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In Vivo MRI of Functionalized Iron Oxide Nanoparticles for Brain Inflammation
Microglia are intrinsic components of the brain immune system and are activated in many central nervous system disorders. The ability to noninvasively image these cells would provide valuable information for both research and clinical applications. Today, most imaging probes for activated microglia...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6036843/ https://www.ncbi.nlm.nih.gov/pubmed/30079001 http://dx.doi.org/10.1155/2018/3476476 |
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author | Tang, Tang Valenzuela, Anthony Petit, Fanny Chow, Sarah Leung, Kevin Gorin, Fredric Louie, Angelique Y. Dhenain, Marc |
author_facet | Tang, Tang Valenzuela, Anthony Petit, Fanny Chow, Sarah Leung, Kevin Gorin, Fredric Louie, Angelique Y. Dhenain, Marc |
author_sort | Tang, Tang |
collection | PubMed |
description | Microglia are intrinsic components of the brain immune system and are activated in many central nervous system disorders. The ability to noninvasively image these cells would provide valuable information for both research and clinical applications. Today, most imaging probes for activated microglia are mainly designed for positron emission tomography (PET) and target translocator proteins that also reside on other cerebral cells. The PET images obtained are not specific for microglia-driven inflammation. Here, we describe a potential PET/MRI multimodal imaging probe that selectively targets the scavenger receptor class A (SR-A) expressed on activated microglia. These sulfated dextran-coated iron oxide (SDIO) nanoparticles are avidly taken up by microglia and appear to be nontoxic when administered intravenously in a mouse model. Intravenous administration of this SDIO demonstrated visualization by T(2)(∗)-weighted MRI of microglia activated by intracerebral administration of tumor necrosis factor alpha (TNF-α). The contrast was significantly enhanced by SDIO, whereas there was little to no contrast change in animals treated with nontargeted nanoparticles or untreated controls. Thus, SR-A targeting represents a promising strategy to image activated microglia in the brain. |
format | Online Article Text |
id | pubmed-6036843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-60368432018-08-05 In Vivo MRI of Functionalized Iron Oxide Nanoparticles for Brain Inflammation Tang, Tang Valenzuela, Anthony Petit, Fanny Chow, Sarah Leung, Kevin Gorin, Fredric Louie, Angelique Y. Dhenain, Marc Contrast Media Mol Imaging Research Article Microglia are intrinsic components of the brain immune system and are activated in many central nervous system disorders. The ability to noninvasively image these cells would provide valuable information for both research and clinical applications. Today, most imaging probes for activated microglia are mainly designed for positron emission tomography (PET) and target translocator proteins that also reside on other cerebral cells. The PET images obtained are not specific for microglia-driven inflammation. Here, we describe a potential PET/MRI multimodal imaging probe that selectively targets the scavenger receptor class A (SR-A) expressed on activated microglia. These sulfated dextran-coated iron oxide (SDIO) nanoparticles are avidly taken up by microglia and appear to be nontoxic when administered intravenously in a mouse model. Intravenous administration of this SDIO demonstrated visualization by T(2)(∗)-weighted MRI of microglia activated by intracerebral administration of tumor necrosis factor alpha (TNF-α). The contrast was significantly enhanced by SDIO, whereas there was little to no contrast change in animals treated with nontargeted nanoparticles or untreated controls. Thus, SR-A targeting represents a promising strategy to image activated microglia in the brain. Hindawi 2018-06-25 /pmc/articles/PMC6036843/ /pubmed/30079001 http://dx.doi.org/10.1155/2018/3476476 Text en Copyright © 2018 Tang Tang et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Tang, Tang Valenzuela, Anthony Petit, Fanny Chow, Sarah Leung, Kevin Gorin, Fredric Louie, Angelique Y. Dhenain, Marc In Vivo MRI of Functionalized Iron Oxide Nanoparticles for Brain Inflammation |
title |
In Vivo MRI of Functionalized Iron Oxide Nanoparticles for Brain Inflammation |
title_full |
In Vivo MRI of Functionalized Iron Oxide Nanoparticles for Brain Inflammation |
title_fullStr |
In Vivo MRI of Functionalized Iron Oxide Nanoparticles for Brain Inflammation |
title_full_unstemmed |
In Vivo MRI of Functionalized Iron Oxide Nanoparticles for Brain Inflammation |
title_short |
In Vivo MRI of Functionalized Iron Oxide Nanoparticles for Brain Inflammation |
title_sort | in vivo mri of functionalized iron oxide nanoparticles for brain inflammation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6036843/ https://www.ncbi.nlm.nih.gov/pubmed/30079001 http://dx.doi.org/10.1155/2018/3476476 |
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