The expression of Foxp3 protein by retroviral vector-mediated gene transfer of Foxp3 in C57BL/6 mice.
- Author:
Insun HWANG
1
;
Danbee HA
;
So Jin BING
;
Kyong Leek JEON
;
Ginnae AHN
;
Dae Seung KIM
;
Jinhee CHO
;
Jaehak LIM
;
Sin Hyeog IM
;
Kyu Kye HWANG
;
Youngheun JEE
Author Information
1. College of Veterinary Medicine and Applied Radiological Institute, Jeju National University, Jeju 690-756, Korea. yhjee@jejunu.ac.kr
- Publication Type:Original Article
- Keywords:
Foxp3;
regulatory T cells;
retroviral vector;
gene transfer
- MeSH:
Animals;
Autoimmune Diseases;
Brain;
Gene Expression;
Heart;
Immune Tolerance;
Inflammation;
Kidney;
Liver;
Lung;
Mice;
Muscles;
Spinal Cord;
Spleen;
T-Lymphocytes;
T-Lymphocytes, Regulatory;
Transcription Factors;
Transgenes;
Zidovudine
- From:Korean Journal of Veterinary Research
2012;52(3):183-191
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
The maintenance of peripheral immune tolerance and prevention of chronic inflammation and autoimmune disease require CD4+CD25+ T cells (regulatory T cells). The transcription factor Foxp3 is essential for the development of functional, regulatory T cells, which plays a prominent role in self-tolerance. Retroviral vectors can confer high level of gene transfer and transgene expression in a variety of cell types. Here we observed that following retroviral vector-mediated gene transfer of Foxp3, transductional Foxp3 expression was increased in the liver, lung, brain, heart, muscle, spinal cord, kidney and spleen. One day after vector administration, high levels of transgene and gene expression were observed in liver and lung. At 2 days after injection, transductional Foxp3 expression level was increased in brain, heart, muscle and spinal cord, but kidney and spleen exhibited a consistent low level. This finding was inconsistent with the increase in both CD4+CD25+ T cell and CD4+Foxp3+ T cell frequencies observed in peripheral immune cells by fluorescence-activated cell-sorting (FACS) analysis. Retroviral vector-mediated gene transfer of Foxp3 did not lead to increased numbers of CD4+CD25+ T cell and CD4+Foxp3+ T cell. These results demonstrate the level and duration of transductional Foxp3 gene expression in various tissues. A better understanding of Foxp3 regulation can be useful in dissecting the cause of regulatory T cells dysfunction in several autoimmune diseases and raise the possibility of enhancing suppressive functions of regulatory T cells for therapeutic purposes.
