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Screening of Differential Expression Proteins in Rat Brain Tissues after DAI by iTRAQ-LC-MS/MS

Authors :
CHEN QING, BAI JIE, ZHANG WEN-FANG
Source :
Fayixue Zazhi, Vol 33, Iss 4, Pp 348-352 (2017)
Publication Year :
2017
Publisher :
Editorial Office of Journal of Forensic Medicine, 2017.

Abstract

Objective To screen for the differential expression proteins in brain tissues of SD rat after diffuse axonal injury (DAI) by isobaric tag for relative and absolute quantification-liquid chromatograph-mass spectrometer/mass spectrometer (iTRAQ-LC-MS/MS), and to explore potential biomarkers available for the diagnosis of DAI. Methods Animal models of DAI were established with the Marmarou method as reference, and the subjects were divided into blank control group (n=4), sham strike group (n=4) and fatal strike group (n=4), respectively. The proteins in rat brain tissues were detected by iTRAQ-LC-MS/MS, and bioinformatics analysis and verification were performed on the results and screened for the differential expression proteins. Results A total of 2 016 proteins were identified and quantified. The bioinformatics analysis revealed that the proteins had wide distribution and function, and participated in different biological processes. There were 16 proteins showed differential expression in fatal strike group, including one up-regulated expression protein and 15 down-regulated expression proteins. The results of iTRAQ-LC-MS/MS were confirmed by Western blotting method. Conclusion Multiple differential expression proteins in rat brain tissues after DAI can be screened by iTRAQ-LC-MS/MS. This not only indicates a research direction for exploring the pathogenesis of DAI, but also provides potential biomarkers available for the diagnosis of DAI.

Details

Language :
Chinese
ISSN :
10045619
Volume :
33
Issue :
4
Database :
Directory of Open Access Journals
Journal :
Fayixue Zazhi
Publication Type :
Academic Journal
Accession number :
edsdoj.9ef2db77f71f4cd29843ee189fe1fc28
Document Type :
article
Full Text :
https://doi.org/10.3969/j.issn.1004-5619.2017.04.003