Expression of Sodium/iodide Symporter Transgene in Neural Stem Cells.
- Author:
Yun Hui KIM
1
;
Dong Soo LEE
;
Joo Hyun KANG
;
Yong Jin LEE
;
June Key CHUNG
;
Myung Chul LEE
Author Information
1. Program in Neuroscience, Seoul National University College of Medicine, Seoul, Korea. dsl@plaza.snu.ac.kr
- Publication Type:Original Article
- Keywords:
neural stem cell;
human sodium/iodide symporter;
promoter methylation;
histone deacetylation
- MeSH:
Azacitidine;
Cell Culture Techniques;
Cell Line;
Epigenomics;
Gene Expression;
Gyeonggi-do;
Histone Deacetylase Inhibitors;
Histones;
Humans;
Ion Transport*;
Liposomes;
Methylation;
Neural Stem Cells*;
Ribosomes;
RNA, Messenger;
Stem Cells;
Transgenes*
- From:Korean Journal of Nuclear Medicine
2004;38(1):99-108
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: The ability to noninvasively track the migration of neural progenitor cells would have significant clinical and research implications. We generated stably transfected F3 human neural progenitor cells with human sodium/iodide symporter (hNIS) for noninvasively tracking F3. In this study, the expression patterns of hNIS gene in F3-NIS were examined according to the cultured time and the epigenetic modulation. MATERIALS AND METHODS: F3 human neural stem cells had been obtained from Dr. Seung U. Kim (Ajou University, Suwon, Korea). hNIS and hygromycin resistance gene were linked with IRES (Internal Ribosome Entry Site) under control of CMV promoter. This construct was transfected to F3 with Liposome. To investigate the restoration of hNIS gene expression in F3-NIS, cells were treated with demethylating agent (5-Azacytidine) and Histone deacetylase inhibitor (Trichostatin A: TSA). The expression of hNIS was measured by I-125 uptake assay and RT-PCR analysis. RESULTS: The iodide uptake of the F3-NIS was higher 12.86 times than F3 cell line. According to the cell passage number, hNIS expression in F3-NIS gradually diminished. After treatment of 5-Azacytidine and TSA with serial doses (up to 20micro M, up to 62.5nM, respectively) for 24 hours, I-125 uptake and mRNA of hNIS in F3-NIS were increased. CONCLUSION: These results suggest that hNIS transfected F3 might undergo a change in its biological characters by cell passage. Therefore, the gene expression of exogenous gene transferred human stem cell might be affected to the epigenetic modulation such as promoter methylation and Histone deacetylation and to the cell culture conditions.
