Transcriptional expression patterns of the cortical morphometric similarity network in progressive supranuclear palsy

被引:2
作者
Qu, Junyu [1 ]
Qu, Yancai [2 ]
Zhu, Rui [1 ]
Wu, Yongsheng [1 ]
Xu, Guihua [1 ]
Wang, Dawei [1 ,3 ,4 ]
机构
[1] Shandong Univ, Qilu Med Imaging Inst, Dept Radiol, Qilu Hosp, Jinan, Peoples R China
[2] Tradit Chinese Med Hosp Muping Dist, Dept Neurosurg, Yantai, Peoples R China
[3] Shandong Univ, Magnet Field free Med & Funct Imaging, Res Inst, Jinan, Peoples R China
[4] Shandong Key Lab, Magnet Field free Med & Funct Imaging MF, Jinan, Peoples R China
基金
中国博士后科学基金;
关键词
gene expression; imaging transcriptomics; morphometric similarity network; neurotransmitter receptor; progressive supranuclear palsy; transcriptional signatures; HUMAN CEREBRAL-CORTEX; NOREPINEPHRINE TRANSPORTER; FUNCTIONAL-ORGANIZATION; STRUCTURAL NETWORKS; PARKINSONS-DISEASE; GENE-EXPRESSION; SCHIZOPHRENIA; CONNECTIVITY; CONNECTOME; SYSTEM;
D O I
10.1111/cns.14901
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
BackgroundIt has been demonstrated that progressive supranuclear palsy (PSP) correlates with structural abnormalities in several distinct regions of the brain. However, whether there are changes in the morphological similarity network (MSN) and the relationship between changes in brain structure and gene expression remain largely unknown.MethodsWe used two independent cohorts (discovery dataset: PSP: 51, healthy controls (HC): 82; replication dataset: PSP: 53, HC: 55) for MSN analysis and comparing the longitudinal changes in the MSN of PSP. Then, we applied partial least squares regression to determine the relationships between changes in MSN and spatial transcriptional features and identified specific genes associated with MSN differences in PSP. We further investigated the biological processes enriched in PSP-associated genes and the cellular characteristics of these genes, and finally, we performed an exploratory analysis of the relationship between MSN changes and neurotransmitter receptors.ResultsWe found that the MSN in PSP patients was mainly decreased in the frontal and temporal cortex but increased in the occipital cortical region. This difference is replicable. In longitudinal studies, MSN differences are mainly manifested in the frontal and parietal regions. Furthermore, the expression pattern associated with MSN changes in PSP involves genes implicated in astrocytes and excitatory and inhibitory neurons and is functionally enriched in neuron-specific biological processes related to synaptic signaling. Finally, we found that the changes in MSN were mainly negatively correlated with the levels of serotonin, norepinephrine, and opioid receptors.ConclusionsThese results have enhanced our understanding of the microscale genetic and cellular mechanisms responsible for large-scale morphological abnormalities in PSP patients, suggesting potential targets for future therapeutic trials. MSN in PSP patients was mainly decreased in frontal and temporal cortex but increased in occipital cortex. In longitudinal studies, these are mainly in frontal and parietal regions. The expression pattern associated with MSN changes in PSP involves genes implicated in astrocytes, excitatory, and inhibitory neurons and is functionally enriched in neuron-specific biological processes. MSN were negatively correlated with the levels of serotonin, norepinephrine, and opioid receptors.image
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页数:15
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