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Negr1基因缺陷小鼠的外周基因失调:对与情感行为可能联系的见解。

Peripheral gene dysregulation in Negr1-deficient mice: insights into possible links with affective behavior.

作者信息

Maigoro Abdulkadir Yusif, Kim Jangrae, Cho Seoyeon, Yoo Ara, Lee Soojin

机构信息

Department of Microbiology and Molecular Biology, Chungnam National University, Daejeon, Republic of Korea.

出版信息

Front Mol Neurosci. 2025 Jul 8;18:1602201. doi: 10.3389/fnmol.2025.1602201. eCollection 2025.

DOI:10.3389/fnmol.2025.1602201
PMID:40698360
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12279845/
Abstract

INTRODUCTION

Neuronal growth regulator 1 (NEGR1) is a brain-enriched membrane protein with mild expression in peripheral tissues such as adipose tissue and skeletal muscle. Genome-wide association studies have implicated NEGR1 as a risk factor for human diseases including obesity, autism, and depression, but its molecular function remains poorly understood.

METHODS

To explore NEGR1's role in peripheral-to-brain communication, we conducted RNA-seq analysis on four peripheral tissues-intestine, skeletal muscle, liver, and epididymal white adipose tissue-collected from knockout mice. Differentially expressed genes (DEGs) were identified and subjected to Gene Ontology (GO) enrichment analyses.

RESULTS

The DEG analysis revealed dysregulation of ion channels and transporters, potentially contributing to AP-1-mediated inflammatory responses in peripheral tissues. Additionally, interleukin (IL)-17 signaling emerged as a key pathway that may mediate systemic inflammation in -deficient mice.

DISCUSSION

These findings suggest a novel role for NEGR1 in modulating peripheral inflammatory responses and support the hypothesis that peripheral immune dysregulation may contribute to depressive-like behaviors in -deficient mice. This work enhances our understanding of NEGR1's function in peripheral tissues and its possible involvement in peripheral-central immune crosstalk relevant to psychiatric disorders.

摘要

引言

神经元生长调节因子1(NEGR1)是一种在大脑中高度表达的膜蛋白,在脂肪组织和骨骼肌等外周组织中表达较弱。全基因组关联研究表明,NEGR1是包括肥胖症、自闭症和抑郁症在内的人类疾病的危险因素,但其分子功能仍知之甚少。

方法

为了探究NEGR1在外周与大脑通讯中的作用,我们对从基因敲除小鼠收集的四种外周组织——肠道、骨骼肌、肝脏和附睾白色脂肪组织进行了RNA测序分析。鉴定出差异表达基因(DEG)并进行基因本体(GO)富集分析。

结果

差异表达基因分析揭示了离子通道和转运体的失调,这可能导致外周组织中AP-1介导的炎症反应。此外,白细胞介素(IL)-17信号通路成为可能介导基因敲除小鼠全身炎症的关键途径。

讨论

这些发现表明NEGR1在调节外周炎症反应中具有新的作用,并支持外周免疫失调可能导致基因敲除小鼠出现抑郁样行为的假说。这项工作增进了我们对NEGR1在外周组织中的功能及其可能参与与精神疾病相关的外周-中枢免疫串扰的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c9/12279845/54c57b761001/fnmol-18-1602201-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c9/12279845/a29fb417595e/fnmol-18-1602201-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c9/12279845/dbe402bbb2a0/fnmol-18-1602201-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c9/12279845/a04dd3bc300f/fnmol-18-1602201-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c9/12279845/cf57d114d26c/fnmol-18-1602201-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c9/12279845/daf94c3424f0/fnmol-18-1602201-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c9/12279845/54c57b761001/fnmol-18-1602201-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c9/12279845/a29fb417595e/fnmol-18-1602201-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c9/12279845/dbe402bbb2a0/fnmol-18-1602201-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c9/12279845/a04dd3bc300f/fnmol-18-1602201-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c9/12279845/cf57d114d26c/fnmol-18-1602201-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c9/12279845/daf94c3424f0/fnmol-18-1602201-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42c9/12279845/54c57b761001/fnmol-18-1602201-g006.jpg

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