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Pilot Study of (64)CuCl(2) for PET Imaging of Inflammation
Copper(II) ion (Cu(2+)) is the essential element for numerous pathophysiological processes in vivo. Copper transporter 1 (CTR1) is mainly responsible for maintaining Cu(2+) accumulation in cells, which has been found to be over-expressed in inflammatory tissues. Therefore, we explored the potential...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017813/ https://www.ncbi.nlm.nih.gov/pubmed/29495260 http://dx.doi.org/10.3390/molecules23020502 |
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author | Jiang, Lei Song, Dongli Chen, Hao Zhang, Ao Wang, Huoqiang Cheng, Zhen |
author_facet | Jiang, Lei Song, Dongli Chen, Hao Zhang, Ao Wang, Huoqiang Cheng, Zhen |
author_sort | Jiang, Lei |
collection | PubMed |
description | Copper(II) ion (Cu(2+)) is the essential element for numerous pathophysiological processes in vivo. Copper transporter 1 (CTR1) is mainly responsible for maintaining Cu(2+) accumulation in cells, which has been found to be over-expressed in inflammatory tissues. Therefore, we explored the potential application of (64)CuCl(2) for PET imaging of inflammation through targeting CTR1. The animal models of H(2)O(2) induced muscle inflammation and lipopolysaccaharide induced lung inflammation were successfully established, then imaged by small animal PET (PET/CT) post-injection of (64)CuCl(2), and PET images were quantitatively analyzed. H&E and immunohistochemical (IHC) staining and western blot experiments were performed for evaluating CTR1 levels in the inflammatory and control tissues. Both inflammatory muscle and lungs can be clearly imaged by PET. PET image quantitative analysis revealed that the inflammatory muscle and lungs showed significantly higher (64)Cu accumulation than the controls, respectively (p < 0.05). Furthermore, IHC staining and western blot analysis demonstrated that compared with the controls, CTR1 expression was increased in both the inflammatory muscle and lungs, which was consistent with the levels of (64)Cu(2+) accumulation in these tissues. (64)CuCl(2) can be used as a novel, simple, and highly promising PET tracer for CTR1 targeted imaging of inflammation. |
format | Online Article Text |
id | pubmed-6017813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-60178132018-11-13 Pilot Study of (64)CuCl(2) for PET Imaging of Inflammation Jiang, Lei Song, Dongli Chen, Hao Zhang, Ao Wang, Huoqiang Cheng, Zhen Molecules Article Copper(II) ion (Cu(2+)) is the essential element for numerous pathophysiological processes in vivo. Copper transporter 1 (CTR1) is mainly responsible for maintaining Cu(2+) accumulation in cells, which has been found to be over-expressed in inflammatory tissues. Therefore, we explored the potential application of (64)CuCl(2) for PET imaging of inflammation through targeting CTR1. The animal models of H(2)O(2) induced muscle inflammation and lipopolysaccaharide induced lung inflammation were successfully established, then imaged by small animal PET (PET/CT) post-injection of (64)CuCl(2), and PET images were quantitatively analyzed. H&E and immunohistochemical (IHC) staining and western blot experiments were performed for evaluating CTR1 levels in the inflammatory and control tissues. Both inflammatory muscle and lungs can be clearly imaged by PET. PET image quantitative analysis revealed that the inflammatory muscle and lungs showed significantly higher (64)Cu accumulation than the controls, respectively (p < 0.05). Furthermore, IHC staining and western blot analysis demonstrated that compared with the controls, CTR1 expression was increased in both the inflammatory muscle and lungs, which was consistent with the levels of (64)Cu(2+) accumulation in these tissues. (64)CuCl(2) can be used as a novel, simple, and highly promising PET tracer for CTR1 targeted imaging of inflammation. MDPI 2018-02-24 /pmc/articles/PMC6017813/ /pubmed/29495260 http://dx.doi.org/10.3390/molecules23020502 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Jiang, Lei Song, Dongli Chen, Hao Zhang, Ao Wang, Huoqiang Cheng, Zhen Pilot Study of (64)CuCl(2) for PET Imaging of Inflammation |
title | Pilot Study of (64)CuCl(2) for PET Imaging of Inflammation |
title_full | Pilot Study of (64)CuCl(2) for PET Imaging of Inflammation |
title_fullStr | Pilot Study of (64)CuCl(2) for PET Imaging of Inflammation |
title_full_unstemmed | Pilot Study of (64)CuCl(2) for PET Imaging of Inflammation |
title_short | Pilot Study of (64)CuCl(2) for PET Imaging of Inflammation |
title_sort | pilot study of (64)cucl(2) for pet imaging of inflammation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017813/ https://www.ncbi.nlm.nih.gov/pubmed/29495260 http://dx.doi.org/10.3390/molecules23020502 |
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