Proteomic Analysis of a Rat Cerebral Ischemic Injury Model after Human Cerebral Endothelial Cell Transplantation.
10.3340/jkns.2016.59.6.544
- Author:
Tae Min CHOI
1
;
Misun YUN
;
Jung Kil LEE
;
Jong Tae PARK
;
Man Seok PARK
;
Hyung Seok KIM
Author Information
1. Department of Neurosurgery, Gwangju Christian Hospital, Gwangju, Korea.
- Publication Type:Original Article
- Keywords:
Brain;
Ischemia;
Cell therapy;
Proteomics;
2-dimensional electrophoresis
- MeSH:
Animals;
Blotting, Western;
Brain;
Brain Ischemia;
Cell Transplantation;
Cell- and Tissue-Based Therapy;
Electrophoresis;
Endothelial Cells*;
Fingers;
Humans*;
Ischemia;
Mass Spectrometry;
Neurons;
Proteomics;
Rats*;
Real-Time Polymerase Chain Reaction;
Stroke;
Transplants
- From:Journal of Korean Neurosurgical Society
2016;59(6):544-550
- CountryRepublic of Korea
- Language:English
-
Abstract:
OBJECTIVE: Cerebral endothelial cells have unique biological features and are fascinating candidate cells for stroke therapy. METHODS: In order to understand the molecular mechanisms of human cerebral endothelial cell (hCMEC/D3) transplantation in a rat stroke model, we performed proteomic analysis using 2-dimensional electrophoresis and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Protein expression was confirmed by quantitative real-time PCR and Western blot. RESULTS: Several protein spots were identified by gel electrophoresis in the sham, cerebral ischemia (CI), and CI with hCMEC/D3 treatment cerebral ischemia with cell transplantation (CT) groups, and we identified 14 differentially expressed proteins in the CT group. Proteins involved in mitochondrial dysfunction (paraplegin matrix AAA peptidase subunit, SPG7), neuroinflammation (peroxiredoxin 6, PRDX6), and neuronal death (zinc finger protein 90, ZFP90) were markedly reduced in the CT group compared with the CI group. The expression of chloride intracellular channel 4 proteins involved in post-ischemic vasculogenesis was significantly decreased in the CI group but comparable to sham in the CT group. CONCLUSION: These results contribute to our understanding of the early phase processes that follow cerebral endothelial cell treatment in CI. Moreover, some of the identified proteins may present promising new targets for stroke therapy.
