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

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 t...

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Autores principales: Martins-de-Souza, Daniel, Gattaz, Wagner F, Schmitt, Andrea, Novello, José C, Marangoni, Sérgio, Turck, Christoph W, Dias-Neto, Emmanuel
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2684104/
https://www.ncbi.nlm.nih.gov/pubmed/19405953
http://dx.doi.org/10.1186/1471-244X-9-17
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author Martins-de-Souza, Daniel
Gattaz, Wagner F
Schmitt, Andrea
Novello, José C
Marangoni, Sérgio
Turck, Christoph W
Dias-Neto, Emmanuel
author_facet Martins-de-Souza, Daniel
Gattaz, Wagner F
Schmitt, Andrea
Novello, José C
Marangoni, Sérgio
Turck, Christoph W
Dias-Neto, Emmanuel
author_sort Martins-de-Souza, Daniel
collection PubMed
description 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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spelling pubmed-26841042009-05-20 Proteome analysis of schizophrenia patients Wernicke's area reveals an energy metabolism dysregulation Martins-de-Souza, Daniel Gattaz, Wagner F Schmitt, Andrea Novello, José C Marangoni, Sérgio Turck, Christoph W Dias-Neto, Emmanuel BMC Psychiatry Research Article 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. BioMed Central 2009-04-30 /pmc/articles/PMC2684104/ /pubmed/19405953 http://dx.doi.org/10.1186/1471-244X-9-17 Text en Copyright © 2009 Martins-de-Souza et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Martins-de-Souza, Daniel
Gattaz, Wagner F
Schmitt, Andrea
Novello, José C
Marangoni, Sérgio
Turck, Christoph W
Dias-Neto, Emmanuel
Proteome analysis of schizophrenia patients Wernicke's area reveals an energy metabolism dysregulation
title Proteome analysis of schizophrenia patients Wernicke's area reveals an energy metabolism dysregulation
title_full Proteome analysis of schizophrenia patients Wernicke's area reveals an energy metabolism dysregulation
title_fullStr Proteome analysis of schizophrenia patients Wernicke's area reveals an energy metabolism dysregulation
title_full_unstemmed Proteome analysis of schizophrenia patients Wernicke's area reveals an energy metabolism dysregulation
title_short Proteome analysis of schizophrenia patients Wernicke's area reveals an energy metabolism dysregulation
title_sort proteome analysis of schizophrenia patients wernicke's area reveals an energy metabolism dysregulation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2684104/
https://www.ncbi.nlm.nih.gov/pubmed/19405953
http://dx.doi.org/10.1186/1471-244X-9-17
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