TY - JOUR
T1 - Cellular sources of TSPO expression in healthy and diseased brain
AU - Nutma, Erik
AU - Ceyzériat, Kelly
AU - Amor, Sandra
AU - Tsartsalis, Stergios
AU - Millet, Philippe
AU - Owen, David R.
AU - Papadopoulos, Vassilios
AU - Tournier, Benjamin B.
N1 - Funding Information: The authors thank the MS Society of Great Britain and Northern Ireland. Authors K.C. and B.B.T. are supported by the Velux Foundation (project n. 1123). Author S.T. received support from the Swiss National Science Foundation (Early PostDoc.Mobility Scholarship, no. P2GEP3_191446), the Prof Dr Max Cloetta Foundation (Clinical Medicine Plus scholarship), and the Jean and Madeleine Vachoux Foundation. Author D.R.O. is supported by the MRC (MR/N008219/1). Author V.P. was supported by the John Stauffer Dean?s Chair in Pharmaceutical Sciences (University of Southern California). This work was supported by the Swiss National Science Foundation (no. 320030-184713). Funding Information: The authors thank the MS Society of Great Britain and Northern Ireland. Authors K.C. and B.B.T. are supported by the Velux Foundation (project n. 1123). Author S.T. received support from the Swiss National Science Foundation (Early PostDoc.Mobility Scholarship, no. P2GEP3_191446), the Prof Dr Max Cloetta Foundation (Clinical Medicine Plus scholarship), and the Jean and Madeleine Vachoux Foundation. Author D.R.O. is supported by the MRC (MR/N008219/1). Author V.P. was supported by the John Stauffer Dean’s Chair in Pharmaceutical Sciences (University of Southern California). This work was supported by the Swiss National Science Foundation (no. 320030-184713). Publisher Copyright: © 2021, The Author(s).
PY - 2021/12/1
Y1 - 2021/12/1
N2 - 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.
AB - 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.
KW - Astrocytes
KW - Microglia
KW - Positron emission tomography
KW - TSPO
UR - http://www.scopus.com/inward/record.url?scp=85121753936&partnerID=8YFLogxK
U2 - https://doi.org/10.1007/s00259-020-05166-2
DO - https://doi.org/10.1007/s00259-020-05166-2
M3 - Review article
C2 - 33433698
SN - 1619-7089
VL - 49
SP - 146
EP - 163
JO - European journal of nuclear medicine and molecular imaging
JF - European journal of nuclear medicine and molecular imaging
IS - 1
ER -