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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...

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Autores principales: Nutma, Erik, Ceyzériat, Kelly, Amor, Sandra, Tsartsalis, Stergios, Millet, Philippe, Owen, David R., Papadopoulos, Vassilios, Tournier, Benjamin B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
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.
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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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