Proteome analysis of schizophrenia patients Wernicke's area reveals an energy metabolism dysregulation

被引:113
作者
Martins-de-Souza, Daniel [1 ,2 ,3 ]
Gattaz, Wagner F. [1 ]
Schmitt, Andrea [4 ]
Novello, Jose C. [2 ]
Marangoni, Sergio [2 ]
Turck, Christoph W. [3 ]
Dias-Neto, Emmanuel [1 ,5 ]
机构
[1] Univ Sao Paulo, Lab Neurociencias, Inst Psiquiatria, Fac Med, BR-05403010 Sao Paulo, Brazil
[2] Max Planck Inst Psychiat, D-80804 Munich, Germany
[3] Univ Estadual Campinas, Dept Bioquim, Inst Biol, BR-13083970 Campinas, SP, Brazil
[4] Univ Gottingen, Dept Psychiat, D-37075 Gottingen, Germany
[5] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
基金
巴西圣保罗研究基金会;
关键词
ANTERIOR CINGULATE CORTEX; GENE-EXPRESSION; TEMPORAL CORTEX; AUDITORY HALLUCINATIONS; MICROARRAY ANALYSIS; PREFRONTAL CORTEX; BIPOLAR DISORDER; BRAIN PROTEINS; LINKAGE; MATTER;
D O I
10.1186/1471-244X-9-17
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: Schizophrenia is likely to be a consequence of DNA alterations that, together with environmental factors, will lead to protein expression differences and the ultimate establishment of the illness. The superior temporal gyrus is implicated in schizophrenia and executes functions such as the processing of speech, language skills and sound processing. Methods: We performed an individual comparative proteome analysis using two-dimensional gel electrophoresis of 9 schizophrenia and 6 healthy control patients' left posterior superior temporal gyrus (Wernicke's area - BA22p) identifying by mass spectrometry several protein expression alterations that could be related to the disease. Results: Our analysis revealed 11 downregulated and 14 upregulated proteins, most of them related to energy metabolism. Whereas many of the identified proteins have been previously implicated in schizophrenia, such as fructose-bisphosphate aldolase C, creatine kinase and neuron-specific enolase, new putative disease markers were also identified such as dihydrolipoyl dehydrogenase, tropomyosin 3, breast cancer metastasis-suppressor 1, heterogeneous nuclear ribonucleoproteins C1/C2 and phosphate carrier protein, mitochondrial precursor. Besides, the differential expression of peroxiredoxin 6 (PRDX6) and glial fibrillary acidic protein (GFAP) were confirmed by western blot in schizophrenia prefrontal cortex. Conclusion: Our data supports a dysregulation of energy metabolism in schizophrenia as well as suggests new markers that may contribute to a better understanding of this complex disease.
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页数:8
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