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Proteomic Analysis of Human Brain Microvascular Endothelial Cells Reveals Differential Protein Expression in Response to Enterovirus 71 Infection

2D DIGE technology was employed on proteins prepared from human brain microvascular endothelial cells (HBMEC), to study the differentially expressed proteins in cells at 0 h, 1 h, 16 h, and 24 h after infection. Proteins found to be differentially expressed were identified with matrix-assisted laser...

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Autores principales: Luo, Wenying, Zhong, Jiayu, Zhao, Wei, Liu, Jianjun, Zhang, Renli, Peng, Liang, Hong, Wenxu, Huang, Sheng He, Cao, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4363668/
https://www.ncbi.nlm.nih.gov/pubmed/25821824
http://dx.doi.org/10.1155/2015/864169
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author Luo, Wenying
Zhong, Jiayu
Zhao, Wei
Liu, Jianjun
Zhang, Renli
Peng, Liang
Hong, Wenxu
Huang, Sheng He
Cao, Hong
author_facet Luo, Wenying
Zhong, Jiayu
Zhao, Wei
Liu, Jianjun
Zhang, Renli
Peng, Liang
Hong, Wenxu
Huang, Sheng He
Cao, Hong
author_sort Luo, Wenying
collection PubMed
description 2D DIGE technology was employed on proteins prepared from human brain microvascular endothelial cells (HBMEC), to study the differentially expressed proteins in cells at 0 h, 1 h, 16 h, and 24 h after infection. Proteins found to be differentially expressed were identified with matrix-assisted laser desorption/ionization time-of-flight/time-of-flight mass spectrometry (MALDITOF/TOF MS) analysis. We identified 43 spots showing changes of at least 2.5 fold up- or downregulated expressions in EV71-infected cells at different time when comparing to control, and 28 proteins could be successfully identified by MALDI TOF/TOF mass spectrometry analysis. 4 proteins were significantly upregulated, and 6 proteins were downregulated, another 18 proteins were different expression at different incubation time. We identified changes in the expression of 12 cellular metabolism-related proteins, 5 molecules involved in cytoskeleton, 3 molecules involved in energy metabolism, 2 molecules involved in signal transduction, 1 molecule involved in the ubiquitin-proteasome pathway, 1 molecule involved in cell cycle, 1 molecule involved in apoptosis-related protein, 1 molecular chaperone, and 2 unknown proteins. These findings build up a comprehensive profile of the HBMEC proteome and provide a useful basis for further analysis of the pathogenic mechanism that underlies EV71 infections to induce severe neural complications.
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spelling pubmed-43636682015-03-29 Proteomic Analysis of Human Brain Microvascular Endothelial Cells Reveals Differential Protein Expression in Response to Enterovirus 71 Infection Luo, Wenying Zhong, Jiayu Zhao, Wei Liu, Jianjun Zhang, Renli Peng, Liang Hong, Wenxu Huang, Sheng He Cao, Hong Biomed Res Int Research Article 2D DIGE technology was employed on proteins prepared from human brain microvascular endothelial cells (HBMEC), to study the differentially expressed proteins in cells at 0 h, 1 h, 16 h, and 24 h after infection. Proteins found to be differentially expressed were identified with matrix-assisted laser desorption/ionization time-of-flight/time-of-flight mass spectrometry (MALDITOF/TOF MS) analysis. We identified 43 spots showing changes of at least 2.5 fold up- or downregulated expressions in EV71-infected cells at different time when comparing to control, and 28 proteins could be successfully identified by MALDI TOF/TOF mass spectrometry analysis. 4 proteins were significantly upregulated, and 6 proteins were downregulated, another 18 proteins were different expression at different incubation time. We identified changes in the expression of 12 cellular metabolism-related proteins, 5 molecules involved in cytoskeleton, 3 molecules involved in energy metabolism, 2 molecules involved in signal transduction, 1 molecule involved in the ubiquitin-proteasome pathway, 1 molecule involved in cell cycle, 1 molecule involved in apoptosis-related protein, 1 molecular chaperone, and 2 unknown proteins. These findings build up a comprehensive profile of the HBMEC proteome and provide a useful basis for further analysis of the pathogenic mechanism that underlies EV71 infections to induce severe neural complications. Hindawi Publishing Corporation 2015 2015-03-02 /pmc/articles/PMC4363668/ /pubmed/25821824 http://dx.doi.org/10.1155/2015/864169 Text en Copyright © 2015 Wenying Luo et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under 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
Luo, Wenying
Zhong, Jiayu
Zhao, Wei
Liu, Jianjun
Zhang, Renli
Peng, Liang
Hong, Wenxu
Huang, Sheng He
Cao, Hong
Proteomic Analysis of Human Brain Microvascular Endothelial Cells Reveals Differential Protein Expression in Response to Enterovirus 71 Infection
title Proteomic Analysis of Human Brain Microvascular Endothelial Cells Reveals Differential Protein Expression in Response to Enterovirus 71 Infection
title_full Proteomic Analysis of Human Brain Microvascular Endothelial Cells Reveals Differential Protein Expression in Response to Enterovirus 71 Infection
title_fullStr Proteomic Analysis of Human Brain Microvascular Endothelial Cells Reveals Differential Protein Expression in Response to Enterovirus 71 Infection
title_full_unstemmed Proteomic Analysis of Human Brain Microvascular Endothelial Cells Reveals Differential Protein Expression in Response to Enterovirus 71 Infection
title_short Proteomic Analysis of Human Brain Microvascular Endothelial Cells Reveals Differential Protein Expression in Response to Enterovirus 71 Infection
title_sort proteomic analysis of human brain microvascular endothelial cells reveals differential protein expression in response to enterovirus 71 infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4363668/
https://www.ncbi.nlm.nih.gov/pubmed/25821824
http://dx.doi.org/10.1155/2015/864169
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