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...

Full description

Bibliographic Details
Main Authors: Jiantu Che, Mikhail Doubrovin, Inna Serganova, Ludmila Ageyeva, Pat Zanzonico, Ronald Blasberg
Format: Article
Language:English
Published: Hindawi - SAGE Publishing 2005-04-01
Series:Molecular Imaging
Online Access:https://doi.org/10.1162/15353500200504193
id doaj-871ab4eaee1f4505b50a5628f05c0e3c
record_format Article
spelling 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
work_keys_str_mv AT jiantuche dualreportergeneimaging
AT mikhaildoubrovin dualreportergeneimaging
AT innaserganova dualreportergeneimaging
AT ludmilaageyeva dualreportergeneimaging
AT patzanzonico dualreportergeneimaging
AT ronaldblasberg dualreportergeneimaging
_version_ 1721553244077948928