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M177. THE PROTEOME OF OLIGODENDROCYTES DIFFERENTIATED FROM NEURAL STEM CELL DERIVED FROM SCHIZOPHRENIA PATIENTS

BACKGROUND: Oligodendrocytes constitute the majority of the cells in white matter and alterations in this region have been reported in patients with schizophrenia. The myelin sheath is produced exclusively by mature oligodendrocytes. Thus, a dysfunction during the maturation of these cells could lea...

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Autores principales: Teles Rodrigues, Caroline, Martins-De-Souza, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7234532/
http://dx.doi.org/10.1093/schbul/sbaa030.489
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author Teles Rodrigues, Caroline
Martins-De-Souza, Daniel
author_facet Teles Rodrigues, Caroline
Martins-De-Souza, Daniel
author_sort Teles Rodrigues, Caroline
collection PubMed
description BACKGROUND: Oligodendrocytes constitute the majority of the cells in white matter and alterations in this region have been reported in patients with schizophrenia. The myelin sheath is produced exclusively by mature oligodendrocytes. Thus, a dysfunction during the maturation of these cells could lead to a change in normal myelination processes, causing the hypomyelination observed in patients with schizophrenia. In this manner, functional studies are needed for a better connection of these different aspects of the disease in order to understand the pathophysiology of schizophrenia in an integrated manner. Thus, our aim was to evaluate the differences between the proteome of oligodendrocytes derived from neural stem cells (NSCs) from patients with schizophrenia and controls. METHODS: The cells were differentiated using the protocol described by Yan, Shin, Jha and collaborators (Yan, Shin, Jha, et al., 2013). After 14 days, the proteins were extracted and proteomic analyses were performed in a two-dimensional microUPLC coupled to nano ESI-Q-IM-TOF mass spectrometer. Progenesis® QI software was used in order to identify and quantify the proteins. RESULTS: On average, 2046 proteins were identified and 444 had alterations in the expression levels. These differentially expressed proteins were related most with metabolism, RNA transport, spliceosome machinery, vesicular transport, and signal transduction. DISCUSSION: The proteins and canonical pathways found here may contribute to understanding the biochemical mechanisms involved in the disorder, which may provide new targets for the development of more effective treatments, improving the schizophrenic patient’s quality of life.
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spelling pubmed-72345322020-05-23 M177. THE PROTEOME OF OLIGODENDROCYTES DIFFERENTIATED FROM NEURAL STEM CELL DERIVED FROM SCHIZOPHRENIA PATIENTS Teles Rodrigues, Caroline Martins-De-Souza, Daniel Schizophr Bull Poster Session II BACKGROUND: Oligodendrocytes constitute the majority of the cells in white matter and alterations in this region have been reported in patients with schizophrenia. The myelin sheath is produced exclusively by mature oligodendrocytes. Thus, a dysfunction during the maturation of these cells could lead to a change in normal myelination processes, causing the hypomyelination observed in patients with schizophrenia. In this manner, functional studies are needed for a better connection of these different aspects of the disease in order to understand the pathophysiology of schizophrenia in an integrated manner. Thus, our aim was to evaluate the differences between the proteome of oligodendrocytes derived from neural stem cells (NSCs) from patients with schizophrenia and controls. METHODS: The cells were differentiated using the protocol described by Yan, Shin, Jha and collaborators (Yan, Shin, Jha, et al., 2013). After 14 days, the proteins were extracted and proteomic analyses were performed in a two-dimensional microUPLC coupled to nano ESI-Q-IM-TOF mass spectrometer. Progenesis® QI software was used in order to identify and quantify the proteins. RESULTS: On average, 2046 proteins were identified and 444 had alterations in the expression levels. These differentially expressed proteins were related most with metabolism, RNA transport, spliceosome machinery, vesicular transport, and signal transduction. DISCUSSION: The proteins and canonical pathways found here may contribute to understanding the biochemical mechanisms involved in the disorder, which may provide new targets for the development of more effective treatments, improving the schizophrenic patient’s quality of life. Oxford University Press 2020-05 2020-05-18 /pmc/articles/PMC7234532/ http://dx.doi.org/10.1093/schbul/sbaa030.489 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Poster Session II
Teles Rodrigues, Caroline
Martins-De-Souza, Daniel
M177. THE PROTEOME OF OLIGODENDROCYTES DIFFERENTIATED FROM NEURAL STEM CELL DERIVED FROM SCHIZOPHRENIA PATIENTS
title M177. THE PROTEOME OF OLIGODENDROCYTES DIFFERENTIATED FROM NEURAL STEM CELL DERIVED FROM SCHIZOPHRENIA PATIENTS
title_full M177. THE PROTEOME OF OLIGODENDROCYTES DIFFERENTIATED FROM NEURAL STEM CELL DERIVED FROM SCHIZOPHRENIA PATIENTS
title_fullStr M177. THE PROTEOME OF OLIGODENDROCYTES DIFFERENTIATED FROM NEURAL STEM CELL DERIVED FROM SCHIZOPHRENIA PATIENTS
title_full_unstemmed M177. THE PROTEOME OF OLIGODENDROCYTES DIFFERENTIATED FROM NEURAL STEM CELL DERIVED FROM SCHIZOPHRENIA PATIENTS
title_short M177. THE PROTEOME OF OLIGODENDROCYTES DIFFERENTIATED FROM NEURAL STEM CELL DERIVED FROM SCHIZOPHRENIA PATIENTS
title_sort m177. the proteome of oligodendrocytes differentiated from neural stem cell derived from schizophrenia patients
topic Poster Session II
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7234532/
http://dx.doi.org/10.1093/schbul/sbaa030.489
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