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About:
Quantitative Analysis of Cellular Proteome Alterations in CDV-Infected Mink Lung Epithelial Cells
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Quantitative Analysis of Cellular Proteome Alterations in CDV-Infected Mink Lung Epithelial Cells
Creator
Cao, Zhigang
Cheng, Shipeng
Cheng, Yuening
Li, Shuang
Lin, Peng
Sun, Yaru
Tong, Mingwei
Wang, Jianke
Yi, Li
Li, J
Sun, Na
Adachi, Akio
Sarute, Nicolas
Cheng, Sun
Wang, Cao
Source
PMC
abstract
Canine distemper virus (CDV), a paramyxovirus, causes a severe highly contagious lethal disease in carnivores, such as mink. Mink lung epithelial cells (Mv.1.Lu cells) are sensitive to CDV infection and are homologous to the natural host system of mink. The current study analyzed the response of Mv.1.Lu cells to CDV infection by iTRAQ combined with LC–MS/MS. In total, 151 and 369 differentially expressed proteins (DEPs) were markedly up-regulated or down-regulated, respectively. Thirteen DEPs were validated via real-time RT-PCR or western blot analysis. Network and KEGG pathway analyses revealed several regulated proteins associated with the NF-κB signaling pathway. Further validation was performed by western blot analysis and immunofluorescence assay, which demonstrated that different CDV strains induced NF-κB P65 phosphorylation and nuclear translocation. Moreover, the results provided interesting information that some identified DEPs possibly associated with the pathogenesis and the immune response upon CDV infection. This study is the first overview of the responses to CDV infection in Mv.1.Lu cells, and the findings will help to analyze further aspects of the molecular mechanisms involved in viral pathogenesis and the immune responses upon CDV infection.
has issue date
2017-12-22
(
xsd:dateTime
)
bibo:doi
10.3389/fmicb.2017.02564
bibo:pmid
29312244
has license
cc-by
sha1sum (hex)
c5157f9976942d166a600cb570a5a8fa9ab91e57
schema:url
https://doi.org/10.3389/fmicb.2017.02564
resource representing a document's title
Quantitative Analysis of Cellular Proteome Alterations in CDV-Infected Mink Lung Epithelial Cells
has PubMed Central identifier
PMC5743685
has PubMed identifier
29312244
schema:publication
Front Microbiol
resource representing a document's body
covid:c5157f9976942d166a600cb570a5a8fa9ab91e57#body_text
is
schema:about
of
named entity 'INFECTED'
named entity 'QUANTITATIVE ANALYSIS'
named entity 'MINK'
named entity 'MOLECULAR'
named entity 'SIGNALING PATHWAY'
named entity 'CDV'
named entity 'DEMONSTRATED'
named entity 'OVERVIEW'
named entity 'IMMUNE RESPONSE'
named entity 'CARNIVORES'
named entity 'PROVIDED'
named entity 'CDV'
named entity 'CANINE DISTEMPER VIRUS'
named entity 'DIFFERENT'
named entity 'NETWORK'
named entity 'PERFORMED BY'
named entity 'NUCLEAR TRANSLOCATION'
named entity 'PARAMYXOVIRUS'
named entity 'DOWN-REGULATED'
named entity 'REAL-TIME RT-PCR'
named entity 'MECHANISMS'
named entity 'PATHWAY'
named entity 'CAUSES'
named entity 'MARKEDLY'
named entity 'REGULATED'
named entity 'VALIDATION'
named entity 'TOTAL'
named entity 'RESPONSES'
named entity 'COMBINED'
named entity 'THIRTEEN'
named entity 'ALTERATIONS'
named entity 'CELLULAR'
named entity 'INFECTION'
named entity 'BAB'
named entity 'ITRAQ'
named entity 'DISEASE'
named entity 'HELP'
named entity 'SEVERE'
named entity 'NATURAL'
named entity 'ANALYZED'
named entity 'LUNG'
named entity 'FINDINGS'
named entity 'POSSIBLY'
named entity 'HIGHLY'
named entity 'EXPRESSED'
named entity 'RESPONSE'
named entity 'CELLS'
named entity 'CURRENT'
named entity 'LC-MS'
named entity 'ASSOCIATED WITH'
named entity 'UP-REGULATED'
named entity 'EPITHELIAL CELLS'
named entity 'INTERESTING'
named entity 'IDENTIFIED'
named entity 'IMMUNOFLUORESCENCE ASSAY'
named entity 'MINK'
named entity 'DEPS'
named entity 'SYSTEM'
named entity 'KEGG'
named entity 'P65'
named entity 'RESULTS'
named entity 'LETHAL'
named entity 'SENSITIVE TO'
named entity 'INDUCED'
named entity 'STUDY'
named entity 'REVEALED'
named entity 'PATHOGENESIS'
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