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视交叉上核中胃泌素释放肽产生神经元的功能作用:对光诱导同步和昼夜节律调节的见解

Functional Roles of Gastrin-Releasing Peptide-Producing Neurons in the Suprachiasmatic Nucleus: Insights into Photic Entrainment and Circadian Regulation.

作者信息

Li Ruoshi, Inoue Ran, Mori Hisashi, Hirano Arisa, Sakurai Takeshi

机构信息

Institute of Medicine, University of Tsukuba, Tsukuba, Ibaraki 305-8575, Japan.

International Institute for Integrative Sleep Medicine (WPI-IIIS), University of Tsukuba, Tsukuba, Ibaraki 305-8575, Japan.

出版信息

J Neurosci. 2025 Jun 18;45(25):e0065252025. doi: 10.1523/JNEUROSCI.0065-25.2025.

DOI:10.1523/JNEUROSCI.0065-25.2025
PMID:40404352
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12178279/
Abstract

The suprachiasmatic nucleus (SCN) serves as the central circadian clock in mammals, coordinating daily rhythms in both behavior and physiology. In the SCN, gastrin-releasing peptide (GRP)-producing neurons (GRPNs) are predominantly located in the core region, suggesting their possible involvement in photic entrainment. However, the specific contribution of GRPNs to the regulation of circadian rhythms remains poorly understood. This study utilized a Cre-driver mouse line, knock-in (KI) mice, in which Cre recombinase is exclusively expressed in GRPNs, allowing the selective manipulation of SCN GRPNs to investigate their characteristics and functional roles in circadian regulation. All experiments were conducted in adult male mice. Anatomical tracing revealed that SCN GRPNs primarily project to the thalamus and hypothalamus, whereas input mapping demonstrated that SCN GRPNs receive most synaptic inputs from within the SCN. Behavioral analyses revealed that neither GRP deficiency nor ablation of SCN GRPNs significantly affected circadian locomotor activity rhythms or photic entrainment. However, chemogenetic stimulation of the SCN GRPNs is sufficient to induce phase shifts in behavioral rhythms. Additionally, calcium imaging with fiber photometry indicated that SCN GRPNs quickly responded to photic stimulation, with increased neural activity following retinal exposure to white light. These findings suggest that SCN GRPNs play a role in photic entrainment, albeit potentially redundant with other neuronal populations such as vasoactive intestinal peptide-producing neurons.

摘要

视交叉上核(SCN)是哺乳动物的中央昼夜节律时钟,协调行为和生理方面的日常节律。在SCN中,产生胃泌素释放肽(GRP)的神经元(GRPNs)主要位于核心区域,表明它们可能参与光诱导同步化。然而,GRPNs对昼夜节律调节的具体作用仍知之甚少。本研究利用一种Cre驱动小鼠品系,即敲入(KI)小鼠,其中Cre重组酶仅在GRPNs中表达,从而能够选择性地操纵SCN中的GRPNs,以研究它们在昼夜节律调节中的特征和功能作用。所有实验均在成年雄性小鼠中进行。解剖学追踪显示,SCN GRPNs主要投射到丘脑和下丘脑,而输入图谱显示,SCN GRPNs接收来自SCN内部的大部分突触输入。行为分析表明,GRP缺乏或SCN GRPNs的消融均未显著影响昼夜运动活动节律或光诱导同步化。然而,对SCN GRPNs进行化学遗传刺激足以诱导行为节律的相位偏移。此外,采用光纤光度法进行的钙成像表明,SCN GRPNs对光刺激有快速反应,视网膜暴露于白光后神经活动增强。这些发现表明,SCN GRPNs在光诱导同步化中发挥作用,尽管可能与其他神经元群体(如产生血管活性肠肽的神经元)功能冗余。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e156/12178279/de2584097757/jneuro-45-e0065252025-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e156/12178279/7a680d8baffe/jneuro-45-e0065252025-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e156/12178279/67ce08377536/jneuro-45-e0065252025-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e156/12178279/8f8b1927f99e/jneuro-45-e0065252025-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e156/12178279/922bc920a7a7/jneuro-45-e0065252025-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e156/12178279/601784508c4b/jneuro-45-e0065252025-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e156/12178279/d849740f453e/jneuro-45-e0065252025-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e156/12178279/d8e9a84d5361/jneuro-45-e0065252025-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e156/12178279/9b9237cf255a/jneuro-45-e0065252025-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e156/12178279/de2584097757/jneuro-45-e0065252025-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e156/12178279/7a680d8baffe/jneuro-45-e0065252025-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e156/12178279/67ce08377536/jneuro-45-e0065252025-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e156/12178279/8f8b1927f99e/jneuro-45-e0065252025-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e156/12178279/922bc920a7a7/jneuro-45-e0065252025-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e156/12178279/601784508c4b/jneuro-45-e0065252025-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e156/12178279/d849740f453e/jneuro-45-e0065252025-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e156/12178279/d8e9a84d5361/jneuro-45-e0065252025-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e156/12178279/9b9237cf255a/jneuro-45-e0065252025-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e156/12178279/de2584097757/jneuro-45-e0065252025-g009.jpg

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