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Tracking of dendritic cell migration into lymph nodes using molecular imaging with sodium iodide symporter and enhanced firefly luciferase genes

We sought to evaluate the feasibility of molecular imaging using the human sodium iodide symporter (hNIS) gene as a reporter, in addition to the enhanced firefly luciferase (effluc) gene, for tracking dendritic cell (DCs) migration in living mice. A murine dendritic cell line (DC2.4) co-expressing h...

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Autores principales: Lee, Ho Won, Yoon, Seung Yun, Singh, Thoudam Debraj, Choi, Yoon Ju, Lee, Hong Je, Park, Ji Young, Jeong, Shin Young, Lee, Sang-Woo, Ha, Jeoung-Hee, Ahn, Byeong-Cheol, Jeon, Yong Hyun, Lee, Jaetae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4431315/
https://www.ncbi.nlm.nih.gov/pubmed/25974752
http://dx.doi.org/10.1038/srep09865
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author Lee, Ho Won
Yoon, Seung Yun
Singh, Thoudam Debraj
Choi, Yoon Ju
Lee, Hong Je
Park, Ji Young
Jeong, Shin Young
Lee, Sang-Woo
Ha, Jeoung-Hee
Ahn, Byeong-Cheol
Jeon, Yong Hyun
Lee, Jaetae
author_facet Lee, Ho Won
Yoon, Seung Yun
Singh, Thoudam Debraj
Choi, Yoon Ju
Lee, Hong Je
Park, Ji Young
Jeong, Shin Young
Lee, Sang-Woo
Ha, Jeoung-Hee
Ahn, Byeong-Cheol
Jeon, Yong Hyun
Lee, Jaetae
author_sort Lee, Ho Won
collection PubMed
description We sought to evaluate the feasibility of molecular imaging using the human sodium iodide symporter (hNIS) gene as a reporter, in addition to the enhanced firefly luciferase (effluc) gene, for tracking dendritic cell (DCs) migration in living mice. A murine dendritic cell line (DC2.4) co-expressing hNIS and effluc genes (DC/NF) was established. For the DC-tracking study, mice received either parental DCs or DC/NF cells in the left or right footpad, respectively, and combined I-124 PET/CT and bioluminescence imaging (BLI) were performed. In vivo PET/CT imaging with I-124 revealed higher activity of the radiotracer in the draining popliteal lymph nodes (DPLN) of the DC/NF injection site at day 1 than DC injection site (p < 0.05). The uptake value further increased at day 4 (p < 0.005). BLI also demonstrated migration of DC/NF cells to the DPLNs at day 1 post-injection, and signals at the DPLNs were much higher at day 4. These data support the feasibility of hNIS reporter gene imaging in the tracking of DC migration to lymphoid organs in living mice. DCs expressing the NIS reporter gene could be a useful tool to optimize various strategies of cell-based immunotherapy.
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spelling pubmed-44313152015-05-22 Tracking of dendritic cell migration into lymph nodes using molecular imaging with sodium iodide symporter and enhanced firefly luciferase genes Lee, Ho Won Yoon, Seung Yun Singh, Thoudam Debraj Choi, Yoon Ju Lee, Hong Je Park, Ji Young Jeong, Shin Young Lee, Sang-Woo Ha, Jeoung-Hee Ahn, Byeong-Cheol Jeon, Yong Hyun Lee, Jaetae Sci Rep Article We sought to evaluate the feasibility of molecular imaging using the human sodium iodide symporter (hNIS) gene as a reporter, in addition to the enhanced firefly luciferase (effluc) gene, for tracking dendritic cell (DCs) migration in living mice. A murine dendritic cell line (DC2.4) co-expressing hNIS and effluc genes (DC/NF) was established. For the DC-tracking study, mice received either parental DCs or DC/NF cells in the left or right footpad, respectively, and combined I-124 PET/CT and bioluminescence imaging (BLI) were performed. In vivo PET/CT imaging with I-124 revealed higher activity of the radiotracer in the draining popliteal lymph nodes (DPLN) of the DC/NF injection site at day 1 than DC injection site (p < 0.05). The uptake value further increased at day 4 (p < 0.005). BLI also demonstrated migration of DC/NF cells to the DPLNs at day 1 post-injection, and signals at the DPLNs were much higher at day 4. These data support the feasibility of hNIS reporter gene imaging in the tracking of DC migration to lymphoid organs in living mice. DCs expressing the NIS reporter gene could be a useful tool to optimize various strategies of cell-based immunotherapy. Nature Publishing Group 2015-05-14 /pmc/articles/PMC4431315/ /pubmed/25974752 http://dx.doi.org/10.1038/srep09865 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Lee, Ho Won
Yoon, Seung Yun
Singh, Thoudam Debraj
Choi, Yoon Ju
Lee, Hong Je
Park, Ji Young
Jeong, Shin Young
Lee, Sang-Woo
Ha, Jeoung-Hee
Ahn, Byeong-Cheol
Jeon, Yong Hyun
Lee, Jaetae
Tracking of dendritic cell migration into lymph nodes using molecular imaging with sodium iodide symporter and enhanced firefly luciferase genes
title Tracking of dendritic cell migration into lymph nodes using molecular imaging with sodium iodide symporter and enhanced firefly luciferase genes
title_full Tracking of dendritic cell migration into lymph nodes using molecular imaging with sodium iodide symporter and enhanced firefly luciferase genes
title_fullStr Tracking of dendritic cell migration into lymph nodes using molecular imaging with sodium iodide symporter and enhanced firefly luciferase genes
title_full_unstemmed Tracking of dendritic cell migration into lymph nodes using molecular imaging with sodium iodide symporter and enhanced firefly luciferase genes
title_short Tracking of dendritic cell migration into lymph nodes using molecular imaging with sodium iodide symporter and enhanced firefly luciferase genes
title_sort tracking of dendritic cell migration into lymph nodes using molecular imaging with sodium iodide symporter and enhanced firefly luciferase genes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4431315/
https://www.ncbi.nlm.nih.gov/pubmed/25974752
http://dx.doi.org/10.1038/srep09865
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