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Cellular sources of TSPO expression in healthy and diseased brain

  • Erik Nutma
  • , Kelly Ceyzériat
  • , Sandra Amor
  • , Stergios Tsartsalis
  • , Philippe Millet
  • , David R. Owen
  • , Vassilios Papadopoulos
  • , Benjamin B. Tournier*
  • *Corresponding author for this work
  • University of Geneva
  • Queen Mary University of London
  • Imperial College London
  • University of Southern California

Research output: Contribution to journalReview articleAcademicpeer-review

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Abstract

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.
Original languageEnglish
Pages (from-to)146-163
Number of pages18
JournalEuropean journal of nuclear medicine and molecular imaging
Volume49
Issue number1
DOIs
Publication statusPublished - 1 Dec 2021

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Astrocytes
  • Microglia
  • Positron emission tomography
  • TSPO

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