Acetylcholine release from basal forebrain promotes cortical synaptic plasticity via somatostatin interneurons
2024-01-12
状态已发表
摘要

Basal forebrain (BF) cholinergic projections densely innervate the neocortex, releasing acetylcholine (ACh) to modulate neuronal excitability, thereby influencing sensory processing and cognitive functions. However, the synaptic basis of such ACh-induced effects in vivo remains elusive. To investigate how ACh release from BF regulates synaptic dynamics in the neocortex, we selectively stimulated BF cholinergic neurons in mice, and used two-photon microscopy to track structural changes of dendritic spines on cortical pyramidal neurons. We found that optogenetic and chemogenetic stimulation of BF cholinergic neurons rapidly induced spine formation in layer 5 pyramidal neurons in the auditory cortex and the posterior parietal cortex. Selective blockage of ACh receptors (AChRs) demonstrated that nicotinic AChRs are required for the ACh-induced spine formation. We also found that Ach-induced spine formation of pyramidal neurons requires the activity of cortical somatostatin-expressing inhibitory interneurons. Together, our study revealed ACh-induced synaptic plasticity in the cortical microcircuit in vivo, providing a synaptic mechanism for cortical neuronal plasticity and functional changes associated with BF ACh release.

DOI10.1101/2023.07.05.547662
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出处bioRxiv
WOS记录号PPRN:87075705
WOS类目Neurosciences
资助项目Ministry of Science and Technology of China[
文献类型预印本
条目标识符https://kms.shanghaitech.edu.cn/handle/2MSLDSTB/349890
专题生命科学与技术学院
生命科学与技术学院_PI研究组_杨扬组
生命科学与技术学院_博士生
作者单位
1.ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai 201210, Peoples R China
2.Univ Calif San Diego, Dept Neurobiol, Dept Neurosci, La Jolla, CA 92093, USA
3.Univ Calif San Diego, Ctr Neural Circuits & Behav, La Jolla, CA 92093, USA
4.Univ Virginia, Dept Biol, Charlottesville, VA 22904, USA
推荐引用方式
GB/T 7714
Zhao, Xueyang,Zhang, Yu E.,Yang, Lu,et al. Acetylcholine release from basal forebrain promotes cortical synaptic plasticity via somatostatin interneurons. 2024.
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