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作为孤独感函数的人类伏隔核中的差异转录组表达

Differential transcriptome expression in human nucleus accumbens as a function of loneliness.

作者信息

Canli T, Wen R, Wang X, Mikhailik A, Yu L, Fleischman D, Wilson R S, Bennett D A

机构信息

Integrative Neuroscience, Department of Psychology, Stony Brook University, Stony Brook, NY, USA.

Department of Applied Mathematics and Statistics, Stony Brook University, Stony Brook, NY, USA.

出版信息

Mol Psychiatry. 2017 Jul;22(7):1069-1078. doi: 10.1038/mp.2016.186. Epub 2016 Nov 1.

DOI:10.1038/mp.2016.186
PMID:27801889
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5411331/
Abstract

Loneliness is associated with impaired mental and physical health. Studies of lonely individuals reported differential expression of inflammatory genes in peripheral leukocytes and diminished activation in brain reward regions such as nucleus accumbens, but could not address gene expression in the human brain. Here, we examined genome-wide RNA expression in post-mortem nucleus accumbens from donors (N=26) with known loneliness measures. Loneliness was associated with 1710 differentially expressed transcripts and genes from 1599 genes (DEGs; false discovery rate P<0.05, fold change ⩾|2|, controlling for confounds) previously associated with behavioral processes, neurological disease, psychological disorders, cancer, organismal injury and skeletal and muscular disorders, as well as networks of upstream RNA regulators. Furthermore, a number of DEGs were associated with Alzheimer's disease (AD) genes (that was correlated with loneliness in this sample, although gene expression analyses controlled for AD diagnosis). These results identify novel targets for future mechanistic studies of gene networks in nucleus accumbens and gene regulatory mechanisms across a variety of diseases exacerbated by loneliness.

摘要

孤独与身心健康受损有关。对孤独个体的研究报告了外周血白细胞中炎症基因的差异表达以及大脑奖赏区域(如伏隔核)的激活减弱,但未能研究人类大脑中的基因表达情况。在此,我们检测了已知孤独程度测量值的捐赠者(N = 26)死后伏隔核中的全基因组RNA表达。孤独与1710个差异表达的转录本和来自1599个基因(差异表达基因;错误发现率P<0.05,变化倍数⩾|2|,控制混杂因素)相关,这些基因先前与行为过程、神经疾病、心理障碍、癌症、机体损伤以及骨骼和肌肉疾病,以及上游RNA调节因子网络有关。此外,一些差异表达基因与阿尔茨海默病(AD)基因相关(在本样本中与孤独相关,尽管基因表达分析对AD诊断进行了控制)。这些结果为未来伏隔核基因网络的机制研究以及孤独加剧的各种疾病中的基因调控机制确定了新的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4007/5411331/d25487a3dc33/nihms788656f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4007/5411331/7b31f9dc24a2/nihms788656f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4007/5411331/7c97b4012356/nihms788656f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4007/5411331/d25487a3dc33/nihms788656f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4007/5411331/7b31f9dc24a2/nihms788656f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4007/5411331/7c97b4012356/nihms788656f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4007/5411331/d25487a3dc33/nihms788656f3.jpg

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