Differential activation of immune/inflammatory response-related co-expression modules in the hippocampus across the major psychiatric disorders

被引:54
作者
Kim, S. [1 ]
Hwang, Y. [2 ]
Webster, M. J. [1 ]
Lee, D. [2 ]
机构
[1] Stanley Med Res Inst, Stanley Brain Res Lab, 9800 Med Ctr Dr, Rockville, MD 20850 USA
[2] Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Daejeon, South Korea
基金
新加坡国家研究基金会;
关键词
MESSENGER-RNA EXPRESSION; BIPOLAR DISORDER; GENE-EXPRESSION; NEUROPATHOLOGY-CONSORTIUM; TRANSCRIPTOMIC ANALYSIS; NETWORK ANALYSIS; DOWN-REGULATION; SCHIZOPHRENIA; DEPRESSION; BRAIN;
D O I
10.1038/mp.2015.79
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Stanley Neuropathology Consortium Integrative Database (SNCID, http://sncid.stanleyresearch.org) is a data -mining tool that includes 379 neuropathology data sets from hippocampus, as well as RNA-Seq data measured in 15 well -matched cases in each of four groups: schizophrenia, bipolar disorder (BPD), major depression (MD) and unaffected controls. We analyzed the neuropathology data from the hippocampus to identify those abnormalities that are shared between psychiatric disorders and those that are specific to each disorder. Of the 379 data sets, 20 of them showed a significant abnormality in at least one disorder as compared with unaffected controls. GABAergic markers and synaptic proteins were mainly abnormal in schizophrenia and the two mood disorders, respectively. Two immune/inflammation-related co -expression modules built from RNA-seq data from both schizophrenia and controls combined were associated with disease status, as well as negatively correlated with the GABAergic markers. The correlation between immune -related modules and schizophrenia was replicated using microarray data from an independent tissue collection. Immune/inflammation-related co -expression modules were also built from RNA-seq data from BPD cases or from MD cases but were not preserved when using data from control cases. Moreover, there was no overlap in the genes that comprise the immune/inflammation response -related modules across the different disorders. Thus, there appears to be differential activation of the immune/inflammatory response, as determined by co -expression of genes, which is associated with the major psychiatric disorders and which is also associated with the abnormal neuropathology in the disorders.
引用
收藏
页码:376 / 385
页数:10
相关论文
共 60 条
[1]   RNA-sequencing of the brain transcriptome implicates dysregulation of neuroplasticity, circadian rhythms and GTPase binding in bipolar disorder [J].
Akula, N. ;
Barb, J. ;
Jiang, X. ;
Wendland, J. R. ;
Choi, K. H. ;
Sen, S. K. ;
Hou, L. ;
Chen, D. T. W. ;
Laje, G. ;
Johnson, K. ;
Lipska, B. K. ;
Kleinman, J. E. ;
Corrada-Bravo, H. ;
Detera-Wadleigh, S. ;
Munson, P. J. ;
McMahon, F. J. .
MOLECULAR PSYCHIATRY, 2014, 19 (11) :1179-1185
[2]   Effects of Antipsychotics on the Inflammatory Response System of Patients with Schizophrenia in Peripheral Blood Mononuclear Cell Cultures [J].
Al-Amin, Md. Mamun ;
Uddin, Mir Muhammad Nasir ;
Reza, Hasan Mahmud .
CLINICAL PSYCHOPHARMACOLOGY AND NEUROSCIENCE, 2013, 11 (03) :144-151
[3]   Transcriptional profiling reveals evidence for signaling and oligodendroglial abnormalities in the temporal cortex from patients with major depressive disorder [J].
Aston, C ;
Jiang, L ;
Sokolov, BP .
MOLECULAR PSYCHIATRY, 2005, 10 (03) :309-322
[4]   Cognitive deficits in depression - Possible implications for functional neuropathology [J].
Austin, MP ;
Mitchell, P ;
Goodwin, GM .
BRITISH JOURNAL OF PSYCHIATRY, 2001, 178 :200-206
[5]   The expression of proapoptosis genes is increased in bipolar disorder, but not in schizophrenia [J].
Benes, FM ;
Matzilevich, D ;
Burke, RE ;
Walsh, J .
MOLECULAR PSYCHIATRY, 2006, 11 (03) :241-251
[6]   Two gene co-expression modules differentiate psychotics and controls [J].
Chen, C. ;
Cheng, L. ;
Grennan, K. ;
Pibiri, F. ;
Zhang, C. ;
Badner, J. A. ;
Gershon, E. S. ;
Liu, C. .
MOLECULAR PSYCHIATRY, 2013, 18 (12) :1308-1314
[7]   Altered cortical glutamatergic and GABAergic signal transmission with glial involvement in depression [J].
Choudary, PV ;
Molnar, M ;
Evans, SJ ;
Tomita, H ;
Li, JZ ;
Vawter, MP ;
Myers, RM ;
Bunney, WE ;
Akil, H ;
Watson, SJ ;
Jones, EG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (43) :15653-15658
[8]   Hippocampal neurogenesis as a target for the treatment of mental illness: A critical evaluation [J].
DeCarolis, Nathan A. ;
Eisch, Amelia J. .
NEUROPHARMACOLOGY, 2010, 58 (06) :884-893
[9]   DAVID: Database for annotation, visualization, and integrated discovery [J].
Dennis, G ;
Sherman, BT ;
Hosack, DA ;
Yang, J ;
Gao, W ;
Lane, HC ;
Lempicki, RA .
GENOME BIOLOGY, 2003, 4 (09)
[10]   A genome-wide association study identifies IL23R as an inflammatory bowel disease gene [J].
Duerr, Richard H. ;
Taylor, Kent D. ;
Brant, Steven R. ;
Rioux, John D. ;
Silverberg, Mark S. ;
Daly, Mark J. ;
Steinhart, A. Hillary ;
Abraham, Clara ;
Regueiro, Miguel ;
Griffiths, Anne ;
Dassopoulos, Themistocles ;
Bitton, Alain ;
Yang, Huiying ;
Targan, Stephan ;
Datta, Lisa Wu ;
Kistner, Emily O. ;
Schumm, L. Philip ;
Lee, Annette T. ;
Gregersen, Peter K. ;
Barmada, M. Michael ;
Rotter, Jerome I. ;
Nicolae, Dan L. ;
Cho, Judy H. .
SCIENCE, 2006, 314 (5804) :1461-1463