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突触Gα12/13信号传导建立海马体小清蛋白抑制性回路。

Synaptic Gα12/13 signaling establishes hippocampal PV inhibitory circuits.

作者信息

Garbett Krassimira, Tosun Baris, Lopez Jaybree M, Smith Cassandra M, Honkanen Kelly, Sando Richard C

机构信息

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

出版信息

Proc Natl Acad Sci U S A. 2024 Dec 24;121(52):e2407828121. doi: 10.1073/pnas.2407828121. Epub 2024 Dec 18.

Abstract

Combinatorial networks of cell adhesion molecules and cell surface receptors drive fundamental aspects of neural circuit establishment and function. However, the intracellular signals orchestrated by these cell surface complexes remain less understood. Here, we report that the Gα12/13 pathway lies downstream of several GPCRs with critical synaptic functions. Impairment of the Gα12/13 pathway in postnatal hippocampal neurons diminishes inhibitory inputs without altering neuronal morphology or excitatory transmission. Gα12/13 signaling in hippocampal CA1 neurons in vivo selectively regulates PV interneuron synaptic connectivity, supporting an inhibitory synapse subtype-specific function of this pathway. Our studies establish Gα12/13 as a signaling node that shapes inhibitory hippocampal circuitry.

摘要

细胞粘附分子和细胞表面受体的组合网络驱动神经回路建立和功能的基本方面。然而,由这些细胞表面复合物精心编排的细胞内信号仍不太为人所知。在这里,我们报告Gα12/13通路位于几个具有关键突触功能的GPCR下游。出生后海马神经元中Gα12/13通路的损伤会减少抑制性输入,而不会改变神经元形态或兴奋性传递。体内海马CA1神经元中的Gα12/13信号选择性地调节PV中间神经元的突触连接,支持该通路的抑制性突触亚型特异性功能。我们的研究将Gα12/13确立为塑造海马抑制性回路的信号节点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04fe/11670215/8fdc50671c6b/pnas.2407828121fig01.jpg

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