很重要的信号通路。这些结果确定了一条对特定抑制性突触亚型具有选择性的孤儿受体信号通路,并扩展了我们对建立海马体抑制性回路的信号机制的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d16d/12324398/539ae38fc0ec/nihpp-2025.07.30.667713v1-f0001.jpg

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