Differential gene regulation in the anterior cingulate cortex and superior temporal cortex in schizophrenia: A molecular network approach

被引:4
|
作者
Gebicke-Haerter, Peter J. [1 ,2 ]
Leonardi-Essmann, Fernando [2 ]
Haerter, Jan O. [3 ]
Rossner, Moritz J. [4 ]
Falkai, Peter [4 ]
Schmitt, Andrea [4 ,5 ]
Raabe, Florian J. [4 ,6 ]
机构
[1] Univ Chile, Inst Biomed Sci, Program Immunol, Fac Med, Av Independencia 1027, Santiago, Chile
[2] Heidelberg Univ, Cent Inst Mental Hlth, Inst Psychopharmacol, Fac Med, J 5, D-68159 Mannheim, Germany
[3] Univ Copenhagen, Niels Bohr Inst, Copenhagen, Denmark
[4] Ludwig Maximilians Univ Munchen, Univ Hosp, Dept Psychiat & Psychotherapy, Nubaumstr 7, D-80336 Munich, Germany
[5] Univ Sao Paulo, Inst Psychiat, Lab Neurosci LIM27, Rua Dr Ovidio Pires de Campos 785, BR-05453010 Sao Paulo, SP, Brazil
[6] Int Max Planck Res Sch Translat Psychiat IMPRS TP, Kraepelinstr 2-10, D-80804 Munich, Germany
关键词
Postmortem; Schizophrenia; Gene expression; Anterior cingulate cortex; Molecular networks; PREFRONTAL CORTEX; MICROGLIAL ACTIVATION; BRAIN; EXPRESSION; PROTEIN; METAANALYSIS; RISK; MIND; RISPERIDONE; UBIQUITIN;
D O I
10.1016/j.schres.2021.04.014
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
The closely connected anterior cingulate cortex (ACC) and superior temporal cortex (STC) are important for higher cognitive functions. Both brain regions are disturbed in schizophrenia, i.e., functional and structural alterations have been reported. This postmortem investigation in brains from patients with schizophrenia and controls compared gene expression in the left ACC and left STC. Most differentially expressed genes were unique to each brain region, but some clusters of genes were equally dysregulated in both, giving rise to a more general disease-specific pattern of gene regulation. The data was used to construct a molecular network of the genes identically expressed in both regions as primary nodes and the metabolically connected genes as secondary nodes. The network analysis identified downregulated clusters of immune-associated gene products and upregulated clusters belonging to the ubiquitin-proteasome system. These findings could help to identify new potential therapeutic targets for future approaches. (c) 2021 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 10
页数:10
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