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Cellular sources of TSPO expression in healthy and diseased brain
The 18 kDa translocator protein (TSPO) is a highly conserved protein located in the outer mitochondrial membrane. TSPO binding, as measured with positron emission tomography (PET), is considered an in vivo marker of neuroinflammation. Indeed, TSPO expression is altered in neurodegenerative, neuroinf...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8712293/ https://www.ncbi.nlm.nih.gov/pubmed/33433698 http://dx.doi.org/10.1007/s00259-020-05166-2 |
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author | Nutma, Erik Ceyzériat, Kelly Amor, Sandra Tsartsalis, Stergios Millet, Philippe Owen, David R. Papadopoulos, Vassilios Tournier, Benjamin B. |
author_facet | Nutma, Erik Ceyzériat, Kelly Amor, Sandra Tsartsalis, Stergios Millet, Philippe Owen, David R. Papadopoulos, Vassilios Tournier, Benjamin B. |
author_sort | Nutma, Erik |
collection | PubMed |
description | The 18 kDa translocator protein (TSPO) is a highly conserved protein located in the outer mitochondrial membrane. TSPO binding, as measured with positron emission tomography (PET), is considered an in vivo marker of neuroinflammation. Indeed, TSPO expression is altered in neurodegenerative, neuroinflammatory, and neuropsychiatric diseases. In PET studies, the TSPO signal is often viewed as a marker of microglial cell activity. However, there is little evidence in support of a microglia-specific TSPO expression. This review describes the cellular sources and functions of TSPO in animal models of disease and human studies, in health, and in central nervous system diseases. A discussion of methods of analysis and of quantification of TSPO is also presented. Overall, it appears that the alterations of TSPO binding, their cellular underpinnings, and the functional significance of such alterations depend on many factors, notably the pathology or the animal model under study, the disease stage, and the involved brain regions. Thus, further studies are needed to fully determine how changes in TSPO binding occur at the cellular level with the ultimate goal of revealing potential therapeutic pathways. |
format | Online Article Text |
id | pubmed-8712293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-87122932022-01-11 Cellular sources of TSPO expression in healthy and diseased brain Nutma, Erik Ceyzériat, Kelly Amor, Sandra Tsartsalis, Stergios Millet, Philippe Owen, David R. Papadopoulos, Vassilios Tournier, Benjamin B. Eur J Nucl Med Mol Imaging Review Article The 18 kDa translocator protein (TSPO) is a highly conserved protein located in the outer mitochondrial membrane. TSPO binding, as measured with positron emission tomography (PET), is considered an in vivo marker of neuroinflammation. Indeed, TSPO expression is altered in neurodegenerative, neuroinflammatory, and neuropsychiatric diseases. In PET studies, the TSPO signal is often viewed as a marker of microglial cell activity. However, there is little evidence in support of a microglia-specific TSPO expression. This review describes the cellular sources and functions of TSPO in animal models of disease and human studies, in health, and in central nervous system diseases. A discussion of methods of analysis and of quantification of TSPO is also presented. Overall, it appears that the alterations of TSPO binding, their cellular underpinnings, and the functional significance of such alterations depend on many factors, notably the pathology or the animal model under study, the disease stage, and the involved brain regions. Thus, further studies are needed to fully determine how changes in TSPO binding occur at the cellular level with the ultimate goal of revealing potential therapeutic pathways. Springer Berlin Heidelberg 2021-01-12 2021 /pmc/articles/PMC8712293/ /pubmed/33433698 http://dx.doi.org/10.1007/s00259-020-05166-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Article Nutma, Erik Ceyzériat, Kelly Amor, Sandra Tsartsalis, Stergios Millet, Philippe Owen, David R. Papadopoulos, Vassilios Tournier, Benjamin B. Cellular sources of TSPO expression in healthy and diseased brain |
title | Cellular sources of TSPO expression in healthy and diseased brain |
title_full | Cellular sources of TSPO expression in healthy and diseased brain |
title_fullStr | Cellular sources of TSPO expression in healthy and diseased brain |
title_full_unstemmed | Cellular sources of TSPO expression in healthy and diseased brain |
title_short | Cellular sources of TSPO expression in healthy and diseased brain |
title_sort | cellular sources of tspo expression in healthy and diseased brain |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8712293/ https://www.ncbi.nlm.nih.gov/pubmed/33433698 http://dx.doi.org/10.1007/s00259-020-05166-2 |
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