Dual Reporter Gene Imaging
The human and rodent sodium iodide symporters ( NIS ) have recently been cloned and are being investigated as potential therapeutic and reporter genes. We have extended this effort by constructing an internal ribosomal entry site (IRES)-linked human NIS (hNIS) -enhanced green fluorescent protein ( e...
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2005-04-01
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Series: | Molecular Imaging |
Online Access: | https://doi.org/10.1162/15353500200504193 |
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doaj-871ab4eaee1f4505b50a5628f05c0e3c2021-04-02T17:48:47ZengHindawi - SAGE PublishingMolecular Imaging1536-01212005-04-01410.1162/1535350020050419310.1162_15353500200504193 Dual Reporter Gene ImagingJiantu CheMikhail DoubrovinInna SerganovaLudmila AgeyevaPat ZanzonicoRonald BlasbergThe human and rodent sodium iodide symporters ( NIS ) have recently been cloned and are being investigated as potential therapeutic and reporter genes. We have extended this effort by constructing an internal ribosomal entry site (IRES)-linked human NIS (hNIS) -enhanced green fluorescent protein ( eGFP ) hybrid reporter gene for both nuclear and optical imaging. A self-inactivating retroviral vector, termed pQCNIG, containing hNIS-IRES-eGFP dual reporter gene, driven by a constitutive CMV promoter, was constructed and used to generate RG2-pQCNIG cells and RG2-pQCNIG tumors. 131 I-iodide and 99m TcO 4 -pertechnetate accumulation studies plus fluorescence microscopy and intensity assays were performed in vitro, and gamma camera imaging studies in RG2-pQCNIG and RG2 tumor-bearing athymic rats were performed. RG2-pQCNIG cells expressed high levels of hNIS protein and showed high intensity of eGFP fluorescence compared with RG2 wild-type cells. RG2-pQCNIG cells accumulated Na 131 I and 99m TcO 4 – to a 50:1 and a 170:1 tissue/medium ratio at 10 min, compared with 0.8:1.2 tissue/medium ratio in wild-type RG2 cells. A significant correlation between radiotracer accumulation and eGFP fluorescence intensity was demonstrated. RG2-pQCNIG and RG2 tumors were readily differentiated by in vivo gamma camera imaging; radiotracer uptake increased in RG2-pQCNIG but declined in RG2 tumors over the 50-min imaging period. Stomach and thyroid were the major organs of radionuclide accumulation. The IRES-linked hNIS-eGFP dual reporter gene is functional and stable in transduced RG2-pQCNIG cells. Optical and nuclear imaging of tumors produced from these cell lines provides the opportunity to monitor tumor growth and response to therapy. These studies indicate the potential for a wider application of hNIS reporter imaging and translation into patient studies using radioisotopes that are currently available for human use for both SPECT and PET imaging.https://doi.org/10.1162/15353500200504193 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jiantu Che Mikhail Doubrovin Inna Serganova Ludmila Ageyeva Pat Zanzonico Ronald Blasberg |
spellingShingle |
Jiantu Che Mikhail Doubrovin Inna Serganova Ludmila Ageyeva Pat Zanzonico Ronald Blasberg Dual Reporter Gene Imaging Molecular Imaging |
author_facet |
Jiantu Che Mikhail Doubrovin Inna Serganova Ludmila Ageyeva Pat Zanzonico Ronald Blasberg |
author_sort |
Jiantu Che |
title |
Dual Reporter Gene Imaging |
title_short |
Dual Reporter Gene Imaging |
title_full |
Dual Reporter Gene Imaging |
title_fullStr |
Dual Reporter Gene Imaging |
title_full_unstemmed |
Dual Reporter Gene Imaging |
title_sort |
dual reporter gene imaging |
publisher |
Hindawi - SAGE Publishing |
series |
Molecular Imaging |
issn |
1536-0121 |
publishDate |
2005-04-01 |
description |
The human and rodent sodium iodide symporters ( NIS ) have recently been cloned and are being investigated as potential therapeutic and reporter genes. We have extended this effort by constructing an internal ribosomal entry site (IRES)-linked human NIS (hNIS) -enhanced green fluorescent protein ( eGFP ) hybrid reporter gene for both nuclear and optical imaging. A self-inactivating retroviral vector, termed pQCNIG, containing hNIS-IRES-eGFP dual reporter gene, driven by a constitutive CMV promoter, was constructed and used to generate RG2-pQCNIG cells and RG2-pQCNIG tumors. 131 I-iodide and 99m TcO 4 -pertechnetate accumulation studies plus fluorescence microscopy and intensity assays were performed in vitro, and gamma camera imaging studies in RG2-pQCNIG and RG2 tumor-bearing athymic rats were performed. RG2-pQCNIG cells expressed high levels of hNIS protein and showed high intensity of eGFP fluorescence compared with RG2 wild-type cells. RG2-pQCNIG cells accumulated Na 131 I and 99m TcO 4 – to a 50:1 and a 170:1 tissue/medium ratio at 10 min, compared with 0.8:1.2 tissue/medium ratio in wild-type RG2 cells. A significant correlation between radiotracer accumulation and eGFP fluorescence intensity was demonstrated. RG2-pQCNIG and RG2 tumors were readily differentiated by in vivo gamma camera imaging; radiotracer uptake increased in RG2-pQCNIG but declined in RG2 tumors over the 50-min imaging period. Stomach and thyroid were the major organs of radionuclide accumulation. The IRES-linked hNIS-eGFP dual reporter gene is functional and stable in transduced RG2-pQCNIG cells. Optical and nuclear imaging of tumors produced from these cell lines provides the opportunity to monitor tumor growth and response to therapy. These studies indicate the potential for a wider application of hNIS reporter imaging and translation into patient studies using radioisotopes that are currently available for human use for both SPECT and PET imaging. |
url |
https://doi.org/10.1162/15353500200504193 |
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