TY - JOUR
T1 - Vascular endothelium-selective gene induction by Tie2 promoter/enhancer in the brain and retina of a transgenic rat
AU - Ohtsuki, Sumio
AU - Kamiya, Naoko
AU - Hori, Satoko
AU - Terasaki, Tetsuya
N1 - Funding Information:
We would like to thank Dr. Sato for kindly supplying the Tie2/GFP vector and Dr. Watanabe for kindly supplying the anti-GLUT1 antibody. We also thank Dr. Ueda and Dr. Shiota in the YS Institute for their valuable suggestions. This study was supported, in part, by a Grant-in-Aid for Scientific Research and a grant for the 21st Century Center of Excellence (COE) Program Special Research Grant from the Japan Society for the Promotion of Science and by the Industrial Technology Research Grant Program from New Energy and the Industrial Technology Development Organization (NEDO) of Japan.
Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.
PY - 2005/6
Y1 - 2005/6
N2 - Purpose. To produce a transgenic rat harboring the Tie2 promoter/enhancer linked green fluorescence protein (GFP) gene and investigate the blood-brain barrier (BBB)- and inner blood-retinal barrier (iBRB)-selective GFP expression in the brain and retina. Methods. Transgenic rats were produced by the microinjection of mouse Tie2/GFP gene into fertilized oocytes of Wistar rats. The expression of GFP was observed in tissue slices by confocal microscopy. Results. One of the obtained transgenic lines showed intense GFP expression in vascular endothelial cells throughout the brain. After double immunostaining with glucose transporter 1, the GFP was found to be localized in the cytoplasmic compartment of brain capillary endothelial cells. In contrast, no fluorescence was observed in neural cells. In the retina of transgenic rats, intense GFP expression was detected in retinal capillary endothelial cells. No fluorescence was detected in other cells. In kidney and liver, GFP expression was detected in vascular endothelial cells, whereas the expressed region was limited. Conclusions. Mouse Tie2 promoter/enhancer has the ability to induce gene expression selectively in vascular endothelial cells in the brain and retina of transgenic rats.
AB - Purpose. To produce a transgenic rat harboring the Tie2 promoter/enhancer linked green fluorescence protein (GFP) gene and investigate the blood-brain barrier (BBB)- and inner blood-retinal barrier (iBRB)-selective GFP expression in the brain and retina. Methods. Transgenic rats were produced by the microinjection of mouse Tie2/GFP gene into fertilized oocytes of Wistar rats. The expression of GFP was observed in tissue slices by confocal microscopy. Results. One of the obtained transgenic lines showed intense GFP expression in vascular endothelial cells throughout the brain. After double immunostaining with glucose transporter 1, the GFP was found to be localized in the cytoplasmic compartment of brain capillary endothelial cells. In contrast, no fluorescence was observed in neural cells. In the retina of transgenic rats, intense GFP expression was detected in retinal capillary endothelial cells. No fluorescence was detected in other cells. In kidney and liver, GFP expression was detected in vascular endothelial cells, whereas the expressed region was limited. Conclusions. Mouse Tie2 promoter/enhancer has the ability to induce gene expression selectively in vascular endothelial cells in the brain and retina of transgenic rats.
KW - Blood-brain barrier
KW - Green fluorescence protein
KW - Inner blood-retinal barrier
KW - Tie2 promoter/enhancer
KW - Transgenic rats
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U2 - 10.1007/s11095-005-4579-y
DO - 10.1007/s11095-005-4579-y
M3 - Article
C2 - 15948028
AN - SCOPUS:21244483145
SN - 0724-8741
VL - 22
SP - 852
EP - 857
JO - Pharmaceutical Research
JF - Pharmaceutical Research
IS - 6
ER -