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Proteome analysis of biomarkers in the cerebrospinal fluid of neuromyelitis optica patients
PURPOSE: To better understand the pathophysiological mechanisms underlying neuromyelitis optica (NMO), we developed a proteomics platform for biomarker discovery in the cerebrospinal fluid (CSF) of patients with NMO. METHODS: Two-dimensional electrophoresis (2-DE) and matrix-assisted laser desorptio...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Molecular Vision
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2730746/ https://www.ncbi.nlm.nih.gov/pubmed/19710940 |
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author | Bai, Shumei Liu, Shilian Guo, Xuxiao Qin, Zhaoyu Wang, Banqin Li, Xiaohong Qin, Yanjiang Liu, Yi-Hsin |
author_facet | Bai, Shumei Liu, Shilian Guo, Xuxiao Qin, Zhaoyu Wang, Banqin Li, Xiaohong Qin, Yanjiang Liu, Yi-Hsin |
author_sort | Bai, Shumei |
collection | PubMed |
description | PURPOSE: To better understand the pathophysiological mechanisms underlying neuromyelitis optica (NMO), we developed a proteomics platform for biomarker discovery in the cerebrospinal fluid (CSF) of patients with NMO. METHODS: Two-dimensional electrophoresis (2-DE) and matrix-assisted laser desorption ionization time of flight mass spectrometry (MALDI-TOF MS) were used to compare the CSF proteome of NMO patients with that of controls. A subsequent ELISA and western blot analysis were performed to verify the results of the proteomic analysis. Pathway Studio 5.0 software was used to determine possible functional interactions among these differentially expressed proteins. RESULTS: Using 2-DE and MALDI-TOF MS, we identified 11 differentially expressed proteins and two isoforms of these same proteins. The expression of four proteins was enhanced, whereas the expression of seven proteins was reduced in the NMO group in comparison to the control group. These differences in protein expression were confirmed by performing ELISA and western blot analyses (p<0.01). Protein network analyses revealed biologic interactions and cross-talks among these differentially expressed proteins. CONCLUSIONS: Because of their unique expression profile in NMO CSFs, these proteins are candidate biomarkers for NMO. Thus, our findings may have important implications for both the diagnosis of NMO and the further understanding of its pathogenesis. |
format | Text |
id | pubmed-2730746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Molecular Vision |
record_format | MEDLINE/PubMed |
spelling | pubmed-27307462009-08-26 Proteome analysis of biomarkers in the cerebrospinal fluid of neuromyelitis optica patients Bai, Shumei Liu, Shilian Guo, Xuxiao Qin, Zhaoyu Wang, Banqin Li, Xiaohong Qin, Yanjiang Liu, Yi-Hsin Mol Vis Research Article PURPOSE: To better understand the pathophysiological mechanisms underlying neuromyelitis optica (NMO), we developed a proteomics platform for biomarker discovery in the cerebrospinal fluid (CSF) of patients with NMO. METHODS: Two-dimensional electrophoresis (2-DE) and matrix-assisted laser desorption ionization time of flight mass spectrometry (MALDI-TOF MS) were used to compare the CSF proteome of NMO patients with that of controls. A subsequent ELISA and western blot analysis were performed to verify the results of the proteomic analysis. Pathway Studio 5.0 software was used to determine possible functional interactions among these differentially expressed proteins. RESULTS: Using 2-DE and MALDI-TOF MS, we identified 11 differentially expressed proteins and two isoforms of these same proteins. The expression of four proteins was enhanced, whereas the expression of seven proteins was reduced in the NMO group in comparison to the control group. These differences in protein expression were confirmed by performing ELISA and western blot analyses (p<0.01). Protein network analyses revealed biologic interactions and cross-talks among these differentially expressed proteins. CONCLUSIONS: Because of their unique expression profile in NMO CSFs, these proteins are candidate biomarkers for NMO. Thus, our findings may have important implications for both the diagnosis of NMO and the further understanding of its pathogenesis. Molecular Vision 2009-08-19 /pmc/articles/PMC2730746/ /pubmed/19710940 Text en http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Bai, Shumei Liu, Shilian Guo, Xuxiao Qin, Zhaoyu Wang, Banqin Li, Xiaohong Qin, Yanjiang Liu, Yi-Hsin Proteome analysis of biomarkers in the cerebrospinal fluid of neuromyelitis optica patients |
title | Proteome analysis of biomarkers in the cerebrospinal fluid of neuromyelitis optica patients |
title_full | Proteome analysis of biomarkers in the cerebrospinal fluid of neuromyelitis optica patients |
title_fullStr | Proteome analysis of biomarkers in the cerebrospinal fluid of neuromyelitis optica patients |
title_full_unstemmed | Proteome analysis of biomarkers in the cerebrospinal fluid of neuromyelitis optica patients |
title_short | Proteome analysis of biomarkers in the cerebrospinal fluid of neuromyelitis optica patients |
title_sort | proteome analysis of biomarkers in the cerebrospinal fluid of neuromyelitis optica patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2730746/ https://www.ncbi.nlm.nih.gov/pubmed/19710940 |
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